Professional Documents
Culture Documents
(Database on EDPs)
I
II
Table of Contents
(DATABASE ON EDPS) .............................................................................................................I
III
APPENDIX 6. INVENTORY OF PATENTS ........................................................................ 411
6.1 PHOTODEGRADABLE POLYOLEFINS PATENTS ................................................................. 411
6.2 BIODEGRADABLE POLYOLEFINS ..................................................................................... 412
6.3 PATENTS ON PACKAGING, HYGINE AND NON-PHARMACEUTICAL APPLICATIONS........... 414
6.4 PHARMACEUTICAL AND AGRICULTURAL PATENTS ......................................................... 415
6.5 MICROBIAL, CHEMICAL METHODS, SYNTHESIS AND DEGRADATION PATENTS .............. 417
6.6 BLENDING, COMPOSITION AND PLASTICIZER PATENTS .................................................. 419
6.7 PATENTS ON POLYHYDROXYALKANOATES IN CHRONOLOGICAL ORDER ........................ 420
6.8 OTHER RELEVANT PATENTS ........................................................................................... 435
6.9 PATENTS IN MEDICAL AND PHARMACEUTICAL APPLICATIONS ....................................... 437
APPENDIX 7. LIST OF R&D INSTITUTIONS ON EDPS ................................................. 491
IV
Appendix 1. Commonly Used Abbreviations
Abbreviation of Polymers
AU poly(ester-urethane)
BPA bisphenol A
CA, CDA cellulose acetate, diacetate
CAP, CAB cellulose acetate propionate, -butylate
CMC Carboxymethylcellulose
CMHEC Carboxymethylhydroxyethylcellulose
CMMC Carboxymethylmethylcellulose
DETOSU 3,9-bis(ethylidene- 2,4,8,10-tetraoxaspiro[5,5] undecane)
DIVEMA poly(maleic anhydride-co-divinylether)
EU poly(ether urethane)
HA Hyaluronic acid
HEC hydroxyethylcellulose
HMC hydroxymethylcellulose
HPC hydroxypropylcellulose
MC Methylcellulose
MEEP poly[bis(methoxyethoxyethoxy)phosphazene
MDI 4,4'-diphenylmethane diisocyanate
Nylon2 polyglycine
Nylon6 poly(epsilon-aminocaproic acid)
PBA poly(butylene adipate)
PBLA poly(beta-benzyl-L-aspartate)
PBS poly(butylene succinate)
PBSA poly(butylene succinate adipate)
PCL polycaprolacton
PCL-PET polycaprolacton-co-poly(ethylene terephthalate)
PCPA poly(p-carboxyphenoxy acetic acid)
PCPP poly[1,3-bis(p-carboxyphenoxy)propane]
P(CPP/A7SA) poly[bis(p-carboxyphenoxy)propane-co-sebacic acid]
PDLA poly(D-lactide)
PDLLA poly(DL-lactide)
1
PDLLA-PCL poly(DL-lactide-co-caprolactone)
PDO-PGA poly(p-dioxanone-co-glycolide)
PDO-PGA-TMC poly(p-dioxanone-co-glycolide-co-1,3-trimethylenecarbonate)
PDS, PDO poly(p-dioxanone)
PEA polyethylene adipate
PES poly(ethylene succinate)
PET polyethlene terephthalate, modified
PGA polyglycolide, polyglycolic acid, polyglycolate
PGA-PCL poly(glycolide-co-caprolactone)
PGA-TMC poly(glycolide-co-trimethylcarbonate)
PGCA poly(1,3-trimethylene carbonate-co-glycolide)
PHA poly(beta-hydroxy alkanoate), poly(beta-hydroxy acid)
PHA/PET poly(beta-hydroxy alkanoate)-co-poly(ethylene terephthalate)
PHB poly(3-hydroxybutyrate)
PHB/PCL poly(3-hydroxybutyrate-co-caprolactone)
PHB/PEO poly(3-hydroxybutyrate-co-ethylene glycol)
PHB/A30PVAc poly(3-hydroxybutyrate-co-vinyl acetate)
PHBB poly(3-hydroxybutyrate-co-4- hydroxybutyrate)
PHBH poly(3-hydroxybutyrate-co-3-hydroxyhexnoate)
PHBP poly((3-hydroxybutyrate-co-3-hydroxypropionat)
PHBV poly(3-hydroxybutyrate-co-3-hydroxyvalerate)
PHBV/CAB poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-co-(cellulose acetate butyrate)
PHBV/CAP poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-co-(cellulose acetate phthlate)
PHEA poly{α,β-[N-(2-hydroxyethyl)-D,L-aspartamide]}
PHV poly(3-hydroxyvalerate)
PLA polylactide, poly(lactic acid), polylactate
PLA/PVOH poly(lactide-co-vinyl alcohol)
PLLA poly(L-lactide)
PLLA/PDLLA poly(L-lactide-co-D,L-lactide)
PLAGA poly(glycolide-co-lactide)
PLCA poly(lysine citramide)
PMDI polymeric isocyanate
PMLA poly(β-malic acid), poly(malate)
Poly(Glu) poly(glutamic acid)
Poly(Glu-Lys-Tyr) poly(glutamic acid-co-lysine-co-tyrosine)
Poly(Lys) polylysine
PPDA poly(phenylene dipropionic acid)
PPG polypropylene glycol
PSA poly(sebacic acid)
PSA-HDA poly(sebacic acid-hexadecandioic acid)
PSA-PEG poly(sebacic anhydride-co-polyethylene glycol)
PTMEG polytetramethylene ether glycol
PTMS poly(tetramethylene succinate)
PTPA-SA poly(terephthalic acid-sebacic acid)
PUR polyurethane
PUU Polyurethane ureas
PVOH polyvinylalcohol
TDI toluene diisocyanate
TPU thermoplastic polyurethane
2
Major Used Degradable Polymers
3
Appendix 2. Standards
ISO 846-78 Plastics - Determination of behavior under the action of fungi and bacteria -
Evaluation by visual examination or measurement of change in mass or
physical properties.
ISO/DIS 14851 Evaluation of the Ultimate Aerobic Biodegradability of Plastic Materials in an
Aqueous Medium - Method by Determining the Oxygen Demand in a Closed
Respirometer (TC61/SC5 N 798)
ISO/DIS 14852 Plastics - Evaluation of the Ultimate Aerobic Biodegradability in an Aqueous
Medium - Method by Analysis of Released Carbon Dioxide
ISO/CD 14853 Plastics Evaluation of Ultimate Anaerobic Biodegradation of Plastic Materials
in an Aqueous System. Method by Analysis of Carbon Conversion to Carbon
Dioxide and Methane
ISO/DIS 14855 Plastics - Evaluation of the Ultimate Aerobic Biodegradability and
Disintegration Under Controlled Composting Conditions - Method by
Analysis of Released Carbon Dioxide
ISO-TC61/SC5 N 5025 Evaluation of Ultimate Anaerobic Biodegradability and Disisntegration of
Plastics Under High-Solids Anaerobic Digestion Conditions
status: to be considered
ISO-TC61/SC5 N 5026 Evaluation of the Compostability and Biological Treatability of Plastics - Test
Scheme for Final Acceptance
status: to be considered
ISO/CD 15985 Plastics-Evaluation of the ultimate anaerobic biodegradability and
disintegration of plastics under high solids anaerobic digestion conditions-
Method by analysis of released biogas (TC61/SC5 N 861). This is based on
ASTM Standard “Standard test method for determining anaerobic
biodegradation of plastic materials under high-solids anaerobic digestion
conditions [D5511-94]
ISO/CD 15986 Plastics-Evaluation of the compostability-Test scheme for final acceptance
(TC61/SC5 N 862). This is based on ASTM Standard “Standard Guide to
assess the compostability of environmentally degradable plasticsD6002-96]”.
COMPOSTING ENVIRONMENT
1. [D 5209-91] Standard test method for determining the aerobic biodegradation of plastic
materials in the presence of municipal sewage sludge
2. [D5338-93, D5338-98 el] Standard test method for determining the aerobic
biodegradation of plastic materials under controlled composting conditions
3. [D5509-94] Standard practice for exposing plastics to a simulated compost environment
4. [D5512-94] Standard practice for exposing plastics to a simulated compost environmnet
using an externally heated reactor
5. [D6003-96] Standard test method for determining weight loss from plastic materials
exposted to a simulated municipal solid waste aerobic compost environment
6. [D5988-96] Standard test method for determining the aerobic biodegradation in soil of
4
plastic materials or residual plastic materials after composting
7. [D6002-96] Standard Guide for Assessing the Compostability of Environmentally
Degradable Plastics
8. [D6340-98] Standard Test Method for Determining Aerobic Biodegradation of
Radiolabeled Plastic Materials in an Aqueous or Compost Environment
9. [D6400-99] Standard Specification for Compostable Plastic
10. [D5951-96] Standard practice for preparing residual solids obtained after
biodegradability standard methods for plastics in solid waste for toxicity and
compost quality testing
11. [D5152-91] Standard practice for water extraction of residual solids from degraded
plastics for toxicity testing– Fate & Effect testing
ANAEROBIC DIGESTION/PROCESSES
12. [D5988-96] Standard test method for determining the aerobic biodegradation of plastic
materials or residual plastic materials after composting in contact with soil
13. [D5271-92] Standard test method for assessing the aerobic biodegradation of plastic
materials in an activated-sludge-wastewater-treatment system
14. [D 5210-91] Standard test method for determining the anaerobic biodegradation of
plastic materials in the presence of municipal sewage sludge
15. [D5511-94] Standard test method for determining anaerobic biodegradation of plastic
materials under high-solids anaerobic digestion conditions
16. [D5526-94] Standard Test Method for Determining Anaerobic Biodegradation of Plastic
Materials Under Accelerated Landfill Conditions
17. [D5525-94A] Standard Practice for Exposing Plastics to a Simulated Landfill
Environment
OTHER
18. [D 5437-93] Standard Practice for Weathering of Plastics Under Marine Floating
Exposure
19. [D 5247-92] Standard test method for determining the aerobic biodegradability of
degradable plastics by specific microorganisms
20. [D5510-94] Standard practice for heat aging of oxidatively degradable plastics
21. [ D6118] Standard test method for determining hydrolytic degradation of plastic
materials in an aqueous solution
22. [D6094-97] Standard Guide to Assess the Compostability of Environmentally
Degradable Nonwoven Fabrics
23. [D3826-98] Standard Practice for Determining Degradation End Point in Degradable
Polyethylene and Polypropylene Using a Tensile Test
5
PHOTODEGRADATION ENVIRONMENT
24. [D5071-91] Practice for operating Xenon arc-type exposure apparatus with water for
exposure of photodegradable plastics
25. [D5071-99] Standard Practice for Exposure of Photodegradable Plastics in a Xenon Arc
Apparatus
26. [D5208-91] Practice for operating fluorescent UV and condensation apparatus for
exposure of photodegradable plastics
27. [D5272-92] (1999) Standard Practice for Outdoor Exposure Testing of Photodegradable Plastics
6
2.4 ISO Biodegradation Test Methods
7
Appendix 3. EDPs Manufacturing and Application Companies
8
Union Carbide TONE®P-787 Poly (caprolactone) (PCL)
USDA - Agritech EAA/starch Extrusionable Starch Materials
Warner & Lambert Fluntera Plast Extrusionable Starch Materials
Willow Ridge Polystarch® Polyethylene + starch
9
Septicin™ antibacterial bone implant polyanhydride
SURETAC® suture anchor Acufex Microsurgical, Inc. TMC/PG
Surgicel© hemostat oxidized cellulose
SYSORB® interference screw SYNOS DL-PL
VICRYL® suture Ethicon PGL
* To be updated
10
Arkelsedijk 46, P.O. Box 21, 4200 AA Gorinchem, The Netherlands
Phone +31 183 695 695
Fax +31 183 695 600
http://www.purac.com/
E-mail pnl@purac.com
PURAC is the world's largest manufacturer of natural L (+)-lactic acid and lactates, with factories in Brazil,
Spain and the Netherlands - plus a worldwide sales network. PURAC, a subsidiary of CSM - a renowned
Dutch multinational specializing in the production and marketing of food ingredients and foodstuffs - is
represented in more than 100 countries. PURAC works according to the GMP method and is ISO certified.
For customers in highly sophisticated medical and pharmaceutical areas worldwide, the Biomaterials
Business Unit offers lactide and glycolide monomers and biodegradable polymers and copolymers.
PURASORB lactide and/ or glycolide polymers and copolymers have been developed to provide materials
for a variety of medical devices and pharmaceutical applications, like wound closure products, orthopaedic
implants and controlled drug delivery systems.
SBU Caprolactones
Solvay Interox Ltd
Baronet Road, Warrington, CheshireWA4 6HB, UK
Telephone:+44 (0) 1925 651277
Fax: +44 (0) 1925 232207
Internet: http://www.solvay.com/capa
Solvay Caprolactones provides caprolactone monomer and polymers. CAPA® is the Solvay trademark for
its range of caprolactones, comprising monomer and polymers of varying molecular weight. The main
CAPA® R&D facilities are located in the UK but with significant support provided by Central R&D
laboratories of Solvay in Brussels.
11
3.4 Commercially Available Degradable Polyolefins
Common description Composition Trade name Manufacture
Photosensitising/Photo- Ferric tiolates Plastor Plastopil (Israel)
(sometimes with Polydress (Germany)
activating additives other metal
Antioxidant-Photo-activator tiolates in Green Plastigone EniChem Agricultural (Italy)
(Scott-Gilead process) polyethylene) Plastigone Technologies Inc. (US)
Alkermes, Inc.
64 Sidney Street, Cambridge, Massachusetts 02139, USA
Telephone: 617 4940171
12
Fax: 617 4949263
For polymer information, contact our Polymer Customer Service Department at:
Alkermes, Inc.
6960 Cornell Road, Cincinnati, Ohio 45242 , USA
Telephone: 513 4890294 , Fax: 513 4897244
Alkermes diversified technology currently consists of four proprietary delivery systems:
ProLease® and Medisorb® injectable sustained release systems; RingCapTM and Dose Sipping oral
delivery technologies; AIRTM pulmonary delivery systems and; Cereport® bloodbrain barrier
permeabilizer. In addition, the Company manufactures and supplies Medisorb® Polymers a wide range of
standard and custom developed pharmaceutical grade, bioabsorbable PLG polymers.
ARTHREX
2885 South Horseshoe Drive, Naples, FL 34104, USA
Phone 8009344404
Fax 8006439310
Quality engineered products and educational services for orthopaedic surgeons.
The TissueTak provides a new, bioabsorbable, sutureless solution for arthroscopic SLAP and Bankart
repairs. The Headed BioAbsorbable Corkscrew is a sutureless solution to rotator cuff repairs. The
BioFASTak is a 3 mm diameter suture anchor designed for cortical bone and incorporates a suture eyelet
which virtually eliminates suture drag to significantly improve the performance of sliding knots. The
BioCorkscrew Suture Anchor with a braided suture eyelet molded into the body of the implant is another
concept for bioabsorbable soft tissue repair.
The Bionx Implants Inc. Bankart Tack is a simple, sutureless design for the arthroscopic and open fixation
of Bankart lesions of the shoulder, acute anterior shoulder instability due to tears in the labrumligament
13
complex or capsular shift procedures. The Bionx Implants, Inc. SelfReinforced absorbable fixation screws
are indicated for a variety of orthopaedic applications. The SmartScrew is made of SelfReinforced PLLA
polymer, which imparts to the material an ultrahigh strength microstructure and a unique ability to resist
shear, flexion and torque while the fracture, osteotomy or fusion site is healing. The Bionx Implants, Inc.
SelfReinforced absorbable fixation pins are indicated for a variety of orthopaedic applications. The Bionx
Implants SmartTack is indicated for the repair of ruptures involving the Ulnar Collateral Ligament of the
Thumb of the first metacarpophalangeal joint, ferred to as "Gamekeeper's Thumb" or "Skier's" tear.
DePuy Orthopaedics
P.O. Box 988, 700 Orthopaedic Drive, Warsaw, IN 465810988, USA
Tel: +1 (800) 3668143
Fax: +1 (219) 2677196
DePuy is a manufacturer of orthopaedic implants in the United States.
The Biostop® G Bone Cement Restrictor is a bioresorbable plug designed to seal the medullary canal
before introducing bone cement during surgery with a cemented prosthesis.
Ethicon, Inc.
Sommerville, New Jersey
ETHICON, INC., a Johnson & Johnson company, is a world's marketer of surgical sutures, hemostats, and,
through its Mitek Products division, suture anchors. ETHICON, INC. is the only U.S. company that offers
an adhesive alternative to sutures for topical skin closure. The company also markets a full line of surgical
mesh products. 10-0 VICRYL (polyglactin 910) suture, An absorbable suture that offers wound integrity
for the first 28 days and is completely absorbed after 70 days
Linvatec Corporation
11311 Concept Boulevard, Largo; Florida 33773-4908, USA
Linvatec Customer Service
Email: cust_serv@linvatec.com
Phone: (800) 2370169
Fax: (727) 3995256
International Fax (727) 397-4540
Linvatec Corporation is a arthroscopy/power surgical instrument equipment manufacturer in the United
States. The Bio-Absorbable Interference Screws both the original screws and the femoral screws are
available in 7, 8 and 9mm dia. by 20mm and 25mm sizes.
14
Bio-Stinger™ meniscal repair
Bio-absorbable PLLA implant
Cannulated implant for precise, one-handed placement
Low profile implant head and built-in countersink minimize condylar contact
Four rows of barbs for increased pull-out strength
Curved and straight instruments allow access to all meniscal zones
MacroMed, Inc.
9520 South State Street, Sandy, Utah 84070, USA
Phone: (801) 565-8561
Fax: (801) 565-8562
R&D Fax: (801) 565-8563
email: macromed@macromed.com
Founded in 1995, MacroMed is a privately held company developing novel drug delivery systems utilizing
proprietary polymer technologies.
Samyang
263 YeonjiDong, ChongnoGu, Seoul 110725, Korea
Tel : 8227407299
Fax : 8227436626
Samyang is one of the Drug Delivery System (DDS) manufacturers in the world. Samyang aims to be an
R&D-oriented company through its cooperation with TheraTech, MacroMed and VivoRx of the United
States in capital participation and joint research. Samyang's Surgisorb is a coated, braided, synthetic and
absorbable suture prepared by utilizing Polyglycolic Acid.
Biomesh GTR barrier
GTR barriers are needed in severe cases of periodontal diseases where patients are at a risk of permanent
loss of tooth due to the removal of the abscess or the infected connective tissues and alveolar bone during
reconstructive surgery.
Acufex Microsurgical
Smith & Nephew
130 Forbes Blvd.
Mansfield, MA 02048
Tel 18003394332; fax 15083394332
15
Smith & Nephew is a global medical device company.
Anatomically Targeted Screws for ACL and PCL Reconstruction
Only one line of bioabsorbable screws gives you techniquespecific screws optimized for all approaches of
both ACL and PCL reconstruction: Screws are designed to hold the graft in place for secure anatomic
aperture reconstruction, allowing patients to resume their active lifestyles. *RotorloC™ Absorbable Rotator
Cuff Suture Anchor RotorloC from Smith & Nephew. Designed exclusively for the humeral head bone, the
RotorloC Absorbable Rotator Cuff Suture Anchor delivers superior deployment and retention in all
humeral head bone densities, including soft bone. RotorloC's propellerlike, selfinserting action creates a
platform and locks the anchor into place for superior retention and stronger fixation. Its twin freesliding
sutures increase the overall strength of the repair by doubling the number of sutures in the tendon.
16
Email: contact@thmbiomedical.com
Located in Duluth, Minnesota, THM was organized in 1990 to commercialize health care applications of its
unique, patented, bioresorbable polymer technology. The core technology, known as OPLA® (Opencell
PolyLactic Acid) can be utilized for a broad range of biomaterials and sustained drug delivery applications.
Research is being conducted by THM in the fields of bone and cartilage repair and regeneration,
chemotherapeutic drugdelivery and dentistry.
Epi-Guide®
Bioresorbable OPLA® Periodontal Barrier
Epi-Guide is indicated for use as an adjunct to periodontal restorative surgeries in the treatment of
periodontal defects following established surgical procedures. Epi-Guide (D, D-L, L-polylactic acid)
functions to support the initial blood clot and maintain competence of collateral circulation.
DRILAC®
Bioresorbable OPLA® surgical dressing
Drilac is indicated for the prevention of alveolar osteitis following mandibular third molar extractions.
Drilac (D, D-L, L-polylactic acid) is a hydrophilic, threee dimensional matrix dressing material resembling
cancellous bone.
GLIADEL® Wafer (polifeprosan 20 with carmustine implant) is a sterile, off-white to pale yellow wafer
approximately 1.45 cm in diameter and 1 mm thick. Each wafer contains 192.3 mg of a biodegradable
polyanhydride copolymer and 7.7 mg of carmustine [1,3-bis (2-chloroethyl)-1-nitrosourea, or BCNU].
Carmustine is a nitrosourea oncolytic agent. The copolymer, polifeprosan 20, consists of poly[bis(p-
carboxyphenoxy) propane: sebacic acid] in a 20:80 molar ratio and is used to control the local delivery of
carmustine. Carmustine is homogeneously distributed in the copolymer matrix.
17
3.6 EDPs Manufacturing Companies
PLLA poly(L-lactide) polyester, poly(alpha- Arthrex (Arthrex): interference screws PLA, Birmingham Polymers (http://www.bpi-sbs.com)
hydroxy acid), microbial Biofix (Bionx, http://www.bionximplants.com), Pins and PLA, Neste (http://www.neste.com)
polyester rods Purasorb PL, PURAC (http://www.purac.com)
Bioscrew (Linvatec, http://www.zimmer.com): Resomer L, Boehringer Ingelheim
interference screws (http://www.resormer.de)
Bio-Statak (Zimmer, http://www.zimmer.com): suture
anchor
Endofix (Acufex): interference screws
Lactasorb (Davis and Geck), Anastomosis clip
SmartScrew (Bionx, http://www.bionximplants.com),
screw
PDLA poly(D-lactide) polyester, poly(alpha-hydroxy acid) Purasorb PD, PURAC (http://www.purac.com)
Resomer R, Boehringer Ingelheim
(http://www.resormer.de)
PDLLA poly(DL-lactide) polyester, poly(alpha- Atrisorb, Atrix (http://www.atrixlabs.com): guided tissue Medisorb, Alkermes (http://www.alkermes.com)
hydroxy acid) Drilac, THM Biomedical: dental Heplon, Chronopol
Guidor, Procordia: guided tissue PDLLA, Birmingham Polymers (http://www.bpi-sbs.com)
Purasorb PDL, PURAC (http://www.purac.com)
PLLA/PD poly(L-lactide-co-D,L- copolyester, poly(alpha- Phusiline, Phusis: interference screws (98%PLLA- Resomer LR (http://www.resormer.de)
LLA lactide) hydroxy acid) 2%PDLA) ; Resor-Pin, Geistlich
(http://www.geistlich.ch): Pins and rods
PGA polyglycolide, polyglycolic polyester, poly(alpha- Biofix, Bionex (http://www.bionximplants.com): Pins Biologically Quiet, Instrument Makar
acid, polyglycolate hydroxy acid) and rods PGA, Birmingham Polymers (http://www.bpi-sbs.com)
Dexon II, Ercadex, Davis and Geck: sutures Purasorb, PURAC (http://www.purac.com)
PGA Suture, Lukens Resomer, Boehringer Ingelheim (http://www.resormer.de)
Valtrac, Davis and Geck: anastomosis ring
18
PLAGA poly(glycolide-co-lactide) copolyester, poly(alpha- Angioseal, AHP: angioplastic plug ProLease, Medisorb, Alkermes (http://www.alkermes.com)
hydroxy acid) Biologically Quiet, Instrument Makar PLAGA, Birmingham Polymers (http://www.bpi-sbs.com)
(http://www.instmak.com): interference screws Purasorb PLG, Purasorb PDLG, PURAC
LactoSorb, Walter Lorenz (http://www.purac.com)
(http://www.lorenzsurgical.com): plates, mesh, screws Resomer RG, Boehringer Ingelheim
Polysorb, US Surgical, sutures (http://www.resormer.de)
Resolut, W.L.Gore (http://www.gorefabrics.com),
guided tissue
Vicryl, Ethicon (http://www.ethiconinc.com): sutures
19
PBA-PCL poly(1,4-butylene copolyester, thermoplastic disposable film, containers
adipate-co-
polycaprolactone)
PDS poly(p-dioxanone) polyether ester LAPRA-TY, PDO: suture clip
ABSOLOK™, PDO: ligating clip
PDS, Ethicon (http://www.ethiconinc.com):
PMLA poly(β-malic acid), polyester medical, pharmaceutical
poly(malate)
poly(alkylene D-tartrate) polyester biomedical Alzamer, Alza (http://www.alza.com)
PGCA poly(1,3-trimethylene copolyester drug delivery
carbonate-co-glycolide) Endofix, Acufex: interference screws
Suretac, Acufex: suture anchor,
Maxon, Davis and Geck: sutures
Ecoflex copolyester packaging BASF (http://www.basf.com), Eastar Bio, Eastman
(http://www.eastman.com)
Eastar Bio copolyester film, coating Eastman
(http://www.eastman.com/ProductFiles/Prod1519.htm)
PET polyethlene polyester packaging Biomax, DuPont (http://www.dupont.com)
terephthalate, modified
PDO/P+ poly(p-dioxanone-co- Polyether ester medical
A37GA glycolide)
PDO/PG poly(dioxanone-co- Polyether ester Biosyn, US Surgical:sutures
A/A39TM glycolide-co-
C trimethylenecarbonate)
poly(iminocarbonates) pseudopoly(amino acids), drug delivery system
based on tyrosine- poly(iminocarbonates)
derivatives
polyaspartate poly(amino acid) dispersants, absorbants and medicals Donlar, Donlar Corporation (http://www.polyaspartate.com)
Poly(Lys) polylysine poly(amino acid) drug delivery system
poly(glutamic acid) poly(amino acid) drug delivery system
PHEA poly[N-(2-hydroxyethyl)- poly(amino acid) drug delivery system
D,L-aspartamide]
PLCA poly(lysine citramide) polyamide drug delivery system
Nylon2- poly(glycine-co- copolyamid packaging
nylon6 aminocaproic acid)
BAK 1095, BAK 2195 poly(ester amide) packaging Bayer (http://www.bayer.com)
P(CPP- poly[bis(p- polyanhydride Biodel, Gliadel: brain tumor implant Guilford Pharmaceuticals, Inc.
SA) carboxyphenoxy)propane (http://www.guilfordpharm.com)
-co-sebacic acid]
20
poly(p-carboxy aliphatic-aromatic drug delivery system
phenoxyalkanoic acids) polyanhydride
PVOH polyvinylalcohol films, fibres, tubing and injection moulded articles, Airvol, Air Products and Chemicals
textile warp sizing, paper industry, (http://www.airproducts.com/airvpoly/html)
Mowial, Hoechst (http://www.hoechst.de)
Hydrolene, Idroplast (http://www.he.net/~tes/hydro)
Aqua-Novon, Novon (http://www.novoninc.com)
Aquadro, Planet Polymers (http://www.planetpolymer.com)
Vinex, Texas Polymer (http://www.aschulman.com)
PVOH/paper pulp laminated film, Shinetsu
(http://www.shinetsu.co.jp/english)
Kuraray (http://www.kuraray.co.jp/en/products/index.html)
21
Casein animal, fibril protein food packaging, drug delivery system Kruse Chemie (http://www.kruse-gruppe.de/uk/casein.htm)
beta-Conglycinine, soybean protein, vegetal protein plastic bags, mulch film, urethane foams, Omnitech
glycinine urethane binders (http://www.omnitechintl.com/soy_program/studies/plastics.html)
Gliadine and Glutenin wheat protein, vegetal protein packaging plastic Polytriticum 200, Midwest Grain
α-Zein vegetal protein coating of food and pharmaceutical tablets, plastic wrap
Heparin polysaccharide, animal medical Heparin-pur-ratiopharm and -pur-forte ratiopharm, MIKA Pharma
GmbH (http://www.mika-pharma.de)
HA Hyaluronic acid polysaccharide, animal scaffold, pharmaceutical, cosmetics, food Chisso (www.chisso.co.jp), Biomatrix (http://www.biomatrix.com)
Carbomer (http://www.carbomer.com/4semisynth.htm)
HYAFF® (scaffold), Fidia Advanced Biopolymers S.p.A.
(http://europa.eu.int/comm/research/press/2000/pr2703-
fidia.html)
Cellulose polysaccharide textile, paper Aquacel, Aqualon, Blanose Cellulose Gum, Aqualon-Hercules
(http://www.herc.com)
CA, CDA Cellulose acetate, polysaccharide, cellulose ester packaging, adhesives, textile, cigarette filters Eastman Chemical Company (http://www.eastman.com)
diacetate EnviroPlastic-Z, Planet Polymer
Rhodia Rhone Poulenc (http://www. Rhone-poulenc.com)
Akzo Noble (http://www.akzonoble.com)
CA sheet products, Mazzucchelli (http://www.mazzucchelli
1849.it)
Celanese (http://www.celanese.com)
Daicel Chemical Industry (http://www/daicel.co.jp)
CAP, CAB Cellulose acetate polysaccharide, cellulose ester ophthalmic, medical, toys/sport goods Eastman Chemical Company (http://www.eastman.com)
propionate, -butylate
22
MC Methylcellulose polysaccharide, cellulose ether excipient, emulsifier, suspending Culminal, Benecel, Aqualon-Hercules
agent,adhesives in foods, cosmetics, (http://www.herc.com/businesses/aqualon/aqualon/htm)
pharmacy Methocel, Celacol, Dow Chemical Company
(http://www.dow.com)
Metolose, Shin-Etsu (http://www.shinetsu.co.jp/english)
Tylose, Clariant (http://www.clariant.com)
Walocel, Wolff-Walsrode-bayer (http://www.bayer.com)
EC Ethylcellulose polysaccharide, cellulose ether adhesives, additives in plastics, lacks and Ethocel, Dow (http://www.dow.com)
pigments. Aqualon EC, Aqualon-Hercules
(http://www.herc.com/businesses/aqualon/aqualon/htm)
EC, Bermocoll (EHEC), Akzo Nobel (http://www.akzonobel.com)
HEC Hydroxyethylcellulose polysaccharide, cellulose ether thickening agent Natrosol, Aqualon-Hercules
B3 (http://www.herc.com/businesses/aqualon/aqualon/htm)
Tylose, Clariant (http://www.clariant.com)
Shin-Etsu (http://www.shinetsu.co.jp/english)
HPC Hydroxypropylcellulose polysaccharide, cellulose ether thickening agents, encapsulation Klucel, Aqualon-Hercules
(http://www.herc.com/businesses/aqualon/aqualon/htm)
Shin-Etsu (http://www.shinetsu.co.jp/english)
Pectin polysaccharide, plant extract coating, gelling agents in foods, pharmacy Herbstreith & Rox (http://www.herbstreith-
fox.de/produkte/englisch/einstplus.htm), Genu (Hercules)
Dextran polysaccharide, fermentation product molecular sieve (Sephadex), drug delivery Pharmachem Corporation (http://www.pharmachemcorp.com)
system
Xanthan polysaccharide, fermentation product emulsifiers and suspending agents Rhodia (http://www.food.us.rhodia.com/prod_info.asp)
Alginate polysaccharide, algae extract thickening, gelling, emusifying agent FMC Biopolymer (http://www.fmcbiopolymer.com/en_US)
Agar/Agarose polysaccharide, algae extract suspending, emulsifying agent, cuture gel Carbomer (http://www.carbomer.com/4semisynth.htm)
Garrageenan polysaccharide, algae extract thickening, stabilizing, emusifying agent FMC Biopolymer (http://www.fmcbiopolymer.com/en_US),
http://www.philexport.org/members/siap/intro.htm
Gum arabic/Aracia gum polysaccharide, gum demulcent, emusifying agent, tablets binder Multikem (http://www.multikem.com/mk/index.html)
Tragacanth gum polysaccharide, gum tablets binder, demulcent Carbomer (http://www.carbomer.com/4semisynth.htm)
Chitosan polysaccharide food coagulant, wastwater treatment, Vanson (http://www.vanson.com/)
coating
Pullulan polysaccharide, plantseed extract food coating Carbomer (http://www.carbomer.com/4semisynth.htm)
Xyloglucan, Amyloid polysaccharide, plantseed extract gelling agent in foods and pharmaceuticals
23
Lignin, lignin sulfonate polysaccharide lignin: adhesives, emulsifiers, dispersing Borregard, Lignotech USA (http://www.ltus.com)
agents; Georgia Pacific (http://www.gp.com)
lignosulfonate or lignin Kraft: paper pate, Northway Lignin (http://duenorth.net/northway)
preparation of polyurethane
Starch polysaccharide paper industry, chemical and pharmaceutical Nadeg by Schulman-Amylum
industry Eridania-Beghin-Say Cerestar (http://www.eridania-beghin-
say.com)
Novo-Nordisk (http://www.novo.dk)
Roquette (http://www.roquette.fr)
Cargill (http://www.cargill.com)
24
3.8 Companies in EDPs Medical Applications
Company Associate Address City State Trademark Application Polymer homepage ref.
Advanced Polymer Heller J. 123 Saginaw Redwood CA 94063, orthopedics poly(ortho)esters http://www.advanced book 05
Systems Research Drive City USA polymer.com/
Institute
Advanced Tissue Bartel, R.; 10933 N. La Jolla CA 92037, Dermagraft® tissue engineering/ skin http://www.advancedt book 12
Sciences, Inc. Mansbridge, Torrey Pines USA issue.com/
J.; Naughton, road
G.K.
Alkermes, Inc. 64 Sidney Cambridge Massachus ProLease® INJECTABLE DRUG poly-(DL-lactide-co- http://www.alkermes.
Street etts 02139, Medisorb® DELIVERY SYSTEMS glycolide) com/
USA
Arthrex, Inc. 2885 South Naples FL 34104, TissueTak™; Headed interference screw; suture PLDLA copolymer http://www.arthrex.co
Horseshoe USA Bio- Absorbable anchor m/flash.htm
Drive Corkscrew™; Bio-
FASTak®; Bio-
Corkscrew™
Atrix Laboratories Dunn, R.L. 2579 Midpoint Fort Collins Colorado ATRIGEL®; BEMA™ Parenteral Drug Delivery poly(a-hydroxy acids)/ www.atrixlabs.com/ book
Drive 80525, System; Bioerodible release 11/
USA Mucoadhesive JBMR
42
Aventis Gliadel® drug delivery poly(CPP-SA) www.gliadel.net;
Pharmaceuticals http://www.aventisph
Products Inc arma-us.com/
Bionix Implants Oy Tormala,P.; P.O.Box 3 FIN 33721 Finland Smartscrew™; PCT Int. Appl. WO http://www.bionximpla CA
Bonfield, W. Tampere Smartpin™; 9911296 A2 11 Mar. nts.com/ 130:21
Smarttack™ 1999/ Bioresorbable 3683
PLLA/PGA Products
American Cyanamid Danbury Connecticu DEXON®; MAXON® suture TMC/PG
Corp., Davis & Geck t, USA
Division of Johnson 700 Warsaw, IN 46581- Biostop® bioresorbable plug http://www.depuy.co
& Johnson, DePuy Orthopaedic 0988, USA m/index.cfm
Orthopaedics Drive
Division of Johnson Jamiolkowski, Somerville New MONOCRYL®; suture; ligating clip; suture PCL/ PLA; poly-p- http://www.ethiconinc. book 11
& Johnson, Ethicon, D.D. Jersey, VICRYL®; clip dioxanone com/
Inc. (endosurgery) USA PANACRYL®;
PDS®; ABSOLOK™;
LAPRA-TY™
Instrument Makar, 2950 East Okemos MI 48864, Biologically Quiet™ interference screw PGL/PLA http://www.instmak.co
Inc. Mount Hope USA m/
25
Linvatec Corp. Perrin, D.E 11311 Concept Largo Florida Bio-Stinger™; Meniscal Fixation Device; PLLA http://www.linvatec.co
Boulevard 33773, BioScrew®; Bio-Absorbable Interference m/
USA BioTwist™ Screws and Delivery
System; Soft Tissue
Fixation Device
Macromed, Inc. Zentner, 9520 South Sandy Utah Oligosphere® drug delivery http://www.macromed
Gaylen. M. State Street 84070, .com/
USA
PHUSIS SA France PHUSILINE interference screw 98%L-PL/2%D-PL
Samyang 263 Yonji- Seoul Korea Surgisorb; BioMesh suture; reconstructive http://www.samyang.
Pharmaceuticals dong, GTR barrier surgery com/english/index.ht
R&D, Samyang Chongno-gu ml
Genex Co.
26
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Pippich B., (1995); EUR 16200 EN, European Commission, Brussels
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Biodegradable Polymers & Plastics, M. Vert, J. Feijen, A. Albertsson, G. Scott and E. Chiellini (Editors). Cambridge
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Biodegradation of Starch-Poly(Beta-hydroxybutyrate-co-valerate) Composites in Municipal Activated Sludge. S. H. Imam, S. H.
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30
Skz, Würzburg 1999, Biologisch abbaubare Werkstoffe Haus der Technik, Essen, Biologisch abbaubare Kunststoffe,
1999.
The use of Agricultural Commodities as a Source of New Plastic Materials - C. Bastioli, V.Bellotti, G. Gilli - APRIA
Conference 10-11/5/90 - Paris
Nuovi materiale a base di amido - C. Bastioli - XLI Convegno Giornate della Chimica: Plastica distruzione o
riutilizzo?
Nuovi materiali biodegradabili da amido - C. Bastioli, V. Bellotti - Agrobiotecnologie e nuove produzioni chimiche
da risorse rinnovabili, Accademia Nazionale dei Lincei - Roma November 26-27 1990
Nuovi materiali biodegradabili da amido - C. Bastioli, V.Bellotti - Materiali e prodotti - March 1991, 258-262
Mater-Bi: Properties and Biodegradability - C. Bastioli - Environmentally Degradable Polymers: Technical, Business,
and Public Perspectives, Univesity of Lowell - August 13 - 15, 1991
Rheology, Processing and Mechanical Properties of a Starch Based Polymer - C. Bastioli, A. Rallis, F.Cangialosi, F.P.
LaMantia, G. Titomanlio, S. Piccarolo - The Polymer Processing Society, European Regional Meeting -
Palermo (Italy) September 15 - 18, 1991
Mater-Bi: Properties and Biodegradability - C.Bastioli, V. Bellotti, G. Gilli, A. Rallis - Plastics Waste Management -
New Orleans, Louisiana - December 9- 12, 1991
Properties and Biodegradability of Mater-Bi Starch Products - C. Bastioli - Corn Utilization Conference IV - St. Louis,
Missouri - June 24 - 26, 1992
Le nuove tecnologie che riducono e agevolano lo smaltimento dei rifiuti - C.Bastioli - Smaltimento Rifiuti Industriali -
Milano, 15 - 16 Marzo 1993 - Cegos
Materiali biodegradabili da amido - C.Bastioli - 3° Settimana della Cultura Scientifica promossa dal Ministero della
Ricerca Scientifica - Foligno, 19 - 24 Aprile 1993
Microstructure and Biodegradability in Starch Based Materials - C.Bastioli - Gordon Research Conferences
Biodegradable Polymers - San Miniato Italy - May 3-7, 1993
Influenza della granulometria negli studi di biodegradazione di materiale plastico - G.Freschi, C.Bastiol i, F.Degli
Innocenti, G.Gilli, G.P.Molinari - Atti Convegno SICA - Ferrara - Settembre 1993
Starch/Vinyl-Alcohol Copolymer Interactions - C.Bastioli, V.Bellotti, M.Camia, L.Del Giudice, A.Rallis - 3rd
International Scientific Workshop on Biodegradable Plastics and Polymers - Osaka - Japan - November 9-11,
1993
The starch based thermoplastics - C.Bastioli - Recycle '94 Davos Global Forum and Exposition - Davos Switzerland
- March 14-18, 1994
Compostable films of Mater-Bi Z grades - C.Bastioli, F.Degli Innocenti, I.Guanella, G.C.Romano - International
Workshop: Controlled Life-Cycle of Polymeric Materials Biodegradable Polymers and Recycling - Stoccolma
Sweden, April 21-23, 1994
Physical state and biodegradation behaviour of starch-polycaprolactone systems - C.Bastioli, A.Cerutti, I.Guanella,
G.C.Romano, M.Tosin - Bio/Environmentally Degradable Polymer Society - Boston Massachusetts - June 6-8,
1994
Starch-Polymer Composites: State of the Art and Future Perspectives - C.Bastioli - Polymers from Renewable Resources
and their Degradation - Stockholm, Sweden, 10-11 November, 1994
Degradation of Mater-Bi ZI01U Sheets in a Composting Pilot - F.Degli Innocenti, S.Piccinini, L.Rossi, C.Bastioli -
Proceedings of the ORCA Congress - January 18, 19, 1995 - Brussels, Belgium
Microstructure of Biodegradable Composite Materials Based on Starch - C.Bastioli, I.Guanella, A.Rallis, M.Trznadel -
Gordon Research Conference on “Biodegradable Polymers” - California, February 19-24, 1995
Polimeri Biodegradabili a base di amido - C.Bastioli - Giornata di Studio AIM su Plastiche biodegradabili - Milano,
23 Marzo 1995
31
Behaviour of Biodegradable Mater-Bi ZI01U plastic layers in a composting pilot plant - S.Piccinini, L.Rossi, F.Degli
Innocenti, M.Tosin, C.Bastioli - International Symposium “The Science of Composting”, May 30th - June, 2rd,
1995
Use of Mater-Bi ZF03U biodegradable bags in source-separated collection and composting of organic waste - C.Bastioli, F.Degli
Innocenti, S.Silvestri, G.Zorzi - International Symposium “The Science of Composting”, May 30th - June, 2rd,
1995
Starch based biodegradable materials in the separate collection and composting of organic waste - C.Bastioli, F.Degli Innocenti
- International Symposium “The Science of Composting”, May 30th - June, 2rd, 1995
Method for the evaluation of biodegradability of packaging in composting conditions proposed by CEN (European Committee for
Standardization): a technical approach - F.Degli Innocenti, M.Tosin, C.Bastioli - International Symposium “The
Science of Composting”, May 30th - June, 2rd, 1995
An overview of the Italian situation on composting - C.Bastioli (BEDPS)
Mater-Bi and the bags for composting - C.Bastioli (ORCA)
Envionmental Conference and Exhibition on the Role of Biodegradable Materials in Waste Management - C.Bastioli -
Biodegradable Materials and the separate/composting of organic waste - Tokyo - June 14, 16, 1995
Raccolta differenziata e compostaggio - Costi e benefici - C.Bastioli - Suno (Novara), October 27, 1995
“OK Compost” label for two Mater-Bi grades” - The Orcazette
Degradation of Mater-Bi ZI01U Sheets in a Composting Pilot - F.Degli Innocenti, S.Piccinini, L.Rossi, C.Bastioli -
Proceedings of the ORCA Congress - January 18, 19, 1995 - Brussels, Belgium
Effect of the Composting Substrate on Biodegradation of Solid Materials Under Controlled Composting Conditions - M.Tosin,
F.Degli Innocenti, C.Bastioli - Journal of Environmental Polymer Degradation, Vol. 4, No. 1, 1996
Starch-polymer composites - C.Bastioli - “Degradable Polymers - Principles & Applications” edited by G.Scott and
D.Gilead - pp. 112-137
Bastoncini cotonati biodegradabili e solubili. Studio della biodegradabilità in laboratorio ed in un impianto di trattamento delle
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PUBLICATION INFORMATION: New York, Cop. 1977.
PUBLICATION YEAR: 1977
ISBN: 99-0130972-7
40
ISBN: 0570-4898
TITLE: Fundamentals of Polymer Degradation and Stabilization
AUTHORS: Allen N. S., Edge M., (Editors)
PUBLICATION INFORMATION: London, Elsevier Applied Science, Cop., 1992.
PUBLICATION YEAR: 1992
ISBN: 1-85166-773-3
41
book 03 Controlled drug delivery Park, K. ACS Professional 0-8412-3418-3 1997
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polymers
book 12 Synthetic Biodegradable Atala, A. and Mooney, D.J.; Birkhauser Boston 0-8176-3919-5 1997
Polymer Scaffolds Vacanti, J.P. and Langer, R.
book 13 Hydrogels and Biodegradable Ottenbridge, R.M.; Huang, ACS Washington 0-8412-3400-0 1996
Polymers for Bioapplications S.J.; Park, K. D.C.
book 14 Biodegradation and Gumargalieva, K.Z.; Zaikov, Nova Science Publ., 1-56072-582-6 1998
Biodeterioration of Polymers: G.E. Inc.; Commack, NY
Kinetical Aspects
book 15 Handbook of Biomaterials von Recum, A.F. Taylor & Francis, 1-56032-479-1 1999
Evaluation: Scientific, Philadelphia
Technical, and Clinical Testing
of Implant Material
book 16 Biodegradable polymers and Vert, M; Feijen, J.; Royal Society of 0-85186-207-1 1992
plastics Albertsson, A.; Scott, G. and Chemistry;
Chiellini, E. Cambridge
book 17 Biomedical Applications of Tsurata, T.; Hayashi, T.; CRC Press 0-8493-4519-7 1993
Polymeric Materials Kataoka, K.; Ishihara, K.;
Kimura, Y.
book 18 The Biomedical Engineering Bronzino, J.D. CRC Press in coop. 0-8493-8346-3 1995
Handbook IEEE Press
book 19 Handbook of Biodegradable Domb, A.J.; Kost, J.; Harwood Academic 90-5702-1530-6 1997
Polymers Wiseman, D.M. Publishers
book 20 Biodegradable hydrogels for Park, K.; Shalaby, W.S.W.; Technomic Publ. Co., 1-56676-004-6 1993
drug delivery Park, H. Inc.
42
4.8 Review articles on medical and pharmaceutical applications (after 1995)
Solid lipid nanoparticles: phagocytic uptake, in vitro cytotoxicity and in vitro biodegradation: 2nd
communication
Muller, Rainer H.; Olbrich, Carsten
Drugs Made Ger. (1999), 42(3), 75-79
Biodegradable materials
Burg, K. J. L.; Shalaby, S. W.
Tissue Eng. Intell. Unit (1999), 1(Tissue Engineering of Vascular Prosthetic Grafts), 505-511
43
Macromol. Symp. (1999), 144(Degradability, Renewability and Recycling—Key Functions for Future
Materials), 33-46
Targeted delivery of antibiotics using liposomes and nanoparticles: research and applications
Pinto-Alphandary, H.; Andremont, A.; Couvreur, P.
Int. J. Antimicrob. Agents (2000), 13(3), 155-168
Solid lipid nanoparticles: phagocytic uptake, in vitro cytotoxicity and in vitro biodegradation. 1st
Communication.
Muller, Rainer H.; Olbrich, Carsten
Drugs Made Ger. (1999), 42(2), 49-53
Polymers in controlled release.Targeted drug delivery. Part 2. Formulation types in targeted delivery
Brannon-Peppas, Lisa; Birnbaum, Duane T.; Kosmala, Jacqueline D.
Polym. News (1999), 24(7), 230-232
The use of natural metabolites in the design of new materials for tissue engineering
Kohn, Joachim
Int. Congr. Ser. (1998), 1169(Tissue Engineering for Therapeutic Use 1), 61-70
44
Peters, Martin C.; Mooney, David J.
Int. Congr. Ser. (1998), 1170(Tissue Engineering for Therapeutic Use 2), 55-65
45
Protein delivery from poly(lactic-co-glycolic acid) biodegradable microspheres: release kinetics and
stability issues
Crotts, G.; Park, Tae Gwan
J. Microencapsulation (1998), 15(6), 699-713
Degradable hydrogels
Chen, Jun; Jo, Seongbong; Park, Kinam
Drug Targeting Delivery (1997), 7(Handbook of Biodegradable Polymers), 203-230
Polyanhydrides
Domb, Abraham J.; Elmalak, Omar; Shastri, Venkatram R.; Ta-Shma, Zeev; Masters, David M.; Ringel,
Israel; Teomim, Doron; Langer, Robert
Drug Targeting Delivery (1997), 7(Handbook of Biodegradable Polymers), 135-159
Poly(ortho esters)
Heller, Jorge
Drug Targeting Delivery (1997), 7(Handbook of Biodegradable Polymers), 99-118
Poly(propylene fumarate)
Peter, Susan J.; Miller, Michael J.; Yaszemski, Michael J.; Mikos, Antonios G.
Drug Targeting Delivery (1997), 7(Handbook of Biodegradable Polymers), 87-97
Polycaprolactone
Perrin, Dana E.; English, James P.
Drug Targeting Delivery (1997), 7(Handbook of Biodegradable Polymers), 63-77
Pre-clinical evaluation and quality control aspects of microparticulate antigen delivery systems
46
Sesardic, Dorothea; Corbel, Michael J.
Drug Targeting Delivery (1997), 8(Antigen Delivery Systems), 227-250
Other polyesters
Shastri, Venkatram R.; Hildgen, Patrice P.; Langer, Robert; Najajrah, Yousef; Ringel, Israel; Domb,
Abraham J.
Drug Targeting Delivery (1997), 7(Handbook of Biodegradable Polymers), 119-134
Synthetic for biodegradable polymers for tissue engineering and drug delivery
Hubbell, Jeffrey A.
Curr. Opin. Solid State Mater. Sci. (1998), 3(3), 246-251
Strategies for site specific, time and rate controlled delivery of drugs, genes, and antigens
Crommelin, D. J. A.; Hennink, W. E.; Storm, G.
Future Strategies Drug Delivery Part. Syst., Lect. Eur. Workshop Part. Syst., 1st (1998), Meeting Date
1997, 147-151. Editor(s): Diederichs, Julia E.; Mueller, Rainer H. Publisher: Medpharm Scientific
Publishers, Stuttgart, Germany.
Nanoencapsulation of hemoglobin and red blood cell enzymes based on nanotechnology and biodegradable
polymer
Chang, T. M. S.; Yu, W. P.
Blood Substitutes (1998), Volume 2, 216-231. Editor(s): Chang, Thomas Ming Swi. Publisher: Karger
Landes Systems, Basel, Switz.
47
Biodegradable polymer microspheres as vaccine adjuvants and delivery systems
Gupta, R. K.; Chang, A. -C.; Siber, G. R.
Dev. Biol. Stand. (1998), 92(Modulation of the Immune Response to Vaccine Antigens), 63-78
Chemical routes to poly(.beta.-malic acid) and potential applications of this water-soluble bioresorbable
poly(.beta.-hydroxy alkanoate)
Vert, Michel
Polym. Degrad. Stab. (1998), 59(1-3), 169-175
Solvent Evaporation Processes for the Production of Controlled Release Biodegradable Microsphere
Formulations for Therapeutics and Vaccines
Cleland, Jeffrey L.
Biotechnol. Prog. (1998), 14(1), 102-107
Dosage and design of leuprorelin acetate microspheres for long-term sustained-release injection
Okada, Hiroaki
Pharm Tech Jpn. (1998), 14(1), 75-78, 81-88
48
Thomasin, Claudio; Nam-Tran, Ho; Merkle, Hans P.; Gander, Bruno
J. Pharm. Sci. (1998), 87(3), 259-268
One- and three-month release injectable microspheres of the LH-RH superagonist leuprorelin acetate
Okada, Hiroaki
Adv. Drug Delivery Rev. (1997), 28(1), 43-70
49
Polymeric carriers of drugs for site-specific therapy
Ulbrich, Karel; Pechar, Michal; Strohalm, Jiri; Subr, Vladimir; Rihova Blanka
Macromol. Symp. (1997), 118, 577-585
Extended release of adenovirus from polymer microspheres: potential use in gene therapy for brain tumors
Beer, Steven J.; Hilfinger, John M.; Davidson, Beverly L.
Adv. Drug Delivery Rev. (1997), 27(1), 59-66
Peptide, protein, and vaccine delivery from implantable polymeric systems. Progress and challenges
Schwendeman, Steven P.; Costantino, Henry R.; Gupta, Rajesh K.; Langer, Robert
Controlled Drug Delivery (1997), 229-267. Editor(s): Park, Kinam.
Publisher: American Chemical Society, Washington, D. C.
Production and novel applications of natural L(+)-lactic acid: food, pharmaceutics and biodegradable
polymers
Bogaert, J.C.
Cerevisia (1997), 22(1), 46-50
Injectable microcapsules prepared with biodegradable poly(.alpha.-hydroxy acids) for prolonged release of
drugs
Ogawa, Yasuaki
J. Biomater. Sci., Polym. Ed. (1997), 8(5), 391-409
Recent contributions of polymers to the design of biomaterials for clinical and surgical applications
Roman, Julio San
An. Quim. Int. Ed. (1997), 93(1, Suppl. 1), S22-S31
50
Drug delivery into the brain using implantable polymeric systems
Menei, P.; Venier-Julienne, M. C.; Benoit, J. P.
S.T.P. Pharma Sci. (1997), 7(1), 53-61
Recent advances in vaccine adjuvants: the development of MF59 emulsion and polymeric microparticles
O'Hagan, Derek T.; Ott, Gary S.; Van Nest, Gary
Mol. Med. Today (1997), 3(2), 69-75
The rationale for peptide drug delivery to the colon and the potential of polymeric carriers as effective tools
Rubinstein, Abraham; Tirosh, Boaz; Baluom, Muhammad; Nassar, Taher; David, Ayelet; Radai, Raphael;
Gliko-Kabir, Irit; Friedman, Michael
J. Controlled Release (1997), 46(1,2), 59-73
Polymeric endoluminal gel paving: hydrogel systems for local barrier creation and site-specific drug
delivery
Slepian, Marvin J.; Hubbell, Jeffrey A.
Adv. Drug Delivery Rev. (1997), 24(1), 11-30
51
Drugs Pharm. Sci.(1996), 77(Microparticulate Systems for the Delivery of Proteins and Vaccines), 279-306
Biodegradable polyurethanes: Biodegradable low adherence films for the prevention of adhesions after
surgery
Rehman, Ihtesham Ur
J. Biomater. Appl. (1996), 11(2), 182-257
Biodegradable polyurethanes
Pkhakadze, G.; Grigorieva, M.; Gladir, I.; Momot, V.
J. Mater. Sci.: Mater. Med. (1996), 7(5), 265-267
Processing and fabrication of bioresorbable implants and devices. State of the art and future perspectives.
Hutmacher, D.; Kirsch, A.; Ackermann, K. L.; Huerzeler, M. B.
52
Carrier for drug formulations and artificial living tissues
Schulz, Michaela; Blunk, Torsten; Gopferich, Achim
Laboratory and field evaluation of biodegradable polyesters for sustained release of isometamidium and
ethidium - Minireview
Geerts, S.; Brandt, J. R. A.; De Deken, R.
The use of natural metabolites in the design of new materials for tissue engineering
Kohn, Joachim
Int. Congr. Ser. (1998), 1169(Tissue Engineering for Therapeutic Use 1), 61-70
Protein delivery from poly(lactic-co-glycolic acid) biodegradable microspheres: release kinetics and
stability issues
Crotts, G.; Park, Tae Gwan
Synthetic for biodegradable polymers for tissue engineering and drug delivery
Hubbell, Jeffrey A.
53
Merkli, A.; Tabatabay, C.; Gurny, R.; Heller, J.
Nanoencapsulation of hemoglobin and red blood cell enzymes based on nanotechnology and biodegradable
polymer
Chang, T. M. S.; Yu, W. P.
Dosage and design of leuprorelin acetate microspheres for long-term sustained-release injection
Okada, Hiroaki
Biodegradable materials
Imai, Yoji
One- and three-month release injectable microspheres of the LH-RH superagonist leuprorelin acetate
Okada, Hiroaki
54
Chiellini, Emo; D'Antone, Salvatore; Solaro, Roberto
Production and novel applications of natural L(+)-lactic acid: food, pharmaceutics and biodegradable
polymers
Bogaert, J.C.
Injectable microcapsules prepared with biodegradable poly(.alpha.-hydroxy acids) for prolonged release of
drugs
Ogawa, Yasuaki
Recent advances in vaccine adjuvants: the development of MF59 emulsion and polymeric microparticles
O'Hagan, Derek T.; Ott, Gary S.; Van Nest, Gary
The rationale for peptide drug delivery to the colon and the potential of polymeric carriers as effective tools
Rubinstein, Abraham; Tirosh, Boaz; Baluom, Muhammad; Nassar, Taher; David,
55
Pradhan, Ram; Shivprakash; Shah, Yamini; Gohel, Mukesh; Shan, Dushyant
56
4.9 Other Books on Degradable Polymers
Title Author/Editor Publisher ISBN year Material Application
Novel Biodegradable Microbial Polymers Dawes, E. A. Kluwer Academic Publishers 0-7923-0949-9 1990
Polymers from Agricultural Coproducts Fishman, M. L., Friedman, R. American Chemical Society, 0-8412-3041-2 1994 polysaccharides, polyamides,
B., Huang, S. J. Washington DC proteins, polyesters, rubbers
Polymer Biomaterials in Solution, as Interfaces and VSP, The Netherlands 90-6764-180-4 1995 Medical
as Solids
Chemistry and Technology of Biodegradable Griffin, G. J. L. Chapman & Hall 0-7514-0003-3 1994
Polymers
Degradability, Renewability and Recycling - Key Functions for Future Materials Wiley-VCH 3-527-29904-1 2000 Plastics Packaging
5th International Scientific Workshop on Biodegradable Plastics and Polymers
Blockcopolymers/polyelectrolytes/biodegradation, Silvestre, F., etc. Springer-Verlag Berlin and Heidelberg 3540631569 1997 Biopolymers Medical
Advances in Polymer Science Vol. 135 GmbH & Co. KG
Biopolymers/PVA Hydrogels/Anionic Polymerisation/ Hassan, C.M., etc. Springer-Verlag Berlin and Heidelberg 3-540-67313-X 2000 Poly(vinyl
Nanocomposites GmbH & Co. KG alcohol), etc
Advances in Polymer Science Vol. 153
Advances in Biodegradable Polymers Rapra review Moore, G. F., Sauders, S. M. Rapra Technology 1-85957-118-2 1997
Report No.98
Degradable Materials: Perspectives, Issues and Barenberg, et al CRC Press 0-849342740 1990
Opportunities
57
Second International Symposium on Natural Capparelli Mattoso, L. H., Embrapa, Sao Carlos ISNaPol 98 1998 Natrural
Polymers and Composites Frollini, E., Leao, A. polymers
Polysaccharides Structural Disversity and Fundtional Chasin, M.; Langer, R. Marcel Dekker, Inc. 0-8247-8344-1 1998 Polysaccharides
Versatility
Polysaccharides in Medical Applications Dimitriu, S. Marcel Dekker, Inc. 1996 Polysaccharides Medical
Biodegradable Polymers and Packaging Ching, C., Kaplan, D. L., Technomoc Publishing 1-56676-008-9 1993 Packaging
Thomas, E. L.
Biosynthesis and Biodegradation of Cellulose Haigler, C., Weimer, R.J., Marcel Dekker 0-8247-8387-5 1990 Cellulose
Haigle, C. H., Weimer, P. J.
Poly(ethylene Glycol) Chemistry Biotechnical and Haigler, C., Weimer, R.J., Plenum Press 0-306-44078-4 1992 PEO
Biomedical Applications Haigle, C. H., Weimer, P. J.
Macromolecular Biomaterials Hastings G. W., Ducheyne P. CRC Press 0-8493-6263-6 1984 General
58
59
4.10 Literatures on polyhydroxyalkanoates
60
61
4.10 Literature on Polyhydroxyalkanoates.xls - page 62
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1. An investigation into the effects of novel DBM and PAM
effectors on
catecholamine metabolism and amidation in adrenal
chromaffin dopamine monooxygenase
Georgia Institute of cell culture. 2. Microbial production of poly-beta- 254 pp. Avail. Univ. Microfilms Int., Order No.: PAM catecholamine adrenal
Technology, Atlanta, hydroxybutyric DA9526142 chromaffin
GA, acid from D-xylose and lactose using Pseudomonas From: Diss. Abstr. Int., B 1995, 56(4), 2006 poly hydroxybutyric acid xylose
1 Young, Frederick Kwai USA cepacia. (English) 1995 1995 lactose Pseudomonas Abstract Unavailable Strains
13C NMR Determination of the degree of cocrystallization
VanderHart; D.L.; Orts; W.J.; in random copolymers of poly(beta-hydroxybutyrate-co-
2 Marchessault; R.H. beta-hydroxyvalerate) Macromolecules 1995; 28:6394-6400 1995 595.
13C Nuclear magnetic resonance studies of Pseudomonas
Huijberts; G.N.M.; DeRijk; C.; putida fatty acid metabolic routes involved in poly(3-
3 DeWaard; P.; Eggink; G. hydroxyalkanoate) synthesis Journal of Bacteriology 1994; 176(6):1661-1666 1994 546.
The metabolism of a, a-
trehalose in the bacterium
Alcaligenes eutrophus H
16 was studied by
Research Laboratory analysis of the 13C NMR
of Resources spectra of intact cells. A.
Utilization, Tokyo eutrophus accumulated
Institute of trehalose together with
Technology, 13C Nuclear magnetic resonance study of trehalose and Alcaligenes eutrophus H 16 - poly(3-hydroxybutyrate)
Nagatsuta, Midori-ku, poly(3-hydroxybutyrate) metabolism in Alcaligenes Ralstonia eutropha H 16 - (P(3(HB)) as intracellular
4 Kawaguchi; Y.; Nakamura; Y.; Doi; Y. Yokohama 227 Japan eutrophus Applied Environmental Microbiology 1990; 1030 1990 trehalose storage compou Strain - Metabolism 309.
Doi; Y.; Kunioka; M.; Nakmaura; Y.; 1H and 13C NMR analysis of poly(beta-hydroxybutyrate)
5 Soga; K. isolated from Bacillus megaterium Macromolecules 1986; 19:1274-1276 1986 578.
Biodegradable patches
made of
polyhydroxybutyrate
(PHB) were recently
shown to limit
postoperative pericardial
adhesions when inserted
into the pericardium in
Department of sheep. The present study
Diagnostic Radiology, A biodegradable patch used as a pericardial substitute postoperative pericardial was carried out to
Duvernoy O, Malm T, Ramstrom J, University Hospital, after cardiac adhesions - Biodegradable evaluate the presence of
7 Bowald S Uppsala, Sweden. surgery: 6- and 24-month evaluation with CT. Thorac Cardiovasc Surg 1995 Oct;43(5):271-4 1995 patches made of PHB post-operative retrosterna Applications
(1) Projektgruppe
Biosignale, Abteilung
Biotechnologie, The analysis of growing or
Fakultät für resting bacterial
Biowissenschaften, populations by flow
cytometry offers several
Pharmazie und advantages over
Psychologie, traditional methods for
Universität Leipzig, determining mean-value
Permoserstraße 15, D- parameters. This method
04318 Leipzig, has been applied here to
measure both the
S. Müller (1), A. Lösche (1), T. Bley (1), Germany A flow cytometric approach for characterization and Applied Microbiology and Biotechnology Abstract distribution of single-cell
11 T. Scheper (2) (2) differentiation of bacteria during microbial processes Volume 43 Issue 1 (1995) pp 93-101 1995 fluoresc
4.10 Literature on Polyhydroxyalkanoates.xls - page 64
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Using a 30-mer
oligonucleotide probe
highly specific for
polyhydroxyalkanoic acid
(PHA) synthase genes,
the respective genes
of Pseudomonas
citronellolis, P.
mendocina, Pseudomonas
Institut fur A general method for identification of polyhydroxyalkanoic sp. DSM 1650 and
Mikrobiologie, Georg- acid synthase Pseudomonas sp.
August-Universitat genes from pseudomonads belonging to the rRNA GP4BH1 were cloned from
12 Timm A, Wiese S, Steinbuchel A Gottingen, Germany. homology group I. Appl Microbiol Biotechnol 1994 Jan;40(5):669-75 1994 genomic libraries
A structured model is
pesented giving a
mathematical description
of batch cultures of
Alcaligenes eutrophus
strain H 16 under
chemolithoautotrophic
growth conditions. A mass-
spectrometer with a
Institut für Alcaligenes eutrophus H 16 - membrane inlet system
Biotechnologie TU A kinetic model for growth and synthesis of poly-á- European J. Appl. Microbiol. Biotechnol. 1980; Ralstonia eutropha H 16 - was used to measure and
13 Heinzle, E.; Lafferty, R. M. Graz hydroxybutyric acid (PHB) in Alcaligenes eutrophus H16 11:42583 1980 chemolithoautotrophic growth - control the con Stain - Kinetics 69.
Deletion studies on
Rhizobium meliloti mega-
plasmid pRmeSU47b
identified a region
required for poly-beta-
hydroxybutyrate (PHB)
Abstr.Gen.Meet.Am.Soc.Microbiol.; (1996) 96 degradation pathway
McGill University, Ste- Meet., 557 intermediates 3-
Anne-de-Bellevue, A megaplasmid-located methylmalonyl-CoA-mutase-like American Society for Microbiology, 96th General hydroxybutyric acid (3HB)
Quebec H9X 3V9, gene is required for operation of the PHB degradation Meeting, New and
Charles T C; Dumont R Canada. pathway in Rhizobium meliloti; poly-beta-hydroxybutyrate Orleans, LA, 19-23 May, 1996. acetoacetic acid (AA)
14 degradation (conference abstract) 1996 as sole C-source. Clo
Comamonas testosteroni
can grow on a variety of
steroid compounds as the
sole carbon and
energy
Departamento de source. In a previous
Bioquimica Clinica, study, we cloned and
Facultad de Ciencias sequenced the
Quimicas, Universidad testosterone-inducible
Nacional de A new Comamonas testosteroni steroid-inducible gene: betahsd
Cabrera JE, Panzetta-Dutari G, cloning and J Steroid Biochem Mol Biol 1997 Sep-Oct;63(1- gene from
18 Pruneda JL, Genti-Raimondi S Cordoba, Argentina. sequence analysis. 3):91-8 1997 C. testosteroni
A protein which is
encoded by protein
sequence (I), or a protein
sequence in with one
amino acid either added,
deleted and/or
replaced, and has
polyhydroxyalkanoate
A new intracellular PHA decomposition enzyme; (PHA)-degrading activity
Chikyu-Kankyo-Sangyo; recombinant enzyme production via vector-mediated gene is
Univ.Kanagawa Japan. transfer and expression in host cell for improved JP 11113574 27 Apr 1999 new. Also claimed
19 polyhydroxyalkanoate production 1999 are: a protein encoded by
To investigate the
metabolic link between
fatty acid de novo
synthesis and
Institut fur polyhydroxyalkanoic
Mikrobiologie, acid (PHA)
Westfalische Wilhelms- synthesis, we isolated
Universitat Munster, mutants of Pseudomonas
Corrensstrabetae 3, A new metabolic link between fatty acid de novo synthesis putida KT2440 deficient in
D- and polyhydroxyalkanoic acid synthesis. The PHAG gene this
48149, Munster, from Pseudomonas putida KT2440 encodes a 3- metabolic
20 Rehm BH, Kruger N, Steinbuchel A Germany. hydroxyacyl-acyl carrier protein-coenzyme a transferase. J Biol Chem 1998 Sep 11;273(37):24044-51 1998 route. The gene
4.10 Literature on Polyhydroxyalkanoates.xls - page 66
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A fragment of genomic
DNA from Sulfolobus
acidocaldarius DSM 639
encoding a lipolytic
enzyme
Lehrstuhl fur Biologie was cloned and
der Mikroorganismen, sequenced. The 314-
Ruhr-Universitat amino acid polypeptide
Bochum, Germany. displays a maximum
A novel heat-stable lipolytic enzyme from Sulfolobus sequence
jeanlouis.arpigny@ruh acidocaldarius DSM 639 displaying similarity to similarity (43%) to a
21 Arpigny JL, Jendrossek D, Jaeger KE r-uni-bochum.de polyhydroxyalkanoate depolymerases. FEMS Microbiol Lett 1998 Oct 1;167(1):69-73 1998 putative
Poly-3-hydroxybutyric acid
is separated from bacterial
cells by drying a finely
divided stream or spray of
an aqueous suspension
of the cells with a gas
HOLMES PAUL ARTHUR; WRIGHT heated to above 100 DEG
LEONARD FREDERICK; ALDERSON C and then extracting the
BARRY; SENIOR PETER A process for the extraction of poly-3-hydroxy-butyric acid PHB, preferably after a
22 JAMES ICI PLC (GB) from microbial cells. EP0015123 1980-09-03 1980 lipid extraction step with
Poly(hydroxyalkanoates)
(PHAs) are bacterial
storage polyesters,
Institut für currently receiving
Biotechnologie, much
Eidgenössische attention because of their
Technische potential as biodegradable
Hochschule, ETH- and renewable plastics.
Hönggerberg, CH Well known
8093 A process for the recovery of poly(hydroxyalkanoates) from Bioprocess Engineering Abstract Volume 17 are
23 G. J. M. de Koning, B. Witholt Zürich, Switzerland Pseudomonads Part 1: Solubilization Issue 1 (1997) pp 7-13 1997 poly(hydroxybutyrate) a
Medium-chain-length
poly(hydroxyalkanoates)
(mcl-PHAs) are storage
polyesters
Braunegg, G.; Sonnleitner, B.; Lafferty, A rapid gas chromatographic method for the determination European J. Appl. Microbiol. Biotechnol. 1978;
25 R.M. of poly-beta-hydroxybutyric acid in microbioal biomass 6:29-37 1978 21.
A rapid spectrophotometric assay of alpha, beta-
26 Slepecky, R. A.; Law, J. H. unsaturated acids and beta-hydroxy acids Ananlytical Chemistry 1960; 32(12):1697-1699 1960 8.
4.10 Literature on Polyhydroxyalkanoates.xls - page 67
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
KOREA INST A recombinant Escherichia coli producing poly-3-
SCIENCE hydroxybutyrate (PHB) and a process for preparing PHB
27 LEE SANG-YUP TECHNOLOGY employing the same AU4835197 1998-06-18 1998 Abstract unavailable.
A new recombinant
plasmid vector contains a
gene cluster encoding
beta-ketothiolase
(acetyl-CoA-
acyltransferase, EC-
2.3.1.16) from
Agency- Alcaligenes eutrophus,
Ind.Sci.Technol.Japan; A recombinant plasmid, a transformed blue-green alga acetoacetyl-CoA-
Chikyu-Kankyo- containing it and preparation of poly-beta-hydroxybutyric reductase (EC-1.1.1.36)
Sangyo acid; Alcaligenes eutrophus acetyl-CoA-acyltransferase, and
LO Japan. acetoacetyl-CoA-reductase and polyhydroxybutyrate- JP 09131186 20 May 1997 polyhydroxybutyrate-
28 polymerase expression in Synechococcu 1997 polymerase, downst
Poly(3-hydroxybutyrate-co-
4-hydroxybutyrate)s
(P(3HB-co-4HB)s) with a
wide range of 4HB
contents were
Department of biosynthesized, and their
Biomolecular crystalline states were
Engineering, Tokyo studied by differential
Institute of scanning calorimetry
Technology, poly(3-hydroxybutyrate), (DSC) and compared with
Nakamura; K.; Yoshie; N.; Sakurai; M.; Nagatsuta, Midori-ku, A structural study of the crystalline state of the bacterial hydroxyalkanoate copolyesters, those of the cold-stretched
33 Inoue; Y. Yokohama 227, Japan copolyester poly(3-hydroxybutyrate-co-4-hydroxybutyrate) Polymer 1994; 35:193-197 1994 molecular mechanics copoly 488.
Biodegradability in soil of
poly-b-hydroxyalkanoate
(PHA) films was
monitored using both light
microscopy and SEM.
PHA films were
buried in a forest soil for
fungi soil polyhydroxyalkanoate up to three months.
Dep. Cienc. film biodegrdn Colonization of the films
Ambientales Recur. A study of biodegradation of poly-b-hydroxyalkanoate microorganism soil by fungal hyphae and
Lopez-Llorca, L. V.; Colom Valiente, M. Nat., Univ. Alicante, (PHA) films in polyhydroxyalkanoate film other microorganizms,
34 F.; Gascon, A. Alicante 03080, Spain soil using scanning electron microscopy. Micron, 24(1), 23-9 (English) 1993 1993 biodegrdn probab
Journal of Environmental Polymer Degradation
35 Sipinen; A.J.; Rutherford; D.R. A study of the oxidative degradation of polyolefins 1993; 1:193 1993 588.
A summary of environmental legislation targeting Journal of Environmental Polymer Degradation
36 Crews; P.C.; Rich; W.; Niemeyer; S. disposable diapers and review of related literature 1994; 2:39 1994 572.
Haywood, G.W.; Anderson, A.J.; A survey of the accumulation of novel poly-beta-
37 Dawes, E.A. hydroxyalkanoates by bacteria Biotechnology Letters 1989; 11(7):471-476 1989 343.
A test method to determine rapidly if polymers are Journal of Environmental Polymer Degradation
38 Tilstra; L.; Johnsonbaugh; D. biodegradable 1993; 1:247 1993 570.
4.10 Literature on Polyhydroxyalkanoates.xls - page 69
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The addition of
poly(ethylene glycol) (Mn
University of = 200 g/mol) (PEG-200) to
Massachusetts-Lowell, the fermentation media of
Department of Alcaligenes eutrophus and
Chemistry, 1 University Alcaligenes latus at
Avenue, Lowell, various stages of
Massachusetts 01854 growth resulted in the
email: Richard A. synthesis of poly(3-
Gross Alcaligenes eutrophus and hydroxybutyrate) (PHB)
(Grossr@woods.uml.e A tunable switch to regulate the synthesis of low and high Alcaligenes latus, molecular with bimodal molecular
39 Ashby; R.D.; Shi; F.; Gross; R.A. du) molecular weight microbial polyesters Biotechnol Bioeng 1999 Jan 5;62(1):106-13 1999 weight weight 680.
40 Winton, J.M. A versatile polymer's delayed debut Chemical week 1985; 28:55-57 1985 No abstract. Others 662.
Poly-beta-
hydroxybuttesäure (HBS)
ist weit verbreitetes
bakterielles Speicherlipid;
ihr Vorkommen ist mit
Ausnahme der Thio- und
Athiorhodaceen auf streng
aerobe Bakterien
beschränkt (Übersichten
Institut für Hydrogenomonas H 16 - bei Forsyth et al. 1958;
Mikrobiologie der Abbau und Wiederverwertung von Polyhydroxybuttersäure Organotrophic growth - Schlegel u. Gottschalk,
41 Hippe, H. Universität Göttingen durch Hydrogenomonas H 16 Archiv f r Mikrobiologie 1976; 56:248-277 1967 Metabolism 1962; Dawe Strain - Metabolism 107.
42 Hartley, P. Abbaubare Polymere aus dem Fermenter BioEngineering 1987; 3:66-68 1987 633.
A number of taxonomically-
related bacteria have
been identified which
accumulate
poly(hydroxyalkanoate)
(PHA) copolymers
containing primarily 3-
hydroxyvalerate (3HV)
Accumulation of a poly(hydroxyalkanoate) copolymer monomer units from a
containing range of unrelated single
Department of Applied primarily 3-hydroxyvalerate from simple carbohydrate carbon sources. One of
Haywood GW, Anderson AJ, Williams Biology, University of substrates by these,
45 DR, Dawes EA, Ewing DF Hull, UK. Rhodococcus sp. NCIMB 40126. Int J Biol Macromol 1991 Apr;13(2):83-8 1991 Rhodococcus
Biodegradable
copolyesters of 3-
hydroxybutyrate-co-3-
hydroxyvalerate (3HB-
3HV) were produced by
Alcaligenes
eutrophus in a two-staged
process, namely growth
stage and nitrogen-
Department of Civil deficient polyester-
and Structural accumulation stage. When
Engineering, Hong Accumulation of biodegradable copolyesters of 3-hydroxy- C5 was
Kong Polytechnic butyrate and Appl Biochem Biotechnol 1998 Spring;70-72:929- used as the sole carbon
46 Chua H, Yu PH, Lo W University, Hung Hom. 3-hydroxyvalerate in Alcaligenes eutrophus. 35 1998 sou
Methylobacterium sp.
KCTC 0048 isolated from
soil, synthesized a
variety of copolyesters
when secondary carbon
substrates were added
to nitrogen-limied cultures
Technol. Res. Inst., contg. methanol as a
Sun major carbon and
Hill Glucose Co., Ltd., Accumulation of PHA and its copolyesters by energy source. The
Kang, Choong K.; Lee, Hyun S.; Kim, Incheon 404-250, S. Methylobacterium sp. Biotechnol. Lett., Methylobacterium copolyester of 3-
48 Jung H. Korea KCTC 0048. 15(10), 1017-20 (English) 1993 1993 polyhydroalkanoate polyester hydroxybutyrate and 449.
4.10 Literature on Polyhydroxyalkanoates.xls - page 71
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
In a limited-scale survey,
55 soil streptomycetes
were screened for the
accumulation of poly (3-
hydroxybutyrate)
[PHB]. Only 18% of
the isolates accumulated
PHB ranging between 1.9-
7.8% of the dry biomass.
Anupam Manna, Rebeca Banerjee, Accumulation of Poly (3-Hydroxybutyric Acid) by Some Soil Curr Microbiol 39:153-158 (1999) The promising
49 Amal K. Paul Streptomyces © 1999 by Springer-Verlag New York, Inc. 1999 isolate DBCC-719, i
Castillo, R.F.; Valera, F.R.; Ramos, Accumulation of Poly(beta-hydroxybutyrate) by
50 J.G.; Berraquero, F.R. Halobacteria Appl. Env. Microbiol. 1986; 51:214-216 1986 293.
Poly-beta-hydroxybutyrate
has been identified in the
cyanobacterium Spirulina
platensis. The addition of
reduced carbon
compounds to the growth
medium was not required
for poly-beta-
hydroxybutyrate
accumulation. Poly-beta-
Campbell, J.; Stevens Jr., S.E.; Balkwill, Accumulation of poly-beta-hydroxybutyrate in Spirulina hydroxybutyrate
51 D.L. platensis. J. Bacteriol. 1982; 149:361-363 1982 accumulated durin 180.
The consumption of
phosphate, formation of
polyphosphate, and the
intracellular ATP level
were compared in the
exponential phase of
poly-b-hydroxybutyrate
Accumulation of polyphosphate and substrate gas (PHB)-accumulating cells
utilization efficiency polyhydroxybutyrate formation of A. eutrophus.
Fac. Agric., Kyushu in PHB accumulation phase of autotrophic batch culture of Alcaligenes phosphate Phosphate consumption
Tanaka, Kenji; Ishizaki, Ayaaki; Univ., Fukuoka 812, Alcaligenes eutrophus ATCC17697T. J. Ferment. Bioeng., 74(5), 288-91 hydrogen metab (mg/g dry cell wt.) by PHB-
52 Stanbury, Peter F. Japan (English) 1992 1992 accumula
4.10 Literature on Polyhydroxyalkanoates.xls - page 72
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
PCT No.
PCT/GB94/01496 Sec.
371 Date Apr. 19, 1996
Sec. 102(e) Date Apr. 19,
1996 PCT Filed Jul. 11,
1994 PCT Pub. No.
WO95/02649 PCT Pub.
Date Jan. 26, 1995A
process of bonding two or
more articles together
using an adhesive
composition
58 KEMMISH DAVID JOHN (GB) ZENECA LTD (GB) Adhesion process US5711842 1998-01-27 1998 comprising at
Novel Alcaligenes
eutrophus strains are
provided which synthesize
PHA polymer more rapidly
than typical
members of
NAYLOR, Linda, Anne , Chemin du MONSANTO the species. Further
Margot 20, B-1380 Ohain, United COMPANY, 800 North ALCALIGENES EUTROPHUS provided are methods of
Kingdom Lindbergh Boulevard, STRAINS WHICH SYNTHESIZE producing PHA polymer
BRIGGS, Helen, Louise , 56 St. Louis, MO 63167, POLYMERS OF by cultivating said
Victoria Embankment, Darlington, Co. United States of HYDROXY ALKANOIC ACIDS Alcaligenes
66 Durham DL1 5JS, United Kingdom America WO9735025 1997-09-25 1997 eutro
The gram-negative
bacteria that are capable
of autotrophic growth by
Department of the use of molecular
Chemical Research, hydrogen as an energy
Hoffmann-La Roche source are currently
Inc., Nutley, New- assigned to the genus
Jersey 07110, and Pseudomonas,
Department of Alcaligenes, Paracoccus,
Zoology, Universiy of Corynebacterium, of
California, Berkely, Alcaligenes latus, a new species of hydrogen-utilizing Alcaligenes latus strain H-4 (= Aquaspirillum. In this
67 Palleroni, N.J.; Palleroni, A.V. California 94720 bacteria Int. J. systematic Bacteriol. 1978; 28:416-424 1978 ATCC 29712) report, the isolati Strain Isolation 176.
The mechanisms of
biodegradation of poly (DL-
lactide), poly (epsilon-
caprolactone), and
copolymers of epsilon-
caprolactone
with DL-dilactide, delta-
valerolactone, and DL-
epsilon-decalactone in
rabbit were shown to be
Aliphatic polyesters II. The degradation of poly (DL- qualitatively similar.
Pitt CG, Gratzl MM, Kimmel GL, Surles lactide), poly However,
68 J, Schindler A (epsilon-caprolactone), and their copolymers in vivo. Biomaterials 1981 Oct;2(4):215-20 1981 the ra
Tanio; T.; Fukui; T.; Shirakura; Y.;
Saito; T.; Tomita; K.; Kaiho; T.; An extracellular poly(3-hydroxybutyrate) depolymerase
69 Masamune; S. from Alcaligenes faecalis Eur.J.Biochem. 1982; 124:71-77 1982 233.
Shuto, H.; Fukui, T.; Saito, T.; An NAD-Linked Acetoacetyl-CoA Reductase from
70 Shirakura, Y.; Tomita, K. Zoogloea ramigera I-16-M Eur. J Biochem. 1981; 118:53-59 1981 402.
4.10 Literature on Polyhydroxyalkanoates.xls - page 76
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The biochemical
mechanisms of the
wastewater treatment
process known as
Advanced Wastewater enhanced biological
Management Centre, phosphorus removal
Departments of (EBPR)
Chemical Engineering are presently described in
and Microbiology, The Anaerobic phosphate release from activated sludge with a metabolic model. We
University of enhanced investigated details of the
Queensland, Brisbane, biological phosphorus removal. A possible mechanism of EBPR model to determine
4072, Australia. intracellular pH the nature of the
73 Bond PL, Keller J, Blackall LL control. Biotechnol Bioeng 1999 Jun 5;63(5):507-15 1999 anaerobic phosphat
Laboratory of
Molecular The polyhydroxyalkanoic
Biotechnology, acid (PHA) granule-
Division of Molecular assocd. 16-kDa protein
Cell, (GA16 protein) of
Graduate School of Paracoccus denitrificans
Bio- and Agro- was identified, and its
Sciences, Nagoya corresponding gene
University, was cloned and analyzed
Maehara, Akira; Ueda, Shunsaku; Nagoya, 464-8601, Analyses of a polyhydroxyalkanoic acid granule-associated at the mol. level. The
Nakano, Hideo; Yamane, Tsuneo Japan 16-kilodalton protein and its putative regulator in the pha J. Bacteriol. (1999), 181(9), 2914-2921 N-terminal amino acid
74 locus of Paracoccus denitrificans 1999 sequence of GA16 p
4.10 Literature on Polyhydroxyalkanoates.xls - page 77
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Laboratory of
Molecular
Biotechnology,
Division of Molecular
Cell Mechanisms, The polyhydroxyalkanoic
Department of acid (PHA) granule-
associated 16-kDa protein
Biological Mechanisms (GA16 protein) of
and Functions, Paracoccus
Graduate School of denitrificans was
Bio- and Agro- Analyses of a polyhydroxyalkanoic acid granule-associated identified, and its
Sciences, Nagoya 16-kilodalton corresponding gene was
protein and its putative regulator in the pha cloned and analyzed at
Maehara A, Ueda S, Nakano H, University, Chikusa-ku, locus of Paracoccus the
75 Yamane T Nagoya denitrificans. J Bacteriol 1999 May;181(9):2914-21 1999 molecular level. The N-
The postulated
posttranslational
modification of the
polyhydroxybutyrate
(PHA) synthase from
Ralstonia eutropha by
Institut fur 4-phosphopantetheine
Mikrobiologie der was investigated. Four
Westfalischen .beta.-alanine
Wilhelms-Universitat Analysis of 4-phosphopantetheinylation of auxotrophic Tn5-
Hoppensack, Astrid; Rehm, Bernd H. Munster, Munster, polyhydroxybutyrate synthase from Ralstonia eutropha: induced mutants of R.
A.; Steinbuchel, Alexander D-48149, Germany generation of .beta.-alanine auxotrophic Tn5 mutants and J. Bacteriol. (1999), 181(5), 1429-1435 eutropha HF39 were
76 cloning of the panD gene region 1999 isolated
The beta-ketothiolase
gene (phaA) and
acetoacetyl-CoA
reductase gene (phaB)
were isolated from
Paracoccus denitrificans.
Nucleotide sequence
analysis showed that they
Department of Applied Analysis of beta-ketothiolase and acetoacetyl-CoA encoded proteins of 391
Biological Sciences, reductase genes of a amino acids with a
Faculty of Agriculture, methylotrophic bacterium, Paracoccus denitrificans, and molecular mass of 40,744
Yabutani T, Maehara A, Ueda S, Nagoya University, their expression Da and
78 Yamane T Japan. in Escherichia coli. FEMS Microbiol Lett 1995 Nov 1;133(1-2):85-90 1995 of 242 amino
Compositions
providing increased
energy content of animal
PIONEER HI-BRED feed using plant crop
PEOPLES, Oliver, P. , 27 Radcliffe INTERNATIONAL, biomass which include a
Road, Arlington, MA 02174, United INC., 400 Locust
States of America Street, 800 Capital polyhydroxyalkanoate
SAUNDERS, Court , 13188 Square, Des Moines, have been developed. In
Pincrest Lane, Clive, IA 50325, United IA one embodiment, the
States of America 50309, compositions can be
NICHOLS, Scott , 6799 United States of ANIMAL NUTRITION prepared using
82 Ceres Circle, Johnston, IA America COMPOSITIONS WO9934687A1 July 15, 1999 1999
4.10 Literature on Polyhydroxyalkanoates.xls - page 79
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The poly-beta-
hydroxybutyrate (PHB)
biosynthesis genes
(phaCAB
genes) of Ralstonia
Univ.Vienna- eutropha that (organized
Inst.Microbiol.Genet. in a single operon)
LO Institute of were cloned in
Microbiology and Escherichia coli using
Genetics, University of Aqueous release and purification of poly(beta- vector plasmid pTZ18U-
Vienna, Dr. hydroxybutyrate) from Escherichia coli; Ralstonia eutropha PHB,
Resch S; Gruber K; Wanner G; Slater Bohrgasse 9, A- recombinant biodegradable thermoplastic preparation by leading to the
S; Dennis D; *Lubtiz W 1030 Vienna, Austria. vector plasmid pTZ18U-PHB-mediated phaCAB gene J.Biotechnol.; (1998) 65, 2-3, 173-82 formation of 50-80%
91 transfer and expression in Escherichia coli 1998 PHB/cell kopiert
The poly(beta-
hydroxybutyrate) (PHB)
biosynthetic genes of
Ralstonia eutropha that
are organized in a single
operon
(phaCAB) have been
cloned in Escherichia coli,
Institute of where the expression of
Microbiology and Aqueous release and purification of poly(beta- the genes in the wild-type
Resch S, Gruber K, Wanner G, Slater Genetics, University of hydroxybutyrate) from pha operon from plasmid
92 S, Dennis D, Lubitz W Vienna, Austria. Escherichia coli. J Biotechnol 1998 Oct 27;65(2-3):173-82 1998 pTZ18U-PHB leads
93 Bogensberger; B. Arbeitsbericht September 1984-März 1985 241.
4.10 Literature on Polyhydroxyalkanoates.xls - page 81
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A convenient
spectrophotometric assay
of bacterial poly-beta-
Department of hydroxybutyric acid has
Chemistry, Harvarrd been devised.
University, Cambridge, Quantitative conversion of
Massachusetts, and poly-beta-hydroxybutyric
Department of acid to crotonic acid by
Biological Sciences, heating in concentrated
Northwestern sulfuric acid and
University, Evanston, Bacillus megaterium KM - determination of the
95 J.H.Law; Slepecky, R.A. Ilinois Assay of poly-beta-hyroxybutyric acid J.Bacteriol. 1961; 82:33-36 1961 spectrophotometric assay ultraviolet abso Analytics 83.
Autotrophic mutants of
Hydrogenomonas
eutropha and H. facilis
requiring utilizable amino
acids were employed to
demonstrate the
Hydrogenomonas eutropha - simultaneous utilization of
Department of Biology, Ralstonia eutropha - Alcaligens H2 and an organic
The Catholic eutrophus - Hydrogenomonas substrate for growth. The
University of America, facilis - Hydrogen - ratio of the cell yields
Washington, D.C. Autotrophic and heterotrophic metabolism of Heterotrophic growth - under dual substrate
99 DeCicco, B.T.; Stukus, P.E. 20017 Hydrogenomonas Journal of Bacteriology 1968; 95:1469-1475 1968 Autotrophic growth - condition Strain - Metabolism 101.
Poly(3-hydroxybutyric
acid) and other structurally
related aliphatic
polyesters from bacteria,
referred to as
polyhydroxyalkanoic
Institut fur acids, form biodegradable
Mikrobiologie, thermoplastics and
Westfalische Wilhelms- elastomers that are
Universitat Munster, currently in use, or being
Germany. steinbu@uni- Bacterial and other biological systems for polyester considered for
103 Steinbuchel A, Fuchtenbusch B muenster.de production. Trends Biotechnol 1998 Oct;16(10):419-27 1998 use, in industry,
4.10 Literature on Polyhydroxyalkanoates.xls - page 83
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Experiments with a
number of bacteria
isolated from activated
sludge have shown that
flocculation is
independent of the
presence of poly-beta-
Laboratory of hydroxybutyrate (PHB) in
Microbiology, the cells. Several strains
Agricultural University, gave flocculent growth
Wageningen, The Bacterial flocculation and production of poly-beta- without any PHB
105 Deinema, M.H. Netherlands hydroxybutyrate Appl Microbiol 1972 Dec;24(6):857-8 1972 floccultation - activated sludge detectable. Other stra Others 110. Korr.
106 Tomita, K.; Saito, T.; Fukui, T. Bacterial metabolism of poly-beta-hydroxybutyrate Biochemistry of Metabolic Processes 1983 1983 195.
Bacterial polyesters containing branched poly(beta-
107 Fritzsche, K.; Lenz, R. W.; Fuller, R. C. hydroxyalkanoate) units Int. J. Biol. Macromol. 1990; 12:92-101 1990 350.
Department of
Chemical Engineering
and BioProcess Polyhydroxyalkanoates
Engineering Research (PHAs) are polyesters of
Center, Korea hydroxyalkanoates (HAs)
Advanced Institute of synthesized by numerous
Science and bacteria as intracellular
Technology, 373-1 carbon and energy
Kusong-dong, Yusong- storage compounds and
gu, Taejon 305-701, polyhydroxyalkanoate; poly(3- accumulated as granules
Korea. hydroxybutyrate); in the cytoplasm of cells.
email: Sang Yup Lee Biotechnology & Bioengineering biodegradable plastic; More than 80 HAs have
(leesy@sorak.kaist.ac. Volume 49, Issue 1, 1996. Pages: 1- biopolymer; fermentation been
108 Lee; S.Y. kr) Bacterial polyhydroxyalkanoates 14 1996 detected as co 602.
Bacterial production of poly(á-hydroxyalkanoates)
Ulmer; H.W.; Gross; R.A.; Posada; M.; containing unsaturated repeating units by Rhodospirillum
109 Weisbach; P.; Fuller; R.C.; Lenz; R.W. rubrum Macromolecules 1994; 27:1676-1679 1994 492.
Organ der (tm)sterreichischen Gesellschaft f r
110 Lukschanderl; , L Bakterien produzieren Kunststoff Natur und Umweltschutz 1983; 3:23 1983 248.
111 Kleiner; D. Bakterien und Ammonium Forum Mikrobiologie 1984; 7:13-19 1984 281.
An optically active
polymer, poly-beta-
hydroxybutyrate (PHB), is
produced in cytoplasm of
various vacteria. The
bending
piezoelectric effect was
observed in oriented films
Institute of Physical of PHB. The coefficient
and Chemical between the electrical
Research, Saitama, Bending piezoelectricity in a microbially produced polarization and the stress
115 Fukada E, Ando Y Japan. poly-beta-hydroxybutyrate. Biorheology 1988;25(1-2):297-302 1988 gradient
Beta-Ketothiolase from Hydrogenomonas eutropha H16
and its significance in the regulation of poly-beta-
116 Oeding; V.; Schlegel; G., H. hydroxybutyrate metabolism Biochem. J. 1973; 143:239-248 1973 630.
Binder-free delayed-
release granules for oral
or parenteral admin.
comprise an opt.
granulated drug coated
with 1-20 wt.%
poly-D(-)-3-
hydroxybutyric acid (PHB).
The PHB has a mol.wt. of
50,000-800,000, esp.
100,000-400,000. The
drug, esp.
118 Binder-free delayed-release pharmaceutical granules DE3871840 1992-07-16 1992 celiprolol.H
4.10 Literature on Polyhydroxyalkanoates.xls - page 85
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxyalkanoic acids
(PHA) represent a
complex class of storage
polyesters that are
synthesized
by a wide range of
Institut fur different gram-positive
Mikrobiologie, and gram-negative
Westfalische Wilhelms- bacteria as well as by
Universitat Munster, Biochemical and genetic analysis of PHA synthases and some
121 Rehm BH, Steinbuchel A Germany. other proteins required for PHA synthesis. Int J Biol Macromol 1999 Jun-Jul;25(1-3):3-19 1999 Archaea and that ar
Pseudomonas lemoignei
has five different
polyhydroxyalkanoate
(PHA) depolymerase
genes (phaZ1 to phaZ5),
which encode
the extracellularly
localized poly(3-
hydroxybutyrate) (PHB)
Institut fur depolymerases C, B, and
D.Jendrossek; Frisse, A.; A.Behrends; Mikrobiologie, Georg- Biochemical and molecular characterisation of D, poly(3-hydroxyvalerate)
Andermann, M.; Kratzin, H.D.; August-Universitat zu Pseudomonas lemoignei polyhydroxyalkanoate (PHV)
122 T.Stanislawsky; H.G.Schlegel Gottingen, Germany. depolymerase system J Bacteriol 1995 Feb;177(3):596-607 1995 depolymerase, and PH 529.
4.10 Literature on Polyhydroxyalkanoates.xls - page 86
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Comamonas acidovorans
YM1609 secreted a
polyhydroxybutyrate
(PHB)
Department of depolymerase into the
Bioengineering, Tokyo culture supernatant when
Institute of it was cultivated on
Technology, poly(3-
Kasuya, Ken-Ichi; Inoue, Yoshio; Faculty of hydroxybutyrate) [P(3HB)]
Tanaka, Takao; Akehata, Takeshi; Bioscience and or poly(3-hydroxybutyrate-
Iwata, Tadahisa; Fukui, Toshiaki; Biotechnology, Biochemical and molecular characterization of the co-3-
Doi, Yoshiharu Kanagawa, 227, Japan polyhydroxybutyrate depolymerase of Comamonas Appl. Environ. Microbiol. (1997), 63(12), 4844- hydroxyvalerate)
123 acidovorans YM1609, isolated from freshwater 4852 1997 [P(3HB-co-3HV)] as the s
Comamonas acidovorans
YM1609, a freshwater
isolate from Lake Biwa,
Polymer Chemistry secreted a
Laboratory, Institute of polyhydroxybutyrate-
Physical and Chemical depolymerase into the
Research (RIKEN), culture
2-1 Hirosawa, Wako- supernatant when
shi, Saitama 351-01, grown on poly-beta-
Japan. Biochemical and molecular characterization of the hydroxybutyrate (P3HB) or
Email: polyhydroxybutyrate-depolymerase of Comamonas a
Kasuya K; Inoue Y; Tanaka T; Akehata ydoi@postman.riken.g acidovorans YM1609, isolated from fresh water; enzyme poly-beta-
T; Iwata T; Fukui T; *Doi Y o.jp purification and gene cloning in Escherichia coli, for poly- Appl.Environ.Microbiol.; (1997) 63, 12, 4844-52 hydroxybutyrate and poly-
124 beta-hydroxybutyrate degradation 1997 beta-hydro
Wheat starch granules
and poly-(beta-
hydroxybutyrate-co-beta-
hydroxyvalerate) [P(HB-co-
HV), (19.1 mol% HV)]
were
blended at 160 degrees C.
Increasing the starch
Departement de Genie content from 0 to 50%
Chimique, Ecole (wt/wt) decreased the
Polytechnique de Biodegradability and mechanical properties of tensile strength of
Ramsay BA, Langlade V, Carreau PJ, Montreal, Quebec, poly-(beta-hydroxybutyrate-co-beta-hydroxyvalerate)- P(HB-co-HV) from 18 MPa
125 Ramsay JA Canada. starch blends. Appl Environ Microbiol 1993 Apr;59(4):1242-6 1993 to 8 M
Biodegradability of blends of poly(3-hydroxybutyrate-co-3-
Gilmore; D.F.; Fuller; R.C.; Schneider; hydroxyvalerate) with cellulose acetate esters in activated Journal of Environmental Polymer Degradation
126 B.; Lenz; R.W.; Lotti; N.; Scandola; M. sludge. 1994; 2:49-57 1994 564.
Biodegradability of polymers in the environment:
complexities and significance of definitions and
127 Swift; G. measurements FEMS Microbiology Reviews 1992; 103:339-346 1992 482.
A biodegradable and
hydrodegradable diblock
copolymer includes a
naturally-occurring
poly(.beta.-alkanoate)
component and
a chemically synthesized
polyester component
formed by ring-opening
Gross; Richard A. (Chelmsford, MA); polymerization. A method
McCarthy; Stephen P. (Tyngsboro, MA); University of of forming the
Reeve; Michael S. Massachusetts Lowell Biodegradable and hydrodegradable diblock copolymers biodegradable
130 (Lowell, MA). (Lowell, MA). composed of poly(.beta . US5439985 Aug. 8, 1995 1995 and hydrode
The present
invention relates to
biodegradable PHA
copolymers
comprising at
least two randomly
repeating monomer units.
The
present
The Procter & Gamble invention further relates to
Company, Cincinnati, a plastic article comprising
131 Noda; Isao OH Biodegradable copolymers USRE036548 Feb. 1, 2000 2000 a
Blends of poly(3-
hydroxybutyrate)-poly(3-
hydroxyvalerate) (PHB-
Research Institute of HV)
Material Science and and polyalcs. have
Technology (INTEMA), been prepd. by solvent
Engineering casting. The polyalcs.
Faculty, Mar del Plata used were castor oil
University, Mar del (CO) and polypropylene
Plata, 7600, Biodegradable films from PHB-8HV copolymers and glycol (PPG400 and
Cyras, V. P.; Fernandez, N. Galego; Argent. polyalcohols blends: crystallinity, dynamic mechanical Polym. Int. (1999), 48(8), 705-712 PPG1000). Thermal
141 Vazquez, A. analysis and tensile properties 1999 behavior, crystallinity,
4.10 Literature on Polyhydroxyalkanoates.xls - page 91
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1Research Institute of
Material Science and
Technology (INTEMA),
Mar del Plata Blends of poly(3-
University, hydroxybutyrate)-poly(3-
Engineering Faculty, J. hydroxyvalerate) (PHB-
B. HV) and polyalcohols
Justo 4302, (7600) have been prepared by
Mar del Plata, solvent
Argentina casting. The polyalcohols
2Laboratory of used were castor oil (CO)
Polymers, Materials blends; polyhydroxyalcanoates; and polypropylene glycol
and Reagents Biodegradable films from PHB-8HV copolymers and castor oil; polypropylene glycol; (PPG400 and PPG1000).
Institute, Havana polyalcohols blends: dynamic mechanical analysis; Thermal
V P Cyras 1, N Galego Fernández 2, A University, Havana crystallinity, dynamic mechanical analysis and tensile Polymer International Volume 48, Issue 8, 1999. miscibility; membrane behaviour, crystallinity,
142 Vázquez 1 * City 1 properties Pages: 705-712 1999 morp
Biodegradable poly(3-hydroxybutyrate-co-4-
hydroxybutyrate) produced from gamma-butyrolactone and
149 Doi; Y.; Segawa; A.; Kunioka; M. butyric acid by Alcaligenes eutrophus Polymer communications 1989; 30:169-171 1989 437.
Cyclic oligo(3-
hydroxybutyrate), oligo(3-
HB), was synthesized and
purified, resulting in
oligolides that contained
three to seven
(R)-3-hydroxybutyrate
units (triolides up to
heptolides). In addition,
Brandl H, Aeberli B, Bachofen R, Universitat Zurich, linear 3-HB octamers
Schwegler I, Muller HM, Burger MH, Institut fur obtained as either tert-
Hoffmann T, Lengweiler UD, Seebach Pflanzenbiologie, Biodegradation of cyclic and substituted linear oligomers of butyl or
154 D Switzerland. poly(3-hydroxybutyrate). Can J Microbiol 1995;41 Suppl 1:180-6 1995
Biodegradation of Microbial Copolyesters: Poly(3-HB-co-3-
155 Doi, Y.; Kanesawa, Y.; Kunioka, M. HV) and Poly(3-HB-co-4-HB) Macromolecules 1990; 23:26-31 1990 356.
4.10 Literature on Polyhydroxyalkanoates.xls - page 94
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The biodegradability of
soln.-cast films of poly(D-(-
)-3-hydroxybutyrate)
(I) blended with the melt-
compatible component
atactic
polyepichlorohydrin (II)
biodegrdn polyhydroxybutyrate was investigated. A
Stn. Sper. Cell. Carta polyepichlorohydrin blend bacterium which produced
Sadocco, Patrizia; Bulli, Chiara; Elegir, Fibre Tess. Veg. Artif., Biodegradation of poly(D(-)-3-hydroxybutyrate)/atactic Aureobacterium saperdae extracellular enzymes that
Graziano; Seves, Alberto; Milan polyepichlorohydrin blends by Aureobacterium saperdae. Makromol. Chem., 194(10), 2675-86 (English) biodegrdn polyhydroxybutyrate degraded I even when
158 Martuscelli, Ezio 20133, Italy 1993 1993 polyepichlorohydrin blended
Urmeneta; J.; Mas-Castella; J.; Biodegradation of poly-beta-hydroxyalkanoates in a lake Applied and Environmental Microbiology 1995;
159 Guerrero; R. sediment sample increases bacterial sulfate reduction 61:2046-2048 1995 514.
Degradation of poly(3-
hydroxybutyrate) and
copolymers with 3-
hydroxyvaleric acid was
investigated in natural
environments,
and the microorganisms
Laboratorium voor involved were isolated and
Microbiologie, identified. The influence of
Universiteit Gent, abiotic and biotic factors
Mergaert J, Anderson C, Wouters A, Belgium. on the degradation is
160 Swings J, Kersters K Biodegradation of polyhydroxyalkanoates. FEMS Microbiol Rev 1992 Dec;9(2-4):317-21 1992 disc
4.10 Literature on Polyhydroxyalkanoates.xls - page 95
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Biodegradable polyesters
such as biol. produced
poly[(R)-3-
hydroxybutyric acid],
(PHB) other
polyhydroxyalkanoic
acids and related
Institut Mikrobiologie chemosynthetic polyesters
Genetik, Georg-August- have attracted
Universitaet, Biological basis of enzyme-catalyzed polyester industrial interest, and
Briese, Bernd Holger; Jendrossek, Goettingen, D- degradation. 59-C-terminal amino acids of poly(3- bacterial produced PHB is
Dieter 37077, Germany hydroxybutyrate) (PHB) depolymerase A from Macromol. Symp. (1998), 130, 205-216 com. available
166 Pseudomonas lemoignei are sufficient for PHB binding 1998
4.10 Literature on Polyhydroxyalkanoates.xls - page 96
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Short-chain complexed
poly-beta-hydroxybutyrate,
130-170 monomer units, is
a ubiquitous constituent of
cells, wherein it is
usually associated with
other macromolecules by
Department of multiple coordinate bonds,
Microbiology, Michigan or by hydrogen bonding
State University, East and hydrophobic
167 Reusch RN Lansing 48824. Biological complexes of poly-beta-hydroxybutyrate. FEMS Microbiol Rev 1992 Dec;9(2-4):119-29 1992 interactions. Thi 470.
The halobacterium H.
mediterranei is an
organism of biotechnol.
potential due to its
capacity as polymer
producer. This
microorganism
accumulates poly-b-
Dep. Genet. Mol. poly beta hydroxybutyrate hydroxybutyrate (PHB) as
Rodriguez-Valera, F.; Garcia Lillo, J. A.; Microbiol., Univ. NATO ASI Ser., Ser. A, 201(Gen. Appl. Aspects prodn Haloferax intracellular granules in
Anton, Josefa; Meseguer, Alicante, Alicante, Biopolymer production by Haloferax mediterranei. Halophilic biopolymer prodn Haloferax very large amts. PHB is
174 Inmaculada Spain Microorg.), 373-80 (English) 1991 1991 an interesting biopolymer
175 Braunegg, G. Biopolymers - Poly(beta-Hydroxyalkanoates) ??? 399.
4.10 Literature on Polyhydroxyalkanoates.xls - page 97
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Most
polyhydroxyalkanoates
(PHAs) reported to date
fall into one of two broad
classes: either
hydroxybutyrate-
hydroxyvalerate
copolymers (typified by
the PHA produced by
Department of Alcaligenes eutrophus), or
Chemical Engineering, Biosynthesis and characterization of hydroxybutyrate- hydroxyoctanoate-rich
Princeton University, hydroxycaproate heteropolymers (typified
181 Caballero KP, Karel SF, Register RA NJ 08544, USA. copolymers. Int J Biol Macromol 1995 Apr;17(2):86-92 1995 by the PHA
Copolyesters of 3-
hydroxybutyrate (3HB)
and 3-hydroxyvalerate
(3HV) were produced by
Burkholderia cepacia D1
at 30
degrees C in nitrogen-free
Department of culture solutions
Biological and containing n-butyric acid
Chemical Engineering, Biosynthesis and characterization of and/or n-valeric acid.
Faculty of Engineering, poly(3-hydroxybutyrate-co-3-hydroxyvalerate) produced by When n-valeric acid was
Gunma University, Burkholderia used as the
182 Mitomo H, Takahashi T, Ito H, Saito T Kiryu, Japan. cepacia D1. Int J Biol Macromol 1999 May;24(4):311-8 1999 sole carbo
4.10 Literature on Polyhydroxyalkanoates.xls - page 98
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Copolyesters of 3-
hydroxybutyrate (3HB)
and 4-hydroxybutyrate
(4HB) were produced by
Alcaligenes eutrophus at
30
degrees C in nitrogen-free
Research Laboratory culture solutions
of Resources containing gamma-
Utilization, Tokyo butyrolactone alone or
Institute of Biosynthesis and characterization of with fructose or butyric
Technology, poly(3-hydroxybutyrate-co-4-hydroxybutyrate) in acid as the
183 Doi Y, Segawa A, Kunioka M Yokohama, Japan. Alcaligenes eutrophus. Int J Biol Macromol 1990 Apr;12(2):106-11 1990 carbon sources. When
Alcaligenes eutrophus
H16 was grown on
mixtures of 1H- and 2H-
acetate as carbon
sources. The
accumulation of
deuterated
poly(3-hydroxybutyrate)
(P(3HB)) was observed.
Department of The deuterium
Biomolecular distributions in the
Engineering, Tokyo Biosynthesis and n.m.r. studies of deuterated poly(3- isolated P(3HB)s were
Yoshie N, Goto Y, Sakurai M, Inoue Y, Institute of hydroxybutyrate) determined from
185 Chujo R, Doi Y Technology, Japan. produced by Alcaligenes eutrophus H16. Int J Biol Macromol 1992 Apr;14(2):81-6 1992 1H and 2H-n.m.r
Biosynthesis and production of poly-D-(-)-3-
186 Braunegg, G. hydroxybutyrate (PHB) 287.
4.10 Literature on Polyhydroxyalkanoates.xls - page 99
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
(1) Department of
Chemical Technology,
College of Pseudomonas sp. A33
Engineering, Seoul and other isolates of
National University, Polyhydroxyalkanoates 3- aerobic bacteria
Seoul hydroxybutyrate · medium- accumulated a complex
151-742, Korea chain-length copolyester
(2) 3- containing 3-
Institut für hydroxyalkanoates · 1 · 3- hydroxybutyric acid (3HB)
Mikrobiologie der butanediol · Pseudomonas sp. and various medium-chain-
Georg-August- Biosynthesis of copolyesters consisting of 3-hydroxybutyric A33 · polyhydroxyalkanoate length
E. Y. Lee (1), D. Jendrossek (2), A. Universität Göttingen, acid and medium-chain-length 3-hydroxyalkanoic acids Applied Microbiology and Biotechnology Abstract synthase · 3-
Schirmer (2), C. Y. Choi (1), A. Grisebachstrasse 8, from 1,3-butanediol or from 3-hydroxybutyrate by Volume 42 Issue 6 (1995) pp 901-909 polyhydroxyalkanoate hydroxyalkanoic acids
189 Steinbüchel (3) Pseudomonas sp. A33 1995 depolymerase · biodegradable (3HAMCL) from 3-hyd 500.
Doi; Y.; Kunioka; M.; Nakamura; Y.; Biosynthesis of copolyesters in Alcaligenes eutrophus H16
190 Soga; K. from 13C-labeled acetate and propionate Macromolecules 1987; 20:2988-2991 1987 324.
Biosynthesis of methyl-branched poly(beta-
191 Hazer; B.; Lenz; R.W.; Fuller; R.C. hydroxyalkanoate)s by Pseudomonas oleovorans Macromolecules 1994; 27:45-49 1994 491.
A series of copolyesters of
3-hydroxybutyrate (3HB)
and 3-hydroxyvalerate
(3HV) was biosynthesized
Department of by Alcaligenes
Biomolecular eutrophus from an amino
Engineering, Tokyo acid, threonine. The 3HV
Institute of content of these
Nakamura K, Goto Y, Yoshie N, Inoue Technology, Japan. polyesters ranged from
194 Y, Chujo R Biosynthesis of poly(3-hydroxyalkanoates) from threonine. Int J Biol Macromol 1992 Apr;14(2):117-8 1992 less than 0.1% to 30%.
(1) Division of
Bioengineering, The
National University of The copolyester of 3-
Yokahama, Hodogaya, hydroxybutyrate and 3-
Kanagawa hydroxyvalerate was
240, synthesized from
Japan. Fax: +81 45 the
331 1704 combined carbon sources
(2) of glucose and sodium
Department of propionate by a
Bioscience, Nishi- filamentaion-defective
M. Takeda (1), H. Matsuoka (2), H. Ban Tokyo University, mutant of
(2), Y. Ohashi (2), M. Hikuma (2), J.-i. Uenohara, Yamanashi Biosynthesis of poly(3-hydroxybutyrate-Co-3- Applied Microbiology and Biotechnology Abstract Sphaerotilus natans,
197 Koizumi (1) 409-01, Japa hydroxyvalerate) by a mutant of Sphaerotilus natans Volume 44 Issue 1/2 (1995) pp 37-42 1995 which i 502.
Biosynthesis of poly(3-hydroxybutyrate-co-3-
hydroxyvalerate) by newly isolated Agrobacterium sp. SH-1
and GW-014 from structurally unrelated single carbon Journal of Fermentation and Bioengineering
198 Lee; E.; Kang; S.H.; Choi; C.Y. substrates 1995; 79:328-334 1995 505.
Keywords: Alcaligenes
eutrophus
Institut fur ; The aim of this study was
Mikrobiologie der Escherichia coli the production of the
Westfalischen ; homopolyester poly(4-
Wilhelms-Universitat Clostridium kluyveri hydroxybutyric acid)
Munster, Germany. ; Biodegradable polyester; (poly(4HB))
* Corresponding Polyhydroxyalkanoic acid; with recombinant strains
author. Tel.: +49 (251) Poly(4-hydrox- of Escherichia coli. Wild-
83-39821; Fax: +49 ybutyric acid); 4-Hydroxybutyric type strains and other
(251) 83-38388; E- Biosynthesis of poly(4-hydroxybutyric acid) by recombinant acid metabolism; PHA widely used
Hein S, Sohling B, Gottschalk G, mail: steinbu@uni- strains of synthase; 4-Hydroxybutyric non-
199 Steinbuchel A muenster.de Escherichia coli. FEMS Microbiol Lett 1997 Aug 15;153(2):411-8 1997 acid-CoA transferase recombinant strai ganze Artikel
Biosynthesis of poly-(R)-3-hydroxyalkanoate: an emulsion Journal of Environmental Polymer Degradation
200 Koning, de; F.J.M.; Maxwell; I.A. polymerization 1993; 1:223-226 1993 581.
Poly-3-hydroxybutyrate
(PHB), a biopolymer of
important commercial
applications, is found in a
wide range of Gram-
negative
and Gram-positive
bacteria and
cyanobacteria. The
Department of Biosynthesis of poly-3-hydroxybutyrate in the luminescent present study has resulted
Biochemistry, McGill bacterium, in the identification of PHB
University, Montreal, Vibrio harveyi, and regulation by the lux autoinducer, in the luminescent
201 Sun W, Cao JG, Teng K, Meighen EA Quebec, Canada. N-(3-hydroxybutanoyl)homoserine lactone. J Biol Chem 1994 Aug 12;269(32):20785-90 1994 marine
Bertrand, J.-L.; Ramsay, B. A.; Ramsay, Biosynthesis of Poly-beta-Hydroxyalkanoates from
202 J. A.; Chavarie, C. Pentoses by Pseudomonas pseudoflava Appl. Env. Microbiol. 1990; 56:3133-3138 1990 355.
4.10 Literature on Polyhydroxyalkanoates.xls - page 102
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Synthesis and
accumulation of poly-b-
hydroxyalkanoate (PHA)
in
Bacillus thuringiensis R-
510 isolated from soil
were investigated. This
organism was resistant to
Department of poly beta hydroxyalkanoate relatively high concn. of
Microbiology, Biosynthesis of poly-b-hydroxyalkanoates by Bacillus manuf Bacillus propionate and had
Lee, Kang Tae; Kim, Jeong Yoon; Chungnam National thuringiensis beta hydroxyalkanoate polymer the capability of
Rhee, Young Ha; Bae, Kyung Sook; University, Daejeon R-510. J. Microbiol. (Seoul), 33(1), manuf Bacillus accumulating copolymers
203 Kim, Young Baek 305-764, S. Korea 59-65 (English) 1995 1995 consis
Biosynthesis of poly-b-hydroxybutyric acid (PHB) by
Alcaligenes
eutrophus H16 (NCIB 11599): an experimental study to
enhance
the synthesis rate of poly-b-hydroxybutyric acid by 302 pp. Avail. Univ.
Alcaligenes Microfilms Int., Order No. BRD-93846 From: polyhydroxybutyrate fermn
Univ. Bradford, eutrophus H16 (NCIB 11599) using ammonium Diss. Abstr. Int. B 1992, Alcaligenes
204 Bitar, Ahed Bradford, UK chloride-supplemented e 52(7), 3749 (English) 1990 1990 Abstract unavailable.
Recombinant strains of
Ralstonia eutropha PHB-
4, which harbored
Aeromonas caviae
Faculty of Engineering, polyhydroxyalkanoates
Department of Applied (PHA) biosynthesis genes
Chemistry, Toyo under the control of a
Kichise, Tomoyasu; Fukui, Toshiaki; University, promoter for R. eutropha
Yoshida, Yasuhiko; Doi, Kawagoe-shi, Saitama, Biosynthesis of polyhydroxyalkanoates (PHA) by phb operon, were
Yoshiharu Japan recombinant Ralstonia eutropha and effects of PHA Int. J. Biol. Macromol. (1999), 25(1-3), 69-77 examd. for PHA prodn.
206 synthase activity on in vivo PHA biosynthesis 1999 from various alkanoic aci
4.10 Literature on Polyhydroxyalkanoates.xls - page 103
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Recombinant strains of
Ralstonia eutropha PHB 4,
which harbored
Aeromonas caviae
polyhydroxyalkanoates
(PHA) biosynthesis genes
Department of Applied Biosynthesis of polyhydroxyalkanoates (PHA) by under the control of a
Chemistry, Faculty of recombinant Ralstonia promoter for R.
Engineering, Toyo eutropha and effects of PHA synthase eutropha
University, Saitama, activity on in vivo PHA phb operon, were
207 Kichise T, Fukui T, Yoshida Y, Doi Y Japan. biosynthesis. Int J Biol Macromol 1999 Jun-Jul;25(1-3):69-77 1999 examined for PHA
Institut für
Mikrobiologie der
Westfälischen A screening identified
Wilhelms-Universität several bacteria that were
Münster, able to use chemically
Corrensstraße 3, D- heterogeneous low-rank
48149 coal
liquefaction products as
Münster, Germany e- complex carbon sources
mail: steinbu@uni- Biosynthesis of polyhydroxyalkanoates from low-rank coal for growth. Pseudomonas
muenster.de Tel.: +49- liquefaction products by Pseudomonas oleovorans and
251-8339821 Fax: +49- oleovorans and Applied Microbiology and Biotechnology Abstract
208 Fuchtenbusch B, Steinbuchel A 251-8338388 Rhodococcus ruber Volume 52 Issue 1 (1999) pp 91-95 1999 Rhodococcus ruber a
Poly-beta-hydroxybutyrate
(PHB) is a widely found
intracellular energy and
carbon reserve polymer in
procaryotic organisms. It
has also been found in
yeast. The biosynthetic
Alcaligenes eutrophus - pathway and regulatory
Lafferty; R.M.; Heinzle; E.; Institute for Ralstonia eutropha - continous mechanisms involved in
Jungschaffer; G.; Sonnleitner; B.; Biotechnology TU Biosynthesis, Extraction and Characterization of Poly-beta- Vienna Symposium of the Federation of culture - extracttion - the synthesis and Strain - Fermentation
213 srienc; F. Graz, Austia hydroxybutyrate in microbial Biomass European Microbiological Societies 1977 chemolithoautotrophic growth reutilization of - Extraction - Kinetics 56.
polyhydroxyalkanoate
poly(hydroxyalkanoate)
Branched poly(hydroxyalkanoate) (PHA) and a salt of a
Board of Trustees polymer salt electrolytic compositions and conductive metal are
Reusch; Rosetta N. , of Okemos, MI operating Michigan method of described.
Reusch; William H. , of State University, East preparation The PHA is a
220 Okemos, MI Lansing, MI USRE035257 May 28, 1996 1996 biodegrada
4.10 Literature on Polyhydroxyalkanoates.xls - page 106
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Compositions and
method for providing a
solid conductive
electrolyte composition
containing a
polyhydroxyalkanoate
(PHA) and
a salt of a conductive
metal are described. The
PHA is biodegradable and
Branched polyhydroxyalkanoate polymer salt electrolytic biocompatible and
REUSCH ROSETTA N (US); REUSCH compositions and method provides a basis for
221 WILLIAM H (US) UNIV MICHIGAN (US) of preparation US5266422 1993-11-30 1993 batteries whi
polyhydroxybutyrate degrdn
Majid, M.; Pouton, C.W.; Notarianni, Catalytic degradation of poly-D(-)-3-hydroxybutyrate (PHB) J. Pharm. hydroxybutyrate polymer
226 L.J. USA in non-aqueous solution Pharmacol., 39(Suppl.), 34P (English) 1987 1987 degrdn 294.
Synthesis of acidic
exopolysaccharides,
neutral dellular
polysaccharides and poly-
beta-hydroxybutyric acid
(PHB) by Rhizobium is
storngly dependent on
cultural conditions and the
strain s used.
Exopolysaccharide
Cellular glycogen, beta-1,2-glucan, poly-beta- production by R.
hydroxybutyric acid and extracellular polysaccharides in leguminosarum, R.
227 Zevenhuizen, L.P.T.M. fast growing species of Rhizobium Antonie van Leeuwenhoek 1981; 47:418-497 1981 PHaseoli 183.
Under growth-limiting
conditions or conditions
which mediate genetic
transformation,
Escherichia coli and
Azotobacter
vinelandii incorporate poly-
Cellular incorporation of poly-beta-hydroxybutyrate into beta-hydroxybutyrate into
plasma their plasma membranes.
membranes of Escherichia coli and Azotobacter vinelandii Genetic transformation
Reusch R, Hiske T, Sadoff H, Harris R, alters native competence of both
228 Beveridge T membrane structure. Can J Microbiol 1987 May;33(5):435-44 1987 bacteria increase
Cellular lipids of a Nocardia grown on propane and n-
229 Davis; J.B. butane Applied Microbiology 1964; 12(4):301-304 1964 310.
We have identified a
range of compounds
which, when present
during poly(3-
hydroxybutyrate)
[P(3HB)]
accumulation by Ralstonia
eutropha (reclassified
Department of Chain termination in polyhydroxyalkanoate synthesis: chain transfer in poly(3- from Alcaligenes
Biological Sciences, involvement of hydroxybutyrate) synthesis - eutrophus), can act
Madden LA, Anderson AJ, Shah DT, The University of Hull, exogenous hydroxy-compounds as chain Ralstonia eutropha as chain
230 Asrar J UK. transfer agents. Int J Biol Macromol 1999 Jun-Jul;25(1-3):43-53 1999 (Alcaligenes eutrophus) transfer agent kopiert
Alcaligenes eutrophus
transformants AER3,
AER4 and AER5
harboring
cloned phbCAB,
phbAB and phbC genes
Department of Genetic (from A. eutrophus
Engineering, College encoding
of Natural Sciences, acetyl-CoA-
Kyungpook acetyltransferase (EC-
National University, Characteristics of cell growth and poly-beta- 2.3.1.16), aceto-acetyl-
Taegu 702-701, South hydroxybutyrate biosynthesis of Alcaligenes eutrophus CoA-
Park J S; Huh T L; *Lee Y H Korea. transformants harboring cloned phb CAB genes; polymer Enzyme Microb.Technol.; (1997) 21, 2, 85-90 reductase and poly-
233 production by fermentation 1997 hydroxybutyrate-synthase)
A pronase-sensitive, 14
kDa component of
bacteroids of
Bradyrhizobium japonicum
I-110ARS was identified
and characterized
using monoclonal
antibodies. This
component was weakly
synthesized
Characterization of a 14 kDa component with low or was missing in
Sikora, Lawrence J.; Kuykendall, David; United State Dep. of expression in a Bradyrhizobium PHB limiting bacteroids of a unique
Dwivedi, Radhey S.; Herman, Agriculture, Beltsville, unique Nod+ Fix- Bradyrhizobium japonicum. Microbiology (Reading, U. K.), 140(10), membrane protein Nod+ Fix- mutant,
237 Eliot M.; Enkiri, Nancy K. MD 20705-2350, USA 2761-7 (English) 1994 1994 ARS252
A bacterium, JS02,
capable of degrading an
aromatic medium-chain-
Department of length
Agricultural Chemistry, polyhydroxyalkanoate
Sunchon National (PHAMCL),
University, Sunchon poly(3-hydroxy-5-
540-742, Korea e-mail: phenylvalerate) (PHPV),
was isolated from
hoon@sunchon.sunch Characterization of an extracellular wastewater-treatment
on.ac.kr Tel.: +82-661- poly(3-hydroxy-5-phenylvalerate) Applied Microbiology and Biotechnology Abstract sludge (Ju
7503294 Fax: +82-661- depolymerase from Volume 53 Issue 3 (2000) pp 323-327 et al.
239 H. Kim, H.-S. Ju, J. Kim 7528011 Xanthomonas sp. JS02 2000 1998),
Characterization of intracellular accumulation of poly-beta-
hydroxybutyrate (PHB) in individual cells of Alcaligenes Biotechnology and Bioengineering Symp. 1984;
240 Srienc; F.; Arnold; B.; Bailey; J.E. eutrophus H16 by flow cytometry 26:982-987 1984 232.
4.10 Literature on Polyhydroxyalkanoates.xls - page 110
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The growth of
Pseudomonas oleovorans
on n-octane was
characterized by the
formation of
intracellular
structures. These
Department of inclusions were isolated
Chemistry, Universiy of Pseudomonas oleovorans - n- and characterized.
Groningen, 9747 AG Characterization of intracellular inclusions formed by octane - poly-beta- Morphologically, they
de Smet MJ, Eggink G, Witholt B, Groningen, The Pseudomonas hydroxyoctanoate - resembled
241 Kingma J, Wynberg H Netherlands oleovorans during growth on octane. J Bacteriol 1983 May;154(2):870-8 1983 characterization the poly-beta- Strain kopiert
Characterization of Intracytoplasmic Hydrocarbon
Inclusions from the Hydrocarbon-Oxidizing Acetinobacter
242 Scott, C. C. L.; Finnerty, W. R. Species HO1-N J Bacteriol. 1976; 127:481-489 1976 374.
Poly-beta-hydroxybutyrate
(PHB) from different
bacterial genera was
Department of studied with regard to its
Bacteriology and crystal structure, infrared
Botany, Biological absorption, intrinsic
Research characterization of PHB - X-ray viscosity, and electron
Laboratories, and diffractometry - crystal microscopy. All PHB
College of Forestry at morphology of PHB - samples precipitated from
Lundgren, D.G.; Alper, R.; Schnaitman, Syracuse University, Characterization of poly-beta-hydroxybutyrate extracted viscosimetry - molecular dilute chloroform solution
243 C.; Marchessault, R.H. Syracuse, New York from different bacteria J. Bacteriol. 1965; 89:245-251 1965 weights gave identica Morphology 80.
The poly(3-
hydroxybutyrate) (PHB)
depolymerase structural
gene of Comamonas sp.
(phaZCsp) was cloned in
Escherichia
Institut fur coli and identified by halo
Mikrobiologie der formation on PHB-
Georg-August- Characterization of the extracellular poly(3- containing solid medium.
Universitat Gottingen, hydroxybutyrate) The nucleotide sequence
Jendrossek D, Backhaus M, Germany. depolymerase of Comamonas sp. and of its structural of a 1719 base pair MboI
244 Andermann M gene. Can J Microbiol 1995;41 Suppl 1:160-9 1995 fragment was determi
Characterization of the Protoplasmic Constituents of
245 Weibull, C. Bacillus megaterium J Bacteriol. 1953; 66:696-702 1953 367.
Poly(3-hydroxybutyrate)
[P(3HB)] and its
copolymers with
hydroxyalkanoates are
Department of naturally occurring
Biomolecular thermoplastic materials
Engineering, Tokyo produced by bacteria.
Institute of There are many potential
Technology, uses for these
Yokohama, Japan. copolyesters owing to
nyoshie@bio.titech.ac. Chemical composition distribution of bacterial Int J Biol Macromol 1999 Jun-Jul;25(1-3):193- their biodegradability and
247 Yoshie N, Inoue Y jp copolyesters. 200 1999 biocompatibility. The
Department of
Chemical Engineering
and BioProcess A novel and efficient
Engineering Research method for the production
Center, Korea of enantiomerically pure
Advanced Institute of (R)-(-)-hydroxycarboxylic
Science and acids by in vivo
Technology, 373-1 chirality; chiral compound; depolymerization of
Kusong-dong, Yusong- polyester; (R)-(-)- microbial polyester
gu, Taejon 305-701, hydroxycarboxylic acid; polyhydroxyalkanoates
Korea email: Sang Yup polyhydroxyalkanoate (PHA); in (PHAs) was developed.
Lee Chiral compounds from bacterial polyesters: Sugars to Biotechnology & Bioengineering vivo Using this method, several
(leesy@sorak.kaist.ac. plastics to fine Volume 65, Issue 3, 1999. Pages: 363- depolymerization; Alcaligenes model
250 Lee SY, Lee Y, Wang F kr) chemicals 368 1999 latus compounds, (R)-(-)-3 Copolyesters kopiert
Marchessault, R. H.; Monasterios, C. J.; Chiral poly(beta-hydroxyalkanoates): an adaptable helix
251 Morin, F. G. influenced by the alkane side-chain Int. J. Biol. Macromol. 1990; 12:158-165 1990 346.
4.10 Literature on Polyhydroxyalkanoates.xls - page 112
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The polyhydroxyalkanoic
acid (PHA) synthase gene
(phaCAc) of a species of
Acinetobacter isolated
from an activated sludge
treatment plant was
Department of Cloning and analysis of the polyhydroxyalkanoic acid cloned by heterologous
Microbiology, Monash synthase gene from complementation in a poly-
University, Clayton, an Acinetobacter sp.: evidence that the gene is both beta-hydroxybutyrate
Victoria, Australia. plasmid and FEMS Microbiol Lett 1994 May 1;118(1-2):145- (PHB) negative mutant of
254 Schembri MA, Bayly RC, Davies JK chromosomally located. 52 1994 Alcaligenes eutrop
The extracellular
polyhydroxybutyrate
(PHB) depolymerase gene
(phaZPst) of
Pseudomonas stutzeri
was cloned and
sequenced.
Graduate School of PhaZPst was
Science and composed of 1728 bp
Engineering, Saitama encoding a protein of 576
University, amino
Urawa, 338-8570, Cloning and characterization of the polyhydroxybutyrate acids. Analyses of the
Ohura, Takeshi; Kasuya, Ken-Ichi; Doi, Japan depolymerase gene of Pseudomonas stutzeri and analysis Appl. Environ. Microbiol. (1999), 65(1), 189-197 N-terminal amino acid
256 Yoshiharu of the function of substrate-binding domains 1999 sequence
Polymer Chemistry
Laboratory and the
RIKEN Group of Japan Two types of
Science and polyhydroxyalkanoate
Technology (PHA) biosynthesis gene
loci (phb and pha) of
Corporation, The
Institute of Physical Pseudomonas sp. strain
and Chemical 61-3, which produces a
Research (RIKEN), 2-1 Cloning and molecular analysis of the Poly(3- blend of poly(3-
Hirosawa, hydroxybutyrate) and hydroxybutyrate) [P(3HB)]
Wako- Poly(3-hydroxybutyrate-co-3-
Matsusaki H, Manji S, Taguchi K, Kato shi, Saitama 351-0198, hydroxyalkanoate) biosynthesis genes in homopolymer and a
260 M, Fukui T, Doi Y Japan. Pseudomonas sp. strain 61-3. J Bacteriol 1998 Dec;180(24):6459-67 1998 random copolymer poly(3
An extracellular poly(3-
hydroxybutyrate)
depolymerase (PHB
depolymerase) producing
bacterium, strain K1, was
isolated from soil
samples and identified as
Tsukuba sequence PHB depolymerase Pseudomonas pickettii.
Research Center, gene Pseudomonas The PHB
Mitsubishi Cloning and nucleotide sequencing of the poly(3- polyhydroxybutyrate depolymerase gene was
Petrochemical Co., hydroxybutyrate) Stud. Polym. Sci., 12(Biodegradable Plastics depolymerase gene cloned from the genomic
Kurusu, Y.; Kohama, K.; Uchida, Y.; Ltd, Inashiki 300-03, depolymerase gene from Pseudomonas pickettii. and Polymers), Pseudomonas DNA of strain K1
263 Saito, T.; Yukawa, H. Japan 357-61 (English) 1994 1994 and th
Pseudomonas acidophila
can grow with CO2 as a
sole carbon source by the
possession of a
recombinant plasmid that
clones
genes that confer
chemolithoautotrophic
growth ability derived from
Faculty of the H2-oxidizing bacterium
Pharmaceutical Cloning and sequence analysis of the poly (3- Alcaligenes
Umeda F, Kitano Y, Murakami Y, Yagi Sciences, Osaka hydroxyalkanoic Appl Biochem Biotechnol 1998 Spring;70-72:341- hydrogenophilus.
264 K, Miura Y, Mizoguchi T University, Japan. acid)-synthesis genes of Pseudomonas acidophila. 52 1998 H2-oxidizin
Eight mutants of A.
eutrophus defective in the
intracellular accumulation
of poly-b-hydroxybutyric
acid (PHB) were isolated
after transposon Tn5
mutagenesis with the
Institut fur suicide vector pSUP5011.
Mikrobiologie, Cloning of the Alcaligenes eutrophus genes for synthesis EcoRI fragments
Universitat Gottingen, of Alcaligenes which harbor Tn5-mob
Schubert, Peter; Steinbuechel, Federal Republic of poly-b-hydroxybutyric acid (PHB) and synthesis of PHB in Journal of Bacteriology 1988; 170(12):5837- polyhydroxybutyrate gene were isolated from pHC79
268 Alexander; Schlegel, Hans G. Germany. Escherichia coli. 5847 1988 cloning c 541.
Polyhydroxyalkanoates
(PHAs) are microbial
polyesters that can be
Department of used as completely
Chemical Engineering,
Korea Advanced biodegradable polymers,
Institute of Science but the high production
and Technology, Cloning of the Alcaligenes latus polyhydroxyalkanoate cost prevents their use in
373-1 biosynthesis genes a wide range of
Kusong-dong, Yusong- and use of these genes for enhanced
gu, Taejon 305-701, production of Appl Environ Microbiol 1998 Dec;64(12):4897- applications. Recombinant
269 Choi JI, Lee SY, Han K Korea. Poly(3-hydroxybutyrate) in Escherichia coli. 903 1998 Escheri kopiert
The polyhydroxyalkanoate
(PHA) synthase gene
(phaCNc) from Nocardia
corallina was
identified in
Cloning of the Nocardia corallina polyhydroxyalkanoate a lambda library on a 6-kb
Department of Biology, synthase gene BamHI fragment. A 2.8-kb
James Madison and production of poly-(3-hydroxybutyrate- XhoII subfragment was
University, co-3-hydroxyhexanoate) and found to
Harrisonburg, VA poly-(3-hydroxyvalerate-co-3- contain the intact PHA
270 Hall B, Baldwin J, Rhie HG, Dennis D 22807, USA. hydroxyheptanoate). Can J Microbiol 1998 Jul;44(7):687-91 1998 synthas
4.10 Literature on Polyhydroxyalkanoates.xls - page 117
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The polyhydroxyalkanoic
acid synthase gene from
Chromobacterium
violaceum (phaC(Cv)) was
cloned and bacterial
characterized. A 6.3-kb genes. An
BamHI fragment was equilibrium
Biology Department, found to contain both effect is
James Madison Cloning, molecular analysis, and expression of the phaC(Cv) and proposed to
University, polyhydroxyalkanoic the explain the
Harrisonburg, Virginia acid synthase (phaC) gene from polyhydroxyalkanoic acid unexpected
271 Kolibachuk D, Miller A, Dennis D 22807, USA. Chromobacterium violaceum. Appl Environ Microbiol 1999 Aug;65(8):3561-5 1999 (P existence of
Institute of
Biotechnology, ETH
Hönggerberg, CH-
8093 Zürich,
Switzerland Pseudomonas putida
email: Bernard Witholt KT2442 is able to
(bw@biotech.biol.ethz. accumulate medium-chain-
ch) length poly(3-
hydroxyalkanoates) (mcl-
PHAs) as
*Correspondence to intracellular inclusions on
Bernard Witholt, a variety of fatty acids and
Institute of Closed-loop control of bacterial high-cell-density fed-batch many other carbon
Biotechnology, ETH cultures: polyhydroxyalkanoates; poly(3- sources. Some of these
Hönggerberg, CH- Production of mcl-PHAs by Pseudomonas putida KT2442 Biotechnology & Bioengineering hydroxyalkanoate) (PHA); substrates, such as
Michele B. Kellerhals, Birgit Kessler, 8093 Zürich, under Volume 65, Issue 3, 1999. Pages: 306- LABVIEW; closed-loop control; octanoic
273 Bernard Witholt * Switzerland single-substrate and cofeeding conditions 315 1999 remote control; acid, alkenoic aci
Inst.Phys.Chem.Res.S
aitama
LO RIKEN Group of
Japan Science and
Technology Escherichia coli 3-ketoacyl-
Corporation, The ACP-reductase,
Institute of designated fabGEc (I),
Physical and Chemical was cloned using a
Research (RIKEN), 2-1 polymerase chain reaction
Hirosawa, technique to study
Wako-shi, Saitama the metabolic link
351-0198, Japan. Co-expression of 3-ketoacyl-ACP-reductase and between fatty acid
Email: polyhydroxyalkanoate- synthase genes induces PHA metabolism and
Taguchi K; Aoyagi Y; Matsusaki H; ydoi@postman.riken.g production in Escherichia coli HB101 strain; useful for the polyhydroxyalkanoate
Fukui T; *Doi Y o.jp production of polyhydroxyalkanoate by accumulation in FEMS Microbiol.Lett.; (1999) 176, 1, 183-90 (PHA) production. 3
276 bacterium 1999 Plasmids, pl
Polyhydroxyalkanoate
biosynthesis genes of
Aeromonas caviae were
expressed in Escherichia
coli LS5218
Polymer Chemistry (fadR atoC(Con)), and the
Laboratory, Institute of Co-expression of polyhydroxyalkanoate synthase and (R)- polyhydroxyalkanoate-
Physical and Chemical enoyl-CoA producing ability of the
Research (RIKEN), hydratase genes of Aeromonas caviae
Fukui T, Yokomizo S, Kobayashi G, Doi Saitama, establishes copolyester biosynthesis recombinants was
277 Y Japan. pathway in Escherichia coli. FEMS Microbiol Lett 1999 Jan 1;170(1):69-75 1999 investigated. A LS
Summary. Polyhydroxamic
acid (PHA) was prepared
from polyacrylamide (PAA)
and from
polymethacrylamide
(1) Petroleum Polyhydroxamic acid; (PMAA). It was found that
Research Institute, Comparison Between the Electric Conductivity of Polyacrylamide; PHA from PAA has the
Nasr City, Cairo Polyhydroxamic Acids of Different Origin Polymethacrylamide; Electrical properties of a
Wafaa M. Sayed (1) (*), Yahia M. Abed (2) Vergleich der elektrischen Leitfähigkeit von properties; semiconductor when
(1), El-Shafie A. M. Gad (1), Tousson A. National Research Polyhydroxamsäuren verschiedenen Monatshefte fuer Chemie/Chemical Monthly it reacts
280 Salem (2) Center, El-Dokki, Cairo Ursprungs Abstract Volume 129 Issue 3 (1998) pp 245-252 1998 Semiconductors. with some met
PHB-depolymerase
degraded poly[(3-
hydroxybutyric
acid)-co-(3-
hydroxyvaleric acid)]
(PHB/V) significantly. No
other
Department of enzyme used in this
Chemistry, University study showed activity
of Puerto Rico, Comparison of the catalytic activity of PHB-depolymerase, toward PHB/V. Wt. loss
Batista, Adalgisa; Aponte, Maria A.; Mayaguez, yeast lipase, and papain on poly(ethylene adipate), and gel permeation
Diaz, Emilio; Reyes, Hector R. 00681-9019, P. R. poly(ethylenesuccinate), and poly(3-hydroxybutyric acid)- J. Polym. Sci., Part A: Polym. Chem. (1999), chromatog. studies
281 co-(3-hydroxyvaleric acid) 37(14), 2581-2585 1999 suggested that enzym
In order to increase the
miscibility in the blend of
poly(<beta>-
hydroxybutyrate) [PHB]
Department of and
Chemical Engineering,
Korea Advanced poly(<epsilon>-
Institute of Science Compatibilizing capability of caprolactone) [PCL],
and Technology, 373-1 poly(<beta>-hydroxybutyrate-,co-<epsilon>- PHB/PCL copolyesters
Kusong caprolactone) in were used as
Dong, the blend of poly(<beta>-hydroxybutyrate) compatibilizers. These
Yusong Gu, Taejon, and Polymer Bulletin Abstract Volume 41 Issue 6 PHB/PCL
282 Bong Oh Kim, Seong Ihl Woo (*) Korea poly(<epsilon>-caprolactone) (1998) pp 707-712 1998 copolyesters w
Poly-beta-
hydroxyalkanoate (PHA)
from crotonate-grown
cutures of
Syntrophominas wolfei
contained only the D-
isomer of beta-
Department of Botany hydroxybutyrate. The PHA
and Microbiology, from cultures grown with
University of trans-2-pentenoate of one
Oklahoma, 770 Van Composition of poly-beta-hydroxyalkanoate from Anaerobic syntrophic bacteria - of several hexenoates as
Vleet Oval, Norman, Syntrophomonas wolfei grown on unsaturated fatty acid Syntrophomonas - Unsaturated the substrate also Strain - Precursor -
285 Amos; D.A.; McInerney; M.J. OK 73019-02450 USA substrates Arch.Microbiol. 1991; 155:103-106 1991 fatty acids contained sm Copolyester 420.
A poly-3-hydroxybutyrate
metabolic pathway
essential for Helicobacter
pylori survival in a host is
provided. A novel
Helicobacter
pylori Coenzyme A
transferase (Hp CoA-t),
thiolase and PHB
CORTHESY COMPOSITIONS AND METHODS RELATING TO DRUG synthase as well as
THEULAZ IRENE DISCOVERY AND DETECTION methods for their
CORTHESY-THEULAZ (CH); KIETA AND TREATMENT OF GASTROINTESTINAL WO9738110 preparation and use are
286 IRENE (CH) HOLDINGS S A (CH) DISEASES 1997-10-16 1997
Conformational analysis of poly(beta-hydroxybutyrate) in
Doi, Y.; Kunioka, M.; Nakamura, Y.; Alcaligenes eutrophus by solid-state 13C NMR Makromol. Chem.,Rapid Commmun. 1986; 7:661-
287 Soga, K. spectroscopy 664 1986 258.
Conformational isimorphism. A general 21 helical
288 Cornibert; J.; Marchessault; R.H. conformation for poly(beta-alkanoates) Macromolecules 1975; 8:296- 1975 209.
4.10 Literature on Polyhydroxyalkanoates.xls - page 121
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Some mathematical
calculations were done
that provided information
about the structure and
biochemistry of
polyhydroxyalkanoic acid
(PHA) granules and about
Institut fur the amounts of the
Steinbuchel A, Aerts K, Babel W, Mikrobiologie der different constituents that
Follner C, Liebergesell M, Madkour MH, Westfalischen Considerations on the structure and biochemistry of contribute to the PHA
Mayer F, Pieper-Furst U, Pries A, Wilhelms-Universitat bacterial granules. The data
289 Valentin HE, et al Munster, Germany. polyhydroxyalkanoic acid inclusions. Can J Microbiol 1995;41 Suppl 1:94-105 1995 obtained f
Polarographic oxygen
electrodes, a mass
spectrometer with a
membrane inlet system,
and a redox electrode
were used to measure
Polarographic oxygen dissolved H2, O2, and
electrodes- mass spectrometry - CO2 continuously during
redox electrode - chemolithoautotrophic
Institut für Continuous mass spectrometric measurement of dissolved chemolithoautotrophic growth - cultivation of Alcaligenes
Biotechnologie, TU H2, O2, and CO2 during chemolithoautotrophic growth of European J. Appl. Microbiol. Biotechnol. 1980; Alcaligenes eutrophus H 16 - eutrophus H 16. A mass
291 Heinzle, E.; Lafferty, R. M. Graz Alcaligenes eutrophus strain H 16 11:17-22 1980 Ralstonia eutropha H 16 spectromete Analytics 68.
Continuous
biotechnology process for
the preparation of poly
beta -hydroxybutyric acid
(PHB), comprises reacting
methylobacterium or
paracoccus species of
bacteria with heterotropic
substrates selected from
UFZ glucose, fructose,
ACKERMANN JOERG-UWE DR (DE); UMWELTFORSCHUN DE19633858 glycerol,
292 BABEL WOLFGANG PROF DR (DE) GSZENTRUM LE (DE) Continuous preparation of poly:hydroxy:butyric acid 1998-02-19 1998 ethanol and/
4.10 Literature on Polyhydroxyalkanoates.xls - page 122
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Kinetics of poly(-D(-)-3-
hydroxyalkanoate) (PHA)
prodn. were studied in
Alcaligenes eutrophus
H16 (ATCC 17699) fed-
batch culture using
butyric acid and valeric
acid as carbon sources.
Control of molecular weight distribution and mole fraction In
in Stud. poly(-D(-)-3-
Shimizu, Hiroshi; Tamura, Shinji; Fac. Eng., Osaka poly(-D(-)-3-hydroxyalkanoate) (PHA) production by Polym. Sci., 12(Biodegradable Plastics and hydroxybutyric acid)
Ishihara, Yoshiyuki; Shioya, Suteaki; University, Suita 565, Alcaligenes Polymers), 365-72 polyhydroxyalkanoate fermn (PHB) prodn., at the
300 Suga, Ken-ichi Japan eutrophus. (English) 1994 1994 Alcaligenes mol wt distribution conditions o
To control molecular
weight of poly-beta-
Laboratory of hydroxybutyric acid (PHB)
Bioreaction produced in a fed-batch
Engineering, culture of Protomonas
Department of Food extorquens, the effects of
Science and cultural temperature, pH,
Technology, Faculty of molar ratio of methanol
Agriculture, Nagoya Control of molecular weight of poly-beta-hydroxybutyric and ammonia, and
Suzuki, R.; Deguchi, H.; Yamane, T.; University, Chikusa-ku, acid produced in fed-batch culture of Protomanas Protomonas exoterquens - concentration of methanol Strain - Polymer
301 Shimizu, S.; Gekko, K. Nagoya 464, Japan extorquens Appl. Microbiol. Biotechnol. 1988; 27:487-491 1988 molecular weight in the medium on polym "Eigenschaften" 297.
4.10 Literature on Polyhydroxyalkanoates.xls - page 124
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly-beta-hydroxybutyrate
(PHB) synthesis in a
cyanobacterium,
Synechococcus sp. strain
MA19, is controlled at the
enzyme
National Institute of level and is dependent on
Bioscience and Human- the C/N balance in the
Technology, Agency of culture medium. The
Industrial Science and control involves at least
Technology, Tsukuba, Control of poly-beta-hydroxybutyrate synthase mediated by two enzymes. The first
Miyake M, Kataoka K, Shirai M, Asada Ibaraki, acetyl enzyme is
302 Y Japan. phosphate in cyanobacteria. J Bacteriol 1997 Aug;179(16):5009-13 1997 PHB s
The compatibility of a
cryst./cryst. polymer
blend, poly(vinyl alc.)
(PVA)/
polyvinyl alc poly(3-hydroxybutyrate)
polyhydroxybutyrate blend (PHB), was studied by
compatibility high-resoln. solid-state
hydrogen bonding tacticity PVA 13C-NMR and 1H NMR
Dep. Crystallization and compatibility of poly(vinyl blend NMR spectroscopy. The 1H
Biomol. Eng., Tokyo alcohol)/poly(3-hydroxybutyrate) blends: influence of blend crystallinity PVA blend domain spin relaxation time (T1)
Yoshie, Naoko; Azuma, Yoichiro; Inst. Technol., composition and tacticity of poly(vinyl alcohol). J. Appl. size measurements indicate
310 Sakurai, Minoru; Inoue, Yoshio Yokohama 226, Japan Polym. Sci., 56(1), 17-24 (English) 1995 1995 that both the compa
4.10 Literature on Polyhydroxyalkanoates.xls - page 126
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Atactic
polyhydroxybutyrate poly(epichlorohydrin) (I)
polyepichlorohydrin rubber rubber was blended in a
blend crystn wide range of
thermal polyhydroxybutyrate ratios with poly[D(-)3-
polyepichlorohydrin rubber hydroxybutyrate)] (II)
blend isolated from Alcaligenes
morphol polyhydroxybutyrate eutrophus cultures. The
polyepichlorohydrin rubber crystn. and thermal
Dip. Chim. Fis. blend behavior of II/I blends
Dubini Paglia, E.; Beltrame, P. L.; Elettrochim., Univ. Crystallization and thermal behavior of poly(D(-) polyester polyepichlorohydrin were
Canette, M.; Seves, A.; Marcandalli, Milano, Milan, 3-hydroxybutyrate)/poly(epichlorohydrin) blends. rubber blend analyzed by DSC and
315 B.; Martuscelli, E. Italy Polymer, 34(5), 996-1001 (English) 1993 1993 microscopy. All
Kemnitzer; J.E.; Gross; R.A.; McCarthy; Crystallization behavior of predominantly syndiotactic Journal of Environmental Polymer Degradation
318 S.P.; Liggat; J.; Blundell; D.J.; Cox; M. poly(á-hydroxybutyrate) 1995; 3:37-47 1995 568.
Crystallization phenomena in bacterial poly(R)-3-
319 deKoning; G.J.M.; Lemstra; P.J. hydroxybutyrate Polymer 1993; 34(19):4089-4094 1993 555.
deKoning; G.J.M.; Scheeren; A.H.C.;
Lemstra; P.J.; Peeters; M.; Reynaers; Crystallization phenomena in bacterial poly(R)-3-
320 H. hydroxybutyrate Polymer 1994; 35(21):4598-4605 1994 556.
321 Yamane; T. Cultivation engineering of microbial bioplastics production FEMS Microbiology Reviews 1992; 103:257-264 1992 483.
Cybernetic model for synthesis of poly-beta-hydroxybutyric Biotechnology and Bioengineering 1994;
322 Yoo; S.; Kim; W-S. acid in Alcaligenes eutrophus 43:1043-1051 1994 458.
D-(-)-3-Hydroxybutyrat
findet sich im Blut und in
den meisten Organen des
Körpers. Es wird bei
unbehandeltem Diabetes
bei der Acidose in großen
Mengen im Harn
ausgeschieden.
Chemische
analytics of beta-hydroxybutyric Bestimmungsmethoden
acid - beta-hydroxybutyrate beruhen auf der Oxydation
325 Williamson, Dermot H.; Mellanby, Jane D-(-)-3-Hydroxybutyrat dehydrogenase zu Aceton und colorimetri Analytics 52.
A soluble D-(-)-beta-
hydroxybutyric-
dehydrogenase was
isolated from cell-free
extracts of
Hydrogenomonas strain H
16. Maximum enzyme
activity was observed in
the presence of cysteine,
Aus dem Institut für versene and MgCl2. The
Mikrobiologie der D-(-)-beta-Hydroxybuttersäure-Dehydrogenase aus PHB-dehydrogenase - enzyme is stable at low
326 Schindler; J.; Schlegel; H.G. Universität Göttingen Hydrogenomonas H 16 Biochem.Z. 1963; 339:154-161 1963 Hydrogenomonas H 16 temperatures and under w Strain - Enzyme 133. Korr.
D-(-)-Poly-beta-
hydroxybutyrate is a
constituent of the
membranes and the
cytoplasms of genetically
competent Azotobacter
vinelandii, Bacillus
subtilis, and Haemophilus
influenzae cells. Within
each species the
D-(-)-poly-beta-hydroxybutyrate in membranes of concentration of
genetically competent D-(-)-poly-beta-
327 Reusch; R.N.; Sadoff; H.L. bacteria. J Bacteriol 1983 Nov;156(2):778-88 1983 hydroxybuty 271.
328 Thun, E. Das Ende des Plastikzeitalters Wochenpresse ? 189.
Vivo, De; D.C.; Leckie; M.P.; Agrawal; D-beta-Hydroxybutyrate: A major precursor of amino acids
329 H.C. in developing rat brain Journal of Neurochemistry 1975; 161-170 1975 221.
4.10 Literature on Polyhydroxyalkanoates.xls - page 129
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A number of aerobic
pseudomonads capable of
using poly-beta-
hydroxybutyrate as sole
source of carbon have
been partially
characterized. One was
Department of selected for special study
Bacteriology, and described as a new
University of Pseudomonas lemoignei - poly- species. Pseudomonas
Delafield, F.P.; Doudoroff, M; Palleroni, California, Berkeley, Decomposition of poly-beta-hydroxybutyrate by beta-hydroxybutyrate lemoignei Delafield. This
330 N.J.; Lusty, C.J.; Contopoulos, R. California pseudomonads. J Bacteriol 1965 Nov;90(5):1455-66 1965 depolymerisation - hydrolases bacterium cons Strain - Metabolism 122. Korr.
Degradation du lipide poly-beta-hydroxybutyrique par un
Garvard, R.; Dahinger, A.; Hauttecoeur, extrait enzymatique de Bacillus Megatherium I. C. R. Acad. Sc. Paris 1966; 1273-1275 (Article in Isolation and purification of a
331 B.; Reynaud, C. depolymerase A French) 1966 bacterial depolymerase No abstract. Depolymerization 120.
Bacteria capable of
growing on poly(3-
hydroxybutyrate), PHB, as
the
sole source of carbon and
energy were isolated from
various soils, lake
water, activated sludge,
Jendrossek, Dieter; Knoke, Ingrid; Inst. Mikrobiol., and air. Although all
Habibian, Rahim Bahodjb; Georg-August-Univ., Degradation of Poly(3-hydroxybutyrate), PHB, by bacteria polyhydroxybutyrate bacteria utilized a wide
Steinbuechel, Alexander; Schlegel, Goettingen 3400, and purification of novel PHB depolymerase from J. Environ. Polym. depolymerase Comamonas variety of monomeric
332 Hans Guenter Germany Comamonas sp. Degrad., 1(1), 53-63 (English) 1993 1993 substrates for growth 523.
Biodegradable polymeric
microspheres have been
prepared by spray drying,
precipitation, rotary
evaporation and press
grinding methods. Erosion
of microspheres of
Division of Medicinal poly(lactide), poly(3-
and Natural Products hydroxybutyrate),
Chemistry, University copolymers of lactide and
Wang HT, Palmer H, Linhardt RJ, of Iowa, Iowa City glycolide, and
335 Flanagan DR, Schmitt E 52242. Degradation of poly(ester) microspheres. Biomaterials 1990 Nov;11(9):679-85 1990 copolymers o
Par dépolymérisation
chimique partielle du PHB,
on obtient simultanément
des polymères
homologues du PHB mais
à chaine carbonée plus
courte et des oligomères
constituant le spemiers
élèments de la
macromolécule. La
Depolymerisation par voie chimique menagee, du lipide structure chimique de ces
341 Michel, Jolivet; Raymond, Gavard beta-hydroxybutyrique (ou PHB) de Bacillus megaterium. C.R.Acad. Sc. Paris 1975; 2801-2804 1975 Depolymerisation oligomères, al Analytics 55.
Par dépolymérisation
chimique partielle du PHB,
on obtient simultanément
des polymères
homologues du PHB mais
à chaine carbonée plus
courte et des oligomères
constituant les premiers
Dépolymérisation par voie chimique ménagée, du lipide éléments de la
beta-hydroxybutyrique (ou PHB) de Bacillus megaterium. macromolécule. La
Obtention et structure d'oligomères de l'acide D(-)bety- structure chimique de ces
343 Hauttecoeur; B.; Jolivet; M.; Gavard; R. hydroxybutyrique. C.R.Acad.Sc.Paris 1975; 280:2899-2902 SerieD 1975 oligomères, a 145.
Le PHB de Bacillus
megaterium a été
dépolymérisé par voie
chimique dans le but
d'obtenir des produits
homologues du polymère
naturel mais susceptible
d'étre métabolisés par une
enzyme isolée de la
bactèrie. L'utilisation de
Depolymerisation, par voie chimique menagee, du lipide á très basses températures
344 Hauttecoeur; B.; Jolivet; M.; Gavard; R. hydroxybutyrique (ou PHB) de Bacillus megaterium C.R.Acad.Sc.Paris 1972; 274:2729-2732 SerieD 1972 Bacillus megaterium et du 146.
4.10 Literature on Polyhydroxyalkanoates.xls - page 132
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
L'action du mélange BF3-
CH3OH sur des
polymères issus de la
saponification ménagée
du PHB conduit
directement à la
préparation de tous les
esters méthyliques des
oligemères. Soumis au
seul BF3, ces mêmes
polymères permettent
Depolymerisation, par voie chimique menagee, du lipide d'isoler en grandes
345 Hauttecoeur; B.; Jolivet; M.; Gavard; R. beta-hydroxybutyrique (ou PHB) de Bacillus megaterium C.R.Acad.Sc.Paris 1972; 274:1975-1960 SerieC 1972 quantités 144.
Depolymerization of poly-beta-hydroxybutyrate by an
346 Merrick, J.M.; Doudoroff, M. intracellular enzyme system Journal of Bacteriology 1964; 88:60-71 1964 34.
Dissolved hydrogen
concentration in the
culture medium was
determined by the tubing
method during the
Department of cultivation of hydrogen
Biochemical bacteria. Dissolved
Engineering, Faculty of hydrogen gas which
Pharmaceutical diffused through the
Sciences, Osaka membrane of the tube was
University, Yamada Determination of dissolved hydrogen concentration during determined by gas
Ohi; K.; Nishimura; T.; Okazaki; M.; Kami, Suita-shi, Osaka cultivation and assimilation of gaseous substartes by Journal of Fermentation Technology 1979; hydrogen bacteria - gas chromatography. The rate
348 Yoshiharu; M. 565 Alcaligenes hydrogenophilus 57(3):203-209 1979 chromatography o Analytics 63.
Determination of PHB in activated sludge by a gas Eoropean J. Appl. microbiol. Biotechnol 1981;
349 Apostolides, Z.; Potgieter, D. J. J. chromatographic method 13(13):62-63 1981 192.
4.10 Literature on Polyhydroxyalkanoates.xls - page 133
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
IRC Biomedical
Materials, Queen Mary Composites -
and Westfield College, Development of a natural degradable polymer for Polyhydroxybutyrate - Bone-
353 Knowles JC London, UK. orthopaedic use. J Med Eng Technol 1993 Jul-Aug;17(4):129-37 1993 Bonding Application
Mayer, J. M.; Greenberger, M.; Kaplan, Development of Standard Methods for Accelerated
354 D. L.; Gross, R.; McCarthy, S. Degradation Studies of Polymer Films ??? 1990 387.
4.10 Literature on Polyhydroxyalkanoates.xls - page 134
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Knallgasbakterien
vermögen unter
Ausnutzung der
Knallgasreaktion Poly-ß-
hydroxybuttersäure
(PHBS) aus Kohlendioxyd
zu synthetisieren. Acetat
wird ebenfalls in PHBS
eingebaut, und zwar auf
Aus dem Institut für Die Synthese von Poly-beta-hydroxybuttersäure durch direktem Wege. Lactat
Mikrobiologie der Hydrogenomonas H 16: Die zu beta-Hydroxybutyryl- Hydrogen Bacteria - Calvin und Pyruvat werden nach
359 Schindler, J. Universität Göttingen coenzym A führenden Reaktionsschritte Arch. Mikrobiol. 1964; 49:236-255 1964 cycle - Acetate - Metabolism einmaliger und Succin Metabolism 126. Korr.
4.10 Literature on Polyhydroxyalkanoates.xls - page 135
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1. Chemolithotrophically
(with H2 + O2 + CO2)
grown Hydrogenomonas H
16 can adapt itself to
fructose, acetic acid,
glutamic acid and aspartic
acid in air but not under
knallgas. 2. The strain H
Institut für Die Verwertung organischer Substrate durch 16, grown previously on
Mikrobiologie der Hydrogenomonas in Gegenwart von molekularem Biochemische Zeitschriften 1965; 341:260-270 Hydrogenomonas H 16 - fructose (in air), grown
360 Gottschalk, G. Universität Göttingen Wasserstoff (Article in German.) 1965 chemolithotrophic growth arithmetical Strain - Metabolism 49.
Medium chain length
polyhydroxyalkanoates,
MCL-PHAs, produced by
Biomacromolecules bacteria as inclusion
Research Laboratory, bodies or
Department of granules were analyzed in
Microbiology, situ by differential
Gyeongsang National scanning calorimetry
Differential scanning calorimetric study of poly(3- (DSC) without
University, Chinju, hydroxyoctanoate) isolation
361 Song JJ, Yoon SC, Yu SM, Lenz RW South Korea. inclusions in bacterial cells. Int J Biol Macromol 1998 Oct;23(3):165-73 1998 from the cells. The
Alcaligenes latus, a
producer of the
intracellular bioplastic
poly(beta-hydroxybutyric
acid), was disrupted by
chemical and mechanical
means. Chemical lysis
Department of employed sequential
Chemical engineering, treatment with sodium
University of Waterloo, Disruption of Alcaligenes latus for recovery of Poly(beta- dodecyl sulfate (SDS) and
Ontario, Canada N2L hydroxybutyric acid): Comparison of high-pressure sodium hypochlorite. The
365 Tamer; I.M.; Moo-Young; M.; Chisti; Y. 3G1 homogenization, bead milling and chemically induced lysis Ind. Eng. Chem. Res. 1998; 37:1807-1814 1998 SDS t 645 korr
Distribution of poly(beta-hydroxybutyrate) and poly(gamma-
caprolactone) aerobic degrading microorganisms in Journal of Environmental Polymer Degradation
366 Nishida; H.; Tokiwa; Y. different environments 1993; 1:227-233 1993 583.
367 Steinb chel; A.; Valentin; H.E. Diversity of bacterial polyhydroxyalkanoic acid FEMS Microbiology Letters 1995; 128:219-228 1995 648.
A genomic fragment
harboring the gene phaG
was cloned by phenotypic
complementation of
Pseudomonas putida
KT2440
mutants, defective in the
polyhydroxyalkanoic acid
(PHA) synthesis via de
novo fatty acid
biosynthesis but not
KRUEGER NIELS (DE); DNA sequence useful for the production of affected in PHA
368 STEINBUECHEL ALEXAND (DE) MONSANTO CO (US) polyhydroxyalkanoates US5750848 1998-05-12 1998 biosynthesi
4.10 Literature on Polyhydroxyalkanoates.xls - page 137
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A genomic fragment
harboring the gene phaG
was cloned by phenotypic
complementation of
Pseudomonas
MONSANTO putida KT2440 mutants,
KRÜGER, Niels , Esking 4a, D-48727 COMPANY, 800 North defective in the
Billerbeck, Germany Lindbergh Boulevard, polyhydroxyalkanoic acid
STEINBÜCHEL, Alexander , St. Louis, MO 63167, (PHA) synthesis via de
Rönnenthal 27, D-48341 Altenberge, United States of DNA SEQUENCE USEFUL FOR THE PRODUCTION OF novo fatty acid
369 Germany America POLYHYDROXYALKANOATES WO9806854A1 Feb. 19, 1998 1998 biosynthesis but
Preprint of the 6th int. conference on computer
Dynamics and control of the fed-batch production of poly- applications in biotech. Garmisch-Partenkirchen
370 Pomerleau; Y.; Perrier; M.; Bourque; D. beta-hydroxybutyrate 1995; 107-112 1995 646.
Gu; J.-D.; Yang; S.; Welton; R.; Eberiel; Effect of environmental parameters on the degradability of Journal of Environmental Polymer Degradation
378 D.; McCarthy; S.P. polymer films in laboratory-scale composting reactors 1994; 2:129 1994 574.
4.10 Literature on Polyhydroxyalkanoates.xls - page 139
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Pseudomonas
resinovorans produced
poly-beta-
hydroxyalkanoates (PHAs)
when grown on
hydrocarbons but not on
glucose.
In a chemostat culture, the
PHA composition was
Department de Genie beta-hydroxybutyrate (C4)-
Chimique, Ecole beta-hydroxyhexanoate
Polytechnique de Effect of nitrogen limitation on long-side-chain (C6)-beta-
Ramsay BA, Saracovan I, Ramsay JA, Montreal, Quebec, poly-beta-hydroxyalkanoate synthesis by Pseudomonas hydroxyoctanoate (C8)-
379 Marchessault RH Canada. resinovorans. Appl Environ Microbiol 1992 Feb;58(2):744-6 1992 beta-hydrox 441.
Effect of nutrient deficiency on accumulation and relative
Daniel; M.; Choi; J.H.; Kim; J.H.; molecular weight of poly-beta-hydroxybutyric acid by
380 Lebeault; J.M. methylotrophic bacterium, Pseudomonas 135 Appl. Microbiol. Biotechnol. 1992; 37:702-706 1992 608.
Effect of oxygen and nitrogen limitation on poly-beta-
hydroxybutyrate biosynthesis in ammonium-grown
381 Ward, A. C.; Rowley, B. I.; Dawes, E. A. Azotobacter beijerinckii Journal of general microbiology 1977; 102:61-68 1977 3.
Kahimoto; K.; Tsuboi; H.; Iwasaki; S.; Effect of pH on the production of poly-beta-hydroxybutylate Journal of Chemical Engineering of Japan 1993;
383 Shirai; Y. by photosynthetic bacteria, Rhodospirillum rubrum. 26:56-58 1993 487.
60 PHB/PET thermotropic
liq. crystal copolyester
was prepd. by melt
copolymn. of a mixt. of 60
parts p-acetoxybenzoic
acid (PHB) and 40
parts poly(ethylene glycol
phase transition flow liq crystal terephthalate) (PET) at
Effect of phase transition and heat treatment on flow polyester 290° and the
Textile Univ. China, characteristics of heat treatment acetoxybenzoic flowability was measured
Wang, Huaping; Guan, Guihe; Zhang, Shanghai 200051, 60 PHB/PET thermotropic liquid crystal copolyester. Hecheng Xianwei Gongye, acid polyester by a capillary rheometer at
384 Yueting Peop. Rep. China 19(2), 18-22 (Chinese) 1996 1996 25
4.10 Literature on Polyhydroxyalkanoates.xls - page 140
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1 Tsukuba Research
Laboratory, Tokuyama As one of a series of
Soda Co. Ltd., 40 studies concerning the
Wadai Tsukuba, realtionship between the
Ibaraki 300-42, Japan; higher-order structure and
2 Fermentation the biodegradability of a
Research Institute, biodegradable plastsic,
Agency of Industrial the effects of the crystal
Science and Biodegradable plastic - structure of the plastic on
Technology, 1-1-3 Effects of higher-order structure of poly(3-hydroxybutyrate) microbial degradation - crystal microbial degradation
Higashi Tsukuba, on its biodegradation. II. Effects of crystal structure on Journal of Environmental Polymer Degradation sturcture - physiological were investigated. Crystallinity -
394 Nishida; H.1; Tokiwa; Y.2 Ibaraki 305, Japan. microbial dgeradation 1993; 1(1):56-80 1993 behavior Bacterial po Degradation 558.
Effects of propionate on accumulation of poly(beta-
Lee; I.Y.; Kim; M.K.; Chang; H.N.; Park; hydroxybutrate-co-beta-hydroxyvalerate) and excretion of
395 Y.H. pyruvate in Alcaligenes eutrophus Biotechnology Letters 1994; 16:611-616 1994 460.
Biological Process
Technology Institute,
Uni6ersity of
Minnesota, 240
Gortner Laboratories, We have increased the
1479 Gortner A6enue, gene dosage of the poly(3-
St. Paul, hydroxybutyrate)
MN 55108, USA biosynthesis operon in
b Department of Ralstonia eutropha
Chemical Engineering (formerly Alcaligenes
and Materials Science, eutrophus) to test
Uni6ersity of whether PHB synthesis
Minnesota, 240 PHB synthesis rates; Poly(3- rates may be increased by
J. Kurt Jackson a , Friedrich Srienc a,b, Gortner Laboratories, Effects of recombinant modulation of the phbCAB operon J. Biotechnol. (1999), 68(1), 49-60 hydroxybutyrate); Ralstonia recombinant methods.
396 * 1479 copy number on PHB synthesis rates in Ralstonia eutropha 1999 eutropha The native R. eutropha ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 142
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Institute of Poly(3-hydroxyalkanoates)
Biotechnology, ETH (PHA) have the potential
Hönggerberg, CH- to become a
8093 Zürich, biodegradable
Switzerland Tel.: ++41 alternative
1 for conventional plastics.
In order to produce PHA
6333402 Fax: ++41 1 Efficient production of medium-chain-length at competitive costs in
6331051 e-mail: poly(3-hydroxyalkanoates) from octane by comparison
hzu@biotech.biol.ethz. Pseudomonas Applied Microbiology and Biotechnology Abstract with commonly used
401 W. Hazenberg, B. Witholt ch oleovorans: economic considerations Volume 48 Issue 5 (1997) pp 588-596 1997 plastics, eff
The ability of Alcaligenes
eutrophus to grow and
produce
polyhydroxyalkanoates
(PHA) on plant
oils was
Polymer Chemistry evaluated. When olive oil,
Laboratory, Institute of corn oil, or palm oil was
Physical and Chemical Efficient production of polyhydroxyalkanoates from plant fed as a sole carbon
Research (RIKEN), oils by source, the
Saitama, Alcaligenes eutrophus and its recombinant wild-type
402 Fukui T, Doi Y Japan. strain. Appl Microbiol Biotechnol 1998 Mar;49(3):333-6 1998 strain of
Electrospray 'soft'
ionisation (ESI) and
multistep mass
spectrometry (MS(n))
techniques enable
characterisation of a
bioactive polymer,
Electrospray multistep ion trap mass spectrometry for the poly[(R,S)-3-
Polish Academy of structural hydroxybutanoic acid] (a-
Sciences, Centre for characterisation of poly[(R,S)-3- PHB), containing
Polymer Chemistry, 41- hydroxybutanoic acid] containing a Rapid Commun Mass Spectrom 2000;14(4):195- covalently
403 Adamus G, Kowalczuk M 800 Zabrze, Poland. beta-lactam end group. 202 2000 bonded
4.10 Literature on Polyhydroxyalkanoates.xls - page 144
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Encystment and polymer production by Azotobacter
vinelandii in the
404 Lin LP, Sadoff HL presence of beta-hydroxybutyrate. J Bacteriol 1968 Jun;95(6):2336-43 1968 Abstract unavailable.
Engineering and biochemical analysis of the bioconversion 169 pp.
of methane Avail. Univ. Microfilms Int., Order No. methane fermn
Columbia Univ., New into an intracellular polymer: poly-b-hydroxybutyrate DA8710227 From: Diss. Abstr. polyhydroxybutyrate
405 Suk, Julie Suehyun York, NY, USA (PHB). Int. B 1987, 48(1), 204 (English) 1987 1987 Methylcystis Abstract Unavailable
In order to scale up
medium-chain-length
polyhydroxyalkanoate (mcl-
PHA) production in
recombinant
microorganisms, we
Institute of generated and
Biotechnology, ETH Engineering of stable recombinant bacteria for production investigated different (R)-3-
Honggerberg, CH- of chiral recombinant bacteria hydroxybutyryl-
Prieto MA, Kellerhals MB, Bozzato GB, 8093 Zurich, medium-chain-length poly-3- containing a CoA in plant
406 Radnovic D, Witholt B, Kessler B Switzerland. hydroxyalkanoates. Appl Environ Microbiol 1999 Aug;65(8):3265-71 1999 stable regulated expr peroxisomes.
Univ. of Minnesota,
Leaf, Timothy Anders Minneapolis, MN, USA Diss. Abstr. Int., B 1999, 59(8), 4287
407 Engineering yeast for polyhydroxybutyrate production 1999 Abstract unavailable.
Univ.Kyungpook-Nat.; Poly-beta-hydroxybutyrate
Korea- (PHB) and poly-beta-
Res.Inst.Biosci.Biotech hydroxyvalerate or
nol. PHB and poly-gamma-
LO Department of hydroxybutyrate
Genetic Engineering, copolymers were
College of Natural produced using
Sciences, Alcaligenes eutrophus
Kyungpook Enhanced biosynthesis of P(3HB-3HV) and P(3HB-4HB) H16 (ATCC 17699)
National University, by amplification of the cloned PHB biosynthesis genes in transformants AER3,
Taegu 702-701, Alcaligenes eutrophus; metabolic engineering for poly-beta- AER4
Korea. hydroxybutyrate and poly-beta-hydroxyvalerate or poly- and AER5, harboring
408 Lee Y H; Park J S; Huh T L gamma-hydroxybutyrate copolymer pr Biotechnol.Lett.; (1997) 19, 8, 771-74 1997 recombinant plasmids c
1. Using cells of
Hydrogenomonas H 16
after mutagenesis by
nitrous acid about 0.4
percent and by 1-nitoso-3-
nitro-1-methylguanidine
1.5 percent auxotrophic
mutants were found
Hydrogenomonas H 16 - among the survivors. In
Institut für Enrichment and Isolation of Auxotrophic Mutants of Alcaligenes eutrophus H 16 - order to increase the
Mikrobiologie der Hydrogenomonas H 16 / Anreicherung und Isolierung Arch. Mikrobiol. 1969; 67:99-109 (Article in Ralstonia eutropha H 16 - mutant yield an
409 Reh; M.; Schlegel; H.G. Universität Göttingen auxotropher Mutanten von Hydrogenomonas H 16 German) 1969 mutants - colistine enrichment method Strain 94.
4.10 Literature on Polyhydroxyalkanoates.xls - page 145
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Centrifugation through
sucrose gradients was
adapted to separate spore-
forming cells of B.
Departamento de megaterium deficient in
Quimica Biologica, poly-beta-hydroxybutyrate
Facultad de Ciencias synthesis from wild type
Exactas y Naturales, cells. The conditions
Universidad de Enrichment for mutants of Bacillus megaterium deficient in described allowed the
Floccari ME, Tiscornia G, Palmada F, Buenos Aires, the synthesis Rev Argent Microbiol 1991 Jan-Feb;23(1):26-9 detection of mutant clones
410 Mendez BS Argentina. of poly-beta-hydroxybutyrate. [Article in Spanish] 1991 Bacillus megaterium screening a low pe strain
Bacteriology
Department, University
of Edinburgh, Teviot
411 Duguid, J.P.; Wilkinson, J.F. Place, Edinburgh 8 Environmentally induced changes in bacterial morphology 11th Symp. Soc. Gen. Micr. 1961; 64-99 1961 Bacterial morphology No abstract. Others 113. Corr.
A bacterium capable of
degrading poly(3-
hydroxybutyrate) [P(3HB)]
was isolated from
laboratory media and
identified as
Pseudomonas pickettii.
The strain P. pickettii
Polymer Chemistry excreted an extracellular
Laboratory, Institute of poly(hydroxyalkanoate)
Physical and Chemical Enzymatic degradation of poly(hydroxyalkanoates) by (PHA) depolymerase and
Research (RIKEN), Pseudomonas grew
413 Yamada K, Mukai K, Doi Y Saitama, Japan. pickettii. Int J Biol Macromol 1993 Aug;15(4):215-20 1993 on P(3HB) as
Jesudason; J.J.; Marchessault; R.H.; Journal of Environmental Polymer Degradation
414 Saito; T. Enzymatic degradation of poly(R,S)-beta-hydroxybutyrate 1993; 1(2):89-98 1993 560.
4.10 Literature on Polyhydroxyalkanoates.xls - page 146
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The enzyme activity
synthesizing poly-beta-
hydroxybutyrate (PHB)
was mainly localized in
the PHB-containing
particulate
fraction of Zoogloea
ramigera I-16-M, when it
grew flocculatedly in a
medium supplemented
Fukui, T.; Yoshimoto, A.; Matsumoto, with glucose. On the other
M.; Hosokawa, S.; Saito, T.; Nishikawa, Enzymatic synthesis of poly-beta-hydroxybutyrate in hand,
415 H.; Tomito, K. Zoogloea ramigera. Arch Microbiol 1976 Nov 2;110(23):149-56 1976 the enzyme a 10.
Department of
Bacteriology,
University of Enzymatic synthesis of poly-beta-hydroxybutyric acid in
416 Doudoroff, J.M. Merrick M. California, Berkeley bacteria Nature 1961; 189:890-892 1961 No abstract. 74.
A bench-scale fermn.
system with several safety
devices, control
systems, and a specially
designed agitation system
was built for the
safety polyhydroxybutyrate prodn. by Alcaligenes
prodn fermentor Alcaligenes eutrophus of poly-b-
Ishizaki, Ayaaki; Tanaka, Kenji; Dep. Food Sci. polyhydroxybutyrate prodn hydroxybutyric acid (PHB)
Takeshita, Toshihiro; Kanemaru, Technol., Kyushu Equipment and operation for fermentative PHB production fermentor Alcaligenes oxygen from H2, O2, and CO2.
Toshihisa; Shimoji, Takashi; Kawano, Univ., Fukuoka 812, using gaseous substrate to guarantee safety from J. Chem. Eng. Jpn., regulation The new fermentor allows
421 Takeharu Japan explosion 26(2), 225-7 (English) 1993 1993 use o 486.
Estimation of fermentation biomass concentration by Applied and Environmental Microbiology 1978;
422 Zabriskie; D.W.; Humphrey; A.E. measuring culture fluorescence 35(2):337-343 1978 270.
Etudes sur l'autolyse microbienne acidification par
423 Lemoigne; M. formation d'acide á-oxybutyrique Annales de l'institut Pasteur 1925; 39:145-173 1925 216.
Etudes sur l'autolyse microbienne origine de l'acide beta-
424 Lemoigne; M. oxobutyrique forme par autolyse Annales de l'institut Pasteur 1927; 41:149-165 1927 217.
(1) Instituto de
Pesquisas
Tecnológicas do A screening programme
Estado de S. Paulo was developed leading to
S/A-IPT, Caixa Postal the isolation of 75 strains
7141, of soil
CEP gram-
01064-970, São Paulo, negative bacteria which
Brazil. Fax: 55 011 are able to produce
J. G. C. Gomez (1), M. F. A. Rodrigues 869 3566 polyhydroxyalkanoic acids
(1), R. C. P. Alli (1), B. B. Torres (2), C. (2) Evaluation of soil gram-negative bacteria yielding (PHA) from
L. Bueno Departamento de polyhydroxyalkanoic acids from Applied Microbiology and Biotechnology Abstract sugar-cane
Netto (1), M. S. Oliveira Bioquímica, Instituto carbohydrates and Volume 45 Issue 6 (1996) pp 785-791 derivatives. The
425 (1), L. F. da Silva (1) de Química, Universi propionic acid 1996 evaluation
Department of
Microbiology,
University of Sheffield
S10 2TN, England,
and Universität
Konstanz, Fachbereich
Biologie, D-775
Konstanz, Postfach
427 Quayle, J.Rodney; Ferenci, Thomas 7733, West Germany Evolutionary Aspects of Autotrophy Microbiological Reviews 1978; 42(2):251-273 1978 autotrophy No abstract. others 51.
Excretion of metabolites by hydrogen bacteria IV.
Vollbrecht, D.; Schlegel, H.G.; Respiration rate-dependent formation of primary European J. Appl. Microbiol. Biotechnol. 1979;
428 Stoschek, G.; Janczikowski, A. metabolites and of poly-3-hydroxybutanoate 7:267-276 1979 25.
Excretion of metabolites by hydrogen bacteria. III. D(-)- European J. Appl. Microbiol. Biotechnol. 1979;
429 Vollbrecht, D.; Schlegel, H.G. 3hydroxybutanoate 7:259-266 1979 26.
Vollbrecht, D.; El Nawawy, M.A.; Excretion of Metabolites by hydrogen bacteriaI. Autotrophic European J. Appl. Microbiol. Biotechnol. 1978;
430 Schlegel, H.G. and heterotrophic fermentations 6:145-155 1978 184.
Excretion of metabolites by hydrogen bacteriaII. Influences European J. Appl. Microbiol. Biotechnol. 1978;
431 Vollbrecht; D.; Schlegel; H.G. of Aeration, pH,Temperature, and Age of Cells 6:157-166 1978 239.
Mutants of A. eutrophus,
which are defective in the
intracellular
accumulation of poly(b-
hydroxybutyric acid)
(PHB) were cultivated in
the
presence of excess
Excretion of pyruvate by mutants of Alcaligenes eutrophus, carbon source after
Inst. Mikrobiol., which are growth had ceased due to
Georg-August Univ., impaired in the accumulation of poly(b-hydroxybutyric acid) Appl. depletion of ammonium,
Steinbuechel, Alexander; Schlegel, Goettingen D-3400, (PHB), Microbiol. Biotechnol., 31(2), 168-75 (English) Alcaligenes pyruvate excretion sulfate, phosphate,
432 Hans G. Fed. Rep. Ger. under conditions permitting synthesis of PHB. 1989 1989 polyhydroxybutyrate potassium 397.
1 Laboratoire
d´Automatique,
Dynamique et Analyse
des Systèmes
University of Louvain, An experimental
Bâtiment Maxwell B- validation, on a pilot
1348 Louvain-la- bioreactor, of an
neuve, Belgium; 2 asymptotic observer for on
Sovay and Cie, line estimation of biomass
Direction Centrale des Fourth international congress on computer Alcaligenes eutrophus - and product
Recherches, Rue de applications in fermentation technology: Ralstonia eutropha - Kinetic concentrations from CO2
Ransbeek, 310 B-1120 Experimental validation of a methodology for on line state SCI/IFAC symposium on modelling and control of model - Pilot plant reactor - On- measurements is
433 Dochain, D.1;de Buyl, E.2; Bastin, G.1 Bruxelles estimation in bioreactors biotechnological processes 1988 1988 line biomass estimation - presented. Kinetics 295.
4.10 Literature on Polyhydroxyalkanoates.xls - page 149
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Complementation analysis
of a polyhydroxyalkanoate
(PHA)-negative mutant of
Aeromonas
caviae
Polymer Chemistry proved that ORF3 in the
Laboratory, The pha locus (a 402-bp gene
Institute of Physical Expression and characterization of (R)-specific enoyl located downstream of the
and Chemical coenzyme A PHA
Research (RIKEN), hydratase involved in polyhydroxyalkanoate synthase
biosynthesis by Aeromonas gene) participates in PHA
434 Fukui T, Shiomi N, Doi Y Saitama, Japan. caviae. J Bacteriol 1998 Feb;180(3):667-73 1998 bi
The PHA-degrading
isolate, strain P37C, was
enriched from residential
compost for its ability to
hydrolyze the medium
chain
Department of length PHA, poly(beta-
Microbiology, hydroxyoctanoate) (PHO).
University of It was subsequently found
Massachusetts to grow on a wide range of
Quinteros R, Goodwin S, Lenz RW, Amherst, 01003, USA. Extracellular degradation of medium chain length PHAs, including both
436 Park WH poly(beta-hydroxyalkanoates) by Comamonas sp. Int J Biol Macromol 1999 Jun-Jul;25(1-3):135-43 1999 short chai
Enzymatic degradation
processes of microbial
copolyesters, poly(3-
hydroxybutyrate-co-3-
hydroxyvalerate): P(3HB-
co-3HV)
and poly(3-
Research Laboratory hydroxybutyrate-co-4-
of Resources hydroxybutyrate): P(3HB-
Utilization, Tokyo co-4HB), were studied by
Institute of Extracellular poly(hydroxyalkanoate) depolymerases and the weight loss (erosion)
Technology, their inhibitor of
438 Mukai K, Yamada K, Doi Y Yokohama, Japan. from Pseudomonas lemoignei. Int J Biol Macromol 1992 Aug;14(4):235-9 1992 copolyester films. These s
Previous investigations on
the role of the polymerase
in the synthesis of poly-3-
hydroxybutyrate (PHB) are
Polymer Science and reviewed, and the
Engineering results from earlier in vitro
Department, University studies on the activity and
of Massachusetts, selectivity of the
Amherst 01003, USA. Extracellular polymerization of 3-hydroxyalkanoate polymerase of Alcaligenes
Lenz RW, Farcet C, Dijkstra PJ, rwlenz@polysci.umass monomers with the eutrophus are discussed.
439 Goodwin S, Zhang S .edu polymerase of Alcaligenes eutrophus. Int J Biol Macromol 1999 Jun-Jul;25(1-3):55-60 1999 In
Poly-beta-hydroxybutyrate
(PHB) or poly-beta-
hydroxyalkanoate
(PHA) co-polymers are
extracted from Alcaligenes
eutrophus ATCC
17699 (KCTC 1006)
using alkali and protease,
Extraction method of PHB or PHA copolymer using alkali in a method that
Kohap and protease; poly-beta-hydroxybutyrate or poly-beta- involves: (1) washing
Im K B; Kim K J LO Korea. hydroxyalkanoate co-polymer purification from Alcaligenes KR 9502866 27 Mar 1995 strain KCTC 1006 in water
440 eutrophus 1995 a
Poly-(b-hydroxybutyric
acid) (PHB) was produced
by fermn. with S.
natans. The culture
medium contained 0.1%
glucose and 0.1%
peptone, pH 8. After the
cells were isolated by
Shenyang Inst. polyhydroxybutyrate prodn centrifugation, the cells
Appl. Ecol., Acad. Sin., Sphaerotilus were ruptured by freeze-
Zhang, Lixin; Wang, Jinping; Guo, Shenyang 110015, Extraction of PHB from Sphaerotilus natans. Weishengwuxue Zazhi, 13(1), 30-3 (Chinese) PHB extn Sphaerotilus thawing. After
441 Xiujun; Kuai, Jun Peop. Rep. China 1993 1993 centrifugation
4.10 Literature on Polyhydroxyalkanoates.xls - page 151
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly( beta -
hydroxybutyric acid) is
separated from bacterial
cells by drying a finely
divided stream or spray of
an aqueous
suspension of the cells
with a gas heated to
above 100 DEG C. and
then extracting the PHB,
SENIOR PETER J; WRIGHT preferably after a lipid
447 LEONARD F; ALDERSON BARRY ICI LTD Extraction process US4324907 1982-04-13 1982 extraction
ETH Zürich, Arbeitstagung "Aufarbeitung in der
448 Lafferty, R. M.; Heinzle, E. Extraktion eines Thermoplasten aus Bakterien Biotechnologie" 1977 1977 193.
A marine photosynthetic
bacterium,
Rhodopseudomonas sp.
strain
W-1S, accumulated
Faculty of poly-beta-hydroxybutyrate
Pharmaceutical (PHB) to 56% of the
Sciences, Osaka dry cell weight under
University, 1-6 microaerobic and
Chowdhury W Q; Idehara K; Maeda I; Yamada-oka, Factors affecting polyhydroxybutyrate biosynthesis in the photoheterotrophic
Umeda F; *Yagi K; Miura Y; Suita, Osaka 565, marine photosynthetic bacterium Rhodopseudomonas sp. conditions. The
Mizoguchi T Japan. strain W-1S; poly-beta-hydroxybutyric acid production Appl.Biochem.Biotechnol.; (1996) 57-58, 361-66 addition of NaCl and
450 (conference paper) 1996 phosphate was
Following Hartman, who
first suggested the use of
Sudan black B, in the
place of red Sudans, as a
bacterial fat stain
(Hartman, 1910) Burdon,
Department of Stokes, and Kimbrough
Bacteriology and (1942) confirmed the
Immunology, Baylor greater value of this dye
University College of and modified the
Medicine, Houston, Fatty material in bacterial and fungi revealed by staining procedure for
452 Burdon, K.L. Texas dried, fixed slide preparations J. Bacteriol. 1946; 52:665-678 1946 Sudan black - fatty material demonstrating Others 116. Korr.
4.10 Literature on Polyhydroxyalkanoates.xls - page 153
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Continuous fermentation
of Alcaligenes micro-
organisms capable of
accumulating PHB under
limitation of a nutrient
required for
growth, but not PHB
accumulation, so that the
PHB content is above
25% by weight. By means
of this the carbon in the
HUGHES LORENZO (GB); ICI PLC Fermentation process for the production of poly( beta - carbon
455 RICHARDSON KENNETH R (GB) (GB) hydroxy butyric acid) US4433053 1984-02-21 1984
Lafferty; R.M.; Oeding; V.; Robra; K.H.;
456 Schlegel; H.G. Fermentationstechnik mit Knallgasbakterien Dechema-Monographien 1972; 71:37-52 1972 93.
A series of expression
plasmids containing either
the complete insert from
plasmid pUCDBK1
(Peoples et al., 1987) or
sub-fragments thereof
were constructed in a tac
Department of Biology, Fine structural analysis of the Zoogloea ramigera phbA- promoter vector. Analysis
Massachusetts phbB locus of protein lysates of
Institute of encoding beta-ketothiolase and acetoacetyl-CoA induced cultures of these
Technology, reductase: nucleotide clones
459 Peoples OP, Sinskey AJ Cambridge 02139. sequence of phbB. Mol Microbiol 1989 Mar;3(3):349-57 1989 identifie
Azospirillum lipoferum
RG6xx was grown under
1 Department of conditions similar to those
Agronomy, 2 resulting in encystment of
Department of Soil Azotobacter spp.. A.
Science, 3 Department lipoferum produced cells
of Microbiology and of uniform shape when
Cell Science, grown on nitrogen-free
University of Florida, Azospirillum lipoferum RG6xx - beta-hydroxybutyrate
Bleakley, B.H.1; Gaskins, M.H.1; Gainesville, Florida Floc formation by Azospirillum lipoferum grown on Poly- Appl. and environm. Microbiol. 1988; Azotobacter - microflocs - agar. Cells accumulated
462 Hubbell, D.H.2; Zam, S.G.3 32611 beta-hydroxybutyrate 54(12):2986-2995 1988 Encapsulation poly-beta-hydroxybu Strain - Morphology 674.
(1) Institut für
Biochemie, Wilhelm-
Klemm-Straße 2, D-
48149 Münster,
Germany Two fluorometric assays
(2) for the determination of
Institut für poly-<beta>-
Biotechnologie, ETH- hydroxybutyrate
Zürich Hönggerberg, (PHB)
CH-8093 Zürich, inside intact cells are
Switzerland presented in this paper, a
(3) Fluorometric measurement of poly-<beta> spectrofluorometric
Kelco, 2025 A E. hydroxybutyrate in Alcaligenes eutrophus fluorometric measurement - method and one
A. Degelau (1), T. Scheper (1), J. E. Harbor Drive, San by flow Applied Microbiology and Biotechnology Abstract spectrofluorometric method - based on a
463 Bailey (2), C. Guske (3) Diego, cytometry and spectrofluorometry Volume 42 Issue 5 (1995) pp 653-657 1995 laser flow cytometer laser flow cytometer. The Analytics 428.
Formal kinetics of poly-beta-Hydroxybutyric acid (PHB)
production in Alcaligenes eutrophus H 16 and Mycoplana
Sonnleitner, B.; Heinzle, E.; Braunegg, rubra R 14 with respect to the dissolved oxygen tension in European J. Appl. Microbiol. Biotechnol. 1979;
464 G.; Lafferty, R.M. ammonium-limited batch cultures 7:36800 1979 20.
Schlegel, H.G.; Gottschalk, G.; von Formation and utilization of poly-beta-hydroxybutyric acid
465 Bartha, R. by Knallgas bacteria (Hydrogenomonas) Nature 1961; 191:463-465 1961 22.
4.10 Literature on Polyhydroxyalkanoates.xls - page 155
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Recombinant strains of
1 Institut für Pseudomonas oleovorans,
Mikrobiologie der which harbour the poly(3-
Georg-August- hydroxybutyrate)-
Universität Göttingen, biosynthetic genes of
Grisebachstrasse 8, W- Alcaligenes eutrophus,
3400 Göttingen, accumulated
Germany; 2 Imperial poly(hydroxyalkanoates),
chemical Industries, P. Pseudomonas oleovorans - composed of 3-
O. Box 1, Billingham, Formation of blends of various poly(3-hydroxyalkanoic Alcaligenes eutrophus - hydroxyoctanoate (3HO),
Timm, A.1; Byrom, D.2; Steinbüchel, Cleveland TS23 1LB, acids) by a recombinant strain of Pseudomonas Ralstonia eutropha - 3- up to 70 % of the cell dry
466 A.1 UK oleovorans Appl. Microbiol. Biotechnol. 1990; 33:296-301 1990 Hydroxyoctanoate (3HO) - weight if the cells Strain - Copolyesters 414.
1 Institut für
Mikrobiologie der
Georg-August-
Universität Göttingen, The formation of poly(3-
Grisebachstrasse 8, W- hydroxyalkanoic acid),
3400 Göttingen, PHA, by various strains of
Germany; 2 chemolithotrophic and
Department of phototrophic bacteria has
Biochemistry, been examined,
University of Copolyester - Phototrophic Chemolithotrophic
Massachusetts, bacteria - Chromatiaceae - bacteria were grown
Amherstr, MA 01003, Rhodospirillaceae - Sulfur aerobically under nitrogen-
Liebergesell; M.1; Hustede; E.1; Timm; USA; 3 Department of purple bacteria - Non-sulfur limiting conditions on
A.1; Steinbüchel; A.1; Fuller; R.C.2; Polymer Science and Formation of poly(3-hydroxyalkanoates) by phototrophic purple bacteria - various aliphatic organic
468 Lenz; R.W.3; Schlegel; H.G.1 Engineering, Univer and chemolithotrophic bacteria Arch. Microbiol. 1991; 155:415-421 1991 Chemolithotrophic bacteria acid Strains 422.
4.10 Literature on Polyhydroxyalkanoates.xls - page 156
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The acetoacetyl-CoA-
reductase (EC-1.1.1.36)
Univ.Harrisonburg- and the
James-Madison; polyhydroxyalkanoate
Monsanto (PHA)-synthase from
LO Department of Rlastonia eutropha were
Biology, James expressed in
Madison University, Formation of poly(3-hydroxybutyrate-co-3- Escherichia coli,
Harrisonburg, VA hydroxyhexanoate) by PHA-synthase from Ralstonia Klebsiella aerogenes and
22807, USA. eutropha; poly-beta-hydroxybutyrate and 3- PHA-negative mutants
Dennis D; McCoy M; Stangl A; Valentin Email: hydroxyhexanoate copolymer production following of R. eutropha and
H E; Wu Z dennisde@jmu.edu acetoacetyl-CoA-reductase and PHA-synthase gene J.Biotechnol.; (1998) 64, 2-3, 177-86 Pseudomonas putida.
471 expression 1998 Whi
Azotobacter vinelandii
UWD formed
polyhydroxyalkanoate
(PHA) copolymers
containing beta-
hydroxybutyrate and
beta-hydroxyvalerate (HV)
Department of when grown in a medium
Microbiology, containing glucose as the
University of Alberta, primary C source and
Edmonton, Canada. Formation of poly(hydroxybutyrate-co-hydroxyvalerate) by valerate (pentanoate) as a
472 Page WJ, Manchak J, Rudy B Azotobacter vinelandii UWD Appl Environ Microbiol 1992 Sep;58(9):2866-73 1992 precursor. Copolymer was 442.
474 Kannan, L.V. Formation of poly-beta-hydroxybutyrate by Actinomycetes Indian Journal of Biochemistry 1970; 7:126-129 1970 223.
Formation of polyester blends by a recombinant strain of
Preusting; H.; Kingma; J.; Huisman; G.; Pseudomonas oleovorans: different poly(3- Journal of Environmental Polymer Degradation
475 Steinb chel; A.; Witholt; B. hydroxyalkanoates) are stored in seperate granules 1993; 1(1):44501 1993 557.
Formation of polyesters by Pseudomonas oleovorans:
Lageveen, R.E.; Huisman, G.W.; Effect of substrates on formation and composition of poly-
Preusting, H.; Ketelaar, P.; Eggink, G.; (R)-3-hydroxyalkanoates and poly-(R)-3- Applied and Environmental Microbiol. 1988;
476 B.Witholt hydroxyalkenoates 54(12):2924-2932 1988 338.
Pseudomonas oleovorans
accumulates poly(3-
hydroxyalkanoates)
(PHAs) after growth on
medium chain length
hydrocarbons.
Large amounts of this
Institut fur polyester are synthesized
Mikrobiologie der when cells are grown
Georg-August- Formation of polyesters consisting of medium-chain-length under nitrogen-limiting
Universitat Gottingen, 3-hydroxyalkanoic acids from gluconate by Pseudomonas conditions. When nitrogen
Federal Republic of aeruginosa and is
477 Timm A, Steinbuchel A Germany. other fluorescent pseudomonads. Appl Environ Microbiol 1990 Nov;56(11):3360-7 1990 resupplied in t 360.
4.10 Literature on Polyhydroxyalkanoates.xls - page 157
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Blends of atactic
poly[(R,S)-3-
Department of hydroxybutyrate], a-PHB,
Chemistry G. with
Ciamician and Centro poly(.epsilon.-
di Studio per la caprolactone), PCL, and
Fisica delle with poly(L-lactic acid),
Macromolecole del PLLA, were obtained in
CNR, University of Further Evidence of Crystallinity-Induced Biodegradation the form of compression
Focarete, Maria Letizia; Ceccorulli, Bologna, Bologna, of Synthetic Atactic Poly(3-hydroxybutyrate) by PHB- molded films. The
Giuseppina; Scandola, 40126, Italy Depolymerase A from Pseudomonas lemoignei. Blends of phase behavior of the
484 Mariastella; Kowalczuk, Marek Atactic Poly(3-hydroxybutyrate) with Crystalline Polyesters Macromolecules (1998), 31(24), 8485-8492 1998 blends was different: a-PH kopiert
485 K"szegi; B. Gärtank oder Retorte ? Risk kontroll 1982; 4:22-24 1982 275.
Gas chromatographic determination of poly-beta-
hydroxybutyric acid in microbial biomass after hydrochloric
486 Riis, V.; Mai, W. acid propanolysis J of Chromatography 1988; 445:285-289 1988 396.
Gas chromatography-mass spectrometric analysis and its
application to a screening procedure for novel bacterial
polyhydroxyalkanoic acids containing long chain saturated Journal of Fermentation and Bioengineering
487 Lee; E.Y.; Choi; C.Y. and unsaturated monomers 1995; 80(4):408-414 1995 600.
Gaschromatographische Bestimmung der H2-, O2- and
CO2-Konsumptionsraten von Hydrogenomonas eutropha
488 Robra, K. H. Stamm H 16 ? 70.
Nonproteinaceous calcium
channel complexes from
Escherichia coli,
composed of poly-(R)-3-
hydroxybutyrate
(PHB) and inorganic
polyphosphate (polyP),
exhibit two distinct gating
modes (modes 1 and 2) in
Gating Kinetics of E. coli Poly-3- planar lipid
Hydroxybutyrate/Polyphosphate Channels in Planar J. Membrane Biol. 170:135-145 (1999) bilayers. Here we
489 S. Das, R.N. Reusch Bilayer Membranes © 1999 by Springer-Verlag New York, Inc. 1999 report
4.10 Literature on Polyhydroxyalkanoates.xls - page 159
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1Laboratory of
Molecular
Biotechnology, Putative promoters of
Division of Molecular polyhydroxyalkanoate
Cell Mechanisms, (PHA)-synthetic genes of
Department of Paracoccus denitrificans
Biological Mechanisms were identified. Gene
and dosage effects for PHA
Functions, Graduate synthesis were
School of Bio- & Agro- investigated in
Sciences, Nagoya recombinants of P.
University, Chikusa-ku, polyhydroxyalkanoate; denitrificans with
Nagoya 464-01, Japan Gene dosage effects on polyhydroxyalkanoates synthesis methylotroph; biodegradable increased expression
2Laboratory of from n-alcohols in plastics; fed-batch culture; levels of each PHA
490 Maehara A, Ikai K, Ueda S, Yamane T Applied Microbi Paracoccus denitrificans Biotechnol Bioeng 1998 Oct 5;60(1):61-9 1998 molecular weight syntheti
The polyhydroxyalkanoate
(PHA) synthase gene of
Comamonas acidovorans
DS-17 (phaCCa) was
cloned by using the
synthase gene of
Department of Alcaligenes eutrophus as
Biological and a heterologous
Environmental Genetic analysis of Comamonas acidovorans hybridization probe.
Sciences, Saitama polyhydroxyalkanoate Complete sequencing of a
University, Urawa, synthase and factors affecting the incorporation of 4- 4.0-kbp
Saitama 338-0825, hydroxybutyrate SmaI-HindIII (SH40)
494 Sudesh K, Fukui T, Doi Y Japan. monomer. Appl Environ Microbiol 1998 Sep;64(9):3437-43 1998 subfragment rev
Mol. methods were
applied to analyze the A.
eutrophus PHB
biosynthetic pathway. The
genes for b-ketothiolase
(phbA),
NADPH-dependent
acetoacetyl-CoA
reductase (phbB), and
Inst. Mikrobiol., Georg- Genetic and molecular analysis of the Alcaligenes PHB
August-Univ., eutrophus synthase (phbC) are
Goettingen D-3400, poly(hydroxyalkanoate)-biosynthetic genes and NATO ASI Ser., Ser. E, 186(Novel Biodegrad. Alcaligenes presumably organized in 1
Steinbuchel, Alexander; Schubert, Fed. Rep. accumulation of Microb. Polym.), polyhydroxyalkanoate gene operon with phbC
495 Peter; Timm, Arnulf; Pries, Andreas Ger. PHA in recombinant bacteria. 143-59 (English) 1990 1990 cloning Pseudomonas being the 1st ge
4.10 Literature on Polyhydroxyalkanoates.xls - page 161
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Rhizobium etli
accumulates poly-beta-
hydroxybutyrate (PHB) in
symbiosis and in free life.
PHB is a reserve material
that serves
as a carbon and/or
electron sink when optimal
Departamento de growth conditions are not
Ecologia Molecular, met. It has been
Universidad Nacional Genetic and physiological characterization of a Rhizobium suggested that in
Cevallos MA, Encarnacion S, Leija A, Autonoma de Mexico, etli mutant symbiosis PHB can
496 Mora Y, Mora J Morelos, Mexico. strain unable to synthesize poly-beta-hydroxybutyrate. J Bacteriol 1996 Mar;178(6):1646-54 1996 pr
Transgenic suspension
cultures of Black Mexican
Sweet maize (Zea mays
L.) expressing the
Alcaligenes eutrophus
genes
encoding enzymes of the
Department of pathway for biosynthesis
Chemical Engineering Growth kinetics, nutrient uptake, and expression of the of the biodegradable
and Material Science, Alcaligenes polymer poly(beta-
University of eutrophus poly(beta-hydroxybutyrate) synthesis pathway in hydroxybutyrate) (PHB)
Hahn JJ, Eschenlauer AC, Narrol MH, Minnesota, St. Paul transgenic were
503 Somers DA, Srienc F 55108, USA. maize cell suspension cultures. Biotechnol Prog 1997 Jul-Aug;13(4):347-54 1997 established as a tool
Growth of Azotobacter vinelandii UWD in fish peptone
medium and simplified extraction of poly-beta- Appl. Environ. Microbiol. 1993; 59(12):4236-
504 Page; W.J.; Cornish; A. hydroxybutyrate 4244 1993 440.
4.10 Literature on Polyhydroxyalkanoates.xls - page 162
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly(hydroxybutyric acid)
(PHB) was produced by a
selectant of Azotobacter
beijerinckii
in media containing only
organic nitrogen sources
Innovent e.V. such as N substrates. The
Arbeitsgruppe Growth-associated production of poly(hydroxybutyric chosen
Biotechnologie, acid) by Azotobacter beijerinckii from compounds
Göschwitzer Str. 22, D- organic nitrogen Applied Microbiology and Biotechnology Abstract were casein peptone,
505 E. J. Bormann, M. Leißner, B. Beer 07747 Jena, Germany substrates Volume 49 Issue 1 (1998) pp 84-88 1998 yeast
507 Rodriguez-Valera; F.; Lillo; J.A.G. Halobacteria as producers of polyhydroxyalkanoates FEMS Microbiology Reviews 1992; 103:181-186 1992 474.
Strohl, W. R.; Cannon, G. C.; Shively,
J. M.; G de, H.; Hook, L. A.; Lane, C.
508 M.; Larkin, J. M. Heterotrophic Carbon Metabolism by Beggiatoa alba J Bacteriol. 1981; 148:572-583 1981 404.
Preusting; H.; Houten, van; R.; Hoefs; High Cell density Cultivation of Pseudomonas oleovorans:
A.; Langenberghe, van; E.K.; Favre- Growth and Production of Poly(3-hydroxyalkanoates) in Biotechnology and Bioengineering 1993; 41:550- 1993(
510 Bulle; O.; Witholt; B. Two-Liquid Phase Batch and Fed-Batch Systems 556 4?) 451.
4.10 Literature on Polyhydroxyalkanoates.xls - page 163
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Department of
Chemical Engineering
and BioProcess A recombinant
Engineering Research Escherichia coli strain XL1-
Center, Korea Blue harboring a stable
Advanced Institute of high-copy-number plasmid
Science and pSYL107
Technology, 373-1 containing the Alcaligenes
Kusong-dong, Yusong- eutrophus
gu, Taejon 305-701, polyhydroxyalkanoate
Korea biosynthesis genes and
email: Sang Yup Lee High cell density culture of metabolically engineered E. coli the
(leesy@sorak.kaist.ac. for the production of Poly(3-hydroxybutyrate) in a defined Biotechnol Bioeng 1998 Apr 20-May 5;58(2- Escherichia
511 Wang; F.; Lee; S.Y. kr) medium 3):325-8 1998 coli ftsZ gen 681.
Polyhydroxyalkanoate
(PHA) polyester is
extracted from biomass by
dissolving the PHA in a
KURDIKAR, Devdatt, L. , non-
12220 Country Place Drive, Maryland MONSANTO halogenated solvent which
Heights, MO 63043, United States of COMPANY, 800 N. comprises a PHA-poor
America Lindbergh Boulevard, solvent that dissolves less
STRAUSER, Fred, E. , 3006 Saint Louis, MO HIGH TEMPERATURE PHA than 1 % of the PHA at
St. Camella Street, Saint Charles, MO 63167, United States EXTRACTION USING PHA-POOR WO9846783 temperatures
516 63301-0356, United States of Am of America SOLVENTS 1998-10-22 1998 less than the
Methylobacterium
extorquens ATCC 55366
Bioprocess R&D was successfully
Group, Biotechnology cultivated
Research Institute at very high cell densities
(BRI), National in a fed-batch fermn.
Research Council of system using MeOH as
High-cell-density production of poly-b-hydroxybutyrate a sole C and energy
Canada, 6100 (PHB) from source and a completely
Royalmount Avenue, methanol by Methylobacterium extorquens. Production of polyhydroxybutyrate manuf minimal culture medium
Bourque, D.; Pomerleau, Y.; Groleau, Montreal (Quebec), high-molecular-mass PHB. Appl. Microbiol. Biotechnol., 44(3-4), 367-76 methanol Methylobacterium for the prodn. of poly-b-
518 D. Canada H4P 2R2 (English) 1995 1995 hydroxybutyrate (PHB). C 604.
The poly(beta-
hydroxybutyrate) (PHB)
biosynthetic genes of
Alcaligenes eutrophus that
are organized in a single
operon
(phbCAB) have been
Institute of cloned in Escherichia coli,
Microbiology and where the expression of
Genetics, University of High-level poly(beta-hydroxybutyrate) production in the genes in the wild-type
Vienna, Austria. recombinant phb operon from plasmid
519 Kalousek S, Lubitz W Escherichia coli in sugar-free, complex medium. Can J Microbiol 1995;41 Suppl 1:216-21 1995 p4A leads to t
Hydroxy-terminated PHA
is produced by cultivating
a PHA-producing
ASRAR, Jawed , 14949 Royal Brook microorganism in the
Drive, Chesterfield, MO 63017, United presence of an
States of America MONSANTO aliphatic diol or
SHAH, Devang, T. , 719 G. COMPANY, 800 N. an aliphatic polyol. High
Treeside Court, Chesterfield, MO Lindbergh Boulevard, molecular weight hydroxy-
63017, United States of America St. Louis, MO 63189, terminated PHA is
TRAN, Minhtien , 459 Holly United States of HYDROXY-TERMINATED obtainable by the
528 Terrace Co America POLYHYDROXYALKANOATES WO9964617A1 Dec. 16, 1999 1999 disclosed pr
Hydroxyterminated PHA is
produced by cultivating a
PHA-producing
microorganism in the
presence of an aliphatic
diol or an aliphatic
Asrar; Jawed , Chesterfield, MO polyol. High
Shah; Devang T. , molecular weight hydroxy-
Chesterfield, MO Hydroxy-terminated terminated PHA is
Tran; Minhtien , Ballwin, Monsanto Company, polyhydroxyalkanoates obtainable
530 MO St. Louis, MO US5994478 Nov. 30, 1999 1999
The transformation of
Azotobacter vinelandii UW
with A. vinelandii 113 DNA
resulted in the formation
of rifampin-resitant
colonies, 13 % of which
Department of also inherited a previously
Microbiology, unrecognized mutation in
University of Alberta, the respiratoy NADH
Emonton, Alberty, Hyperproduction of Poly-beta-hydroxybutyrate during Azotobacter vinelandii UW - oxidase. These
531 Page, W.J.; Knosp, O. Canada T6G 2E9 exponential growth of Azotobacter vinelandii UWD Appl. Environ. Microbiol. 1989; 55:1134-1339 1989 Azotobacter vinelandii UWD transformants produce Strain - Metabolism 323 korr
4.10 Literature on Polyhydroxyalkanoates.xls - page 167
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1 Institut für
Mikrobiologie der Geor-
August-Universität Twenty-four different
Göttingen, strains of aerobic Gram-
Grisebachtsrasse 8, W- negative bacteria, mainly
3400 Göttingen, Alcaligenes - Paracoccus - belonging to the genera
Germany; 2 Institut für Methylobacterium - Alcaligenes, Paracoccus,
Organische Chemie Pseudomonas - Alcaligenes Pseudomonas and
der Georg-August- eutrophus NCIB 11599 - Methylobacterium, were
Universität Göttingen, Pseudomonas oxalaticus Ox1 - examined with respect to
Tammannstrasse 2, W- terpolyesters - 4-hydroxyvaleric their ability to utilize 4- Strains -
Valentin; E., H1; Schönebaum; A.2; 3400 Göttingen, Identification of 4-hydroxyvaleric acid as a constituent of acid - 4-valerolactone - 3- hydroxybaleric acid (4HV), Copolyesters -
536 Steinbüchel; A.1 Germany biosynthetic polyhydroxyalkanoic acids from bacteria Appl. Microbiol. Biotechnol. 1992; 36:507-514 1992 hydroxypropionic acid 4-valerolactone Substrates 416.
(1) Department of
Biology, James
Madison University,
Harrisonburg, VA A recombinant strain of
22807, USA Pseudomonas putida
(2) GPp104
Institut für Organische (pHP1014::E146), which
Chemie der Georg- expressed
August-Universität the polyhydroxyalkanoic
Göttingen, acid (PHA) synthase of
Tammannstraße 2, Identification of 5-hydroxyhexanoic acid, Thiocapsa pfennigii
D- 4-hydroxyheptanoic acid and 4- exhibiting an
37077 Göttingen, hydroxyoctanoic acid as Applied Microbiology and Biotechnology Abstract unusual
H. E. Valentin (1), A. Schönebaum (2), Germany new constituents of bacterial Volume 46 Issue 3 (1996) pp 261-267 substrate specificity at a
537 A. Steinbüchel (3) polyhydroxyalkanoic acids 1996 high lev
The first
polyhydroxyalkanoic acid
(PHA) synthase gene
(phbCRr) of a Gram-
positive bacterium was
cloned from a genomic
library of Rhodococcus
ruber in the broad-host-
Institut fur range plasmid vector
Mikrobiologie, Georg- Identification, cloning and sequence analysis of the pRK404. The hybrid
August-Universitat poly(3-hydroxyalkanoic acid) synthase gene of the gram- plasmid harboring phbCRr
Gottingen, FRG. positive allowed
542 Pieper U, Steinbuchel A bacterium Rhodococcus ruber. FEMS Microbiol Lett 1992 Sep 1;75(1):73-9 1992 the expression o
4.10 Literature on Polyhydroxyalkanoates.xls - page 170
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Enrichments from an
estuarine sediment with
crotonate as substrate
resulted in the isolation of
a motile, gram-neg.,
obligately anaerobic rod
with pointed ends,
designated strain 10cr1.
The organism was
Dep. Biol. Sci., Univ. Ilyobacter delafieldii sp. nov., a metabolically restricted polyhydroxybutyrate metab asporogenous, did not
Waikato, anaerobic Ilyobacter reduce S0, S2O32-, NO3-,
543 Janssen, Peter H.; Harfoot, C. G. Hamilton, N. Z. bacterium fermenting PHB. Arch. Microbiol., 154(3), 253-9 (English) 1990 1990 O2, Strain 423.
Production of poly(4-
hydroxybutyrate) [P(4HB)]
by Comamonas
acidovorans JCM10181
was
studied by
Department of introducing additional
Biological and copies of its PHA
Environmental Improved production of poly(4-hydroxybutyrate) by synthase gene and the
Sciences, Saitama Comamonas beta-ketothiolase gene.
Sudesh K, Fukui T, Taguchi K, Iwata T, University, Urawa, acidovorans and its freeze-fracture A multi-
547 Doi Y Japan. morphology. Int J Biol Macromol 1999 Jun-Jul;25(1-3):79-85 1999 copy-number broad-
4.10 Literature on Polyhydroxyalkanoates.xls - page 171
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The biodegradation of
samples of poly(3-
hydroxybutyrate)(P(3HB)),
poly(3-hydroxybutyrate-co-
10%-3-
hydroxyvalerate)(P(3HB-
co-10 %-3HV)), and poly
3-hydroxybutyrate-co-20%-
Laboratorium voor 3-hydroxyvalerate)(P(3HB-
Microbiologie, In situ biodegradation of poly(3-hydroxybutyrate) and co-20%- 3HV)) was
Mergaert J, Wouters A, Anderson C, Universiteit Gent, poly(3-hydroxybutyrate-co-3-hydroxyvalerate) in natural investigated in situ in
549 Swings J Belgium. waters. Can J Microbiol 1995;41 Suppl 1:154-9 1995 natural waters. Th
Polyhydroxybutyrate
(PHB) is a polyester made
by many microorganisms
under conditions of
nitrogen deficiency, and is
produced commercially in
bulk by biotechnology. It
has been suggested that
Department of PHB-based materials
Materials, Queen Mary In vitro and in vivo evaluation of polyhydroxybutyrate and (copolymers and
and Westfield College, of composites) could be
550 Doyle C, Tanner ET, Bonfield W London, UK. polyhydroxybutyrate reinforced with hydroxyapatite. Biomaterials 1991 Nov;12(9):841-7 1991 suitab
Kwong, A. K.; Chou, S.; Sefton, A. M.; In vitro and in vivo release of insulin from poly(lactic acid)
551 Goosen, F. A. microbeads and pellets Journal of controlled release 1986; 4 1986 288.
4.10 Literature on Polyhydroxyalkanoates.xls - page 172
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Spherical microporous
reservoir-type
microcapsules, fabricated
using a W/O/W double
emulsion technique with
solvent
evaporation and
composed of 330 kD
Department of poly(beta-hydroxybutyrate-
Pharmaceutical and In vitro biodegradation of polyhydroxybutyrate- hydroxyvalerate (P(HB-
Biological Sciences, hydroxyvalerate HV)) (10.8% HV)/20%
Aston University, microcapsules exposed to Hank's buffer, newborn calf PCL II
Birmingham, UK. serum, pancreatin containing a range of
552 Atkins TW, Peacock SJ and synthetic gastric juice. J Microencapsul 1997 Jan-Feb;14(1):35-49 1997 bovine
Purified recombinant
poly(hydroxyalkanoic acid)
(PHA) synthase from
Chromatium vinosum
(PhaECCv) was used to
examine
in vitro the specific
Institut fur synthase activity, turnover
Mikrobiologie der In vitro biosynthesis of poly(3-hydroxybutyric acid) by using of R-(-)-3-hydroxybutyryl
Westfalischen purified coenzyme A (3HB-CoA)
Wilhelms-Universitat poly(hydroxyalkanoic acid) synthase of Chromatium Appl Microbiol Biotechnol 1998 Mar;49(3):258- and poly(3-hydroxybutyric
553 Jossek R, Reichelt R, Steinbuchel A Munster, Germany. vinosum. 66 1998 acid) formation
The use of
polyhydroxybutyrate
(PHB) and its copolymers
(with
hydroxyvalerate) as
degradable materials for
surgical use is showing
increasing promise due to
Med. Inst., their long degrdn. profile.
Staffordshire Of considerable
Polytech., In vitro degradation of a PHB/PHV copolymer and a new hydroxybutyrate interest were the
Stoke-on-Trent ST4 technique for Biomaterials, 12(2), 210-14 (English) hydroxyvalerate polymer interfacial changes and
554 Knowles, J. C.; Hastings, G. W. 7NY, UK monitoring early surface changes. 1991 1991 degrdn their role
4.10 Literature on Polyhydroxyalkanoates.xls - page 173
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Injection-molded PHB/7%
PHV (mol. mass 580,000)
samples were
placed in buffered saline
at varying pH for long-term
in vitro studies.
Anomalies between
sample mass loss and
Biomed. Eng. Unit, In vitro degradation of a polyhydroxybutyrate valerate Young's modulus were
Med. Inst., poly(hydroxybutyrate)[PHB]/poly(hydroxyvalerate)[PHV] biomaterial degrdn found for the different
Stoke-on-Trent ST4 copolymer. J. Mater. Sci.: Mater. Med., 3(5), 352-8 polyester biomaterial degrdn pHs. The Young's
555 Knowles, J. C.; Hastings, G. W. 7NY, UK (English) 1992 1992 modulus anomaly was
PURPOSE:To increase
the share of PHB
producing microorganisms
in an active sludge to
efficiently recover PHB
from the active
sludge by continuing the
aeration thereof for a
specific number of days
without the supply of a
SAITO YUJI; others: INCREASE OF SHARE OF PHB PRODUCING substrate.
558 04 TAISEI CORP MICROORGANISMS IN ACTIVE SLUDGE JP4131196 1992-05-01 1992 CONSTITUTION:An ac
4.10 Literature on Polyhydroxyalkanoates.xls - page 174
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Synthesis of
polyhydroxyalkanoates
(PHAs) from intermediates
of fatty acid beta-oxidation
was used as a tool to
study fatty
Institut d'Ecologie- acid degradation in
Biologie et Physiologie developing seeds of
Vegetales, Batiment Increased flow of fatty acids toward beta-oxidation in Arabidopsis. Transgenic
de Biologie, Universite developing seeds of plants expressing a
de Lausanne, CH- arabidopsis deficient in diacylglycerol acyltransferase peroxisomal PHA
1015 Lausanne, activity or synthase under the
559 Poirier Y, Ventre G, Caldelari D Switzerland. synthesizing medium-chain-length fatty acids. Plant Physiol 1999 Dec;121(4):1359-66 1999 control of a
Azotobacter chroococcum
MAL-201, when grown
under nitrogen-free
conditions with excess
glucose,
accumulated poly-
beta-hydroxybutyric acid
amounting to 75% of cell
dry weight at the late
Induction of Encystment and Poly-beta-Hydroxybutyric exponential phase. This
Soma Pal, Anupam Manna, Amal K. Acid Production by Azotobacter Curr Microbiol 35:327-330 (1997) led to induction of
563 Paul chroococcum MAL-201 © Springer-Verlag New York Inc. 1997 1997 encystmen
564 Kumar; C.; Patel; N. Industrial ecology Proc. Natl. Acad. Sci. USA 1992; 89:798-799 1992 507.
4.10 Literature on Polyhydroxyalkanoates.xls - page 175
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
565 Hrabak; O. Industrial production of poly-beta-hydroxybutyrate FEMS Microbiology Reviews 1992; 103:251-256 1992 481.
566 Leaversuch, R. Industry weighs need to make polymer degradable Modern Plastics 1987; 52-55 1987 378.
Influence of ammonium salts and cane molasses on growth
Beaulieu; M.; Beaulieu; Y.; Melinard; J.; of Alcaligenes eutrophus and production of Applied and Environmental Microbiology 1995;
567 Pandian; S.; Goulet; J. polyhydroxybutyrate 61:165-169 1995 498.
Production of poly-beta-
hydroxybutyrate (PHB) by
Univ.Laval Alcaligenes
LO Centre STELA, eutrophus DSM 545
Departement de was studied in synthetic
Sciences et culture medium (0.79
Technologie des g/l MgSO4.7H2O, 2.98
Aliments, g/l Na2HPO4, 1.5 g/l
Universite Laval, Influence of ammonium salts and cane molasses on growth KH2PO4, 15 mg/l
Beaulieu M; Beaulieu Y; Melinard J; Cite Universitaire, of Alcaligenes eutrophus and production of FeSO4.7H2O and 24
Pandian S; *Goulet J Quebec, G1K 7P4, polyhydroxybutyrate; culture medium optimization for poly- Appl.Environ.Microbiol.; (1995) 61, 1, 165-69 ml trace element solution)
568 Canada. beta-hydroxybutyrate production 1995 with 3% g
The influence of
phenylacetic acid on the
polymerization of beta-
Istituto di Microbiologia hydroxybutyrate and cell
agraria dell' Università elongation in Azotobacter
di Pisa, Centro di chroococcum has been
Studio per la investigated. The polymer
Microbiologia del Influence of phenylacetic acid on poly- -hydroxybutyrate was extracted by a new
Suolo del Consiglio (PHB) Azotobacter chroococcum - method. Ist molecular
Nazionale delle polymerization and cell elongation in Azotobacter phenylacetic acid - cell weight, calculated by
570 Nuti; M.P.; DeBertholdi; M.; Lepidi; A.A. Ricerche, Pisa, Italy chroococcum Beij. Can.J.Microbiol. 1972; 18:1275-1261 1972 elongation intrinsic viscosity and l Strain - Metabolism 150.
Influence of the endogenous storage lipid poly-á-
hydroxybutyrate on the reducing power availability during
cometabolism of trichloroethylene and naphthalene by Applied an dEnvironmental Microbiology 1993;
571 Henrysson; T.; McCarthx; P.L. resting methanotrophic mixed cultures 59(5):1602-1606 1993 609.
Insulin delivery systems and encapsulation of cells for CRC Critical Reviews in Biocompatibility 1987;
572 Goosen, M. F. A.; Langer, R. medical and industrial use 3:45292 1987 290.
4.10 Literature on Polyhydroxyalkanoates.xls - page 176
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
In a laboratory-scale
system, dentrification
activity of a heterotrophic
microbial starter culture
changed when different
lots of
Universitat poly-3-hydroxybutyrate-co-
Hohenheim, Institut fur 3-hydroxyvalerate (P(HB-
Mikrobiologie, co-HV)) were used as the
Stuttgart, Germany. Interaction between poly-3-hydroxybutyrate-co-3- solid carbon source in the
Biedermann J, Owen AJ, Schloe KT, biederma@uni- hydroxyvalerate and a heterotrophic
573 Gassner F, Sussmuth R hohenheim.de denitrifying Pseudomonas strain. Can J Microbiol 1997 Jun;43(6):561-8 1997 denitrifi
Interrelations between glycogen, poly-beta-hydroxybutyric
acid and lipids during accumulation and subsequent
574 Zevenhuizen; L.P.T.M.; Ebbink; A.G. utilization in a Pseudomonas Antonie van Leeuwenhoek 1974; 40:103-120 1974 222.
Intracellular degradation
of poly(3-hydroxybutyrate)
(PHB) in bacteria is not
yet clear. The properties
of the autodigestion of
native PHB granules from
Department of Zoogloea ramigera I-16-M
Biological Sciences, were examined. The
Faculty of Science, release of D(-)-3-
Kanagawa University, Intracellular degradation of poly(3-hydroxybutyrate) hydroxybutyrate was
Japan. granules of Zoogloea observed
575 Saito T, Saegusa H, Miyata Y, Fukui T ramigera I-16-M. FEMS Microbiol Rev 1992 Dec;9(2-4):333-8 1992 only at pH
Polyhydroxyalkanoate
(PHA) granule associated
proteins from
Pseudomonas oleovorans
Department of Biology, were
James Madison purified and
University, the N-terminal sequences
Harrisonburg, VA, of two major proteins
USA. migrating in sodium
Investigation of the function of proteins associated to dodecyl sulfate
Valentin HE, Stuart ES, Fuller RC, Lenz henry.e.valentin@mon polyhydroxyalkanoate inclusions in
578 RW, Dennis D santo.com Pseudomonas putida BMO1. J Biotechnol 1998 Oct 8;64(2-3):145-57 1998 polyacrylamide gels with
Blends of poly(D-(-)-3-
hydroxybutyrate) (PHB)
and atactic PMMA were
isothermally cold-crystd.
from homogeneous
amorphous samples
Stazione polyhydroxybutyrate PMMA obtained by quenching. X-
Sperimentale Investigation of the phase structure of blend phase structure ray techniques were
Cellulosa, Carta Fibre poly(D(-)3-hydroxybutyrate)/atactic poly(methyl crystal morphol employed to investigate
Vegetali Artificiali, methacrylate) polyhydroxybutyrate PMMA the phase structure of the
Canetti, M.; Sadocco, P.; Siciliano, A.; Milan 20133, blends by small-angle x-ray scattering. blend cold-crystd. blends. The
579 Seves, A. Italy Polymer, 35(13), 2884-7 (English) 1994 1994 lon
580 Widma... Ionenstr"me und Substratfl sse Biologie in unserer Zeit 1985; 15(1):41852 1985 279.
Bluhm; T.L.; Hamer; G.K.;
Marchessault; R.H; C.A., Fyfe; Veregin; Isodimorphism in bacterial poly(beta-hydroxybutyrate-co-
581 R.P. beta-hydroxyvalerate) Macremolecules 1986; 19:2871 1986 210.
A microorganism
(Azotobacter sp.) was
isolated from soil samples
from the Agronomy
Faculty campus and its
ability to
Catedra de accumulate poly-beta-
Microbiologia, hydroxyalkanoate (PHAs)
Facultad de polymers was analyzed.
Agronomia, The isolated strain
Universidad de Isolation and characterization of Azotobacter sp. for the (named No 8)
Buenos Aires, production of Rev Argent Microbiol 1994 Jan-Mar;26(1):21-7 accumulated 8
583 Quagliano JC, Alegre P, Miyazaki SS Argentina. poly-beta-hydroxyalkanoates. [Article in Spanish] 1994 micrograms PHA/m of cul
1. Employing mutagenic
agents (nitrite, 1-nitroso-3-
Institut für nitro-1-methylguanidine,
Mikrobiologie der ethylmethanesulfonate),
Universität Göttingen the colistine
und Institut für counterselection
Mikrobiologie der Hydrogenomonas eutropha H technique and the „pin
Gesellschaft für Isolation and Characterization on Mutants of 16 - Ralstonia eutropha H 16 - point“ colony isolation
Strahlen- und Hydrogeneomonas eutropha Strain H 16 Defective in Alcaligenes eutrophus H 16 - method, mutants of
Umweltforschung Catabolism / Isolierung und Charakterisierung Mutants - Entner-Doudoroff Hydrogenomonas
mbH, München in katabolischer Defektmutanten von Hydrogenomonas pathway - Fructose - Glucose - eutropha strain H 16
584 Bowien, B.; Schlegel, H.G. Göttingen eutropha Stamm H 16 Arch. Mikrobiol. 1972; 87:203-210 1972 Gluconate (ATCC 17 699) and of Strain - Metabolism 97. Korr.
Isolation and culture conditions of a bacterium grown on
585 Kodama, T.; Igarashi, Y.; Minoda, Y. hydrogen and carbon dioxide Agr. Biol. Chem. 1975; 39(1):77-82 1975 47.
Poly(3-hydroxybutyric
acid) granules, which
harbored only four major
granule-associated
proteins as revealed by
SDS
polyacrylamide gel
electrophoresis, were
isolated from crude
Institut fur Isolation and identification of granule-associated proteins cellular extracts of
Mikrobiologie, Georg- relevant for Chromatium vinosum D by
Liebergesell M, Schmidt B, Steinbuchel August-Universitat poly(3-hydroxyalkanoic acid) biosynthesis in Chromatium centrifugation in a
586 A Gottingen, FRG. vinosum D. FEMS Microbiol Lett 1992 Dec 1;78(2-3):227-32 1992 linear sucros
Takahashi, J.; Ichikawa, Y.; Sagae, H.; Isolation and Identification of n-Butane-assimilating
587 Komura, I.; Kanou, H.; Yamada, K. Bacterium Agric. Biol. Chem. 1980; 44:1835-1840 1980 375.
4.10 Literature on Polyhydroxyalkanoates.xls - page 179
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
By using selective
enrichment of
polyhydroxyalkanoate-
degrading bacteria and
Laboratorium voor poly(3-hydroxyvalerate)-
Microbiologie, containing granules
Vakgroep Biochemie, from Chromobacterium
Fysiologie en violaceum as the carbon
Microbiologie, source, 10 new
Universiteit Gent, Pseudomonas lemoignei
Mergaert J, Schirmer A, Hauben L, Mau Belgium. Isolation and identification of poly(3-hydroxyvalerate)- strains were isolated;
M, Hoste B, Kersters K, Jendrossek D, Joris.Mergaert@rug.ac degrading strains these strains
588 Swings J .be of Pseudomonas lemoignei. Int J Syst Bacteriol 1996 Jul;46(3):769-73 1996 were able to de
Isolation and metabolism og glycogen and poly-
betahydroxybutyrate in Nocardia asteroides at different
589 Emeruwa; A.C. developmental stages Ann. Microbiol. (Inst Pasteur) 1981; 132B:13-21 1981 238.
Poly-b-hydroxybutyrate
(PHB), a biodegradable
polymer of com.
importance is produced as
storage granules in many
bacteria grown
under high C:N ratio.
Following enrichment and
Department of Botany, Isolation and screening of poly-b-hydroxybutyrate (PHB) diln. plating on specific
University of Calcutta, producing polyhydroxybutyrate formation media, free-living N2-
Calcutta 700 019, bacteria from soil. Proc. Acad. Environ. Biol., 5(1), 43-48 bacteria soil fixers, pseudomonads,
590 Pal, Soma; Paul, A.K. India (English) 1996 1996 spore-for
Isolation of intracellular
polyhydroxyalkanoate (I)
from a fermentation broth
is effected by (a) removing
at least part of the liq.
BLAUHUT WILFRIED phase, (b) adding a
DIPL ING (AT); GIERLINGER water-immiscible solvent
WOLFGANG (AT); STREMPFL DANUBIA Isolation of poly:hydroxy:alkanoate from fermentation broth with a b.pt. below 100
FRIEDRICH DIPL ING PETROCHEM - by concn., solvent deg. C, (c) stirring at a
591 DR (AT) DEUTSCHLAND (DE) extn. and spraying extract into hot water DE4036067 1992-05-14 1992 temp. between room temp.
4.10 Literature on Polyhydroxyalkanoates.xls - page 180
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Organism isolated from
activated sludge and
identified as Zoogloea
ramigera accumulated
large amounts of
sudanophilic granules as
Wisconsin Agricultural the cultrues
Experiment Station flocculated.The granules
and Engineering were extracted by
Experiment Station, chloroform and
University of precipitated with ether
Crabtree; K.; McCoy; E.; Boyle; W.C.; Wisconsin, Madison, Isolation, identification, and metabolic role of the from acid-hydrolyzed
592 Rohlich; G.A. Wisconsin sudanophilic granules of Zoogloea ramigera Applied Microbiology 1965; 13:218-226 1965 Zoogloea ramigera cells. Id Strain 132. Korr.
study was conducted to
isolate, screen and
identify bacteria for
National Institute of the prodn. of a
Molecular Biology and biodegradable plastic
Biotechnology material called
(BIOTECH), poly-.beta.-
University of the hydroxybutyrate (PHB).
Philippines Los Banos Stud. Environ. Sci. (1997), 66(Global The results of isolating
(UPLB) College, Environmental Biotechnology), bacteria from soils
Laguna, 4031, Isolation, screening and identification of bacteria for poly- 737-748 showed that 78 isolates
593 Reyes, Gloria D.; So, R. S.; Ulep, M. M. Philippines .beta.-hydroxybutyrate (PHB) production 1997 possessed cellu
Kinetics and models for the bioconversion of methane into Biotechnology and Bioengineering Symp. 1985;
598 Asenjo; J.A.; Suk; J.S. an intracellular polymer, poly-beta-hydroxybutyrate 15:225-234 1985 240.
1. Beta-Ketothiolase of
Clostridium pasteurianum
Institut für was purified 130-fold by
Mikrobiologie der ammonium sulphate
Universität Göttingen fractionation and by
und Institut für column
Mikrobiologie der chromatography using
Gesellschaft für DEAE-Sephadex A-50 and
Strahlen- und hydroxylapatite. Subjected
Umweltforschung Kinetics and properties of beta-ketothiolase from Beta-Ketothiolase - Clostridium to gel electrophoresis beta-
mbH, München in Clostridium pasteurianum - Activation by ketothiolase
599 Berndt H, Schlegel HG Göttingen pasteurianum. Arch Microbiol 1975 Mar 12;103(1):21-30 1975 Coenzyme A revealed two distinct b Strain - Enzymology 111. Korr.
Braunegg; G.; Lefebvre; G.; Renner; G.;
Zeiser; A.; Haage; G.; Loidl-Lanthaler; Kinetics as a tool for polyhydroxyalkanoate production
600 K. optimization Can. J. Microbiol. 1995; 41:239-248 1995 517.
604 Bakterien als Kunststoffproduzenten Kosmos Kosmos 1983; 8:48-49 1983 246.
Kulturgefäße zur Aufzucht von Hydrogenomonas H16 mit
605 Rudolph, V. elektrolytischer Knallgaserzeugung Dissertation, Göttingen 1968 1968 46.
4.10 Literature on Polyhydroxyalkanoates.xls - page 182
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Lamellar thickening
behavior of microbial
polyesters, poly(3-
hydroxybutyrate) [P(3HB)],
poly(3-hydroxybutyrate-co-
3-hydroxyvalerate) [P(3HB-
Department of co-3HV)] and poly(3-
Biological and hydroxybutyrate-co-4-
Chemical Engineering, hydroxybutyrate)
Faculty of Engineering, Lamellar thickening and cocrystallization of [P(3HB-co-4HB)]
Gunma University, poly(hydroxyalkanoate)s on annealed at various
606 Mitomo H, Doi Y Kiryu, Gunma, Japan. annealing. Int J Biol Macromol 1999 Jun-Jul;25(1-3):201-5 1999 temperatures was inve
PCT No.
PCT/GB96/00284 Sec.
371 Date Nov. 24, 1997
Sec. 102(e) Date Nov. 24,
SATGURUNATHAN 1997 PCT Filed Feb. 9,
RAJASINGHAM (GB); 1996 PCT Pub. No.
GEORGE NEIL (GB); WO96/24682 PCT Pub.
SATGURUNATHAN HAMMOND TIMOTHY Date Aug. 15, 1996A
RAJASINGHAM (GB); GEORGE NEIL (GB); chiral (R) stereospecific
(GB); HAMMOND TIMOTHY (GB); LIDDELL polyhydroxyalkanoate
LIDDELL JOHN JOHN MACDONALD (PHA) in aqueous latex
MACDONALD (GB); TURNER PETER (GB); TURNER form having
607 DERYK (IE) PETER DERYK (IE) Latex of polyhydroxyalkanoate US5977250 1999-11-02 1999 virgin disp
A rapid and inexpensive
test has been developed
to investigate the
Universität Zürich, influence of elevated
Institut für heavy
Pflanzenbiologie, metal
Abteilung concentrations on the
Mikrobiologie, degradation of
Zollikerstrasse 107, lecture: A rapid method for the determination of metal biodegradable plastics.
CH-8008 toxicity Fresenius' Journal of Analytical Chemistry Using an overlay agar
Zürich, to the biodegradation of water insoluble Abstract Volume 354 Issue 5/6 (1996) pp 760- technique it could
608 Linda Birch, H. Brandl Switzerland polymers 762 1996 be d
Ramsay, J.; Ramsay, B.; Normandin,
609 D.; Chavarie, C.; Braunegg, G. Les Plastiques Biodegradables Interface 1991; Jan/Fev 42309 1991 380.
Department of Polyhydroxybutyrate
Chemistry, (PHB) synthases catalyze
Massachusetts the conversion of beta-
Institute of hydroxybutyryl coenzyme
Technology, 77 A (HBCoA)
Massachusetts to PHB. These enzymes
Avenue, Lipases provide a new mechanistic model for require an active site
polyhydroxybutyrate (PHB) cysteine nucleophile for
Cambridge, synthases: characterization of the functional covalent
Jia Y, Kappock TJ, Frick T, Sinskey AJ, Massachusetts 02139, residues in Chromatium catalysis. A
610 Stubbe J USA. vinosum PHB synthase. Biochemistry 2000 Apr 11;39(14):3927-36 2000 protein BLASTp
4.10 Literature on Polyhydroxyalkanoates.xls - page 183
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
(1) CEIMA-
Universidad Nacional
de la Patagonia San
Juan Bosco, Km 4,
9000 Comodoro Forty psychrophile or
psychrotrophic crude-oil-
Rivadavia, Argentina utilizing marine bacteria
(2) were
Institut für
Mikrobiologie der investigated for their
Westfälischen ability to accumulate lipid
Wilhelms-Universität storage compounds in the
Münster, cytoplasm during
H. M. Alvarez (1)(2), O. H. Pucci (1), A. Corrensstraße 3, Applied Microbiology and Biotechnology Abstract cultivation
612 Steinbüchel (2) Lipid storage compounds in marine bacteria Volume 47 Issue 2 (1997) pp 132-139 1997 under nitrogen-limiting
Metabolic pathway
engineering in cotton has
been accomplished by
introducing modified
Alcaligenes eutrophus
genes encoding the
enzymes acetoacetyl-
CoA reductase and
polyhydroxyalkanoate
Agracetus, Monsanto, Portland Press Proc. (1998), 14(Engineeering (PHA)
Middleton, WI, 53562, Crop Plants for synthase. These two
USA Manipulating metabolic pathways in cotton fiber: synthesis Industrial End Uses), 133-147 enzymes, when produced
616 John, Maliyakal E. of polyhydroxybutyrate 1998 in f
Park; H.C.; Park; J.S.; Lee; Y.H.; Huh; Manipulation of the genes for poly-á-hydroxybutyric acid
617 T.L. synthesis in Alcaligenes eutrophus Biotechnology Letters 1995; 17(7):729-734 1995 619.
Interest in biodegradable
plastics made from
renewable resources has
increased significantly in
recent years. PHBV
(polyhydroxybutyrate-
polyhydroxyvalerate)
copolymers are good
ICI BioProducts and examples of this type of
Fine Chemicals, ICI materials. This paper
Americas, Inc., Proc Natl Acad Sci U S A 1992 Feb 1;89(3):839- provides an
621 Luzier WD Wilmington, DE 19897. Materials derived from biomass/biodegradable materials. 42 1992 overview of the man 509.
Mathematical model for determining the effects of
intracytoplasmic inclusions on volume and density of
622 Mas; J.; Pedros-Alio; C.; Guerrero; R. mocroorganisms Journal of Bacteriology 1985; 164(2):749-756 1985 550.
4.10 Literature on Polyhydroxyalkanoates.xls - page 185
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1CRBA-URA CNRS
1465, Faculté de
pharmacie, Université The present study
de Montpellier I, investigated the in vitro
Montpellier, France mechanism and
2Laboratory of degradation rate of
Experimental Surgery, polyhydroxyoctanoate
Department of (PHO). Solution-cast
Surgery, Laval PHO films were incubated
University, Quebec in either water or
Biomaterial Institute, isoosmotic phosphate-
Pavillon polyhydroxyalkanoates; buffered saline (PBS) for
Yves Marois 1 2, Ze Zhang 2, Michel St-François d'Assise, Mechanism and rate of degradation of Journal of Biomedical Materials Research polyhydroxyoctanoate; periods ranging from 1 to
Vert 1, Xiaoyan Deng 2, Robert Lenz 3, CHUQ, Quebec, polyhydroxyoctanoate films in aqueous Volume 49, Issue 2, 2000. Pages: 216- bacterial polyesters; in vitro 24
625 Robert Guidoin 2 * Quebec, media: A long-term in vitro study 224 2000 study; degradation; hydrolysis months. Physi
Department of Poly-beta-hydroxybutyric
Pharmacy, Kunamoto acid (PHB) microspheres
University Hospital, 1 1- containing aclarubicin
1-1 Honjo, Kunamoto hydrochloride were
860, Japan Faculty of prepared by a solvent-
Pharmaceutical evaporation process. The
Sciences, Josai release rates of the drug
Universiy, 2 1-1 from the microspheres
Keyakidai, Sakado, Mechanism of Enhancement of the release rate of were significantly
Saitama 350-02, aclarubicin from poly-beta-hydroxybutyric acid increased by incorporating
626 Kubota, M.1; Nakano, M.1; Juni, K.2 Japan microspheres by fatty acid esters Chem. Pharm. Bull. 1988; 36:333-337 1988 Microsphere - Aclarubicin ethyl or n-butyl esters Application 672.
4.10 Literature on Polyhydroxyalkanoates.xls - page 186
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Mechanism of protein excretion by gram-negative bacteria:
627 Lory; S.; Phang; C.T.; Davis; B.D. Pseudomonas aeruginosa exotoxin A Journal of Bacteriology 1983; 156(2):695-702 1983 274.
Pseudomonas
saccharophila NRRL B-
628 is capable of utilizing
agricultural lipids for
growth. The organism
exhibited good
growth with triacylglycerol
substrates that contained
saturated fatty acyl
Medium-Chain-Length Poly(beta-Hydroxyalkanoate) moieties such as coconut
Daniel K. Y. Solaiman, Richard D. Synthesis from Triacylglycerols by Curr Microbiol 38:151-154 (1999) © 1999 by oil
628 Ashby, Thomas A. Foglia Pseudomonas saccharophila Springer-Verlag New York, Inc. 1999 (CO; C10-12 fa
271 pp.
Avail. Univ. Microfilms Int., Order No.
McGill Univ., Montreal, Melting and crystallization in poly(beta-hydroxyalkanoate) DANN99997 From: Diss. Abstr. melting crystn
629 Pearce, Robert Patrick PQ, Can. blends. Int., B 1996, 56(10), 5521 (English) 1996 1996 polyhydroxyalkanoate blend Abstract Unavailable
The isocitrate
dehydrogenase leaky
mutant Alcaligenes
eutrophus RM-1 was
isolatet after mutagenesis,
and ist metabolic
Department of Genetic Alcaligenes eutrophus - characteristics were
Engineering, College Ralstonia eutropha - isocitrate investigated. The PHB
of Natural Sciences, dehydrogenase leaky mutant - accumulation was
Kyungpook National Metabolic characteristics of isocitrate dehydrogenase leaky metabolic characteristics - significantly increased due
University, Taegu 702- mutant of alcaligenes eutrophus and its utilization for poly- Journal of Fermentation and Bioengineering Vol poly(3-hydroxybutyrate-3- to the icreased forw of Strain - Metabolism -
630 Park, Jin-Seo; Lee Yong-Hyun 701, Korea beta-hydroxybutyrate production 81, No. 3, 197-205, 1996 1996 hydroxyvalerate) - production carbon to the PHB biosyn Copolyesters kopiert
a Department of
Genetic Engineering, The regulatory
College of Natural mechanisms of the
Sciences, Kyungpook biosynthesis of in vivo
National University, poly- b-hydroxybutyrate
Taegu 702-701, Korea Keywords: Alcaligenes [PHB] and poly(3-
b Technology eutrophus; Metabolic hydroxybutyrate-3-
Appraisal Centers, engineering; Regulation hydroxyval-erate)
Korea Technology Metabolic engineering of Alcaligenes eutrophus through mechanism of PHB and P(3HB- [P(3HB-3HV)] of
Credit Guarantee the 3HV) biosynthesis; phbCAB Alcaligenes eutrophus
Fund, Youido, Seoul transformation of cloned phbCAB genes for genes; b-Ketothiolase; were investigated by using
150-010, Korea * the investigation of the Acetoacetyl-CoA reductase; various transformants with
Young-Mi Jung a , Jin-Seo Park b , Corresponding regulatory mechanism of Enzyme Microb Technol 2000 Feb 1;26(2-4):201- PHB synthase; Granular enzyme activities that
631 Yong-Hyun Lee a, * author.E-mail addre polyhydroxyalkanoate biosynthesis. 208 2000 structure were ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 187
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly(hydroxyalkanoates)
are natural polymers with
thermoplastic properties.
One polymer of this class
with commercial
applicability, poly(3-
hydroxybutyrate-co-3-
hydroxyvalerate) (PHBV)
Slater S, Mitsky TA, Houmiel KL, Hao can be produced by
M, Reiser SE, Taylor NB, Tran M, Cereon Genomics, 45 Metabolic engineering of Arabidopsis and Brassica for bacterial fermentation, but
Valentin HE, Rodriguez DJ, Stone DA, Sidney St., Cambridge, poly(3-hydroxybutyrate-co-3-hydroxyvalerate) copolymer the
632 Padgette SR, Kishore G, Gruys KJ MA 02139, USA. production. Nat Biotechnol 1999 Oct;17(10):1011-6 1999 process is not econ
Poly(3-hydroxyalkanoates)
(PHAs) are a class of
microbially produced
polyesters that have
potential applications as
conventional plastics,
specifically thermoplastic
Metabolix, Inc., elastomers. A wealth of
Cambridge, biological diversity in PHA
Massachusetts 02142, Metabolic engineering of poly(3-hydroxyalkanoates): from formation exists, with at
633 Madison LL, Huisman GW USA. DNA to plastic. Microbiol Mol Biol Rev 1999 Mar;63(1):21-53 1999 least 100 d
California Inst. Metabolic modeling of growth and poly(beta- 375 pp. Avail. Univ. Microfilms Int., Order No.
Technol., Pasadena, hydroxybutyrate) (PHB) DA9137235 polyhydroxybutyrate fermn
CA, production in Alcaligenes eutrophus H16. From: Diss. Abstr. Int. B 1992, 52(10), 5398 Alcaligenes model
634 Guske, Christopher James USA (English) 1990 1992 Abstract unavailable.
A math. model describing
intracellular
polyhydroxybutyrate
(PHB)
Department of synthesis in
Chemical Engineering Alcaligenes eutrophus has
and Materials Science, been constructed. The
Biological Process model
Technology Institute, allows investigation of
University of issues such as the
Minnesota, existence of
St. Paul, MN, rate-limiting enzymic
Leaf, Timothy A.; Srienc, Friedrich 55108, USA Biotechnol. Bioeng. (1998), 57(5), 557-570 steps, possible regulatory
635 Metabolic modeling of polyhydroxybutyrate biosynthesis 1998 m
4.10 Literature on Polyhydroxyalkanoates.xls - page 188
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Heterologous expression
of the phaC1 gene from
Pseudomonas
aeruginosa, which
encodes one
of the
polyhydroxyalkanoic acid
Institut fur Metabolic routing towards polyhydroxyalkanoic acid synthases, in Escherichia
Mikrobiologie, synthesis in coli impaired in fatty acid
Westfalische Wilhelms- recombinant Escherichia coli (fadR): beta-
Universitat, Munster, inhibition of fatty acid beta-oxidation oxidation results in
640 Qi Q, Steinbuchel A, Rehm BH Germany. by acrylic acid. FEMS Microbiol Lett 1998 Oct 1;167(1):89-94 1998 polyhydr
P oleovorans Accumulates
poly(3-hydroxyalkanoates)
(PHAs) after
growth on medium-chain-
length hydrocarbons.
Large amts. of this
Metabolism of poly(3-hydroxyalkanoates) (PHAs) by polyester are synthesized
Pseudomonas when cells are grown
Groningen Biotechnol. oleovorans. Identification and sequences of genes and polyhydroxyalkanoate under N-limiting
Huisman, Gjalt W.; Wonink, Eric; Cent., Univ. function of polymerase depolymerase conditions. When N is
Meima, Rob; Kazemier, Bert; Groningen, Groningen the encoded proteins in the synthesis and degradation of J. Biol. Chem., 266(4), 2191-8 gene sequence resupplied in the medium,
641 Terpstra, Peter; Witholt, Bernard 9747 AG, Neth. PHA. (English) 1991 1991 Pseudomonas the accumulat
648 Budwill, K.; Fedorak, P. M.; Page, W. J. Methanogenic Degradation of Poly(3-Hydroxyalkanoates) Appl. Env. Microbiol. 1992; 58:1398-1401 1992 408.
So far, the
commercialisation on a
large scale of the
environmentally harmless
PHB and PHA
biopolymers has failed
because of
the very high production
costs involved in the
production of these
Method for combining intracellular polyhydroxyalkanoate substances by
KOSMANN JENS DR (DE); INST synthesis in biotechnological
BUETTCHER VOLKER DR (DE); GENBIOLOGISCHE microorganisms with an extracellular polysaccharide fermentation processes.
649 WELSH THOMAS (DE) FORSCHUNG (DE) synthesis DE4420223 1995-05-04 1995 The
4.10 Literature on Polyhydroxyalkanoates.xls - page 190
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
PURPOSE:To easily
monitor the PHB storage
change in activated
sludge by culturing the
activated sludge contg.
many kinds of
microorganisms under
the conditions of limiting
nitrogen sources and
measuring the turbidity of
the culture solution at
METHOD FOR MONITORING PHB STORAGE CHANGE JP4156998 660(nm)
652 SAITO YUJI; others: 04 TAISEI CORP OF ACTIVATED SLUDGE 1992-05-29 1992
ALEXANDER KOREA INST METHOD FOR PRODUCING HIGH DENSITY PHB USING
STEINBUCHER (DE); JANG HO-NAM SCIENCE FED-BATCH CULTURE OF
653 (KR); LEE SANG-YEUP (KR) TECHNOLOGY (KR) RECOMBINANT E. COLI KR122437 1997-11-24 1997 Abstract unavailable.
4.10 Literature on Polyhydroxyalkanoates.xls - page 191
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly-ß-hydroxybutyrate is
produced by providing a
culture of
Escherichia
coli bacterial host cells
transformed by a DNA
sequence
coding for
Method for the improved production and the biosynthetic pathway
James Madison recovery of poly-ß-hydroxybutyrate from of poly-ß-hydroxybutyrate
Dennis; Douglas E. , University, transformed US5512456 and a
661 Weyers Cave, VA Harrisonburg, VA Escherichia coli April 30, 1996 1996
663 KIM KAP-JIN (KR); IM KON-BIN (KR) KOHAP LTD (KR) METHOD OF PRODUCING OF PHB/PHV KR9405653 1994-06-22 1994 Abstract unavailable.
The invention relates to
recombinant
deoxyribonucleic acid
(DNA) technology and,
more particularly, to a
process whereby
polybetahydroxyalkanoate
(PHA) copolymers can be
synthesized in a
recombinant host strain
containing the
DENNIS DOUGLAS E (US); SLATER INNOVATIVE TECH METHOD OF PRODUCTION OF POLY-BETA- WO9306225 poly-beta-
664 STEVEN C (US) CENTER (US) HYDROXYALKANOATE COPOLYMERS 1993-04-01 1993 hydroxybutyrate
4.10 Literature on Polyhydroxyalkanoates.xls - page 194
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxyalkanoate
(PHA) polyester is
extracted from biomass by
dissolving the PHA in a
KURDIKAR, Devdatt, L. , 12220 non-
Country Place Drive, Maryland Heights, halogenated solvent which
MO 63043, United States of MONSANTO comprises a PHA-good
America COMPANY, 800 N. solvent or a mixture
STRAUSER, Fred, E. , 3006 Lindbergh Boulevard, METHODS OF PHA EXTRACTION thereof. Suitable PHA-
St. Camella Street, St. Charles, MO St. Louis, MO 63167, AND RECOVERY USING NON- good
63301-0356, United States of America United States of HALOGENATED solvents can
675 America SOLVENTS WO9846782 1998-10-22 1998 be selected from
A cluster of genes on
megaplasmid
pRmeSU47b, bhbA-D, is
required for growth on the
Russian-Acad.Sci.; Methylobacterium
Polish-Acad.Sci.; extorquens strain P14,
Inst.Catal.Surface.Che which synthesized
m. poly-beta-
Cracow hydroxybutyrate (PHB),
LO Institute of Methylobacterium extorquens strain P14, a new was isolated from
Catalysis and Surface methylotrophic Kaneda's
Chemistry, Polish bacteria producing poly-beta-hydroxybutyrate ( culture medium. The
Academy of ***PHB*** ); cells were Gram-neg.
Sciences, ul. polymer production by a bacterium fed-batch culture motile rods, had polar
Ostafin M; Haber J; Doronina N V; Niezapominajek 1, 30- for use in flagellum and a
Sokolov A P; Trotsenko Y A 239 Cracow, Poland. biodegradable plastic production Acta Microbiol.Pol.; (1999) 48, 1, 39-51 carotenoid pigment, but
678 1999 they did not f
The investigation of
microbial population
Universitaet Leipzig, dynamics gains more and
Fakultaet fuer more importance for
Biowissenschaften, biotechnol. processes
Pharmazie und insofar as people may
Psychologie, Abteilung assume that the individual
Biotechnologie, Methylobacterium rhodesianum cells tend to double the Methylobacterium cells of a population
Ackermann, Joerg-Uwe; Mueller, Permoserstr. 15, DNA content polyhydroxybutyrate fermn contribute differently to
Susann; Loesche, Andreas; Bley, 04318, Leipzig, under growth limitations and accumulate PHB. J. DNA formation the overall productivity.
681 Thomas; Babel, Wolfgang Germany Biotechnol., 39(1), 9-20 (English) 1995 1995 Flow cytometry is known
4.10 Literature on Polyhydroxyalkanoates.xls - page 198
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Microbial Conversion of methane into poly-beta-
hydroxybutyrate (PHB): Growth and intracellular product
682 Asenjo, J.A.; Suk, J.S. accumulation in a type II methanotroph J. Ferment. Technol. 1986; 64(4):271-278 1986 256.
Microbial degradation of an aliphatic polyester with a high Applied and Environmental Microbiology 1995;
683 Pranamuda; H.; Tokiwa; Y.; Tanaka; H. melting point, poly(tetramethylene succinate) 61:1828-1832 1995 513.
In landfills, deposited
waste material is usually
faced with strictly anoxic
conditions. This means
that the design of new
biodegradable polymers
must take into
consideration that
degradation should be
Fakultat fur Biologie, possible especially in the
Universitat Konstanz, Microbial degradation of natural and of new synthetic absence of molecular
684 Schink B, Janssen PH, Frings J FRG. polymers. FEMS Microbiol Rev 1992 Dec;9(2-4):311-6 1992 oxyge
Mergaert; J.; Anderson; C.; Wouters; Microbial degradation of poly(3-hydroxy<butyrate) and Journal of Environmental Polymer Degradation
685 A.; Swings; J. poly(3-hydroxybutyrate-co-3-hydroxyvalerate) in compost 1994; 2:177-183 1994 585.
1 Microbiology and
Genetics Division
Industrial
Technology The population of poly-b-
Development Institute hydroxybutyrate-
Department of degrading microorganisms
Science and and the biodegradation of
Technology PHB in
Bicutan, Tagig local landfill soils were
Metro Manila, examined in vitro and in
1604 Philippines vivo. Forty-two PHB-
degraders consisting of 12
2 University of bacteria, 25
TANSENGCO1, M., DOGMA2, I. Jr. Santo Tomas Microbial Degradation of Poly-b-hydroxybutyrate Using Acta Biotechnologica Vol. 19 (1999) No. 3, pp. actinomycetes and 5
688 Graduate School Landfill Soils 191–203 1999 moulds were iso
689 Sutherland, I.W. Microbial exopolysaccharides TIPS 1979; 55-59 1979 257.
A review with 27 refs.
Traditionally, micro-
organisms are grown in
media where a single
Swiss Federal Institute nutrient is limiting growth.
for Environmental However,
Science and recently also the
Technology Int. Symp. Bact. Polyhydroxyalkanoates (1997), existence of clearly
(EAWAG), Meeting Date 1996, defined double-nutrient-
Dubendorf, CH-8600, Microbial growth under multiple-nutrient-limited cultivation 171-177. Editor(s): Eggink, Gerrit. Publisher: limited growth regimes
Egli, Thomas; Durner, Roland; Zinn, Switz. conditions, with special reference to the accumulation of National Research has been demonstrated
690 Manfred; Witholt, Bernard PHA Council of Canada, Ottawa, Ont. 1996 un
A review with 66 refs.
Polyhydroxyalkanoates
(PHAs), in the form
of metabolic storage
reserves, are assembled
in intracellular
Department of cytoplasmic inclusions,
Biochemistry and often called granules.
Molecular Biology, This review
University of discusses both the
Fuller, R. Clinton Massachusetts, Microbial inclusions with special reference to PHA structure and function of
691 Amherst, MA, USA inclusions and intracellular boundary envelopes Int. J. Biol. Macromol. (1999), 25(1-3), 21-29 1999 this as
Novel thermoplastic
copolymers of
hydroxycarboxylic acids
with useful
properties are manufd.
using microorganisms
expressing the phaC
and phaE genes of the
polyhydroxycarboxylic acid purple bacterium
manuf transgenic bacteria Thiocapsa pfennigii. The
Steinbuechel, Alexander; Liebergesell, phaC phaE gene Thiocapsa compn. of the copolymers
Matthias; Valentin, Henry; Pries, Buck WErke Gmbh Microbial manufacture of polyhydroxycarboxylic acids with Ger. Offen. DE polyester manuf is a function of the
693 Andreas und Co, Germany microorganisms expressing Pha genes of Thiocapsa. 4433134 A1 21 Mar 1996, 25 pp. (Germany) 1996 monomers s
4.10 Literature on Polyhydroxyalkanoates.xls - page 200
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly-beta-hydroxybutyric
acid (PHB) was produced
from xylose and lactose by
using Pseudomonas
cepacia. Approximately 50
% PHB (grams of PHB
School of Chemistry total/grams of biomass
and Biochemistry, total) was produced. With
Georgia Institute of a laser-based fluorescent
Young, Frederick K.; Kastner James R.; Technology, Atlanta, Microbial Production of Poly-beta-Hydroxybutyric Acid form Applied and Environmental Microbiology Nov Pseudomonas cepacia - Xylose probe, beta-galactosidase
694 May Sheldon W. Georgia 30332 D-Xylose and Lactose by Pseudomonas cepacia 1994, 4195-4198 1994 - Lactose activity was s Strain - Substrates kopiert
Microbial synthesis and characterization of poly(3-
695 Hiramitsu; M.; Doi; Y. hydroxybutyrate-co-3-hydroxypropionate) Polymer 1993; 34:4782-4786 1993 489.
Microbial synthesis and characterization of poly(3-
696 Nakamura; S.; Doi; Y.; Scandola; M. hydroxybutyrate-co-4-hydroxybutyrate) Macromolecules 1992; 25:4237-4241 1992 485.
Comamonas acidovorans
DS-17 was isolated from
activated sludge and
found to produce
copolymers of 3-
hydroxybutyrate
(3HB) and 4-
hydroxybutyrate (4HB) at
30 degrees C under
Research Institute of growth-limited conditions.
Innovative Technology Microbial synthesis and properties of poly(3- When 1,4-butanediol or
for the Earth (RITE), hydroxybutyrate-co-4-hydroxybutyrate) in Comamonas 4-hydroxybutyric acid was
697 Saito; Y.; Doi; Y. Saitama, Japan. acidovorans Int J Biol Macromol 1994 Apr;16(2):99-104 1994 used as 616.
Microbial synthesis of poly(beta-hydroxy alkanoates)
containing novel microbial prepn
functional side chain units for advanced material 164 pp. Avail. Univ. polyhydroxyalkanoate
applications Microfilms Int., Order No. DA9618619 From: functional side chainmicrobial
Univ. of Lowell, Lowell, (pseudomonas oleovorans, pseudomonas putida, Diss. Abstr. Int., B 1996, prepn polyhydroxyalkanoate
698 Kim, Ohyoung MA, USA biocatalysts). 57(2), 1119 (English) 1995 1995 functional side chain Abstract Unavailable
358
Microbial synthesis of polymers: Alcaligenes eutrophus pp. Avail. Univ. Microfilms Int., Order No.
Counc. Natl. Acad. and the BRDX88759 From: Diss. Alcaligenes
699 Hardwicke, Philip Ian Awards, London, UK production of poly-b-3-hydroxybutyric acid (PHB). Abstr. Int. B 1990, 51(1), 319 (English) 1989 1989 polyhydroxybutyrate fermn Abstract unavailable.
Poly(3-hydroxybutyric
acid), PHB, is produced by
the aerobic culture of
Methylobacterium
organophilum strains
NCIB 11482 to
11488 inclusive on a
carbon source such as
methanol. Accumulation of
POWELL KEITH ADRIAN; COLLINSON Microbiological process for the production of poly (beta- PHB is favoured by
BARBARA ANN; RICHARDSON hydroxybutyric acid) and EP0015669 culturing in two stages;
700 KENNETH RAYMOND ICI PLC (GB) micro-organisms for use therein. 1980-09-17 1980 the first sta
4.10 Literature on Polyhydroxyalkanoates.xls - page 201
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Microfiltration porous
membranes (flux JH2O =
15,800 L/m2×atm×J, pore
radius = 0.25 mm) and
pervaporation dense
Laboratoire de Chimie membranes for EtOH
Macromoleculaire, hydroxybutyrate polymer dehydration (Jtotal =
Universite des microfiltration pervaporation 0.008 kg/J×m2, selectivity
Sciences et Microfiltration and pervaporation membranes of PHB, P(HB- membrane = 12.6) were prepd. from
Techniques du co-9% ethanol drying polyhydroxybutyrate and
Languedoc, HV), P(HB-co-22% HV). Filtration and surface properties. Eur. Polym. J., 32(4), 435-50 polyhydroxybutyrate membrane poly(hydroxybutyrate-co-
701 Mas, A.; Jaaba, H.; Sledz, J.; Schue, F. Montpellier 34095, Fr. (French) 1996 1996 hy
As a complement to
previous studies of the
enzymic degrdn. of
folded chain lamellar
single crystals of
polyhydroxyalkanoates,
Department of single crystals of a no.
Chemistry, McGill of polyhydroxyalkanoates
University, Montreal, were partially
Nobes, G. A. R.; Marchessault, R. H.; PQ, H3A 2A7, Microscopic visualization of the enzymic degradation of degraded with
Briese, B. H.; Jendrossek, D. Can. poly(3HB-co-3HV) and poly(3HV) single crystals by PHA J. Environ. Polym. Degrad. (1998), 6(2), 99-107 depolymerases from
703 depolymerases from Pseudomonas lemoignei 1998 Pseudomonas lemo
Microstructure and 13C nuclear magnetic relaxation of
bacterial Diss. Abstr. Int. B 1993, 53(12, Pt. carbon NMR bacterial poly beta
McGill Univ., Montreal, poly(b-hydroxyalkanoates). 1), 6324 (English) 1991. DOCUMENT TYPE: hydroxyalkanoate Abstract Unavailable
704 Nedea, Maria Elena PQ, Can. Dissertation 1993
4.10 Literature on Polyhydroxyalkanoates.xls - page 202
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Bacterially synthesized
Department of Polymer copolyersters of 3-
Chemistry, Tokyo hydroxybutyrate (HB) and
Institute of 3-hydroxyvalerate (HV) of
Technology, Meguro- HV mole fraction ranging
ku, Tokyo 152, Japan; from 0 to 93 % were
*Research Laboratory analyzed by NMR
of Resources spectroscopy and
Utilization, Tokyo copolyersters PHB/HV - NMR differential scanning
Institute of spectroscopy - differential calorimetry (DSC). The
Kamiya; N.; Yamamoto; Y.; Inoue; Y.; Technology, Midori-ku, Microstructure of bacterially synthesized poly(3- scanning calorimetry (DSC) - sequence distributions of
705 Chujo; R.; Doi; Y.* Yokohama 227, Japan. hydroxybutyrate-co-3-hydroxyvalerate) Macromolecules 1989; 22:1676-1682 1989 melting behaviour some PHB-HV´ copolyesters 431.
Department of Polymer
Chemistry, Tokyo
Institute of
Technology, Meguro-
ku, Tokyo 152, Japan
Research Laboratory
of Ressources
Utilization, Tokyo
Institute of
Inoue, Y.; Kamiya, N.; Yamamoto, Y.; Technology, Midori-ku, Microstructures of Comercially available poly(3-
707 Chujo, R. Yokohama 227, Japan hydroxybutyrate-co-3-hydroxyvalerate)s Macromolecules 1989; 22:3800-3802 1989 no abstract 658.
4.10 Literature on Polyhydroxyalkanoates.xls - page 203
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Department of
Chemical Engineering
and BioProcess
Engineering Research Polyhydroxyalkanoates
Center, Korea (PHA) have been
Advanced attracting considerable
Institute attention as biodegradable
of Science and substitutes
Technology, 373-1 for conventional polymers.
Kusong-dong, Yusong- To reduce their production
gu, Taejon 305-701, cost, a great deal of effort
Korea e-mail: mini-review: Factors affecting the economics of has been
polyhydroxyalkanoate production by Applied Microbiology and Biotechnology Abstract devoted to
708 J. Choi, S. Y. Lee leesy@sorak.kais bacterial fermentation Volume 51 Issue 1 (1999) pp 13-21 1999 dev
Institute of Applied
Biochemistry, Polyurethane (PUR) is a
University of Tsukuba, polymer derived from the
Tsukuba, Ibaraki, 305- condensation of
8572, Japan e-mail: polyisocyanate and polyol
and
toshi@sakura.cc.tsuku it is widely
ba.ac.jp. (c/o Toshiaki used as a base material in
Nakajima-Kambe) Tel.: various industries. PUR, in
T. Nakajima-Kambe, Y. Shigeno- +81-298-53-6626 Fax: mini-review: Microbial degradation of polyurethane, particular, polyester PUR,
Akutsu, N. Nomura, F. Onuma, T. +81- polyester Applied Microbiology and Biotechnology Abstract is known to be
709 Nakahara 298-53-4605 polyurethanes and polyether polyurethanes Volume 51 Issue 2 (1999) pp 134-140 1999 vu
Miscibility behavior of
poly[D(-)(3-
hydroxybutyrate)] (I)-
poly(ethylene
polyhydroxybutyrate miscibility oxide) (II) and I-PMMA
polyoxyethylene PMMA blends were studied using
glass temp polyhydroxybutyrate DSC and the vapor
blend miscibility sorption technique. The I-
Miscibility of poly[D(-)(3-hydroxybutyrate)] in poly(ethylene interaction parameter II system showed a single
Yoon, Jin San; Choi, Chang Soon; Dep. Poly. Sci. Eng., oxide) polyhydroxybutyrate blend glass transition,
Maing, Sung Jai; Choi, Hyoung Jin; Inha Univ., Incheon and poly(methyl methacrylate). miscibility whereas two glass
713 Lee, Han Sup; Choi, Soon Ja 402-751, S. Korea Eur. Polym. J., 29(10), 1359-64 (English) 1993 1993 transitions were obsd. for
Compositions are
provided which are useful
ASRAR, Jawed , in the production of
14949 Royal Brook polymeric products, such
ASRAR, Jawed , 14949 Royal Brook Drive, Chesterfield, as coatings and
Drive, Chesterfield, MO 63017, United MO 63017, United films, which
States of America States of America comprise branched PHA.
D'HAENE, Pol , D'HAENE, MODIFIED The compositions of the
Pellenbersgstraat 179, B-3010 Kessel- Pol , Pellenbersgstraat POLYHYDROXYALKANOATES FOR invention comprise PHA
Lo, Belgium 179, B-3010 Kessel- PRODUCTION and 0.001 - 0.5
715 Lo, Belgium OF COATINGS AND FILMS WO9914268A1 March 25, 1999 1999 wt.% of a freer
Mole fraction control of poly(3-hydroxybutyric-co-3-
hydroxyvaleric) acid in fed-batch culture of Alcaligenes Journal of Fermentation and Bioengineering
716 Ishihara; Y.; Shimizu; H.; Shioya; S. eutrophus 1996; 81(5):422-428 1996 622.
A 3.6-kb EcoRI-SalI
fragment of Paracoccus
denitrificans DNA
hybridized with a DNA
probe carrying the
poly(3-hydroxyalkanoate)
Department of (PHA) synthase gene
Bioproductive (phaC) of Alcaligenes
Sciences, Faculty of eutrophus. Nucleotide
Agriculture, sequence analysis of this
Utsunomiya University, Molecular analysis of the poly(3-hydroxyalkanoate) region
Ueda S, Yabutani T, Maehara A, Japan. synthase gene from a showed the presence of a
719 Yamane T methylotrophic bacterium, Paracoccus denitrificans. J Bacteriol 1996 Feb;178(3):774-9 1996 1,872-
4.10 Literature on Polyhydroxyalkanoates.xls - page 206
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Fragments of
IInstitut für chromosomal DNA from
Biotechnologie, Alcaligenes latus
Technische Universität DSM1124 were cloned
Graz, Petersgasse 12, into Escherichia coli and
A- 8010 Graz, Austria transformants were
* Corresponding screened for poly(D(-)-3-
author. Tel.: ?43 316 Molecular cloning, sequencing and expression in hydroxybutyrate) [P(3HB)]
8738417; fax: ?43 316 Escherichia coli of the Keywords : Heterologous production during excess
8738434; e-mail: poly(3-hydroxyalkanoate) synthesis genes from expression; NADH oxidase carbon supply. A plasmid
Klaus F. Genser, Gerald Renner, schwab@biote.tu- Alcaligenes latus activity; Polyhydroxyalkanoate harboring a 5.5-kb
722 Helmut Schwab * graz.ac.at DSM1124. J Biotechnol 1998 Oct 8;64(2-3):125-35 1998 synthesis; Regulation insert of A. latus ganze Artikel
Poly-D(-)-3-
hydroxybutyrate (PHB) is
synthesized in large
amounts under certain
physiological conditions in
the cells of various
microorganisms. This
biological polyester acts
as a carbon and energy
Alcaligenes eutrophus H 16 - storage medium for
Molecular weight of bacterially produced poly-D(-)-3- Ralstonia eutropha H 16 - bacteria. The production
727 Bradel, R.; Kleinke, A.; Reichert, K.H. hydroxybutyrate 7. Dechema Jahrestagung 1989 1989 molecular weight of this poly Polymer properties 667.
A biochemical model is
presented that describes
Chemical Engineering growth of Methylosinus
and Biochemistry trichosporium OB3b on
Departments, methane.
University of The model, which was
Groningen, NL-9747 developed to compare
AG NADH-Regulated Metabolic Model for Growth of strategies to alleviate
Methylosinustrichosporium OB3b. Model NADH limitation
Sipkema EM, de Koning W, Ganzeveld Groningen, The Presentation, Parameter resulting
735 KJ, Janssen DB, Beenackers AA Netherlands. Estimation, and Model Validation. Biotechnol Prog 2000 Apr 7;16(2):176-188 2000 from cometaboli
737 Raymond, R. L.; Davis, J. B. n-Alkane Utilization and Lipid Formation by a Nocardia ??? 1960; 8:329-334 1960 371.
Ueda; S.; Matsumoto; S.; Takagi; A.; n-amyl alcohol as a substrate for the production of poly(3-
738 Yamane; T. hydroxybutyrate-co-3-hydroxyvalerate) by bacteria FEMS Microbiology Letters 1992; 98:57-60 1992 467.
739 Fuller, R. C.; Lenz, R. W. Natural Plastics Natural History 1990; 5:82-84 1990 379.
New bacterial copolyester of 3-hydroxyalkanoates and 3-
Abe; C.; Taima; Y.; Nakamura; Y.; Doi; hydroxy-omega-fluoroalkanoates produced by
740 Y. Pseudomonas oleovorans Polymer Communications 1990; 31:404-406 1990 552.
New bacterial copolyesters produced in Alcaligenes
741 Kunioka; M.; Nakamura; Y.; Doi; Y. eutrophus from organic acids Polymer communications 1988; 29:174-176 1988 439.
4.10 Literature on Polyhydroxyalkanoates.xls - page 210
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
PROBLEM TO BE
SOLVED: To obtain a
gene effective for
improving the productivity
of a polyhydroxyalkanoate
RESEARCH in the cell, by
INSTITUTE OF encoding a protein
INNOVATIVE containing a specific
TECHNOLOGY FOR amino acid sequence.
THE EARTH; SOLUTION: This
KANAGAWA intracellular PHA
SAITO MITSUSANE; SAEGUSA JP11113574 decomposition enzyme
742 HARUHISA UNIVERSITY NEW INTRACELLULAR PHA DECOMPOSITION ENZYME 1999-04-27 1999 encodes (i)
Chromatium vinosum D
(DSM 180) poly-beta-
Institut fuer hydroxybutyrate (PHB)
Mikrobiologie der granule isolation in the
Westfaelischen absence of lysozyme (EC-
Wilhelms- 3.2.1.17) and the
Universitaet Munster, identification of an
Corrensstrasse 3, D- New knowledge about the PHA-locus and P(3HB) granule- open reading frame (ORF)
48149 Munster, associated proteins in Chromatium vinosum; poly-beta- 5Cv translational
Liebergesell M; *Steinbuechel A Germany. hydroxybutyrate granule isolation and open reading frame product as a granule-
743 5Cv product identification Biotechnol.Lett.; (1996) 18, 6, 719-24 1996 associated protein wer
PURPOSE:To obtain a
new PHB degrading
enzyme useful for
degrading a
biodegradable plastics
containing
polyhydroxybutyrate
as a component.
CONSTITUTION:This
polyhydroxybutyrate
NEW PHB DEGRADING ENZYME, ITS PRODUCTION degrading enzyme is
TOYODA SHUJI; SNOW BRAND MILK AND MICROORGANISM capable of manifesting the
745 others: 03 PROD CO LTD CAPABLE OF PRODUCING THE SAME ENZYME JP7155180 1995-06-20 1995 following properties: (1) a
4.10 Literature on Polyhydroxyalkanoates.xls - page 211
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A new poly-beta-
hydroxybutyrate-
depolymerase (PHBD) is
derived
from Pseudomonas
sp. 328 (FERM P-13954),
and has the following
properties:
degradation of PHB;
New polyhydroxybutyratase (PHB-ase) production; poly- optimal pH 4.3; pI 8.4;
Snow-Brand-Milk- beta-hydroxybutyrate-depolymerase purification from optimal
Prod. Pseudomonas sp. for use in poly-beta-hydroxybutyrate temp. 40 deg; and
746 degradation JP 07155180 20 Jun 1995 1995 mol.wt. 513,000 (gel filtrati
biodegradable
polyesterurethane-foam
(DegraPol-foam) to
chondrocytes and
Department of osteoblasts. Both
Materials, Institute of
Saad B, Neuenschwander P, Uhlschmid Polymers, ETH, New versatile, elastomeric, degradable polymeric materials Int J Biol Macromol 1999 Jun-Jul;25(1-3):293- chondrocytes and
747 GK, Suter UW Zurich, Switzerland. for medicine. 301 1999 osteoblasts, is
Poly-beta-hydroxybutyrate
granules exhibited a
strong orange
fluorescence when stained
with Nile blue A. Heat-
fixed cells were treated
with 1 % Nile blue A for 10
Department of min and were observed at
Micorbiology, Iowa an excitation wavelength
State University, Ames Nile blue A as a fluorescent stain for poly-á- Nile blue A Poly-beta- of 460 nm. Glycogen and
749 Ostle, A.G.; Holt, J.G. , Iowa 50011 hydroxybutyrate Appl. Environ. Microbiol. 1982; 44:238-241 1982 hydroxybutyrate-stain polyphosphate did Analytic 173.
4.10 Literature on Polyhydroxyalkanoates.xls - page 212
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Nile red, a
benzophenoxazone stain
was attempted for
microscopical
observation of poly-b-
hydroxybutyric acid (PHB)
and other lipid
deposits in bacterial cells.
Coll. Agric. Resour. Nile red fluorescence stain Two kinds of the lipids
and Environ. Sci., bacteria cell were distinct to
Beijing Agric. Nile red, a superior fluorescence stain for detection of PHB polyhydroxybutyric acid lipid some extent with
Univ., Beijing 100094, and other Weishengwu Xuebao, bacteria fluorescence microscopy
750 Wang, Jingguo Peop. Rep. China lipid deposits in bacterial cells. 34(1), 71-5 (Chinese) 1994 1994 after Nile r
Department of
Chemical Engineering
and Material Science,
University of
Minnesota, St. Paul
55108.
757 Jackson DE, Srienc F Novel methods to synthesize polyhydroxyalkanoates. Ann N Y Acad Sci 1994 Nov 30;745:134-48 1994 Abstract unavailable.
Novel feasibility of
fuctionalized poly(3-
hydroxybutanoic acid),
PHB, and its copolymers
synthesis via ring-opening
of
beta-butyrolactone (ROP)
mediated by activated
Polish Academy of anionic initiators or
Sciences, Centre for enzymes in vitro is
Polymer Chemistry, 41- Novel synthesis of functionalized poly(3-hydroxybutanoic Anionic polymerization; presented. Using these
Z. Jedlin ´ ski *, M. Kowalczuk, G. 800 Zabrze, Poland * acid) and its Copolymers; ESI-MS; Lipase; new synthetic
758 Adamus, W. Sikorska, J. Rydz Corresponding author. copolymers. Int J Biol Macromol 1999 Jun-Jul;25(1-3):247-53 1999 Poly(3-hydroxybutanoic acid) approaches ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 214
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Y., Doi.; Kunioka; M.; Nakamura; Y.; Nuclear magnetic resonance studies on unsusual bacterial
762 Soga; K. coplyesters of 3-hydroxybutyrate and 4-hydroxybutyrate Macromolecules 1988; 21:2722-2727 1988 438.
764 Repaske, R. Nutritional requirements for hydrogenomonas eutropha J. Bacteriol. 1962; 83:418-422 1962 29.
4.10 Literature on Polyhydroxyalkanoates.xls - page 215
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
13C-NMR spectra of
whole native cells of
Methylobacterium AM1
show dominant signals
belonging to poly(beta-
hydroxybutyrate) and
trehalose. Fractionation of
the cells demonstrates
University Chemical that the poly(beta-
Laboratory, Lensfield Observation of mobile poly(beta-hydroxybutyrate) in the hydroxybutyrate) is
Road, Cambridge CB storage granules of Methylobacterium AM1 by in vivo 13C- Storage granule - Trehalose - located in the storage
765 Barnard, G.N.; Sanders, J.K.M. 1 EW, England NMR spectroscopy FEBS 1988; 231(1):16-18 1988 Methylobacterium AM1 granules and t Strain - Morphology 296.
Observations on the fine structure of spheroplasts of
766 Boatman; E.S. Rhodospirillum rubrum The Journal of Cell Biology 1964; 20:297-311 1964 219.
Several strains of
photoautotrophically
Istituto di Microbiologia grown Spirulina spp.
Agraria e Tecnica contained poly-beta-
dell'Universita e hydroxybutyrate (PHB) at
Centro di Studio dei concentrations
Microrganismi Autotrofi never exceeding a few
del Consiglio milligrams per gram of dry
Nazionale delle weight. Under mixotrophic
Ricerche, Firenze, growth conditions in the
Vincenzini M, Sili C, de Philippis R, Ena Italy. Occurrence of poly-beta-hydroxybutyrate in Spirulina presence of acetate,
768 A, Materassi R species. J Bacteriol 1990 May;172(5):2791-2 1990 PHB reached v
Poly-beta-hydroxybutyrate
(PHB) from various
representative strains of
the genera Azotobacter,
Beijerinckia, and Derxia
was isolatet and
characterized. During
Department of Azotobacter - Azotomonas - growth in shake culture,
Biochemistry, Beijerinckia - Derxia - with glucose as a carbon
Stockdale, H.; Ribbons, D.W.; Dawes, University of Hull, Hull, Occurrence of poly-beta-hydroxybutyrate in the Beijerinckia fluminensis - and energy source, and
769 E.A. England Azotobacteriaceae J. Bacteriol. 1968; 95:1798-1803 1968 molecular nitrogen - glucose molecular nitrogen as a Strains 73.
4.10 Literature on Polyhydroxyalkanoates.xls - page 216
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Fifty different
polyhydroxyalkanoic acid
(PHA)-accumulating
bacterial strains were
investigated for the
occurrence of phasin
proteins bound to PHA
granules and related to
Institut fur the GA24 protein of
Mikrobiologie der Occurrence of polyhydroxyalkanoic acid granule- Alcaligenes eutrophus
Westfalischen associated proteins H16, by isolating PHA
Wilhelms-Universitat related to the Alcaligenes eutrophus H16 GA24 protein in granules and
771 Wieczorek R, Steinbuchel A, Schmidt B Munster, Germany. other bacteria. FEMS Microbiol Lett 1996 Jan 1;135(1):23-30 1996 Western
Polyhydroxyalkanoates
(PHAs), of which
polyhydroxybutyrate
(PHB) is the most
abundant, are bacterial
carbon and energy
reserve materials of
widespread occurrence.
They are composed of 3-
hydroxyacid monomer
Department of Applied Occurrence, metabolism, metabolic role, and industrial units and exist as a small
Biology, University of uses of bacterial number
772 Anderson AJ, Dawes EA Hull, United Kingdom. polyhydroxyalkanoates. Microbiol Rev 1990 Dec;54(4):450-72 1990 of cytoplasmic 351.
The known
biodegradability of PHB
[26063-00-3] in certain
biol.
environments has led to
its proposed use as a
biodegradable implant
material. Monofilaments
of PHB homopolymer and
poly(hydroxyvalerate)-
Inst. Med. Dent. PHB (PHV-PHB)
Bioeng., Univ. On the biodegradation of poly-b-hydroxybutyrate (PHB) biodegrdn hydroxybutyrate copolymers were studied
Liverpool, homopolymer hydroxyvalerate copolymer in
774 Miller, N. D.; Williams, D. F. Liverpool L69 3BX, UK and poly-b-hydroxybutyrate-hydroxyvalerate copolymers. Biomaterials, 8(2), 129-37 (English) 1987 1987 fiber vivo and in
775 Malik, K.A.; Claus, D. On the changed taxonomic position of Alcaligenes latus Abstract of the 38th meeting of the DGHM 254.
Estimation of biomass
concentration by on-line
fluorimetry was examined
during batch cultivations
of Alcaligenes eutrophus
Biotechnology ATCC 17697, a poly-beta-
Research Institute, Alcaligenes eutrophus ATCC hydroxybutyric acid (PHB)
National Research 17697 - Ralstonia eutropha producer. The results
Council of Canada, On-line culture fluorescence measurement during the ATCC 17697 - Fluorescence - obtained revealed a linear
Groom, C.A.; Luong, J.H.T.; Montreal, Quebec H4P batch cultivation of poly-beta-hydroxybutyrate producing On-line monitoring - Biomass correlation between total
778 Mulchandani, A. 2R2, Canada Alcaligens eutrophus J. Biotechnol. 1988; 8:271-278 1988 concentration culture Strain - Analytics 298.
Optimization of microbial poly(3-hydroxybutyrate) recovery
Hahn; S.K.; Chang; Y.K.; Kim; B.S.; using dispersions of sodium hypochlorite solution and Biotechnology and Bioengineering 1994; 44:265-
779 Chang; H.N. chloroform 261 1994 459.
4.10 Literature on Polyhydroxyalkanoates.xls - page 218
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Goosen, M. F. A.; O'Shea, G. F.;
Gharapetian, H. M.; Chou, S.; Sun, A. Optimization of microencapsulation parameters:
780 M. semipermeable microcapsules as a bioartificial pancreas Biotech. Bioeng. 1985; 27:146-150 1985 289.
Department of
Chemical Engineering,
University of Waterloo Recovery of the
Waterloo, Ontario, intracellular bioplastic
Canada N2L 3G1 poly(<beta>-
(2) Y. hydroxybutyric acid) or
Chisti PHB from fed-batch
(3) cultured
Department of Alcaligenes latus, ATCC
Chemical Engineering, 29713, was examined
University of Almeria E- Optimization of poly(<beta>-hydroxybutyric acid) recovery using combinations of
04071 Almeria, Spain from Alcaligenes latus: combined chemical and mechanical
Fax: mechanical and chemical Bioprocess Engineering Abstract Volume 19 treatments
781 I. M. Tamer, M. Moo-YoungY. Chisti treatments Issue 6 (1998) pp 459-468 1998 t
Optimum growth
conditions and pH control
soln. were obtained in the
biosynthesis of PHB
(poly-.beta.-
hydroxybutyrate) with
Alcaligenes
eutrophus. Optimum
G-Caltex Oil Refinery carbon and nitrogen
Seo, Jeong-Kwi; Yoon, Jeong-Yeol; Oh, Co., Ltd., Chonnam, sources were fructose and
Joon-Taek; Kim, Woo-Sik 550-600, S. Korea Optimum growth conditions and pH control solution for (NH4)2SO4, resp., and
782 PHB biosynthesis in A. eutrophus J. Ind. Eng. Chem. (Seoul) (1998), 4(3), 215-220 1998 optimum additive
This invention relates to a
process for producing
oriented
polyhydroxyalkanoate
(PHA) that requires less
stringent
temperature
MONSANTO control than previous
COMPANY, 800 North processes. The process
Lindbergh Boulevard, comprises melting the
WALDOCK, Paul , 9 Springhill, St. Louis, MO 63167, PHA, shaping preform
Welbury, Northallerton DL6 2SQ, United States of WO9722459 from the
783 United Kingdom America ORIENTED POLYESTER 1997-06-26 1997
4.10 Literature on Polyhydroxyalkanoates.xls - page 219
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxyalkanoate
(PHA) synthase has been
expressed in Escherichia
coli by reengineering the
5'-end of the wild-type (wt)
gene and subsequent
Department of Biology, transformation of this gene
Massachusetts Overexpression and purification of the soluble into protease-deficient E.
Institute of polyhydroxyalkanoate coli UT5600 (ompT-).
Gerngross TU, Snell KD, Peoples OP, Technology, synthase from Alcaligenes eutrophus: evidence for a Induction with IPTG
Sinskey AJ, Csuhai E, Masamune S, Cambridge 02139- required results
784 Stubbe J 4307. posttranslational modification for catalytic activity. Biochemistry 1994 Aug 9;33(31):9311-20 1994 in sol
Inst.Phys.Chem.Res.S
aitama
LO Polymer A Pseudomonas sp. 61-3
Chemistry Laboratory malonyl-CoA-ACP-
and the RIKEN Group transacylase gene
of Japan Science (fabDPs)
and Technology was cloned by
Corporation, The Southern blot
Institute of Physical hybridization using an
and Chemical equivalent gene
Research (RIKEN), of Escherichia coli
2-1 Hirosawa, Wako- Over-expression of 3-ketoacyl-ACP-synthase-III or malonyl- (fabDEc) as a DNA probe.
Taguchi K; Aoyagi Y; Matsusaki H; shi, Saitama 351-0198, CoA-ACP-transacylase genes induces monomer supply for Some recombinant E.
Fukui T; *Doi Y Japan. polyhydroxybutyrate production in Escherichia coli HB101; Biotechnol.Lett.; (1999) 21, 7, 579-84 coli HB101 strains
786 Emai poly-beta-hydroxybutyrate production 1999 harboring fabDPs,
MASSACHUSETTS
PEOPLES OLIVER P; GERNGROSS INST TECHNOLOGY;
787 TILLMAN U; SINSKEY ANTHONY J METABOLIX INC Overproduction and purification of soluble pha synthase AU3322195 1996-03-07 1996 Abstract unavailable.
Purified, soluble
recombinant bacterial long
chain and short chain PHA
synthases are described,
MASSACHUSETTS with methods and
INST TECHNOLOGY materials for
PEOPLES OLIVER P; GERNGROSS (US); METABOLIX INC OVERPRODUCTION AND PURIFICATION OF SOLUBLE overexpression and
788 TILLMAN U; SINSKEY ANTHONY J (US) PHA SYNTHASE WO9605316 1996-02-22 1996 purification.
Purified, soluble
recombinant bacterial long
chain and short chain PHA
synthases are described,
with methods and
PEOPLES OLIVER P (US); MASSACHUSETTS materials for
GERNGROSS TILLMAN U (US); INST TECHNOLOGY overexpression and
789 SINSKEY ANTHONY J (US) (US) Overproduction and purification of soluble PHA synthase US5480794 1996-01-02 1996 purification.
Oxidation of 1-Alkenes to 1,2-Epoxyalkanes by
790 Abbott, B. J.; Hou, C. T. Pseudomonas oleovorans Appl. Microbiol. 1973; 26:86-91 1973 372.
791 Papers presented at the Toronto, Canada meeting polymer reprints 1988; 29(1):593-615 1988 339.
4.10 Literature on Polyhydroxyalkanoates.xls - page 220
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
PURPOSE:To provide an
aid in finding an effective
inhibitor including a
degradation pathway of a
polyhydroxyalkanoate
(PHA)
which is an aliphatic
polyester, expected as a
biodegradable plastic and
CHIKYU KANKYO accumulated by a
SANGYO GIJUTSU microorganism by
SAITO MITSUSANE; KENKYU KIKO; JP6086681 elucidating a PHA
802 others: 01 others: 02 PHA INTRACELLULAR DEGRADING ENZYME 1994-03-29 1994 in
Polyhydroxyalkanoate
synthase (PHA) from
Chromatium vinosum
catalyzes the
Department of conversion of 3-
Chemistry and hydroxybutyryl-CoA (HB-
Department of Biology, CoA) to
Massachusetts polyhydroxybutyrate
Institute of (PHB) and CoA. The
Technology, synthase is composed of a
Mueh, Ute; Sinskey, Anthony J.; Kirby, Cambridge, MA, .apprx.1:1 mixt. of two
Daniel P.; Lane, William S.; 02139, USA PHA Synthase from Chromatium vinosum: Cysteine 149 Is Biochemistry (1999), 38(2), 826-837 subunits, PhaC and PhaE.
808 Stubbe, JoAnne Involved in Covalent Catalysis 1999 Siz
Hypochlorite digestion of
bacterial biomass from
intracellular poly-beta-
hydroxybutyreate (PHB)
has not been used on a
large scale since it has
been reported to severely
hypochlorite extn degrade PHB. In this
Chem. Eng., Ec. polyhydroxybutyrate biomass study, to minimize
Berger, E.; Ramsay, B. A.; Ramsay, J. Polytech., Montreal, PHB recovery by hypochlorite digestion of non-PHB Biotechnol. Alcaligenes biomass degradation, the initial
817 A.; Chavarie, C.; Braunegg, G. PQ H3C 3A7, Can. biomass. Tech., 3(4), 227-32 (English) 1989 1989 polyhydroxybutyrate extn Alcaligenes eutrophu Extraction 299.
Extrusion coating expts.
were carried out in the
pilot line at
Tampere University of
Technol (Institute of Paper
Converting) in
Finland. Com. 3-
Paper Converting hydroxybutyrate/3-
Laboratory, Tampere hydroxyvalerate
University of copolymer
Technology, Polym., Laminations Coat. Conf. (1998), Volume (PHB/V, Biopol) (I) was
Kuusipalo, Jurkka Tampere, Finland PHB/V in extrusion coating of paper and paperboard: study 2, 779-802 provided by Monsanto
818 of functional properties Publisher: TAPPI Press, Atlanta, Ga. 1998 PLC, U
Two amination-deficient
mutants of
Hydrogenomonas
eutropha, characterized
by pH-dependet linear
growth on non-amino
substrates were
investigated to determine
Department of Biology, the exact nature of
The Catholic Hydrogenomonas eutropha - mutation. Glutamate
University of America, pH-conditional, ammonia assimilation-deficient mutants of Ralstonia eutropha - dehydrogenase, the only
Washington D.C. Hydrogenomonas eutropha: Isolation and growth Alcaligenes eutrophus - aminating enzyme found
825 Strenkoski, L.F.; DeCicco, B.T. 20017 characteristics J.Bacteriol. 1971; 105:219-295 1971 Nitrogen assimilation - Mutants in the wil Strain - Metabolism 98.
4.10 Literature on Polyhydroxyalkanoates.xls - page 226
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The polyhydroxyalkanoic
acid (PHA) biosynthetic
gene locus was
cloned and characterized
from an Acinetobacter sp.
isolated from
activated sludge.
phosphate regulation Nucleotide sequence anal.
Department of polyhydroxyalkanoate identified three clustered
Microbiology, Monash Phosphate concentration regulates transcription of the biosynthesis Acinetobacter genes, phaAAc (encoding
Schembri, Mark A.; Bayly, Ronald C.; University, Clayton, Acinetobacter pha gene operon Acinetobacter a b-ketothiolase), phaBAc
826 Davies, John K. Victoria, Australia. polyhydroxyalkanoic acid biosynthetic genes. J Bacteriol 1995 Aug;177(15):4501-7 1995 (enco 538.
Regulatory mechanism in
PHB [poly-
(hydroxybutyrate)]
accumulation by
cyanobacteria, especially
by a thermophilic isolate,
Synechococcus MA19
National Institute of was reviewed in
Bioscience and Human- comparison with a
Technology, Tsukuba, genetically engineered
Ibaraki, Japan. Photosynthetic accumulation of poly-(hydroxybutyrate) by strain. The strain, MA19
Asada Y, Miyake M, Miyake J, Kurane yasada@ccmail.nibh.g cyanobacteria--the metabolism and potential for CO2 accumulates PHB
829 R, Tokiwa Y o.jp recycling. Int J Biol Macromol 1999 Jun-Jul;25(1-3):37-42 1999 under nitrogen s
Marchessault, R.H.; Okamura, K.; Su, Physical properities of poly(beta-hydroxy butyrate). H.
830 C.J. Conformational aspects in solution ? 1970; 3:735-739 1970 224.
4.10 Literature on Polyhydroxyalkanoates.xls - page 227
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Marchessault; R.H.; Morikawa; H.; 316. Und 687
831 Revol; J.F. Physical properties of a naturally occurring polyester Macromolecules 1982; 17:1884 1984 korr
Physical properties of poly-beta -hydroxybutyrate. IV.
Conformational
832 Cornibert J, Marchessault RH analysis and crystalline structure. J Mol Biol 1972 Nov 28;71(3):735-56 1972 Abstract unavailable.
833 Marchessault, J. Cornibert R.H. Physical properties of poly-beta-hydroxybutyrate J. Mol.Biol. 1972; 71:735-765 1972 38.
Phys. properties of a new
polymer blend obtained by
mixing
poly-D(-)(3-
polyhydroxybutyrate hydroxybutyrate) (I), a
polyepichlorohydrin blend phys cryst. polymer with
property interesting
polyester polyepichlorohydrin properties of
blend phys property biodegradability and
glass temp polyhydroxybutyrate biocompatibility, with
Natl. Inst. Sericul. polyepichlorohydrin blend uncrystallizable
Entomol. Sci. Physical properties of miscibility polyhydroxybutyrate atactic
Owashi, Tsukuba 305, poly-D(-)(3-hydroxybutyrate)/poly(epichlorohydrin) blends. Acta Polym., 43(6), 327-30 (English) polyepichlorohydrin blend poly(epichlorohydrin) (II)
834 Tsukada, M.; Romano, M.; Seves, A. Japan 1992 1992 were studied. I-I
The physico-mechanical
properties of degradable
polymers used for medical
applications have been
characterized. The
following polymers were
Department of included in this study:
Chemistry, Rutgers, three samples of
State University of Physico-mechanical properties of degradable polymers poly(ortho esters) derived
New Jersey, New used in medical from 3,9-bis(ethylidene
835 Engelberg I, Kohn J Brunswick. applications: a comparative study. Biomaterials 1991 Apr;12(3):292-304 1991 2,4,8,10-tetraoxaspiro[
Pseudomonas aeruginosa
M60, a mucoid strain, was
grown in continuous
culture (D 0.05 h-1) under
ammonia limitation with
glucose as the carbon
source. Steady-state
alginate production
Department of occurred for only 1-2 d
Biochemistry, Physiological and biochemical changes accompanying the under these conditions
Williams SG, Greenwood JA, Jones University of Leicester, loss of mucoidy [qalginate 0.097
836 CW UK. by Pseudomonas aeruginosa. Microbiology 1996 Apr;142 ( Pt 4):881-8 1996 g algina
837 Lee, C.M.; Schlegel, H.G. Physiological characterization of Pseudoflava GA3 Current Microbiology 1981; 5:333-337 1981 252.
Physiologische Untersuchungen ber den
chemolithotrophen Stoffwechsel neu isolierter
838 Bartha, R. Hydrogenomonas-Stämme Archiv Mikrobiol. 1962; 41:313-350 1962 48.
Physiology and biochemistry of aerobic hydrogen-oxidizing
839 Bowien, B.; Schlegel, H. G. bacteria Ann. Rev. Microbiol. 1981; 35:405-452 1981 191.
4.10 Literature on Polyhydroxyalkanoates.xls - page 228
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The Alcaligenes
eutrophus genes for beta-
ketothiolase, NADPH-
dependent acetoacetyl-
CoA reductase and
poly(beta-hydroxybutyric
acid) synthase (PHB
synthase) which comprise
the three-step PHB-
biosynthetic pathway,
Institut fur Physiology and molecular genetics of poly(beta-hydroxy- were
Mikrobiologie, alkanoic acid) cloned. Molecular studies
840 Steinbuchel A, Schlegel HG Gottingen, Germany. synthesis in Alcaligenes eutrophus. Mol Microbiol 1991 Mar;5(3):535-42 1991 revealed tha
Physiology and polyester formation of Pseudomonas
841 Preusting, H.; Kingma, J.; Witholt, B. oleovorans in continuous two-liquid-phase cultures Enzyme Microb. Technol. 1991; 13:770-780 1991 403.
Alcaligenes eutrophus
NCIMB 40529 was grown
in batch culture at 34
Department of deg in SEII mineral
Biochemistry, salts medium with 2 g/l C-
University of Leicester, source (1 g/l each
Leicester LE1 of cosubstrates).
7RH, UK. Alternatively, the strain
Email: Physiology of poly-3-hydroxybutyrate (PHB) production by was grown in
Henderson R A; *Jones C W cwj1@le.ac.uk Alcaligenes eutrophus growing in continuous culture; poly- Microbiology; (1997) 143, Pt.7, 2361-71 continuous culture at
842 beta-hydroxybutyrate production by fermentation 1997 34 deg and pH 6.8. Poly-
Piezoelectric properties of poly-beta-hydroxybutyrate and
copolymers of beta-hydroxybutyrate and beta-
844 Fukada, E.; Ando, Y. hydroxyvalerate Int. J. Biol. Macromol. 1986; 8:361-366 1986 653.
A mutant of A. latus
DSM1124 with
considerably increased
productivity
was incubated in shake
flasks and further scaled-
up in a 300-L
fermenter. In the next
step the bacteria were
Biotechnologische transferred to the 15-m3
Forschungsgesselsch. Pilot-scale production of poly(hydroxybutyrate) (PHB) with fermenter and grown to
m.b.H., Linz Alcaligenes NATO ASI Ser., Ser. E, 186(Novel Biodegrad. polyhydroxybutyrate manuf high densities. PHB was
846 Haenggi, Urs J. A-4021, Austria latus. Microb. Polym.), 65-70 (English) 1990 1990 Alcaligenes pr 660.korr
Park; J.S.; Park; H.C.; Huh; T.L.; Lee; Production of poly-beta-hydroxybutyrate by Alcaligenes
856 Y.H. eutrophus transformants harbouring cloned phbCAB genes Biotechnology Letters 1995; 17(7):735-740 1995 618.
PCT No.
PCT/KR91/00019 Sec.
371 Date Nov. 18, 1993
Sec. 102(e) Date Nov. 18,
1993 PCT Filed Sep. 16,
1991 PCT Pub. No.
WO92/18553 PCT Pub.
Date Oct. 29, 1992.A new
poly- beta -hydroxy
alkanoate (PHA)
Poly- beta -hydroxy alkanoate (PHA) copolymer, method of copolymer is produced in
LEE YANG-GUL (KR); KOHAP its production, the microbe which produces it, and PHA the cell of
857 YIM GUHN-BEEN (KR) LTD (KR) copolymer blend US5395919 1995-03-07 1995 Pseudomonas ce
4.10 Literature on Polyhydroxyalkanoates.xls - page 231
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
In the present invention a
new poly- beta -hydroxy
alkanoate (PHA)
copolymer is produced in
the cell of Pseudomonas
cepacia
KYG/505 (KCCM 10004)
by the method of its
production, and a variety
POLY- beta -HYDROXY ALKANOATE (PHA) of polymer blends of PHB
COPOLYMER, METHOD OF ITS and PHA are developed.
LEE YANG GUL (KR); YIM GUHN KOHAP PRODUCTION, THE MICROBE WHICH PRODUCES IT, The
858 BEEN (KR) LTD (KR) AND PHA COPOLYMER BLEND WO9218553 1992-10-29 1992 PHA cop
Binding of (i) purified wild-
type poly(3-
hydroxybutyrate) (PHB)
depolymerase PhaZ4 of
Pseudomonas lemoignei,
(ii) a purified
truncated form of PhaZ4,
which lacked 55 C-
terminal amino acids and
Institut fur (iii) commercial lactate
Mikrobiologie, Georg- Poly(3-hydroxybutyrate) depolymerases bind to their dehydrogenase to
August-Universitat substrate by a aqueous
859 Behrends A, Klingbeil B, Jendrossek D Gottingen, Germany. C-terminal located substrate binding site. FEMS Microbiol Lett 1996 Oct 1;143(2-3):191-4 1996 suspensions
Poly(3-hydroxybutyrate)
(PHB) is well-known as a
high molecular weight
homopolymer of R-3-
hydroxybutyrate which
accumulates in storage
granules within the
Department of cytosols of certain
Microbiology, Michigan bacteria. Escherichia coli
State University, East Poly(3-hydroxybutyrate) is associated with specific does not amass these
Lansing, Michigan proteins in the granules; however,
860 Huang R, Reusch RN 48824, USA. cytoplasm and membranes of Escherichia coli. J Biol Chem 1996 Sep 6;271(36):22196-202 1996 small amounts
Department of
Chemical Engineering Recombinant Escherichia
and BioProcess coli strain GCSC 6576,
Engineering Research harboring a high-copy-
Center, Korea number plasmid
Advanced containing the Ralstonia
Institute eutropha
of Science and genes for
Technology (KAIST), polyhydroxyalkanoate
373-1 Kusong-dong, (PHA) synthesis and the
Yusong-gu, Taejon E. coli ftsZ gene, was
305-701, Korea Poly-(3-hydroxybutyrate) production from whey by high- employed to produce
e-mail: density poly-(3-hydroxybutyrate)
861 Wong HH, Lee SY leesy@so cultivation of recombinant Escherichia coli. Appl Microbiol Biotechnol 1998 Jul;50(1):30-3 1998 (PHB) from whe kopiert
4.10 Literature on Polyhydroxyalkanoates.xls - page 232
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Department of
Chemical Engineering
and BioProcess Several recombinant
Engineering Research Escherichia coli strains
Center, Korea harboring the Alcaligenes
Advanced eutrophus
Institute
of Science and polyhydroxyalkanoate
Technology (KAIST), biosynthesis genes were
373-1 Kusong-dong, used to produce poly(3-
Yusong-gu, Taejon hydroxybutyrate), PHB,
305-701, Korea from xylose.
e-mail: Poly(3-hydroxybutyrate) production from xylose by Bioprocess Engineering Abstract Volume 18 By flask
862 Sang Yup Lee leesy@so recombinant Escherichia coli Issue 5 (1998) pp 397-399 1998 culture of TG
POly(3-Hydroxybutyrate) Production with high productivity
and high polymer content by a fed-batch culture of
863 Wang; W.; Lee; S.Y. Alcaligenes latus under nitrogen limitation Appl. Environ. Microbiol. 197; 63(9):3703-3706 1997 641.
To provide 4-
hydroxybutyryl-CoA for
poly(3-hydroxybutyrate-co-
4-hydroxybutyrate)
formation from glutamate
Monsanto Co., 800 in Escherichia
North Lindbergh coli, an acetyl-CoA:4-
Boulevard, St. Louis, hydroxybutyrate CoA
Missouri 63167, USA transferase from
email: Henry E. Clostridium kluyveri, a 4-
Valentin Poly(3-hydroxybutyrate-co-4-hydroxybutyrate) formation hydroxybutyrate
(henry.e.valentin@mo from dehydrogenase from
864 Valentin HE, Reiser S, Gruys KJ nsanto.com) gamma-aminobutyrate and glutamate. Biotechnol Bioeng 2000 Feb 5;67(3):291-9 2000 Ralstonia eutr
Pseudomonas lemoignei
is equipped with at least
five polyhydroxyalkanoate
(PHA)
depolymerase structural
genes (phaZ1 to phaZ5)
Institut fur which enable the
Mikrobiologie der bacterium to utilize
Universitat Stuttgart, extracellular
70550 Stuttgart, Poly(3-hydroxyvalerate) depolymerase of pseudomonas Appl Environ Microbiol 2000 poly(3-hydroxybutyrate)
865 Schober U, Thiel C, Jendrossek D Germany. lemoignei. Apr;66(4):1385-92 2000 (PHB),
Poly(beta-hydroxyalkanoate) biosynthesis and
866 Tombolini; R.; Nuti; M.P. accumulation by different Rhizobium species FEMS Microbiology Letters 1989; 60:299-304 1989 273.
Poly(beta-hydroxyalkanoate) copolymers containing
brominated repeating units produced by Pseudomonas
867 Kim; Y.B.; Lenz; R.W.; Fuller; R.C. oleovorans Macromolecules 1992; 25:1852-1857 1992 484.
Marchessault; R.H.; Bluhm; T.L.;
Deslandes; Y.; Hamer; G.K.; Orts; W.J.;
Sundarajan; P.R.; Taylor; M.G.; Poly(beta-hydroxyalkanoates): biorefinery polymers in Makromol.Chem.,Macromol.Symp. 1988; 19:235-
868 Bloembergen; S.; Holden; D.A. search of applications 254 1988 329.
4.10 Literature on Polyhydroxyalkanoates.xls - page 233
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxyalkanoates
(PHAs) comprise a class
of biodegradable polymers
which offer an
environmentally
Monsanto Company, sustainable
Agricultural Sector, alternative to petroleum-
700 Chesterfield based plastics. Production
Houmiel KL, Slater S, Broyles D, Parkway North, St. of PHAs in plants is
Casagrande L, Colburn S, Gonzalez K, Louis, MO 63198, Poly(beta-hydroxybutyrate) production in oilseed attractive since current
Mitsky TA, Reiser SE, Shah D, Taylor USA. leukoplasts of brassica fermentation technology is
869 NB, Tran M, Valentin HE, Gruys KJ napus. Planta 1999 Oct;209(4):547-50 1999 prohibitively e
U.S. Department of
Agriculture,
Agricultural Research The biosynthesis of
Service, Eastern poly(hydroxyalkanoates)
Regional Research (PHA) by Pseudomonas
Center, 600 E. resinovorans from
triglyceride
Mermaid Lane, substrates was
Wyndmoor, PA 19038, investigated. Each
USA Tel.: +1 215 233 triglyceride, whether
6483 Fax: +1 215 233 animal fat or vegetable oil,
6795 e-mail: supported
Poly(hydroxyalkanoate) biosynthesis from triglyceride Applied Microbiology and Biotechnology Abstract cellular
873 R. D. Ashby, T. A. Foglia rashby@arserrc substrates Volume 49 Issue 4 (1998) pp 431-437 1998 growth
874 Stal; L.J. Poly(hydroxyalkanoate) in cyanobacteria: an overview FEMS Microbiology Reviews 1992; 103:169-180 1992 473.
Dep. Biol.,
Massachusetts Inst. Poly(hydroxybutyrate) (PHB): a model system for NATO ASI Ser., Ser. E,
Technol., Cambridge, biopolymer 186(Novel Biodegrad. Microb. Polym.), 191-202 review polyhydroxybutyrate
876 Peoples, Oliver P.; Sinskey, Anthony J. MA 02139, USA engineering: II. (English) 1990 1990 biopolymer engineering A review with 35 refs.
The biodegradable
polyesters,
poly(hydroxybutyrate)
(PHB) and
poly(hydroxybutyrate-
hydroxyvalerate) (PHBV)
were
investigated for use as
sustained delivery carriers
of a model drug,
Poly(hydroxybutyrate-hydroxyvalerate) microspheres progesterone. Spherical
College of Pharmacy, containing microspheres containing
University of Georgia, progesterone: preparation, morphology and release the drug
877 Gangrade N, Price JC Athens 30602. properties. J Microencapsul 1991 Apr-Jun;8(2):185-202 1991 were prepared by
Laboratorium für
Organische Chemie
der Eidgenössischen
Technische
Hochschule ETH-
Zentrum
Universitätsstrasse 16,
CH-8092 Zürich Poly(hydroxyfettsäureester), eine fünfte Klasse von Angewandte Chemie 1993; 105:483-509 (Article
878 Müller; H-M.; Seebach; D. Schweiz physiologisch bedeutsamen organischen Biopolymeren in German) 1993 Review Abstract unavailable. Review 430.
879 Heller J, Himmelstein KJ Poly(ortho ester) biodegradable polymer systems. Methods Enzymol 1985;112:422-36 1985 Abstract unavailable.
4.10 Literature on Polyhydroxyalkanoates.xls - page 235
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
885 Tezuka, C.; Takeda, K.; Someya, J. poly-beta-hydroxy butyrate of methane oxidizing bacteria japanische Zeitschrift!!! 175.
Nickerson, K.W.; Zarnick, W.J.; Poly-beta-hydroxy butyrate parasporal bodies in Bacillus
886 Kramer, V.C. thuringiensis FEMS Microbiology Letters 1981; 12:327-331 1981 225.
Environmental Science and Technology 1974;
887 Wallen; L.L.; Rohwedder; K. Poly-beta-hydroxyalkanoate from activated sludge 8(6):576-579 1974 313.
Poly-ß-hydroxybuttersäure
(PHBS) scheint der unter
aeroben Bakterien am
weitesten verbreitete
Speicherstoff zu sein. Die
chemische Natur dieses
Reservestoffes wurde von
LEMOIGNE (1926,
1927)an den
Aus dem Institut für Fettteinschlüssen von
Mikrobiologie der Poly-beta-hydroxybuttersäure abbauende Bakterien und Archiv f r Mikrobiologie 1963; 47:167-200 Isolation of PHB-degrading Bacillus megaterium Metabolism -
889 Chowdhury, A.A. Universität Göttingen Exoenzym (Article in German) 1963 bacteria - Depolymerase aufgeklärt. Daß Degradation 127.korr.
Poly-beta-hydroxybuttersäure, ihre Verbreitung, Funktion
890 Schlegel, H.G.; Gottschalk, G. und Biosynthese Angew. Chem. 1962; 74(10):342-347 1962 23.
4.10 Literature on Polyhydroxyalkanoates.xls - page 237
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Die Fähigkeit,
Reservematerial in Form
von Poly-beta-
hydroxybuttersäure (PHB)
vorübergehend
intracellulär anzuhäufen,
ist bei aeroben Bakterien
anscheinend eher die
Regel als eine Ausnahme.
Die Akkumulation erfolgt,
Poly-beta-hydroxybuttersäure-arme und -freie Mutanten Nachrichten der Akademie der Wissenschafren wenn Kohlenstoff- und
891 Schlegel, H.G.; Krauss, I.; Lafferty, R. von Hydrogenomonas H 16 in Göttingen 1969 1969 Energiequellen im 182.
The procaryotic
endogenous storage
material poly-beta-
hydroxybutyrate (PHB)
can be induced to
accumulate the estuarine
detrital microbiota under
Department of Regulation of PHB- conditions which suggest
Biological Science, accumulation in estuarine unbalanced growth, such
Florida State detrital microbiota - Balanced as limitation of a critical
University, Tallahasee, Poly-beta-hydroxybutyrate accumulation as a measure of Applied and enviromental microbiology 1979; and unbalanced growth factor(s) in the presence
895 Nickels, J.S.; King, J.D.; White, D.C. Florida 32306 unbalanced growth of the estuarine detrial microbiota 37(3):495-465 1979 conditions of carb Strain - Metabolism 124. Korr.
Poly-beta-hydroxybutyrate accumulation by facultative
896 Daniel, M.C.; Lebeault, J.M. methylotrophic bacteria Como Tagung 1986 1986 260.
4.10 Literature on Polyhydroxyalkanoates.xls - page 238
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Azotobacter beijerinckii
possesses the enzymes of
both the Enter-Doudoroff
and the oxidative pentose
Azotobacter beijerinckii - phosphate cycle pathways
Entner Doudoroff pathway - of glycose catabolism and
Department of pentose phosphate pathway - both pathways are subject
Biochemistry, regulation of PHB-metabolism - to feedback inhibition by
University of Hull, allosteric regulation - NAD, products of glucose
Kingston upon Hull Poly-beta-hydroxybutyrate biosynthesis and the regulation NADP, ATP, ADP - PHB oxidation. The allosteric
897 Senior, P.J.; Dawes, E.A. HU6 7RX, U.K. of glucose metabolism in Azotobacter beijerinckii Biochem. Journal 1971; 125:55-66 1971 formation as electron sink gluco Strain - Metabolism 125. Korr.
Poly-beta-hydroxybutyrate biosynthesis in Alcaligenes The journal of biological chemistry 1989;
898 Peoples, O.P.; Sinskey, A.J. eutrophus H16 264(26):15293-15297 1989 519.
The poly-beta-
hydroxybutyrate
biosynthetic thiolase gene
from Zoogloea ramigera
was used as a
hybridization probe to
screen
restriction digests of
Biology Department, Alcaligenes eutrophus
Massachusetts Poly-beta-hydroxybutyrate biosynthesis in Alcaligenes H16 DNA. Specific
Institute of eutrophus H16. hybridization signals were
Technology, Characterization of the genes encoding beta-ketothiolase obtained and two
Cambridge 02139. and fragments (a
899 Peoples OP, Sinskey AJ acetoacetyl-CoA reductase. J Biol Chem 1989 Sep 15;264(26):15293-7 1989 2.3-kilobas
Poly-beta-hydroxybutyrate depolymerases of
900 C.J.Lusty; Doudoroff, M. Pseudomonas lemoignei Biochemistry 1966; 56:960-965 1966 33.
901 Szewczyk; E.M. Poly-beta-hydroxybutyrate in staphylococci FEMS Microbiology Reviews 1992; 103:165-168 1992 472.
Staphylococci--
chemoorganotrophic
bacteria whose main
habitats are human and
animal organisms--can
accumulate
Department of poly-beta-hydroxybutyrate
Pharmaceutical (PHB) in their cells. The
Microbiology, Medical polymer is metabolized in
University of Lodz, endogenous turnovers
Poland. preceding degradation of
902 Szewczyk EM Poly-beta-hydroxybutyrate in staphylococci. FEMS Microbiol Rev 1992 Dec;9(2-4):165-8 1992 aminoacids, proteins
Department of
Bacteriology and
Botnay, Syracuse
University, Syracuse, Poly-beta-hydroxybutyrate in the chemolithotrophic Ferrobacillus ferrooxidans -
903 Wang, W.S.; Lundgren, D.G. New York 131 bacterium Ferrobacillus ferrooxidans J.bacteriol. 1969; 97:947-950 1969 heterotrophic growth No abstract. Strain - Metabolism 77.
4.10 Literature on Polyhydroxyalkanoates.xls - page 239
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly-beta-hydroxybutyrate
was determined in lactic
acid bacteria belonging to
the genera Lactobacillus,
Lactococcus,
Pediococcus and
Gazi University, Streptococcus.
Faculty of Arts and Lactobacilli were grown in
Science, Department MRS broth, the others
of Biology, Ankara, were grown in Elliker broth
Aslim B, Caliskan F, Beyatli Y, Gunduz Turkey. Poly-beta-hydroxybutyrate production by lactic acid medium. Cell
908 U bacteria. FEMS Microbiol Lett 1998 Feb 15;159(2):293-7 1998 biomass was obtai
Poly-beta-hydroxybutyrate synthesis in Azotobacter
beijerinkii; the
909 Ritchie GA, Senior PJ, Dawes EA non-involvement of acyl carrier protein. J Gen Microbiol 1969 Nov;58(3):3 1969 Abstract unavailable.
Poly-beta-
hydroxybutyrate/calcium
polyphosphate (PHB-
CaPolyPi) complexes exist
as labile quasi-crystalline
structures in
Department of bacterial plasma
Microbiology and membranes. The
Public Health, composition, structure,
Michigan State and distribution of the
University, East Poly-beta-hydroxybutyrate/calcium polyphosphate complex suggest it may
Lansing. complexes in play a role in the
910 Reusch RN eukaryotic membranes. Proc Soc Exp Biol Med 1989 Sep;191(4):377-81 1989 regulation o
911 Ramsay, B. Poly-beta-Hydroxybutyric Acid (PHB) ??? 383.
4.10 Literature on Polyhydroxyalkanoates.xls - page 240
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly-beta-hydroxybutyric
acid (PHB) was extracted
from various species of
staphylococci isolated
from different sources. IR
and UV spectrophotometry
and NMR analysis
Department of revealed that the
Pharmaceutical compound consisted only
Microbiology, of the beta-
Academy of Medicine, hydroxybutyrate. The
912 Szewczyk E, Mikucki J Lodz, Poland. Poly-beta-hydroxybutyric acid in staphylococci. FEMS Microbiol Lett 1989 Oct 15;52(3):279-84 1989 PHB level in t
Lafferty; R.M.; Braunegg; G.; Korneti; Poly-D-3-hydroxybutyric acid (poly-HB): Biotechnological Third European Congress on Biotechnology
919 L.; Strempfl; F.; Bogensberger; B. production and polymer applications 1984 1984 237.
A polyester composition
comprises at least one
first semi-crystalline or
crystallisable
polyhydroxyalkanoate
(PHA-X) and at least
one second
polyhydroxyalkanoate
ZENECA (PHA-Y) in semi-
LTD (GB); LIGGAT crystalline or crystalline
LIGGAT JOHN JOHN JAMIESON form and having a higher
920 JAMIESON (GB) (GB) POLYESTER COMPOSITION WO9428070 1994-12-08 1994 crystalline melting poi
PCT No.
PCT/GB94/01095 Sec.
371 Date Apr. 17, 1996
Sec. 102(e) Date Apr. 17,
1996 PCT Filed May 20,
1994 PCT Pub. No.
WO94/28070 PCT Pub.
Date Dec. 8, 1994A
polyester composition
comprises at least one
first semi-crystalline or
US5693389 crystallizable
921 LIGGAT JOHN JAMIESON (GB) ZENECA LTD (GB) Polyester composition 1997-12-02 1997 polyhydr
Polyhydroxyalkanoic acids
(PHA) are carbon and
energy storage polymers
that accumulate in
Department of inclusion
Microbiology, bodies in many bacteria
University of and archaea in response
Massachusetts, to environmental
Amherst, Polyhydroxyalkanoate inclusion body-associated proteins conditions. This work
Massachusetts 01003, and coding presents
928 McCool GJ, Cannon MC USA. region in Bacillus megaterium. J Bacteriol 1999 Jan;181(2):585-92 1999 the results o
4.10 Literature on Polyhydroxyalkanoates.xls - page 243
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Transgenic plants
producing peroxisomal
polyhydroxy- alkanoate
(PHA) from intermediates
of fatty acid degradation
were
Institut dEcologie- used to study carbon flow
Biologie et Physiologie through the beta-oxidation
Vegetales, Universite cycle. Growth of
de Lausanne, CH- Polyhydroxyalkanoate synthesis in transgenic plants as a transgenic plants in media
Mittendorf V, Bongcam V, Allenbach L, 1015, Lausanne, new tool to study containing fatty acids
932 Coullerez G, Martini N, Poirier Y Switzerland. carbon flow through beta-oxidation. Plant J 1999 Oct;20(1):45-55 1999 conjugated to Tw
4.10 Literature on Polyhydroxyalkanoates.xls - page 244
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Problem to be solved: To
produce the subject new
decomposing enzyme,
comprising a
polyhydroxyalkanoate(PH
A) decomposing enzyme
having an N-terminal
SAITO YUJI fragment of a specific
ITO MASAKO TAISEI CORP amino
TAKEBE HIDEAKI MEIJI POLYHYDROXYALKANOATE-DECOMPOSING acid sequence
935 MATSUNOBU TOSHIO SEIKA KAISHA LTD ENZYME AND ITS PRODUCTION JP10191980A July 28, 1998 1998 and a specified molecular
Institut fur
Pharmazeutische
Chemie, Karl-Franzens-Polyhydroxyalkanoates as drug carriers for the formulation
Universitat Graz, of tablets Pharmazie 1990 Sep;45(9):691-2 [Article in
936 Korsatko-Wabnegg B, Korsatko W Osterreich. with "quick-release" effect. German] 1990 Abstract unavailable.
4.10 Literature on Polyhydroxyalkanoates.xls - page 245
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Bacterial survival in
natural environments
involves the ability of
scavenging nutrients and
energy sources.
Departamento de Polyhydroxyalkanoates
Quimica Biologica, (PHAs) are intracellular
Facultad de Ciencias polymers that endow
Exactas y Naturales, bacteria with enhanced
Universidad de Polyhydroxyalkanoates degradation affects survival of survival capabilities in
Buenos Aires, Pseudomonas adverse environmental
937 Ruiz JA, Lopez NI, Mendez BS Argentina. oleovorans in river water microcosms. Rev Argent Microbiol 1999 Oct-Dec;31(4):201-4 1999 conditions
Polyhydroxyalkanoates
(PHAs) from which
pyrogen has been
removed are provided for
WILLIAMS, Simon, F. , 28 use in numerous
Deerfield Road, Sherborn, MA 01770, biomedical
United States of America applications. PHAs which
MARTIN, David, P. , 33 METABOLIX, INC., have been chemically
Hemlock Street, Arlington, MA 02174, 303 Third Street, modified to enhance
United States of America Cambridge, MA 02142- physical and/or chemical
GERNGROSS, Tillman , 12 1196, United States of POLYHYDROXYALKANOATES properties, for
938 Ant America FOR IN VIVO APPLICATIONS WO9851812 1998-11-19 1998 tar
Polyhdroxyalkanoates
(PHAs), stored as
bacterial reserve materials
for carbon and energy, are
biodegradable substitutes
to fossil fuel plastics that
can be produced from
Institut fur Polyhydroxyalkanoates, biopolyesters from renewable renewable raw
Biotechnologie, TU resources: materials.
939 Braunegg G, Lefebvre G, Genser KF Graz, Austria. physiological and engineering aspects. J Biotechnol 1998 Oct 27;65(2-3):127-61 1998 PHAs can be pr 640.
941 Babel; W. Polyhydroxyalkans"uren-ein Kapitel umweltprophylaxe Bioworld 1997; 4:16-20 1997 647.
4.10 Literature on Polyhydroxyalkanoates.xls - page 246
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxybutyrate
(PHB) can be used as an
alternative polymer to
polylactide-glycolides for
drug carrier production. It
is a
linear homopolymer
Department of biosynthesized by various
Pharmaceutical strains of bacteria by
Sciences, School of condensation of D(-)-B-
Pharmacy, University hydroxybutyric acid and
of Nottingham, United Crit Rev Ther Drug Carrier Syst 1989;6(2):117- used as
943 Koosha F, Muller RH, Davis SS Kingdom. Polyhydroxybutyrate as a drug carrier. 30 1989 an en
Polyhydroxybutyrate
(PHB) is a thermoplastic
biopolymer posessing
unique properties, such
as biocompatibility and
Institute of biodegradability.
Microbiology and The potential prodn. of
Biotechnology, PHB from renewable
Kizlo, Zulfija; Savenkova, Ludmila; University of Latvia, Proc. Latv. Acad. Sci., Sect. B (1999), 53(2), 117- substrates makes this
Gercberga, Zoja; Kalnins, Riga, LV-1586, Polyhydroxybutyrate biosynthesis by Azotobacter 120 polymer a prospective
944 Martins Latvia chroococcum 23 from renewable unrefined carbon sources 1999 substitute for thermo
4.10 Literature on Polyhydroxyalkanoates.xls - page 247
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxybutyrate
(PHB) offers many
advantages over by adding a
traditional petrochemically carboxy-
derived plastics. In terminal
Department of addition to its complete targeting
Chemistry and biodegradability, PHB is sequence. The
Biochemistry, formed from renewable enzymes
University of resources. It possesses evidently were
California, Santa Cruz better physical transported
95064, USA. Polyhydroxybutyrate: plastic made and degraded by properties than into
949 Hankermeyer CR, Tjeerdema RS microorganisms. Rev Environ Contam Toxicol 1999;159:1-24 1999 PHA, review polypropylene for food p peroxisomes,
Biodegradable polymer
blend compositions are
provided which contain
oligomeric esters. The
oligoester
compounds
ASRAR, Jawed , 14949 Royal Brook MONSANTO can compatibilize blends
Drive, Chesterfield, MO 63017, United COMPANY, 800 N. of two or more
States of America Lindbergh Boulevard, POLYMER BLENDS CONTAINING biodegradable polymers
PIERRE, Jean, R. , Rue des St. Louis, MO 63189, POLYHYDROXYALKANOATES AND resulting in excellent
Trois Bonniers 13, B-5081 Saint-Denis, United States of COMPOSITIONS WITH GOOD RETENTION ductility
950 Belgium America OF ELONGATION WO9923161 1999-05-14 1999 and reduced
951 Schnabel, W. Polymer Degradation ? 1981; 155-177 1981 391.
Reservoir-type
microcapsules were
prepared using a double
emulsion solvent
evaporation process from
a range of different
poly-beta-hydroxybutyrate
Speciality Materials Polymers for biodegradable medical devices. X. homopolymers and
Research Group, Microencapsulation copolymers thereof with 3-
Aston University, studies: control of poly-hydroxybutyrate-hydroxyvalerate hydroxyvalerate (P(HB-
Aston Triangle, microcapsules HV) polymers) blended
961 Embleton JK, Tighe BJ Birmingham, UK. porosity via polycaprolactone blending. J Microencapsul 1993 Jul-Sep;10(3):341-52 1993 with 20 per cent by w
Poly(beta-malic acid) and
poly(beta-3-alkylmalic
acid) derivatives, as
synthetic
Laboratoire de polyhydroxyalkanoates
Recherche sur les (PHAs), present several
Polymeres, UMR advantages as
C7581 CNRS, macromolecular materials
Universite Paris Val de Polymers of malic acid and 3-alkylmalic acid as synthetic for
Marne, PHAs in the temporary
Cammas S, Bear MM, Moine L, Escalup Thiais, France. design of biocompatible hydrolyzable biomedical applications.
962 R, Ponchel G, Kataoka K, Guerin P cammas@glvt-cnrs.fr devices. Int J Biol Macromol 1999 Jun-Jul;25(1-3):273-82 1999 Inde
4.10 Literature on Polyhydroxyalkanoates.xls - page 251
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
964 Stein POolymer recycling: opportunities and limitations Proc. Natl. Acad. Sci USA 1992; 89:835-838 1992 508.
The photosynthetic
bacterium Rhodobacter
capsulatus can grow with
short- to long-chain fatty
Department of Biology, acids as the
Washington sole carbon source (R. G.
University, St. Louis, Kranz, K. K. Gabbert, T.
Missouri 63130, USA. A. Locke, and M. T.
Positive selection systems for discovery of novel polyester Madigan,
kranz@wustlb.wustl.ed biosynthesis Appl.
966 Kranz RG, Gabbert KK, Madigan MT u genes based on fatty acid detoxification. Appl Environ Microbiol 1997 Aug;63(8):3010-3 1997 Environ. Microbio
Possible hydrolysis
products of poly(3-
hydroxybutyrate) (PHB)
include the monomer,
oligomers and derivatives
Department of of these that have been
Bioscience and further modified in side
Biotechnology, reactions. Hauttecoeur at
University of High performance liquid al. reported that oligomers
Strathclyde, Glasgow Preparation and chromatographic analysis of poly(3- chromatography (HPLC) - (2-7 units long) (with
970 McLellan, D.W.; Halling, P.J. G1 1XW (UK) hydroxybutyrate) hydrolysis products J. of Chromatography 1988; 445:251-257 1988 oligomers - crotonic acid methyl ester of the Analytics 679.
PHB [poly(3-
hydroxybutyrate)]
microspheres contg. drug
were prepd.
by the emulsion solvent
evapn. method. The
Dep. Fine Chemicals, release behavior and
Jiangsu Institute content of
Petrochemical progesterone in the
Technology, microspheres depended
Changzhou, Jiangsu Shiyou Huagong Xueyuan Xuebao on the concn.
Chen, Haiqun; Zhang, Hao; Pang, Yixin 213016, Peop. Rep. Preparative conditions of PHB microspheres containing (1997), 9(4), 15-18, 23 of PHB in chloroform,
972 China drug Chinese 1997 the ratio of proges
4.10 Literature on Polyhydroxyalkanoates.xls - page 253
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Oriented films of a
copolymer of 70 mol%
1 Department of beta-hydroxybutyrate and
Industrial Chemistry, 25 mol% beta-
Tokyo University of hydroxyvalerate produced
Agriculture and from microorganism
Technology, Koganei, showed intrinsic shear
Tokyo; 2 The Institute piezoelectricity. Complex
of Physical and piezoelectric constant e =
Ando, Y.1; Minato, M.1; Nishida, K.1; Chemical Research, Primary piezoelectric relaxation in a copolymer of beta- IEEE transactions on Electrical Insulation 1986; e ´ - ie ´´ , elastic constant Copolyesters -
973 Fukada, E.2 Wako, Saitama, Japan hydroxybutyrate and beta-hydroxyvalerate E1-21(3):505-510 1986 Piezoelectricity - Copolyesters c = c´ - ic´´ and dielect Crystallinity 670.
Oriented films of a
copolymer of 70 mol%
1 Department of beta-hydroxybutyrate and
Industrial Chemistry, 25 mol% beta-
Tokyo University of hydroxyvalerate produced
Agriculture and from microorganism
Technology, Koganei, showed intrinsic shear
Tokyo; 2 The Institute piezoelectricity. Complex
of Physical and piezoelectric constant e =
Ando, Y.1; Minato, M.1; Nishida, K.1; Chemical Research, Primary piezoelectric relaxation in copolymers of beta- Proc. 5th intern. Sympl Electrets, Heidelberg, e ´ - ie ´´ , elastic constant Copolyesters -
974 Fukada, E.2 Wako, Saitama, Japan hydroxybutyrate and beta-hydroxyvalerate 1985 1985 Piezoelectricity - Copolyesters c = c´ - ic´´ and dielect Crystallinity 673.
Department of
Chemical Engineering
and BioProcess Several processes for the
Engineering Research production and recovery
Center, Korea of poly(3-hydroxybutyrate)
(PHB)
Advanced Institute of by
Science and Alcaligenes eutrophus,
Technology (KAIST), Alcaligenes latus,
373-1 Kusong-dong, Methylobacterium
Yusong-gu, organophilum, and
Taejon Process analysis and economic evaluation for
305-701, Korea. e- Poly(3-hydroxybutyrate) production by Bioprocess Engineering Abstract Volume 17 recombinant Escherichia
976 Jong-il Choi, Sang Yup Lee mail: leesy@s fermentation Issue 6 (1997) pp 335-342 1997 coli were designed b
The biodegradable
carrier is a mixture of PHB
and PLGA. The capsules
Process for preparing biodegradable microcapsules are obtained by spraying a
containing peptides and suspension, solution or
SCHMIEDEL RAINER DR; SANDOW proteins soluble in water and microcapsules obtained by EP0315875 emulsion of active
977 JURGEN KURT DR HOECHST AG (DE) said process. 1989-05-17 1989 ingredients and carriers.
4.10 Literature on Polyhydroxyalkanoates.xls - page 254
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
polyhydroxyalkanoate
from biological source
material containing the
polyhydroxyalkanoate, the
The Procter & Gamble Process for recovering process comprising: a)
Company, Cincinnati, polyhydroxyalkanoates using centrifugal comminuting the
980 Noda; Isao , Fairfield, OH OH fractionation US5899339 May 4, 1999 1999 b
PCT No.
PCT/GB96/00293 Sec.
371 Date Dec. 1, 1997
Sec. 102(e) Date Dec. 1,
1997 PCT Filed Feb. 9,
1996 PCT Pub. No.
WO96/25509 PCT Pub.
Date Aug. 22, 1996A
process for producing poly-
3-hydroxyalkanoate (PHA)
NAYLOR LINDA ANNE by culturing Alcaligenes
(GB); WOOD JOHN CHRISTOPHER US5871980 on a
986 (GB) MONSANTO CO (US) Process for the microbiological production of pha-polymers 1999-02-16 1999 low water-
PCT No.
PCT/GB95/01926 Sec.
371 Date Jun. 16, 1997
Sec. 102(e) Date Jun. 16,
1997 PCT Filed Aug. 15,
1995 PCT Pub. No.
WO96/06179 PCT Pub.
Date Feb. 29, 1996A
hydroxyalkanoic acid
(PHA)is recovered from
matter derived from living
LIDDELL JOHN US5894062 organisms
987 MACDONALD (GB) MONSANTO CO (US) Process for the recovery of polyhydroxyalkanoic acid 1999-04-13 1999 by disso
PCT No.
PCT/GB95/01925 Sec.
371 Date Jul. 7, 1997 Sec.
102(e) Date Jul. 7, 1997
PCT Filed Aug. 15, 1995
PCT Pub. No.
WO96/06178 PCT Pub.
Date Feb. 29, 1996A
process of recovering
PHA from a suspension
GEORGE NEIL (GB); which comprises particles
HALL ALAN (GB); LIDDELL JOHN US5952460 of PHA in
988 MACDONALD (GB) MONSANTO CO (US) Process of recovering polymers of hydroxyalkanoic acids 1999-09-14 1999 a liquid wh
4.10 Literature on Polyhydroxyalkanoates.xls - page 257
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxyalkanoate
(PHA) polyester is
recovered from vegetable
matter associated with its
production in
MONSANTO transgenic
COMPANY, 800 North plants. The process
Lindbergh Boulevard, involves contacting the
LIDDELL, John, Macdonald , 678 Yarm St. Louis, MO 63167, PROCESS TO RECOVER vegetable matter with one
Road, Eaglescliffe, Stockton on Tees, United States of POLYESTERS FROM TRANSGENIC WO9717459 or more reagents inactive
989 Cleveland TS16 0DP, -- America PLANTS 1997-05-15 1997 toward
Poly(hydroxybutyrate) (I)
and hydroxybutyrate-
hydroxyvalerate
copolymer (II) with
Department of different contents of
Chemical Engineering, hydroxy-valerate were
Tsinghua University, successfully prepd. by
Beijing, Azotobacter Vinelandii
Hu, Ping; Chen, Guoqiang; Zhang, 100084, Peop. Rep. UWD in beet molasses
Zengmin; Wu, Qiong China Production and characterization of biodegradable plastics - Hecheng Shuzhi Ji Suliao (1997), 14(2), 45-49 media contg. valerate
993 polyhydroxyalkanoates (PHA) Chinese 1997 of different concns. The
4.10 Literature on Polyhydroxyalkanoates.xls - page 258
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Alcaligenes eutrophus
mutant strain R3, which is
a spontanious revertant to
prototrophy of an
Institut für isoleucine-auxotrophic
Mikrobiologie der Alcaligenes eutrophus H 16 - mutant of the wild-type
Georg-August- Ralstonia eutropha H 16 - strain H 16, accumulated
Universität Göttingen, Alcaligenes eutrophus R3 - a copolyester consisting of
Grisebachstrasse 8, W- Production of a copolyester of 3-hydroxybutyric acid and 3- fructose - gluconate - succinate 3-hydroxybutyric acid
3400 Göttingen, hydroxyvaleric acid from single unrelated carbon sources - lactate - acetate - (3HB), i.e. poly(3HB-co- Strain - Copolyesters
999 Steinbüchel; A.; Pieper; U. Germany by a mutant of Alcaligenes eutrophus Appl. Microbiol. Biotechnol. 1992; 37:36678 1992 copolyesters - P(3HB-co3HV) 3HV), as the on - Substrates 417.
PCT No.
PCT/GB96/00305 Sec.
371 Date Jan. 6, 1998
Sec. 102(e) Date Jan. 6,
1998 PCT Filed Feb. 12,
1996 PCT Pub. No.
WO96/25452 PCT Pub.
Date Aug. 22, 1996A
process of making a
polyhydroxyalkanoate
GEORGE NEIL (GB); PHA latex comprises
LIDDELL JOHN MACDONALD (GB); making a
1003 TURNER PETER DERYCK (IE) MONSANTO CO (US) Production of a polymer composition US5891936 1999-04-06 1999 liquid-form solution of
Production of beta -
hydroxybutyrate polymers
(PHB) by microbial
cultivation wherein at least
part of the carbon source
is derived
from cell material
obtained by separation of
PHB from PHB-containing
EP0114086 micro-organism cells: i.e.
1004 RICHARDSON KENNETH RAYMOND ICI PLC (GB) Production of beta-hydroxybutyrate polymers. 1984-07-25 1984 the non-PHB cell materia
Senior, P. J.; Collins, S. H.; Kenneth, K. Production of beta-hydroxybuyric acid-beta-hydroxyvaleric
1005 R. acid copolymers Eur. Pat. Appl. EP 204.442 1986 1986 292.
Poly[beta-hydroxybutyrate-
co-beta-hydroxyvalerate]
co-polymer, PHBV, is a
polyhydroxyalkanoate
(PHA) that has greater
utility as a biodegradable
thermoplastic polyester
Department of than poly-beta-
Agronomy and Plant hydroxybutyrate, PHB. In
Genetics, University of Production of heteropolymeric polyhydroxyalkanoate in order to produce PHBV, a
Eschenlauer AC, Stoup SK, Srienc F, Minnesota-St. Paul Escherichia coli system
1010 Somers DA 55108-6026, USA. from a single carbon source. Int J Biol Macromol 1996 Aug;19(2):121-30 1996 of pathways is
Production of medium
chain length poly-3-
hydroxyalkanoates (mcl-
PHAs) in Escherichia coli
is reported for the first
time. To
produce PHA in E. coli, a
PHA polymerase encoding
gene (phaC2) of
Production of medium chain length poly-3-hydroxy Pseudomonas oleovorans
EIDGENOESS TECH alkanoates in Escherichia coli, EP0881293 GPo1 was introduced into
1011 HOCHSCHULE (CH) and monomers derived therefrom 1998-12-02 1998 various E. c
Production of medium
EIDGENÖSSISCHE chain length poly-3-
TECHNISCHE hydroxyalkanoates (mcl-
WITHOLT, Bernard , ETH HOCHSCHULE PHAs) in Escherichia coli
Hönggerberg, HPT, CH-8093 Zürich, ZÜRICH INSTITUT is reported for
United States of America FÜR the first time.
REN, Qun , ETH BIOTECHNOLOGIE, PRODUCTION OF MEDIUM CHAIN To produce PHA in E. coli,
Hönggerberg, HPT, CH-8093 Zürich, ETH LENGTH POLY-3-HYDROXY a PHA polymerase
China ALKANOATES encoding gene (phaC2) of
KESSLER, Birgit , ETH Hönggerberg, HPT, INESCHERICHIA COLI, AND MONOMERS Pseudomonas
Hönggerberg, HPT, CH-8093 Zürich, CH-8093 Zürich, DERIVED olevorans
1012 Germany Switzerland THEREFROM WO9854329A1 Dec. 3, 1998 1998 GPo1 w
Plant metabolic
engineering has recently
enabled the synthesis of a
range of
polyhydroxyalkanoates as
Institut d'Ecologie- well as a protein-based
Biologie et Physiologie polymer. These novel
Vegetales, Universite compounds can be
deLausanne, CH-1015 harvested from plants as a
Lausanne, renewable source of
Switzerland. environmentally friendly
yves.poirier@ie- polymers or
1013 Poirier Y bpv.unil.ch Production of new polymeric compounds in plants. Curr Opin Biotechnol 1999 Apr;10(2):181-5 1999 can be
4.10 Literature on Polyhydroxyalkanoates.xls - page 262
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Recombinant Escherichia
coli XL1-Blue harboring a
high-copy-number plasmid
containing the
Department of Alcaligenes
Chemical Engineering, eutrophus
Korea Advanced polyhydroxyalkanoate
Institute of Science Production of poly(3-hydroxybutyrate) by fed-batch culture synthesis genes could
and Technology, of efficiently synthesize
Taejon, filamentation-suppressed recombinant poly(3-
1023 Wang F, Lee SY Korea. Escherichia coli. Appl Environ Microbiol 1997 Dec;63(12):4765-9 1997 hydroxybutyrate) (PHB) i kopiert
4.10 Literature on Polyhydroxyalkanoates.xls - page 264
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Department of
Molecular Biology and
Microbiology, Case
Western Reserve
University, Cleveland,
Ohio 44106-4960,1
and Department of
Chemistry2 and
Department of
Biology,3 James
Madison University,
Harrisonburg, Virginia Production of Poly(3-hydroxybutyrate-co-4-
1027 Hiramitsu; M.; Koyama; N.; Doi; Y. 22807 hydroxybutyrate) by Alcaligenes latus Biotechnology Letters 1993; 15:-3 1993 448.
Production of poly(3-hydroxybutyrate-co-4- Food technol. biotechnol. 1996; 34:91-95
1028 Renner; G.; Pongratz; K.; Braunegg; G. hydroxybutyrate) by Comamonas testeronii A3 36587? 1996 624.
4.10 Literature on Polyhydroxyalkanoates.xls - page 265
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A number of Escherichia
coli strains including K12,
B, W, XL1-Blue, DH5
alpha, HB101, JM109, and
C600 were
transformed with the
Department of stable high-copy-number
Chemical Engineering, plasmid pSYL105
Korea Advanced containing the Alcaligenes
Institute of Science eutrophus
and Technology, Production of poly(3-hydroxybutyric acid) by recombinant polyhydroxyalkanoic
Yusong-gu, Taejon. Escherichia acid biosynthesis genes,
1032 Lee SY, Chang HN coli strains: genetic and fermentation studies. Can J Microbiol 1995;41 Suppl 1:207-15 1995 and w
Production of poly(3-hydroxybutyric-co-3-hydroxyvaleric
Kim; B.S.; Lee; S.C.; Lee; S.Y.; Chang; acid) by fed-batch culture of Alcaligenes eutrophus with
1033 H.N.; Y.K., Chang; Woo; S.I. substrate control using on-line glucose analyzer Enzyme Microb. Technology. 1994; 16:556-561 1994 462.
Production of poly(beta-hydroxybutyrate-co-beta-
Lee; I.Y.; Kim; M.K.; Kim; F.J.; Chang; hydroxyvalerate) from glucose and valerate in Alcaligenes
1034 H.N.; Y.H., Park eutrophus Biotechnology Letters 1995; 17:571-574 1995 515.
4.10 Literature on Polyhydroxyalkanoates.xls - page 266
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
BioProcess
Engineering Research
Center, Korea
Advanced Institute of
Science and Production of poly(beta-hydroxybutyric acid) by
Technology, Yusung- recombinant Escherichia
1035 Lee SY, Chang HN, Chang YK gu, Taejon. coli. Ann N Y Acad Sci 1994 May 2;721:43-53 1994 Abstract unavailable.
Alcaligenes latus,
Alcaligenes eutrophus,
Bacillus cereus,
Pseudomonas
pseudoflava,
Pseudomonas cepacia,
and Micrococcus
Department of halodenitrificans were
Chemical Engineering, found to accumulate poly-
Ecole Polytechnique (beta-hydroxybutyric-co-
de Montreal, Quebec, beta-hydroxyvaleric) acid
Ramsay BA, Lomaliza K, Chavarie C, Canada. Production of poly-(beta-hydroxybutyric-co-beta- [P(HB-co-HV)]
1036 Dube B, Bataille P, Ramsay JA hydroxyvaleric) acids. Appl Environ Microbiol 1990 Jul;56(7):2093-8 1990 copolymer when supplie
A bench-scale recycled-
gas, closed-circuit culture
Univ.Kyushu; Saibu- system was
Gas developed for
LO Department of production of poly-beta-
Food Science and hydroxybutyrate by high
Technology, Kyushu cell
University, density autotrophic
Hakozaki, Higashi- Production of poly(D-3-hydroxybutyrate) from CO2, H2, cultivation of Alcaligenes
Tanaka K; *Ishizaki A; Kanamaru T; ku, Fukuoka 812, and O2 by high cell density autotrophic cultivation of eutrophus ATCC
Kawano T Japan. Alcaligenes eutrophus; impeller design effect on kLa Biotechnol.Bioeng.; (1995) 45, 3, 268-75 17697. The specially-
1038 during poly-beta-hydroxybutyrate production 1995 designed agitation syste
Hydrogen-oxidizing
bacterium, Alcaligenes
eutrophus autotrophically
produces biodegradable
plastic material, poly(D-3-
hydroxybutyrate),
P(3HB), from carbon
dioxide, hydrogen, and
Dep. Food Sci. Production of poly(D-3-hydroxybutyrate) from CO2, H2, oxygen. In autotrophic
Tanaka, Kenji; Ishizaki, Ayaaki; Technol., Kyushu and O2 by cultivation of the
Kanamaru, Toshihisa; Kawano, Univ., Fukuoka 812, high cell density autotrophic cultivation of Alcaligenes Biotechnol. Bioeng., 45(3), 268-75 (English) fermn polyhydroxybutyrate microorganism, it is
1039 Takeharu Japan eutrophus. 1995 1995 Alcaligenes essential to 497.
4.10 Literature on Polyhydroxyalkanoates.xls - page 267
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly(hydroxyalkanoic
acid) [PHA] is
accumulated by numerous
microorganisms as an
energy reserve material
under
Department of unbalanced growth
Chemical Engineering, conditions in the presence
Korea Advances of excess carbon source.
Institute of Science In spite of being a good
and Technology, candidate for
Daeduk Science Town, biodegradable
1040 Lee SY, Chang HN Taejon. Production of poly(hydroxyalkanoic acid). Adv Biochem Eng Biotechnol 1995;52:27-58 1995 thermoplastics, their
Methylobacterium sp.
ZP24, isolated from a
local pond, is able to grow
in a medium containing 12
g l-1 lactose as a sole
source of carbon, giving
Department of 5.25 g l-1 biomass yield
Microbiology and and poly-3-
Biotechnology Centre, hydroxybutyrate (PHB) up
Faculty of Science, Production of poly-3-hydroxybutyrate from lactose and to 59% of its dry weight in
M.S. University of whey by Methylobacterium sp. ZP24 - 40 h. The
1043 Yellore V, Desai A Baroda, India. Methylobacterium sp. ZP24. Lett Appl Microbiol 1998 Jun;26(6):391-4 1998 cheese whey isolate wa Strain - Substrates kopiert
Poly-beta-hydroxybutyric
acid (PHB) and similar
bacterial polyesters are
National Research promising candidates for
Council of Canada, the development of
Biotechnology environment-friendly,
Research Institute, totally biodegradable
6100, Royalmount plastics. The use of
Avenue, Montreal Production of poly-beta-hydroxybutyrate from methanol: methanol, one of the
Bourque; D.; Oullette; B.; Andre; G.; (Quebec) Canada H4P characterization of a new isolate of Methylobacterium Methylobacterium extorquens - cheapest noble substrates
1052 Groleau; D. 2R2 extorquens Appl. Microbiol. Biotechnol. 1992; 37:36867 1992 isolation - methanol available, may help to red Strain - Substrates 418.
Rees, G.N.; Vasiliadis, G.; May, J.W.; Production of poly-beta-hydroxybutyrate in Acinetobacter
1053 Bayly, R.C. spp. isolated from activated sludge Appl. Microbiol. Biotechnol. 1993; 38:734-737 1993 445.
4.10 Literature on Polyhydroxyalkanoates.xls - page 269
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly-beta-hydroxybutyrate
(PHB) was produced by
recombinant
Escherichia coli
HMS174 (plasmid pTZ18u-
Department of PHB) on beet molasses as
Chemical Engineering, a
Ohio University, sole C-source instead
Athens, OH of glucose. Fermentation
45701, USA. Production of poly-beta-hydroxybutyrate on molasses by with molasses was
Liu F; Li W; Ridgway D; *Gu T Email: recombinant Escherichia coli; polymer production following Biotechnol.Lett.; (1998) 20, 4, 345-48 cheaper than with
1055 gu@ohiou.edu plasmid pTZ18u-PHB expression in bacterium 1998 glucose. The plasmid carr
Production of poly-beta-hydroxybutyrate: poly-beta-
1056 Byrom; D. hydroxyvalerate copolymers FEMS Microbiology Reviews 1992; 103:247-250 1992 480.
Refractile granules of
poly-beta-hydroxybutyric
acid are produced by
Micrococcus
halodenitrificans during
the exponential growth
phase in a nitrogenous
medium. The amount
Division of Applied Micrococcus halodenitrificans - produced varied from
Biology, National effect of glycerol, pyruvate and about 1% of the salt-free
Research Council, Production of poly-beta-hydroxybutyric acid granules in Canadian Journal of Microbiology 1961; 8:249- acetate on polymer dry weight during vigorous
1059 Sierra, G.; Gibbons, N.E. Ottawa, Canada Micrococcus halodenitrificans 253 1961 accumulation aeration Strain - Metabolism 123. Korr.
A new microorganism, A.
chroococcum PHA (CECT
4435), obtained
by mutation with
nitrosoguanidine and
capable of growth on
waste olive
exudate, and its use for
the prodn. of poly(3-
hydroxybutyrate) and
poly(3-hydroxybutyrate/3-
Gonzalez Lopez, Jesus; Martinez Production of polyhydroxyalkanoates by Azotobacter hydroxyvalerate) are
Toledo, M. Victoria; Salmeron Miron, Universidad de chroococcum Span. ES 2061405 A2 1 polyhydroxyalkanoate fermn claimed
1065 Victoriano Granada, Spain PHA. Dec 1994, 8 pp. (Spain) 1994 Azotobacter
4.10 Literature on Polyhydroxyalkanoates.xls - page 272
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
In response to problems
associated with plastic
waste and its effect on the
environment, there has
been
Carnegie Institution of considerable interest in
Washington, the development and
Department of Plant production of
Biology, Stanford, CA Production of polyhydroxyalkanoates, a family of biodegradable plastics.
94305-1297, biodegradable plastics
1068 Poirier Y, Nawrath C, Somerville C USA. and elastomers, in bacteria and plants. Biotechnology (N Y) 1995 Feb;13(2):142-50 1995 Polyhydroxyalkanoates 501.
Institut für
Mikrobiologie der
Westfälischen
Wilhelms-Universität Screening experiments
Münster, identified several bacteria
Corrensstrasse 3, D- which were able to use
48149 residual oil from
Poly-beta-hydroxybutyrate
(PHB) production from
Environmental petrochemical
Sciences and Applied activated sludge by
Biology Division, Bacillus sp. IPCB-403 was
Research investigated. Cells
Center, Indian were cultivated at 30
Petrochemicals deg in a 250 ml
Corporation Limited, Erlenmeyer shake flask
Baroda 391 346, Production of polyhydroxybutyrate by petrochemical with
Dave H; Ramakrishna C; *Desai J D India. activated sludge and Bacillus sp. IPCB-403; poly-beta- Indian J.Exp.Biol.; (1996) 34, 3, 216-19 100 ml of medium
1071 hydroxybutyrate production and waste-water treatment 1996 containing (g/l) 3 yeast
Polyhydroxybutyrate
(PHB) was produced by
Ralstonia eutropha DSM
11348 (formerly
Alicaligenes eutrophus) in
media contg. 20-30 g l-1
Innovent casein peptone or
e.V./Biomaterialien, casamino acids as sole
Bormann, E. J.; Leissner, M.; Roth, M.; Jena, D-07747, Appl. Microbiol. Biotechnol. (1998), 50(5), 604- sources of nitrogen. In
Beer, B.; Metzner, K. Germany Production of polyhydroxybutyrate by Ralstonia eutropha 607 fermns. using media
1072 from protein hydrolyzates 1998 based on casein pepto
Poly-beta-
Innovent; hydroxybutyrate (PHB)
Tech.Coll.Jena; Hans- was produced by
Knoll- Ralstonia eutropha
Inst.Natur.Prod.Res.Je DSM 11348 (formerly
na; Alicaligenes eutrophus)
BSL-Olefinverbund when it was grown in a
LO Innovent culture medium
e.V./Biomaterialien, Production of polyhydroxybutyrate by Ralstonia eutropha containing 20-30 g/l
Felsbachstrasse 5, D- from protein hydrolyzates; the effect of casein peptone and casein peptone or
Bormann E J; Leissner M; Roth M; Beer 07747 Jena, casamino acid N-source on the production of poly-beta- casamino
B; Metzner K Germany. hydroxybutyrate by a bacterium, for use in biodegradable acids as a sole N-
1073 plastic Appl.Microbiol.Biotechnol.; (1998) 50, 5, 604-07 1998 source. The cells we
A group of 13 bacterial
species from the rRNA
superfamily III were tested
for their
Institute of ability to
Biotechnology, produce the
Technical University of biodegradable polyesters
Graz, Petersgasse 12, poly(3-hydroxybutyrate-co-
A-8010 Graz, Austria. Production of short-side-chain polyhydroxyalkanoates 4-hydroxybutyrate)
by various bacteria from the rRNA Applied Microbiology and Biotechnology Abstract [P(3-HB-co-
1075 G. Renner, G. Haage, G. Braunegg Fax:+43316811050 superfamily III Volume 46 Issue 3 (1996) pp 268-272 1996 4-HB)] and poly(3-h
4.10 Literature on Polyhydroxyalkanoates.xls - page 274
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
To synthesize layered
granules consisting of
selected phases of
polyhydroxybutyrate
(PHB)
Azotobacter salinestris, a
sodium-dependent,
microaerophilic N2-fixing
Department of soil
Biological Sciences, bacterium,
University of Alberta, formed
Edmonton, Alberta, polyhydroxyalkanoate
T6G 2E9, copolymers comprised of
Canada Production of <beta>-hydroxybutyric
Tel.: (403) 492 4782 poly(<beta>-hydroxybutyrate-<beta>- acid
Fax: (403) 492 2216 e- hydroxyvalerate) and 9-12
W. J. Page, N. Bhanthumnavin, J. mail: copolymer from sugars by Azotobacter Applied Microbiology and Biotechnology Abstract mol% <beta>-
1079 Manchak, M. Ruman Bill.Page@Ualberta.ca salinestris Volume 48 Issue 1 (1997) pp 88-93 1997 hydroxyvaleric acid
The prodn. of PHB and
Gellan gum has been
studied by using the
Lab. of Environmental fermenter with novel
Biotechnology, School axial impellers on the
of Biotechnology, Wuxi basis of the research
University of Light on the mixing and
Industry, Wuxi, Huaxue Fanying Gongcheng Yu Gongyi (1999), mass transfer effect of the
Fu, Weimin; Chen, Jian; Ruan, 214036, Peop. Rep. 15(1), 79-84 axial impellers. It
Wenquan; Zhan, Xiaobei; Qi, Rufeng; China Production on PHB and Gellan gum by using the fermenter Chinese was indicated from
1080 Lun, Shiyi with axial impellers 1999 exptl. results that the a
Doi, Y.; Kunioka, M.; Kawaguchi, Y.; Production, properties, and biodegradation of microbial
1081 Segawa,, A. copolyesters of 3-hydroxybutyrate an 4-hydroxybutyrate Polymer preprints 1989; 30:1 1989 666.
4.10 Literature on Polyhydroxyalkanoates.xls - page 275
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Ultra-high-molecular-
weight poly[(R)-3-
hydroxybutyrate] (P(3HB))
(Mw = 3-11 x 10(6)) was
produced
from glucose by a
recombinant Escherichia
coli XL1-Blue (pSYL105)
Properties and biodegradability of ultra-high-molecular- harboring
Akebono Brake R&D weight Ralstonia
Centre, Ltd., Saitama, poly[(R)-hydroxybutyrate] produced by a eutropha H16
1082 Kusaka S, Iwata T, Doi Y Japan recombinant Escherichia coli. Int J Biol Macromol 1999 Jun-Jul;25(1-3):87-94 1999 polyhydroxya
Microcapsules of poly(3-
hydroxybutyric acid) [PHB]
and its copolymers with
hydroxyvalerate [HV] were
prepared by the
solvent evaporation
technique and loaded with
Properties and drug release behaviour of poly(3- a model drug, 2,7-
Middle East Technical hydroxybutyric acid) and dichlorofluorescein.
University, Department various poly(3-hydroxybutyrate-hydroxyvalerate) Microcapsules were also
of Biological Sciences, copolymer prepared from
1083 Gursel I, Hasirci V Ankara, Turkey. microcapsules. J Microencapsul 1995 Mar-Apr;12(2):185-93 1995 the same polyme
Kita; K.; Ishimaru; K.; Teraoka; M.; Properties of poly(3-hydroxybutyrate) depolymerase from a Applied and Environmental Microbiology 1995;
1084 Yanase; H.; Kato; N. marine bacterium Alcaligenes faecalis AE122 61:1727-1730 1995 512.
A soluble hydrogenase
from cell-free extracrs of
Hydrogenomonas H 16
Institut für has been purified 45-fold
Mikrobiologie der up to a specific activity of
Universität Göttingen 36 500 units per g protein.
und Institut für The enzyme catalyzes the
Mikrobiologie der reduction of NAD with
Gesellschft für Properties of The NAD-Specific Hydrogenase from molecular hydrogen, It
Pfitzner; J.; Linke; H.A.B.; Schlegel; Strahlen forschung Hydrogenomonas H 16 / Eigenschaften der NAD- Hydrogenomonas H 16 - does not require
1087 H.G. mbH München spezifischen Hydrogenase aus Hydrogenomonas H 16 Arch.Mikrobiol. 1970; 71:67-78 1970 Hydrogenase cofactors. The N Strain - Metabolsim 160.
4.10 Literature on Polyhydroxyalkanoates.xls - page 276
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxyalkanoate
(PHA) cellular inclusions
consist of polyesters,
phospholipids, and
proteins. Both the
Department of polymerase and
Biochemistry and the depolymerase
Molecular Biology, enzymes are active
University of components of the
Massachusetts, structure. Recently,
Amherst, USA. proteins associated with
Stuart ES, Tehrani A, Valentin HE, esstuart@bio.umass.e Protein organization on the PHA inclusion cytoplasmic these inclusions have
1090 Dennis D, Lenz RW, Fuller RC du boundary. J Biotechnol 1998 Oct 8;64(2-3):137-44 1998 been descr
4.10 Literature on Polyhydroxyalkanoates.xls - page 277
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polyhydroxyalkanoate
Univ.Massachusetts; (PHA) cellular inclusions
Univ.Harrisonburg- consist of
James-Madison polyesters,
LO Department of phospholipids and
Biochemistry and proteins. Both the
Molecular Biology, polymerase and
University of the depolymerase
Massachusetts, enzymes are active
Amherst, MA, USA. Protein organization on the PHA inclusion cytoplasmic components of the
Stuart E S; Tehrani A; Valentin H E; Email: boundary; polyhydroxyalkanoate production by Ralstonia structure.
Dennis D; Lenz R W; Fuller R esstuart@bio.umass.e eutropha poly-beta-hydroxybutyrate biosynthesis operon In order to further
C du phaCAB gene transfer to Pseudomonas putida and J.Biotechnol.; (1998) 64, 2-3, 137-44 clarify the structure and
1091 Escherichia coli 1998 fun
Kinetics of poly-HB
accumulation in
Pseudomonas 2F, a
recently isolated and new
strain, differ considerably
from the behaviour found
hitherto with other strains.
Institute for After a period of carbon
Biotechnology, Graz limitation of 1 hour,
University of Pseudomonas 2 F: Kinetics of Growth and Accumulation of Pseudomonas 2 F - Carbon- without the application of
1092 Braunegg, G.; Korneti, L. Technology, Austria. Poly-D(-)-3-Hydroxybutyric Acid (Poly-HB) Biotechnol. Lett. 1984; 6:825-829 1984 overcompensation growth-limiting con Strain - Metabolism 410.
Four
polyhydroxyalkanoate
(PHA) depolymerases
were purified from
the culture fluid of
Pseudomonas lemoignei:
poly(3-hydroxybutyrate)
Institut (PHB), depolymerase A
fuer Mikrobiologie, (Mr, 55,000), and PHB
Georg-August- Pseudomonas lemoignei has five poly(hydroxyalkanoic polyhydroxyalkanoate depolymerase B (Mr,
Universitaet, acid) (PHA) depolymerase gene sequence 67,000) were specific for
Briese, Bernd Holger; Schmidt, Goettingen 37077, depolymerase genes: a comparative study of bacterial and J. Environ. Polym. Degrad., 2(2), 75-87 (English) Pseudomonas PHB and copolymers of 3-
1093 Bernhard; Jendrossek, Dieter Germany eukaryotic PHA depolymerases. 1994 1994 hydroxyb 526.
Pseudomonas oleovorans as a source of poly(beta-
Btandl; H.; Gross; R.A.; Lenz; R.W.; hydroxyalkanoates) for potential applications as Applied and Environmental Microbiology 1988;
1094 Fuller; R.C. biodegradable polyesters 54(8):1977-1982 1988 328.
4.10 Literature on Polyhydroxyalkanoates.xls - page 278
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Agrotechnological
Research Institute The biosynthesis of poly(3-
(ATO-DLO), P.O. Box hydroxyalkanoates)
17, 6700 AA (PHAs) by Pseudomonas
Wageningen,1 and putida KT2442 during
Groningen growth on carbohydrates
Biotechnology Center, was studied, PHAs
Department of isolated from P. putida
Biochemistry, cultivated on glucose,
University of fructose, and glycerol
Huijberts, G. N. M.1; Eggink, G1; de Groningen 9747 AG Pseudomonas putida KT2442 Cultivated on Glucose were found to have a very Strain -Metabolsim -
Waard, P.1; Huisman, G. W.2; Witholt, Groningen,2 The Accumulates PHAs Consisting of Saturated and Copolyesters - Pseudomonas similar monomer Copolyesters -
1095 B.2 Netherlands Unsaturated Monomers Appl. Env. Microbiol. 1991; 58:536-544 1992 putida KT2442 composition. Analytics 406.
Citrate-synthase (EC-
Institute of 4.1.3.7) was isolated and
Biochemistry and purified to
Physiology of homogeneity from the
Microorganisms, methylotrophic producer of
Pushchino, poly-beta-
Moscow Region hydroxybutyrate (PHB),
142292 Russia. Methylobacterium
Email: Purification and characterization of citrate-synthase from extorquens 15.
Belova L L; Sokolov A P; Morgunov I G; trotsenko@ibpn.serpu Methylobacterium extorquens, methylotrophic producer of Purification included
Trotsenko Yu A khov.su polyhydroxybutyrate; enzyme for use in poly-beta- Biokhimiya; (1997) 62, 1, 85-90 streptomycin sulfate
1098 hydroxybutyrate production Russian 1997 treatment of cell-free
Purification and characterization of D(-)-beta-
hydroxybutyrate dehydrogenase from Azospirillum Journal of General Microbiology 1990; 136:645-
1099 Tal; S.; Smirnoff; P.; Okon; Y. brasilense Cd 649 1990 306.
Shiraki; M.; Shimada; T.; Tatsumichi; Purification and characterization of extracellular poly(3- Journal of Environmental Polymer Degradation
1100 M.; Saito; T. hydroxybutyrate) depolymerases 1995; 3:13-21 1995 567.
4.10 Literature on Polyhydroxyalkanoates.xls - page 279
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
An NADP-linked
acetoacetyl-CoA
reductase was purified to
electrophoretic
homogeneity from
Deparmtent of Health Zoogloea ramigera I-16-M,
chemistry, Faculty of a poly(3-hydroxybutyrate)-
Pharmaceutical accumulating bacterium.
Sciences, Kyoto The purified enzyme
Universiy, Yoshida, NADP-linked acetoacety-CoA showed specific activity of
Sakyo-ku, Kyoto Purification and characterization of NADP-linked Biochimica et Biophysica Acta 1987; 917:365- reductase - Zoogloea ramigera 412 Mmol acetoacetyl-
1101 Fukui, T.; Ito, M.; Saito, T.; Tomita, K. (Japan) acetoacetyl-CoA reductase from Zoogloea ramigera I-16-M 371 1987 I-16-M - CoA reduced per min Strain -Metabolsim 425. corr.
D(-)-beta-Hydroxybutyrate
dehydrogenase was
purified from Zoogloea
ramigera I-16-M to
Poly(3-hydroxybutyrate)
depolymerase was
purified to homogeneity
from the culture filtrate of
Paecilomyces lilacinus
D218 by column
chromatography on CM-
Purification and Properties of Poly(3-Hydroxybutyrate) Toyopearl 650M and
Depolymerase Curr. Microbiol. 34:230-232 (1997)
Yuji Oda, Hidekazu Osaka, Teizi from the Fungus Paecilomyces lilacinus © Springer-Verlag New York, Inc. hydroxylapatite. The
1107 Urakami, Kenzo Tonomura D218 1997 1997 molecular weig
Purification and properties of poly(3-hydroxyvaleric acid)
1108 B.M ller; D.Jendrossek depolymerase from Pseudomonas lemoignei Appl. Microbiol Biotechnol 1993; 38:487-492 1993 525.
4.10 Literature on Polyhydroxyalkanoates.xls - page 280
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1. Phosphoribulokinase
was purified 286-fold from
extracts of autotrophically
grown cells. 2. The
enzyme had a molecular
weight of 237 000 and
Institut für showed a pH optimum of
Mikrobiologie der Hydrogenomonas eutropha H 9.0 in both crude extracts
Universität Göttingen, 16 - Ralstonia eutropha H 16 - and purified preparation.
3400 Göttingen, West Purification and regulatory properties of fructose-1,6- Alcaligenes eutrophus H 16 - MgCl2 was required for
1111 Abdelal; A.T.; Schlegel; H.G. Germany diphosphatase from Hydrogenomonas eutropha Journal of Bacteriology 1974; 120(1):304-310 1974 phosphoribulokinase activiey; ful Strain - Metabolism 158.
Fructose diphosphatase of
Hydrogenomonas
eutropha H 16, produced
during autotrophic growth,
was purified 247-fold from
extracts of cells. The
Institut für molecular weight of the
Mikrobiologie der Hydrogenomonas eutropha H enzyme was estimated to
Universität Göttingen, 16 - Ralstonia eutropha H 16 - be 170 000. The enzyme
3400 Göttingen, West Purification and regulatory properties of Alcaligenes eutrophus H 16 - showed a pH optimum of
1112 Abdelal; A.T.H.; Schlegel; H.G. Germany phosphoribulokinase from Hydrogenomonas eutropha H 16 Biochem.J. 1974; 139:481-489 1974 fructose 1,6-diphosphatase 8.5 in both crude e Strain - Metabolism 159.
Purification of poly-beta-hydroxybutyrate by density
1113 Nickerson, K. W. gradient centrifugation in sodium bromide Appl. Environ. Microbiol. 1982; 43:1208-1209 1982 190.
4.10 Literature on Polyhydroxyalkanoates.xls - page 281
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A poly-beta-
hydroxybutyrate complex
extracted from the plasma
membranes of genetically
competent Escherichia
coli
contained
polyhydroxybutyrate:polyp
Department of hosphate:calcium in molar
Microbiology and ratios approximating
Public Health, 1:1:0.5. The chain length
Michigan State Putative structure and functions of a poly-beta- of the
University, East hydroxybutyrate/calcium Proc Natl Acad Sci U S A 1988 Jun;85(12):4176- polyhydroxybutyrate was
1114 Reusch RN, Sadoff HL Lansing 48824. polyphosphate channel in bacterial plasma membranes. 80 1988 es
1115 Morikawa; H.; Marchessault; R.H. Pyrolysis of bacterial polyalkanoates Can.J.Chem. 1981; 59:2306 1981 208.
Pseudomonas
United States resinovorans produces a
Department of medium-chain-length
Agriculture, Eastern poly(hydroxyalkanoate)
Regional Research (MCL-PHA) copolymer
Center, Wyndmoor, PA when grown on
19038, USA. tallow (PHA-tal). This
* Corresponding polymer had a repeat unit
author. Tel.: ?1 215 Keywords : Medium-chain- composition ranging from
2336483; fax: ?1 215 length poly(hydroxyalkanoate); C4 to C14 with some
2336795; e-mail: Radiation crosslinking of a bacterial medium-chain-length Pseudomonas resino6orans; mono-unsaturation in the
1119 Ashby RD, Cromwick AM, Foglia TA rashby@arserrc.gov poly(hydroxyalkanoate) elastomer from tallow. Int J Biol Macromol 1998 Jul;23(1):61-72 1998 Radiation crosslinking C12 and C14 alkyl side ganze Artikel
Recovery of polyhydroxy
acids (PHAs) from waste
containing high molecular
weight polyhydroxy acid
polymer by
depolymerizing
BRAKE LOREN D the PHA in water at
(US); SUBRAMANIAN NARAYANAN S US5229528 elevated temperature and
1121 (US) DU PONT (US) Rapid depolymerization of polyhydroxy acids 1993-07-20 1993 pressure.
Rapid determination of poly-beta-hydroxybutyric acid in
1122 Mee, J. M. L. blood and milk gas chromatography Journal of Chromatography 1974; 101:414-416 1974 41.
Niel, van; E.W.J.; Robertson; L.A.; Rapid short-term poly-beta-hydroxybutyrate production by Enzyme and Microbial Technology 1995; 17:977-
1123 Kuenen; J.G. Thiospora pantotropha in the presence of excess acetate 982 1995 599.
Poly(3-hydroxybutyrate)
Department of [P(3HB)] and other
Chemical Engineering polyhydroxyalkanoates
and BioProcess (PHAs) have been
Engineering Research drawing
Center, Korea much
attention as biodegradable
Advanced Institute of substitutes for
Science and conventional
Technology, Taejon, nondegradable plastics.
South Korea. Recent advances in polyhydroxyalkanoate production by For the
leesy@sorak.kaist.ac.k bacterial economical
1125 Lee SY, Choi J, Wong HH r fermentation: mini-review. Int J Biol Macromol 1999 Jun-Jul;25(1-3):31-6 1999 production of P
A combined SDS-NaClO
method to recover PHB
from recombinant E. coli
HMS 174 (pTZ18u-
PHB) was studied. The
adding order of SDS and
NaClO affected the
result of this method and
Dep. Chem. Eng., the reason was
Tsinghua Univ., Shengwu Gongcheng Xuebao (1998), 14(3), 342- analyzed. A new
Yin, Jin; Yu, Hinmin; Li, Hongqi; Shen, Beijing, 100084, Peop. Recovering PHB from recombinant Escherichia coli by a 344 Chinese process that the cell was
1129 Zhongyao Rep. China combined SDS-NaClO treatment 1998 treate
4.10 Literature on Polyhydroxyalkanoates.xls - page 284
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
We studied recovery of
poly(3-hydroxybutyric
acid) (PHB) from
Alcaligenes eutrophus and
a recombinant Escherichia
coli
BioProcess strain harboring the A.
Engineering Research eutrophus poly(3-
Center, Korea hydroxyalkanoic acid)
Advanced Institute of biosynthesis genes. The
Science and Recovery and characterization of poly(3-hydroxybutyric amount of PHB degraded
Technology, Taejon. acid) synthesized to a
1130 Hahn SK, Chang YK, Lee SY in Alcaligenes eutrophus and recombinant Escherichia coli. Appl Environ Microbiol 1995 Jan;61(1):34-9 1995 lower-molecular-weigh 499.
Ramsay, J.A.; Berger, E.; Ramsay, Recovery of poly-3-hydroxyalkanoic acid granules by y
1131 B.A.; Chavarie, C. surfactant-hydrochlorite tratment Biotechnology techniques 1990; 4:221-226 1990 531.
Recovery of Poly-beta-Hydroxybutyrate from Estuarine Applied and Enviromental Microbiology 1978;
1132 Herron, J.S.; King, J.D.; White, D.C. Microflora 35:251-257 1978 14.
Polyhydroxyacid (PHA) is
recovered by heating
under pressure in the
presence of a C1-C6
BRAKE LOREN D DU alcohol, and optionally
1133 (US) PONT (US) Recovery of polyhydroxy acids US5264614 1993-11-23 1993 also water.
a Department of
Biological Sciences, Abstract Sequence
University of Durham, analysis of several cDNAs
Durham, DH13LE, UK encoding the
b Imperial Cancer phasin protein of
Research Fund, Ralstonia eutropha
London, WC2A 3PX, indicated that the carboxyl
UK terminus of the resulting
*Corresponding derived protein sequence
Steven Zachary Hanley a; *, Darryl J.C. author. Fax: +44 (191) Key words: Alcaligenes is different
Pappin b , Dinah Rahman b , Andrew J. 377 2417. Re-evaluation of the primary structure of Ralstonia eutrophus; Ralstonia eutropha; from that reported
White a , E-mail: eutropha phasin and Polyhydroxyalkanoic acid previously. This was
Kieran M. Elborough a , Antoni R. s.z.hanley@durham.ac implications for polyhydroxyalkanoic acid granule; Phasin; Biodegradable confirmed by: (1)
1135 Slabas a .uk granule binding. FEBS Lett 1999 Mar 19;447(1):99-105 1999 polyester sequenc ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 285
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A novel poly-beta-
hydroxybutyrate (PHB)
production system in
Department of Biology, which
James Madison the expression and
University, gene dosage of the
Harrisonburg, Alcaligenes eutrophus pha
Virginia 22807, biosynthetic operon
USA. Regulated expression of the Alcaligenes eutrophus pha were effectively regulated
Email: biosynthesis genes in Escherichia coli; poly-beta- by temp. was
FAC_DENNIS@VAX1. hydroxybutyrate production by recombinant Escherichia constructed in
Kidwell J; Valentin H E; *Dennis D ACS.JMU.EDU coli with temp.-dependent gene regulation under fed-batch Appl.Environ.Microbiol.; (1995) 61, 4, 1391-98 Escherichia coli. The pha
1136 culture conditions 1995 oper
A novel poly-b-
hydroxybutyrate (PHB)
prodn. system in which the
expression and gene
dosage of the Alcaligenes
eutrophus pha
biosynthetic operon were
Department effectively regulated by
Biology, James cultivation temp. was
Madison University, Regulated expression of the Alcaligenes eutrophus pha constructed in Escherichia
Kidwell, John; Valentin, Henry E.; Harrisonburg, VA biosynthesis Appl. Environ. Microbiol., 61(4), 1391-8 (English) Alcaligenes operon pha cloning coli. The pha operon was
1137 Dennis, Douglas 22807, USA genes in Escherichia coli. 1995 1995 regulation fused
Institut für
Mikrobiologie Regulation of PHB-Metabolism -
Abteilung Regulation des Poly-beta-hydroxybuttersäure- Hydrogenomonas H 16 -
Bakterienphysiologie Stoffwechsels bei Hydrogenomonas eutropha Stamm H 16 Ralstonia eutropha H 16 -
1138 Oeding; V. Göttingen und PHBS-freie Mutanten Dissertation 1972 1972 Alcaligenes eutrophus H 16 Abstract unavailable. Strain - Metabolism 156.
The intracellular
concentration of CoA
metabolites and
nucleotides was
determined in batch
cultures of
Sachsisches Institut Methylobacterium
fur Angewandte rhodesianum grown on
Biotechnologie (SIAB), methanol and shifted to
Universitat Leipzig, growth on fructose. The
Permoserstrasse 15, D- Regulation of poly(beta-hydroxybutyrate) synthesis in intracellular concentration
04318 Leipzig, Methylobacterium of CoA decreased from a
1145 Mothes G, Ackermann JU, Babel W Germany. rhodesianum MB 126 growing on methanol or fructose. Arch Microbiol 1998 Apr;169(4):360-3 1998 high value of
Regulation of the Pyruvate Kinase from Alcaligenes
1146 D.Wilke; H.G.Schlegel eutrophus H 16 in vitro and in vivo Arch. Microbiol.1975; 105:109-115 1975 13.
Regulation of the tricarboxylic acid cycle and poly-á-
hydroxybutyrate metabolism in Azobacter beijerinckii Journal of General Microbiology 1976; 97:303-
1147 Jackson, F.A.; Dawes, e.d. grown under nitrogen or oxygen limitation 313 1976 37.
4.10 Literature on Polyhydroxyalkanoates.xls - page 287
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1Bioprocess
Technology Research
Group, Korea Regulatory roles of
Research Institute of nicotinamide nucleotides
Bioscience and and three key enzymes, -
Biotechnology, Yusong- ketothiolase (KT), NADPH-
gu, Taejon dependent
305-600, Korea acetoacetyl-CoA
2Department of reductase (AAR), and
Chemical Engineering citrate synthase (CS), on
and BioProcess poly(3-hydroxybutyrate)
Engineering Research Regulatory effects of cellular nicotinamide nucleotides and poly(3-hydroxybutyrate); (PHB) synthesis in
Center, KAIST, 373-1 enzyme activities Biotechnology & Bioengineering Escherichia coli; PHB recombinant
In Young Lee 1, Mi Kyoung Kim 1, Kusong-dong, on poly(3-hydroxybutyrate) synthesis in recombinant Volume 52, Issue 6, 1996. Pages: 707- synthesis; regulation; Escherichia coli harboring
1148 Young Hoon Park 1, Sang Yup Lee 2 * Yusong-gu, Taejo Escherichia coli 712 1996 nicotinamide nucleotides a pl kopiert
1150 Bradley DF Relation between structure and activity of biopolymers. Trans N Y Acad Sci 1966 Apr;28(6):788-95 1966 Abstract unavailable.
Wild-type cells of
Rhodobacter sphaeroides
and Rhodospirillum
rubrum strains Ha and S1
as well as mutant cells
defective in the
synthesis of poly-(3-
hydroxybutyric acid)
Inst. (PHB) were used to study
Mikrobiol., Georg- Relationship between the photoproduction of hydrogen the
August-Univ., and the Appl. hydrogen formation purple competition between PHB
Hustede, Eilert; Steinbuechel, Goettingen W-3400, accumulation of PHB in non-sulfur purple bacteria. Microbiol. Biotechnol., 39(1), 87-93 (English) bacteria polyhydroxybutyrate accumulation and
1152 Alexander; Schlegel, Hans G. Germany 1993 1993 photoprodn. of
Synchronous cultures of
Alcaligenes eutrophus
(Hydrogenomonas
eutropha H 16) were
prepared by a size
selection method which
gave high synchrony
Department of Alcaligenes eutrophus H 16 - indices (0,70 to 0,85).
Biochemistry, School Hydrogenomonas eutropha H Unlike the smooth
of Biological Sciences, Respiratory properties of synchronous cultures of 16 - Ralstonia eutropha H 16 - exponentioal increase
University of Leicester, Alcaligenes eutrophus H16 prepared by a continuous-flow Journal of General Microbiology 1977; 99:383- Respiration rates - which was observed in
1155 Edwards, C.; Jones, C.W. Leicester LE1 7RH size selection method 388 1977 Synchronous cultures exponentially growing cul Strain - Metabolism 115. Corr.
Aspects of thermal,
morphol., and rheol.
properties of
biodegradable
poly[D(-)(3-
hydroxybutyrate)] (PHB)
blended with
poly(ethylene oxide)
(PEO) have been studied.
Dep. Thermal properties and
Polymer Science morphol. of the
Engineering, Inha Rheological study on poly-D-(-)(3-hydroxybutyrate) and its blends were examd. by
Choi, H. J.; Park, S. H.; Yoon, J. S.; Univ., Inchon 402-751, blend with polyoxybutyrate DSC and SEM, resp. A
1160 Lee, H-S.; Choi, S. J. S. Korea poly(ethylene oxide). Polym. Eng. Sci., 35(20), 1636-42 (English) 1995 1995 polyoxyethylene blend rheol rotatio
Recombinant fadR
(negative fatty acid
Univ.Kyung-Hee oxidation regulator) and
LO Department of atoC(Con) (positive
Biology, James fatty acid uptake
Madison University, regulator) mutant
Harrisonburg, VA Escherichia coli
22807, USA. Role of fadR and atoC(Con) mutations in poly(3- LS5218 with poly-beta-
Email: hydroxybutyrate)-co- 3-hydroxyvalerate) synthesis in hydroxyalkanoate (PHA)
fac_dennis@vax1.acs.j recombinant pha+ Escherichia coli; poly-beta- biosynthesis genes
Rhie H G; *Dennis D mu.edu hydroxybutyrate and poly-beta-hydroxyvalerate copolymer Appl.Environ.Microbiol.; (1995) 61, 7, 2487-92 from Alcaligenes
1163 overproduction using genes from Alcaligenes eutrophus 1995 eutrophus on a plas kopiert
Department of
Bacteriology and Miller
Institute, Universiy of Role of poly-beta-hydroxybutyric acid in the assimilation of
1165 Doudoroff, M.; Stanier, R.Y. California, Berkeley organic carbon by bacteria Nature 1959; 183:1440-1442 1959 No abstract. 75.
4.10 Literature on Polyhydroxyalkanoates.xls - page 291
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The polyhydroxybutyrate
(PHB) synthase gene of
the bacterium Alcaligenes
eutrophus was used to
construct a yeast plasmid
which enabled expression
Department of of the functional synthase
Chemical Engineering enzyme in
and Materials Science, Saccharomyces
University of cerevisiae. Cells
Minnesota, St Paul Saccharomyces cerevisiae expressing bacterial transformed with the
Leaf TA, Peterson MS, Stoup SK, 55108, USA. polyhydroxybutyrate synthase
1166 Somers D, Srienc F synthase produces poly-3-hydroxybutyrate. Microbiology 1996 May;142 ( Pt 5):1169-80 1996 plasmid ac
(1) Department of
Chemistry, University
of Malaya, 50603 The synthesis of
Kuala Lumpur, polyhydroxyalkanoates
Malaysia (PHA) by Pseudomonas
(2) putida PGA1,
Polymer Program, using
PennState University, saponified palm kernel oil
State College, PA (SPKO), was investigated.
16081 USA The PHA produced from
(3) Saponified palm kernel oil and its major free fatty acids SPKO
I. K. P. Tan (3), K. Sudesh Kumar (3), Institute of Advanced as carbon substrates for the production of Applied Microbiology and Biotechnology Abstract was
M. Theanmalar (3), S. N. Gan (1), B. Studies, University of polyhydroxyalkanoates in Pseudomonas Volume 47 Issue 3 (1997) pp 207-211 compared with those
1168 Gordon III. (2) Malaya, putida PGA1 1997 produced by the major fr
Sheppard; J.D.; Marchessault; P.;
1169 Whalen; T.; Barrington; S.F. Scale-up of a Cyclone Bioreactor J. Chem. Tech. Biotechnol. 1994; 59:83-89 1994 490.
4.10 Literature on Polyhydroxyalkanoates.xls - page 292
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Seventy-three bacterial
strains were isolated from
a clay-loam soil and
screened for poly-beta-
hydroxybutyric acid
(PHB) production.
When grown in a nitrogen-
free, carbon-rich medium,
Screening of Soil Bacteria for Poly-beta-Hydroxybutyric 23 strains produced PHB
Acid Production and Its Role in Microb Ecol 35:94-101 (1998) homopolymer.
1171 J.G. Wang, L.R. Bakken the Survival of Starvation © 1998 by Springer-Verlag New York, Inc. 1998 The pseudomonads,
Poly-beta-hydroxbutate
Innovent-Jena; Hans- (PHB) is a member of a
Knoll- family of polyesters
Inst.Natur.Prod.Res.Je in which more than 40
na; different hydroxyalkanoic
Univ.Jena- acids are
Friedrich-Schiller constituents (poly-beta-
LO Innovent e. V., hydroxyalkanoates). PHB
Biomaterialien, is a
Felsbachstr. 5, D- Selection of capsule deficient strains of Methylobacterium biodegradable
Bormann E J; Roth M; Linss W; 07745 Jena, rhodesianum producing polyhydroxybutyrate; poly-beta- thermoplastic polyester.
Leissner M Germany. hydroxybutyrate production Biotechnol.Tech.; (1999) 13, 8, 539-44 Such homo and
1173 1999
4.10 Literature on Polyhydroxyalkanoates.xls - page 293
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A Strain of Sphaerotilus
natans from 6 polluted
water samples was
isolated. The strain
had some main features
Department of Biology, as follows: bacillus,
Qingyang College, 0.85- 1.2 x 2.0-5.0
Xifeng, 745000, Peop. .mu.m, Gram-neg.
Rep. bacteria, it had sheath that
Xue, Lingui; Wang, Weiguo; Jiang, China Selection of high-yield PHB producing strain by technique Weishengwuxue Tongbao (1999), 26(3), 172- cells were in it, the
1174 Shuanglin of protoplasts 175 Chinese 1999 hypha was very long
Hypochlorite digestion of
bacterial biomass to
recover intracellular poly-
beta -hydroxylalkanoic
acid (PHA) has not been
used on
RAMSAY BRUCE A (CA); RAMSAY a large scale since it has
JULIANA (CA); BERGER ERIC (FR); been widely reported to
CHAVARIE CLAUDE (CA); severely degrade the
BRAUNEGG GERHART ECOLE POLYTECH Separation of poly- beta -hydroxyalkanoic acid from polymer. The process of
1178 (AT) (CA) microbial biomass US5110980 1992-05-05 1992 the invention proposes t
4.10 Literature on Polyhydroxyalkanoates.xls - page 294
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
When Pseudomonas
oleovorans was grown on
a mixture of 5-
phenylvaleric acid, PVA,
and nonanoic acid, NA,
the reserve
polyester produced
included both a
Department of Polymer homopolymer and a
Science and copolymer. The
Engineering, homopolymer poly-3-
University of Sequential production of two different polyesters in the hydroxy-5-phenylvalerate,
Massachusetts, inclusion bodies of PHPV, contained only 3-
1180 Curley JM, Lenz RW, Fuller RC Amherst 01003, USA. Pseudomonas oleovorans. Int J Biol Macromol 1996 Jul;19(1):29-34 1996 hyd
(1) Department of
Biological Sciences
and Biotechnology,
Tsinghua University, Polyhydroxyalkanoates
Beijing 100084, China (PHA) are synthesized by
e-mail: many bacteria as inclusion
bodies, and their
microbes@public3.bta.
net.cn Tel.: +8610- biodegradability and
62783844 Fax: +8610- structural diversity have
62788784 short contribution: A rapid method for detecting bacterial been studied with a view
(2) polyhydroxyalkanoates in intact cells by to their potential
K. Hong (1) (1), S. Sun (2), W. Tian (1), Analysis Centre, Fourier transform Applied Microbiology and Biotechnology Abstract application as
1181 G. Q. Chen (1), W. Huang (3) Tsinghua infrared spectroscopy Volume 51 Issue 4 (1999) pp 523-526 1999 biodegrad
4.10 Literature on Polyhydroxyalkanoates.xls - page 295
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Polymer Chemistry
Laboratory, The
Institute of Physical The ability of Alcaligenes
and Chemical eutrophus to grow and
Research (RIKEN), produce
Hirosawa 2-1, polyhydroxyalkanoates
Wako- (PHA) on plant
shi, Saitama 351-0198, oils was
Japan Tel.: +81 48 467 evaluated. When olive oil,
9402 Fax: +81 48 462 corn oil, or palm oil was
4667 e-mail: short contribution: Efficient production of fed as a sole carbon
polyhydroxyalkanoates from plant oils by Applied Microbiology and Biotechnology Abstract source, the wild-type
ydoi@postman.riken.g Alcaligenes eutrophus Volume 49 Issue 3 (1998) pp 333-336 strain
1182 T. Fukui, Y. Doi o and its recombinant strain 1998 o
1) Innovent
e.V./Biomaterialien,
Felsbachstr. 5, D-
07747 Jena, Germany Polyhydroxybutyrate
Tel.: +49-36-41-28-25- (PHB) was produced by
22 Fax: Ralstonia eutropha DSM
+49-36- 11348 (formerly
41-28-25-30
(2) Alicaligenes eutrophus) in
Fachhochschule Jena, media containing 20-30 g l-
Bereich 1 casein peptone or
Wirtschaftsingenieurw casamino acids as sole
esen, D-07743 Jena, short contribution: Production of polyhydroxybutyrate by sources of
E. J. Bormann (1), M. Leißner (2), M. Germany Ralstonia eutropha from protein Applied Microbiology and Biotechnology Abstract nitrogen. In
1183 Roth (3), B. Beer (1), K. Metzner (4) hydrolysates Volume 50 Issue 5 (1998) pp 604-607 1998 ferme
Middelberg; A.P.J.; Lee; S.Y.; Martin; Size analysis of poly(3-hydroxybutyric acid) granules
1186 J.; Williams; D.R.G.; Chang; H.N. produced in recombinant Escherichia coli Biotechnology Letters 1995; 17(2):205-210 1995 620.
4.10 Literature on Polyhydroxyalkanoates.xls - page 296
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly-b-hydroxybutyrate
(PHB) has emerging
potential for use as a
biodegradable
thermoplastic. In its extn.
from the bacterial source,
the
Department of polymer remains in
Chemical Engineering, granular form. Hence the
University of Cape final stages of extn.
Town, Rondebosch Spec. Publ. - R. Soc. Chem., 158(Separations polyhydroxybutyrate extn froth require its rigorous
Cilliers, J. J.; Johnson, L. S.; Harrison, 7700, S. solid-liquid separation of PHB by froth flotation. for Biotechnology flotation washing and dewatering.
1188 S. T. L. Afr. 3), 113-19 (English) 1994 1994 Ini
Poly(3-hydroxybutyrate)
(PHB) is a completely
biodegradable
polyester, produced by
bacterial fermn. Because
of poor thermal
stability, melt
Macromol. Symp. (1998), 127(Rolduc Polymer processing of the material
Meeting 10: "Petro" is accompanied by
Luepke, Thomas; Radusch, Hans Martin-Luther-Univ., Polymers vs. "Green" Polymers, 1997), 227- thermal degrdn. and
Joachim; Metzner, Klaus Halle/Saale, D-06099, 240 poor mech. properties. To
1189 Germany Solid-state processing of PHB powders 1998 prevent
Akita, S.; Einaga, Y.; Miyaki, Y.; Fujita, Solution properties of PHB. 1. biosynthesis and
1190 H. Characterization Macromolecules 1976; 9:774-780 1976 5.
SOLVENT EXTRACTION OF
POLYHYDROXYALKANOATES FROM
BIOMASS
THE PROCTER & FACILITATED BY THE USE OF A MARGINAL
1198 NODA, Isao GAMBLE COMPANY NONSOLVENT FOR PHA EP846184A1 June 10, 1998 1998 Abstract unavailable.
1199 Dunlop; W.F.; Robards; A.W. Some artifacts of the freeze-etching technique J. Ultrastructural Research 1972; 40:391-400 1972 212.
1200 Bongers, L. Some aspects of continuous cultures of hydrogen bacteria Develop. Ind. Microbiol. 1970; 11:241-255 1970 45.
Chiellini; E.; Cioni; F.; Solaro; R.; Starch-filled polyethylene in a composting environment: Journal of Environmental Polymer Degradation
1207 Vallini; G.; Corti; A.; Pera; A. evidence for polyethylene matrix oxidation 1993; 1:167 1993 569.
Stereoregular Poly-beta-hydroxyalkanoates: Produced by
1208 R.W.Lenz Bacteria or prepared from á-Lactones 654.
Poly[(R)-3-hydroxybutyric
acid] and its copolymers
were prepared by
biosynthetic and
chemosynthetic methods.
The films of
polyesters were prepared
Polymer Chemistry by both the solution-cast
Laboratory, The and melt-crystallized
Institute of Physical techniques. The
and Chemical enzymatic degradation of
Research (RIKEN), Structural effects on enzymatic degradabilities for polyester
1215 Abe H, Doi Y Saitama, Japan. poly[(R)-3-hydroxybutyric acid] and its copolymers. Int J Biol Macromol 1999 Jun-Jul;25(1-3):185-92 1999 films was
A membrane surrounding
Department of poly-beta-hydroxybutyrate
Bacteriology and (PHB) granules isolated
Botany, Syracuse from both Bacillus cereus
University, Syracuse, and B. megaterium has
New York, USA; been demonstrated by the
Department of carbon-replica technique
Biochemistry, and electron microscopy.
Universiy of Buffalo, PHB-granules - Bacillus Some general features
Lundgren, D.G.; Pfister, R.M.; Merrick, Buffalo, New York, megaterium - Bacillus cereus - and properties of both the
1220 J.M. USA Structure of poly-beta-hydroxybutyric acid granules J.gen.Microbiol. 1964; 34:441-446 1964 membrane membrane a Strain - Morphology 76.
Bloembergen; S.; Holden; D.A.; Hamer; Studies of composition and crystallinity of bacterial poly-(á-
1221 G.K.; Bluhm; T.H.; Marchessault; R.H. hydroxybutyrate-co-á-hydroxyvalerate) Macromolecules 1986; 19:2865- 1986 319.
Rhodococcus ruber
NCIMB 40126 synthesizes
copolyesters
(polyhydroxyalkanoates)
of 3-hydroxybutyrate
(3HB) and 3-
a Department of hydroxyvalerate (3HV),
Applied Biology, containing primarily 3HV
School of Life Rhodococcus ruber - monomer units, from a
Sciences and b School Studies on copolyester synthesis by Rhodococcus ruber methylobacterium extorquens - variety of single,
of Chemistry, and factors influencing the molecular mass of alcaligenes eutrophus - chemically unrelated
Anderson; A.J.a; Williams; D.R.a; Taidi; University of Hull, Hull, polyhydroxyburyrate accumulated by Methylobacterium copolyester synthesis - substrates. The 3HV
1223 B.a; Dawesa; E.A.; Ewing; D.F.b UK extorquens and Alcaligenes eutrophus FEMS Microbiology Reviews 1992; 103:93-102 1992 molecular mass content of th 468.
Studies on Membrane Synthesis in Bacillus megaterium
1224 Morrison, D. C.; Morowitz, H. J. KM J Mol. Biol. 1970; 49:441-459 1970 369.
4.10 Literature on Polyhydroxyalkanoates.xls - page 303
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The degrdn. by
microorganisms in marine
and freshwater
biofouling environments
polyhydroxyalkanoate water of polyhydroxyalkanoate
SEM (PHA) films made from
bacterial polyester biodegrdn exts. of halobacteria
water was studied. SEM
Dep. de Cienc. hyphal track bacterial polyester observations showed that
Ambientales y Recur. degrdn PHA films, both in sea-
Nat., Univ. de Alicante, Study of biofouling of polyhydroxyalkanoate (PHA) films in etching biofouling bacterial and freshwater, were
Lopez-Llorca, Luis V.; Colom-Valiente, Alicante water by polyester degrdn rapidly colonized by
1225 Maria F.; Carcases, Maria J. 03080, Spain scanning electron microscopy. Micron, 25(1), 45-51 (English) 1994 1994 bacteria a
Poly(3-hydroxybutyrate)
(PHB) quantification has
been developed mostly
using acidic methanolysis
followed by GC analysis of
the 3-hydroxybutyrate
Laboratorie de Genie methyl ester. However,
Cellulaire, Faculte des under our experimental
Sciences, Universite conditions, only 62% of
Jan S, Roblot C, Goethals G, Courtois de Picardie Jules Study of parameters affecting poly(3-hydroxybutyrate) the ester was detected by
J, Courtois B, Saucedo JE, Seguin JP, Verne, Amiens, quantification by GC
1226 Barbotin JN France. gas chromatography. Anal Biochem 1995 Mar 1;225(2):258-63 1995 analysis.
The fermn. expts. of
recombinant Ecc13B-1 for
the prodn. of PHB
using sucrose as the C
source were carried out to
achieve high cell
Inst. Chemical d. in 15L Air-lift Loop
Mo, Haitao; Sheng, Qin; Chen, Bingyu; Metallurgy, CAS, Huaxue Fanying Gongcheng Yu Gongyi (1998), Reactor. The exptl.
Xia, Linpei; Yang, Lianfu; Beijing, 100080, Peop. 14(1), 92-96 results showed that
Li, Jilun; Tian, Jiesheng; Wu, Baihe Rep. China Study on high cell density cultivation of PHB fermentation Chinese the cell d. can reach
1227 in 15L airlift loop reactor 1998 57.9g/cm3 in 53 h in
Institut für
Mikrobiologie, During cultivation under
Westfälische Wilhelms- storage conditions with
Universität Münster, BG11 medium containing
Corrensstraße 3, D- acetate as a carbon
48149 Münster, Synechocystis sp. PCC6803 · source,
Biodegradable polyester · Synechocystis sp.
Germany Tel.: +49- Polyhydroxyalkanoic acid · PCC6803 accumulated
251-83-39821; Fax: Synechocystis sp. PCC6803 possesses a two-component Poly(3- poly(3-hydroxybutyrate)
+49-251-83-38388 e- polyhydroxyalkanoic acid synthase similar hydroxybutyric acid) · PHA- up to 10% (w/w) of the cell
mail: steinbu@uni- to that of anoxygenic Archives of Microbiology Abstract Volume 170 synthase · PhaE · PhaC dry
1242 Hein S, Tran H, Steinbuchel A muenster.de purple sulfur bacteria Issue 3 (1998) pp 162-170 1998 weight. Our
Synthese der Enzyme des Tricarbonsäure-Cyclus in
1243 Glaeser; H.; Schlegel; H.G. Hydrogenomonas eutropha Stamm H16 Arch.Mikrobiol. 1972; 86:315-325 1972 148.
Synthese von Poly-D-(-)-3-hydroxybutters"ure und
Sniene, F.; Braunegg, G.; Lafferty, R. Ausscheidung organischer S"uren durch Alcaligenes
1244 M. eutrophus H16/M7 ? 286.
Polyhydroxyalkanoate
(PHA) is a family of
polymers composed
primarily of R-3-
hydroxyalkanoic acids.
These polymers have
Institut de Biologie et properties of
Physiologie Vegetales, biodegradable
Batiment de Biologie, thermoplastics and
Universite de Synthesis of medium-chain-length polyhydroxyalkanoates elastomers. Medium-chain-
Lausanne, CH-1015 in arabidopsis length PHAs (MCL-PHAs)
Mittendorf V, Robertson EJ, Leech RM, Lausanne, thaliana using intermediates of peroxisomal fatty acid beta- Proc Natl Acad Sci U S A 1998 Nov are synthesized in
1257 Kruger N, Steinbuchel A, Poirier Y Switzerland. oxidation. 10;95(23):13397-402 1998 bacteria by using int
In order to obtain
functional expression of
PHA synthase gene
phaC2
from Pseudomonas
aeruginosa in Escherichia
coli, the coding region
of phaC2 was
subcloned, including the
Inst. Microbiol. Synthesis of poly(3-hydroxyalkanoates) in Escherichia coli ribosomal binding site,
Qi, Qingsheng; Rehm, Bernd H. A.; Shandong Univ., expressing the PHA synthase gene phaC2 from into
Steinbuchel, Alexander Jinan, 250100, Peop. Pseudomonas aeruginosa: comparison of PhaC1 and FEMS Microbiol. Lett. (1997), 157(1), 155-162 pBluescript SK-
1260 Rep. China PhaC2 1997 collinear to the lac p
4.10 Literature on Polyhydroxyalkanoates.xls - page 309
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Department of
Chemical Engineering
and BioProcess Several recombinant
Engineering Research Escherichia coli strains,
Center, Korea including XL1-Blue,
Advanced Institute of JM109, HB101, and DH5
Science and harboring a stable
Technology, 373-1 high-copynumber plasmid
Kusong-dong, Yusong- pSYL105 containing the
gu, Taejon 305-701, Alcaligenes eutrophus
Korea polyhydroxyalkanoate
email: Kang Sub Yim Synthesis of poly-(3-hydroxybutyrate-co-3- Biotechnology & Bioengineering poly-(3-hydroxybutyrate-co-3- (PHA) biosynthesis genes
Kang Sub Yim *, Sang Yup Lee, Ho (Teesy@sorak.kaist.ac hydroxyvalerate) by recombinant Volume 49, Issue 5, 1996. Pages: 495- hydroxyvalerate); Escherichia were constructed. These
1262 Nam Chang .kr) Escherichia coli 503 1996 coli; propionate; valerate recombi 614.
Synthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)
from methanol and n.amyl alcohol by the methylotrophic
Ueda; S.; Matsumoto; S.; Takagi; A.; bacteria Paracoccus denitrificans and Methylobacterium Applied and Environmental Microbiology 1992;
1263 Yamane; T. extorquens 58(11):3574-3579 1992 611.
División
"Macromoleculas",
Instituto de Poly(D-beta-
Investigaciones hydroxybutyric acid) is
Fiscoquimicas one of the few
Teóricas y Aplicadas biopolymers which can be
Casilla de Correo No. synthesized also in vitro.
16. Sucursal 4, La This offers the rare
Plata (Universidad possibility to compare the
Naccional de La polymerization kinetics
Plata), Diagonal 113, and the physico-chemical
Esqu. 64, La Plata, poly-DL-beta-hydroxybutarate - and physical properties of
1264 Jorge, Vergara; Victor, Figini Ruben Argentina Synthesis of Poly(DL-beta-hydroxybutyric acid) Makromolekulare Chemie 1977; 178:267-270 1977 in vitro polymerization - an in vivo and an in vitro p others 53.
The fluorescent
pseudomonads are
classified as a group, one
characteristic of which is
that they do not
Department of accumulate
Biochemistry, poly-3-hydroxybutyrate
Groningen (PHB) during nutrient
Biotechnology Center, starvation in the presence
University of Synthesis of poly-3-hydroxyalkanoates is a common of excess carbon source.
Huisman GW, de Leeuw O, Eggink G, Groningen, The feature of fluorescent In this paper we show that
1265 Witholt B Netherlands. pseudomonads. Appl Environ Microbiol 1989 Aug;55(8):1949-54 1989 prototype strain
Huisman, G.W.; De Leeuw, O.; Eggit, Synthesis of poly-beta-hydroxalkanoates is a common Applied and Entvironmental Microbiol. 1989;
1266 G.; Withholt, B. feature of fluorescent Pseudomonads 55(8):1949-1954 1989 340.
4.10 Literature on Polyhydroxyalkanoates.xls - page 310
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Alcaligenes eutrophus H
16 (A.T.T.C. 17699;
Institut für D.S.M. 428) synthesizes
Mikrobiologie der the lipid-storage material
Gesellschaft für poly-beta-hydroxybutyrate
Strahlen- und under autotrophic
Umweltforschung mbH Alcaligenes eutrophus H 16 - conditions in the absence
München in 3400 Ralstonia eutropha H 16 - beta- of a N2 source. The
Göttingen, Synthesis of Poly-beta-hydroxybutyrate in vivo and ketothiolase - Azotobacter synthesis of the polymer
Grisebachstraße 8, Kinetics of beta-Ketothiolase in vitro in Alcaligenes Biochemical Society Transactions, 58th Meeting beijerinckii - autotrophic growth starts from acetyl-CoA
1267 Eva-Maria, Ruhr; G., Schlegel Hans Germany eutrophus H 16 Edinborough - (Gottschalk, 1964 Arch Strain - Metabolsim 54.
Synthesis of poly-beta-hydroxybutyric acid in Alcaligenes
Schubert, P.; Steinb chel, A.; Schlegel, eutrophus, its genetic localization and conjugational Nachrichten der Akademie der Wissenschaften
1268 H.G. transfer of the genes in Göttingen 1988; 4 1988 669.
Targeting of the polyhydroxybutyrate biosynthetic pathway
to the plastids of Arabidopsis thaliana results in high levels Proc. Natl. Acad. Sci. USA 1994; 91:12760-
1269 Nawrath; C.; Poirier; Y.; Somerville; C. of polymer accumulation 12764 1994 510.
In the bacterium
Alcaligenes eutrophus,
three genes encode the
enzymes necessary to
catalyze the synthesis of
poly[(R)-(-)-3-
hydroxybutyrate] (PHB)
Department of Plant from acetyl-CoA. In order
Biology, Carnegie Targeting of the polyhydroxybutyrate biosynthetic pathway to target these enzymes
Institution of to the plastids into the plastids of higher
Washington, Stanford, of Arabidopsis thaliana results in high levels of polymer Proc Natl Acad Sci U S A 1994 Dec plants,
1270 Nawrath C, Poirier Y, Somerville C CA 94305. accumulation. 20;91(26):12760-4 1994 the genes were modifi
The poly(3-
hydroxyalkanoate) (PHA)
degrading isolate K10 was
identified as Streptomyces
exfoliatus. This bacterium
is
distinguished from other
Institut fur PHA-degrading strains by
Mikrobiologie der Taxonomic identification of Streptomyces exfoliatus K10 its ability to utilize both
Georg-August- and poly(3-hydroxybutyrate)
Klingbeil B, Kroppenstedt RM, Universitat Gottingen, characterization of its poly(3-hydroxybutyrate) FEMS Microbiol Lett 1996 Sep 1;142(2-3):215- (PHB) and
1271 Jendrossek D Germany. depolymerase gene. 21 1996 poly(3-hydroxyoctanoate)
4.10 Literature on Polyhydroxyalkanoates.xls - page 311
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Whereas poly-beta-
hydroxybutyrate (PHB)
production by
Pseudomonas species is
rare,
synthesis of
medium-chain-length poly-
beta-hydroxyalkanoates
(mcl-PHAs) other than
Institute of Taxonomic implications of synthesis of poly-beta- PHB, has
Biotechnology, ETH- hydroxybutyrate and been
Honggerberg, HPT, other poly-beta-hydroxyalkanoates by observed in fluorescent
1272 Kessler B, Palleroni NJ Zurich, Switzerland. aerobic pseudomonads. Int J Syst Evol Microbiol 2000 Mar;50 Pt 2:711-3 2000 and n
The changes of
parameters of the unit cell
of biopolymer
poly(b-hydroxybutyrate)
(PHB) during heating from
room temp. to the
melting temp. are
measured and results are
Faculty Sciences, Temperature influence on changes of parameters of the polyhydroxybutyrate unit cell presented here. The
Univ. Novi Sad, Novi unit cell of polyester hydroxybutyric acid considerable increase of
Sad biopolymer PHB. crystallinity value of parameter a with
1275 Skrbic, Z.; Divjakovic, V. 21000, Yugoslavia Polymer, 37(3), 505-7 (English) 1996 1996 increase of tem
4.10 Literature on Polyhydroxyalkanoates.xls - page 312
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1 University of Zürich,
Institute of Plant
Biology, Zollikerstraße In recent years industrial
107, CH-8008 Zürich, interest has been
Switzerland; 2 focussed on the
University of lowell, evaluation of poly(3-
Department of hydroxyalkanoates) (PHA)
Chemistry, Lowell, MA as potentially
01854, USA; 3 biodegradable plastics for
University of a wide range of technical
Massachusetts, applications. Studies have
Department of Polymer been carried out in order
Brandl; H.; Gross; R.A.; Lenz; R.W.; Science and The accumulation of poly(3-hydroxyalkanoates) in Rhodobacter sphaereoides - 3- to optimize growth and
1276 Lloyd; R.; Fuller; R.C. Engineering, Amhe Rhodobacter sphaeroides Arch. Microbiol. 1991; 155:337-340 1991 hydroxyvalerate cult Strain - Copolyester 421.
Gross, R.A.; Brandl, H.; Ulmer, H.W.; The biosynthesis and characterization of new poly(beta-
1283 M.A; Posada; Fuller, R.C.; Lenz, R.W. hydroxyalkanoates) 659.
Microbiological
Research
Establishment, Porton, The chemical composition of micro-organisms as a Chemical composition of mircro-
1284 Herbert, D. Wiltshire function of their enviroment 11th Symp. Soc. Gen. Micr. 1961; 391-416 1961 organisms No abstract. Others 112. korr.
329 pp. Avail. Univ. Microfilms Int., Order No.
The degradation of PHB and P(HB/HV) copolymers and BRDX81854 From:
Univ. Bath, Claverton their uses in Diss. Abstr. Int. B 1988, 49(5), 1720 (English)
1285 Majid, Mohamed Isa bin Abd Down/Bath, UK drug delivery. 1988 1988 polymer degrdn drug delivery Abstract Unavailable
4.10 Literature on Polyhydroxyalkanoates.xls - page 313
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Poly(b-hydroxybutyric
acid) (PHB) has been
proposed as a
biodegradable implant
polyhydroxybutyrate fiber material on the basis of its
degrdn known degrdn.
polyhydroxypentanoate characteristics in certain
polyhydroxybutyrate fiber biol. environments.
degrdn Monofilaments of PHB
Inst. Med. Dent. prosthetic homopolymer and PHB-
Bioeng., Univ. polyhydroxypentanoate hydroxypentanoic acid
Liverpool, Adv. Biomater., 7(Biomater. Clin. Appl.), 471-6 polyhydroxybutyrate fiber (PHV) copolymers were
1286 Williams, D. F.; Miller, N. D. Liverpool, UK The degradation of polyhydroxybutyrate (PHB). (English) 1987 1987 392.
In Escherichia coli
carrying the poly(3-
hydroxyalkanoate) (PHA)
biosynthesis pathway on a
plasmid (pha+), the
function of the ackA
(acetate kinase) and pta
(phosphotransacetylase)
Dep. of Biology, Kyung genes is necessary
Hee Univ., The function of ackA and pta genes is necessary for Escherichia for efficient incorporation
Seoul 130-701, S. poly(3-hydroxybutyrate-co-3-hydroxyvalerate) synthesis in Can. J. Microbiol., 41(Suppl. 1), 200-6 polyhydroxybutyratehydroxyval of 3-hydroxyvalerate (3-
1293 Rhie, Ho Gun; Dennis, Douglas Korea recombinant pha+ Escherichia coli. (English) 1995 1995 erate formation HV)
Azotobacter vinelandii
produces two polymers:
the extracellular
Departamento de polysaccharide alginate
Microbiologia and the
Molecular, Instituto de intracellular
Biotecnologia, polyester poly-beta-
Universidad Nacional hydroxybutyrate (PHB). A
cosmid clone (pSMU588)
Autonoma de Mexico, The GacS sensor kinase regulates alginate and poly-beta- from an
Castaneda M, Guzman J, Moreno S, Cuernavaca Morelos hydroxybutyrate A. vinelandii
1294 Espin G 62250, Mexico. production in azotobacter vinelandii. J Bacteriol 2000 May;182(9):2624-8 2000 gene libr
4.10 Literature on Polyhydroxyalkanoates.xls - page 315
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
A. eutrophus can
accumulate poly-3-
hydroxybutyrate (PHB) or
polyhydroxyalkanoate
(PHA) contg. only 3-
hydroxybutyrate (HB) and
3-hydroxyvalerate (HV)
units. Granule-assocd.
polyhydroxybutyrate synthase PHB-synthase was
Sch. Life Sci., Univ. polyhydroxyalkanoate active with D(-)-3-
Haywood, G. W.; Anderson, A. J.; Hull, Hull HU6 7RX, The importance of PHB-synthase substrate specificity in FEMS Microbiol. Lett., 57(1), 1-6 (English) formation hydroxybutyryl-CoA and
1296 Dawes, E. A. UK polyhydroxylalkanoate synthesis by Alcaligenes eutrophus. 1989 1989 Alcaligenes D(-)-3-hydroxyvaleryl-C 390.
(1) Agricultural
Research Service, The bacteria
United States Pseudomonas oleovorans,
Department of P. resinovorans, P. putida,
Agriculture, Eastern and P.
Regional citronellolis
were evaluated for their
Research Center, 600 ability to grow and
East Mermaid Lane, produce
Wyndmoor, PA 19038, poly(hydroxyalkanoates)
USA. Fax: + 1 215 233 (PHA)
A.-M. Cromwick (1), T. Foglia (1), R. W. 6795 The microbial production of poly(hydroxyalkanoates) Applied Microbiology and Biotechnology Abstract using tallow free fatty
1312 Lenz (2) (2) from tallow Volume 46 Issue 5/6 (1996) pp 464-469 1996 acids and tall
Zhao; S.; Fan; C.; Hu; X.; Chen; J.; The microbial production of polyhydroxybutyrate from Applied Biochemistry and Biotechnology 199;
1313 Feng; H. methanol 39(40):191-199 1993 610.
4.10 Literature on Polyhydroxyalkanoates.xls - page 317
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
1314 Dawes, E.A.; Senior, P.J. The nature of Poly-beta-Hydroxybutyrate ? 17.
Dipartimento di
Chimica 'G. Ciamician'
dell'Universitá di
Bologna and Centro di
Studio per la Fisica
delle Macromolecule
del C.N.R., Via Selmi The physical aging of bacterial poly(D-beta- Makromol. Chem., rapid Commun. 1989; 10:47-
1316 Scandola, M.; Ceccorulli, G.; Pizzoli, M. 2, 40216 Bologna, Italy hydroxybutyrate) 50 1989 Crystallization - Physical aging No abstract. Crystallization 664.
1317 Schlegel, H.G. The physiology of hydrogen bacteria Antonie van Leeuwenhoek 1976; 42:181-201 1976 24.
1318 Bernard, G.N.; Sanders, J.K.M. The poly-beta-hydroxybutyrate granule in vivo J. biol. chem. 1989; 264:3286-3291 1989 341.
Pseudomonas oleovorans
is a soil bacterium capable
of degrading medium-
chain aliphatic
Groningen hydrocarbons. The
Biotechnology Center enzymes for this catabolic
University of activity are encoded by
Groningen Nijenborgh the alk genes of the 500
Withold, B.; Lageveen, R.G.; Huisman, 16 9747 AG Pseudomonas oleovorans - kb OCT-plasmid. We have Strains - Metabolism -
G.W.; Preusting, H.; Nijenhuis, A.; Groningen The The production of polyalkanoates by pseudomonas medium chain length (MSCL) - studied the genetics and Genetics -
1320 Kingma, J.; Tijsterman, A.; Eggink, G. Netherlands oleovorans Polymer Preprints 1989; 1:592-593 1989 Copolyesters - Fine chemicals regulation of alkane oxid Copolyesters 661.
Azotobacter beijerinckii
was grown in ammonia-
free glucose-mineral salts
media in batch culture and
in chemostat cultures
limited by the supply of
Department of glucose, oxygen or
Biochemistry, The role of oxygen limitation in the formation of poly-beta- molecular nitrogen. In
University of Hull, hydroxybutyrate Azotobacter beijerinckii - effect batch culture poly-beta-
Senior PJ, Beech GA, Ritchie GA, Kingston upon Hull during batch and continuous culture of Azotobacter of nitrogen and oxygen- hydroxybutyrate was
1327 Dawes EA HU6 7RX, U.K. beijerinckii. Biochem J 1972 Aug;128(5):1193-201 1972 limitation on PHB accumulation formed towards the end Strain - Metabolsim 131. Korr.
The synthesis of beta-hydroxy acids using beta-lihtiated
1328 Moersch; G.W.; Burkett; A.R. carboxylic acid salts J.Org.Chem. 1971; 36(8):1149-1151 1971 311.
The thermal
decomposition of some
polyhydroxyalkanoates
(PHA) has been
1Department of investigated by means of
Physical Chemistry, thermogravimetry and
Faculty of Chemistry, differential
University of Havana, thermogravimetry. The
Cuba thermal stability of the
2Laboratory of poly(-hydroxyalkanoates); studied polyesters
Polymers, Institute of thermal stability; decreases slightly with
Materials and thermogravimetry; differential increasing
Reagents, University Polymer International Volume 48, Issue 12, thermogravimetry; cis- hydroxyvalerate
1330 Norma Galego 1 *, Chavati Rozsa 2 of Havana, Cuba Thermal decomposition of some poly(-hydroxyalkanoates) 1999. Pages: 1202-1204 1999 elimination mechanism (HV) c
Bacterial genes
responsible for the
synthesis of the aliph.
polyester compd., poly-
D-(-)-3- hydroxybutrate
(PHB) were
introduced into cotton
MATECH Associates, (Gossypium hirsutum L.
150 E. Grove Street, Cv DP50) through
Scranton, PA, 18510, particle bombardment.
USA Thermal evaluation of transgenic cotton containing Thermochim. Acta (1998), 313(1), 43-53 The resulting transgenic
1331 Chowdhury, B.; John, Maliyakal E. polyhydroxybutyrate 1998 cotton cont
BACKGROUND: Ovine
pulmonary valve leaflets
and pulmonary arteries
have been tissue-
Department of engineered (TE) from
Cardiovascular autologous
Surgery, Children's cells and biodegradable
Hospital, Harvard polyglycolic acid (PGA)-
Shum-Tim D, Stock U, Hrkach J, Medical School, polyglactin copolymers.
Shinoka T, Lien J, Moses MA, Stamp A, Boston, Tissue engineering of autologous aorta using a new Use of this cell-polymer
Taylor G, Moran AM, Landis W, Massachusetts 02115, biodegradable Ann Thorac Surg 1999 Dec;68(6):2298-304; construct in the systemic
1334 Langer R, Vacanti JP, Mayer JE Jr USA. polymer. discussion 2305 1999 circulation resul
The interface in
poly(hydroxybutyrate)/PA
N- and
poly(hydroxybutyrate)/PET
fibers model composites
has been
investigated by
Faculty of Technology polarizing optical and
and Metallurgy, SEM. Under certain
University "Sv. Kiril i melting/cooling
Metodij", Skopje, Compos. Interfaces (1998), Volume Date 1998, conditions in the PAN fiber
Grozdanov, Anita; Bogoeva-Gaceva, Yugoslavia Transcrystallinity phenomena in PET and PAN 5(2), 179-189 system a transcryst.
1338 Gordana fibers/polyhydroxybutyrate matrix systems 1998 inte
A fiber-producing plant
comprising in its genome
a heterologous genetic
construct is disclosed.
This genetic construct
comprises
a fiber-specific promoter
and a coding sequence
selected from the group
TRANSGENIC COTTON PLANTS PRODUCING WO9412014 consisting of sequences
1339 MALIYAKAL JOHN AGRACETUS (US) HETEROLOGOUS BIOPLASTIC 1994-06-09 1994 encoding bioplastic-produ
A fiber-producing plant
comprising in its genome
a heterologous genetic
construct is disclosed.
This genetic construct
comprises
a fiber-specific promoter
and a coding sequence
selected from the group
JOHN MALIYAKAL Transgenic cotton plants producing heterologous US5602321 consisting of sequences
1340 (US) MONSANTO CO (US) polyhydroxy(e) butyrate bioplastic 1997-02-11 1997 encoding bioplastic-produ
4.10 Literature on Polyhydroxyalkanoates.xls - page 322
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Transmembrane ion
transport, a critical
process in providing
energy for cell functions,
Department of is carried
Microbiology, Giltner out by pore-
Hall, Michigan State forming macromolecules
University, East capable of discriminating
Lansing, MI, 48824, among very similar ions
USA. Transmembrane Ion Transport by and
rnreusch@pilot.msu.e Polyphosphate/Poly-(R)-3-hydroxybutyrate responding
1342 Reusch RN du Complexes. Biochemistry (Mosc) 2000 Mar;65(3):280-295 2000 to changes
Poly-beta-hydroxybutyrate
(PHB) is an amphiphilic
lipid that has been found
to be a ubiquitous
component of the cellular
membranes of bacteria,
Department of plants and animals. The
Microbiology and distribution of PHB in
Public Health, human plasma was
Michigan State investigated using
University, E. Lansing chemical and
1343 Reusch RN, Sparrow AW, Gardiner J 48824. Transport of poly-beta-hydroxybutyrate in human plasma. Biochim Biophys Acta 1992 Jan 3;1123(1):33-40 1992 immunological m
Poly-beta-hydroxybutyrate
(PHB) accumulation by
Alcaligenes
Department of Applied eutrophus NCIMB
Biology, School of Life 40529 was investigated to
Sciences, University determine whether the
of Hull, Hull HU6 decline in molecular
7RX, UK. Turnover of poly(3-hydroxybutyrate) (PHB) and its mass of PHB during batch
Email: influence on the molecular mass of the polymer fermentation could
A.J.Anderson@appbiol accumulated by Alcaligenes eutrophus during batch be explained by
.hull.ac.uk culture; poly-beta-hydroxybutyrate accumulation and turnover of the polymer.
1344 Taidi B; Mansfield D A; *Anderson A J turnover FEMS Microbiol.Lett.; (1995) 129, 2-3, 201-06 1995 A. eut
4.10 Literature on Polyhydroxyalkanoates.xls - page 323
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The freeze-etching
technique was used to
examine the effects of
fracturing and etching on
the appearance of poly-
beta-hydroxybutyrate
granules from Bacillus
Department of Biology, cereus. These granules
University of York, were examined in extracts
Heslington, York, Ultrastructural studies of poly-beta-hydroxybutyrate Bacillus cereus - freeze-etching isolated by hypochlorite or
1349 Dunlop; W.F.; Robards; A.W. England granules from Bacillus cereus Journal of Bacteriology 1973; 114(3):1271-1280 1973 - PHB granules by sonic tratment, an Strain - Granules 134. Korr.
The chemolithotroph,
Hydrogenomonas
eutropha, was tested für
Department of ist ability to utilize a
Biochemistry, School variety of single nitrogen
of Medicine, and sources during growth in
Space Sciences an atmosphere of H2-O2-
Research Center, Hydrogenomonas eutropha - CO2. The present data
University of Missouri, Ralstonia eutropha - show that H. eutropha can
Columbia, Missouri Utilization of organic nitrogen compounds by Alcaligenes eutrophus - organic utilize the nitrogen from
1358 Wixom, R.K.; Sheng, Y.B.; Becker, R.S. 65201 Hydrogenomonas eutropha Biotechnol. Bioeng. 1972; 14:985-1006 1972 nitrogen sources many, but not all, a Strain - Metabolsim 67.
Chemie Linz
Aktiengesellschaft, St.
Peter-Strasse 25, A-
4020 Linz (AT); Letia
GesmbH,
Arabellastrasse 4
Postfach 810508 D-
8000 München 81 Verfahren zur biotechnologischen Herstellung von Poly-D(-
1359 Lafferty, Robert M.; Braunegg Gerhart (DE) )-3-hydroxybuttersäure DE3343551 1983-12-01 Abstract unavailable.
Verfahren zur Herstellung einer optisch aktiven
1360 Carbonsäuren ? ? 196.
Versuche zur Polyphosphat-šberkompensation in
1361 Liss; E.; Langen; P. Hefezellen nach Phosphatveratmung Archiv f r Mikrobiologie 1962; 41:383-392 1962 243.
Als fakultativ
chemolithotrophe
Mikroorganismen wachsen
die Knallgasbakterien
sowohl unter einer
Atmosphäre von Knallgas
und Kohlendioxyd als
auch auf einer Reihe von
organischen Substraten.
So werden von den
Aus dem Institut für Hydrogenomonas - Ralstonia Hydrogenomonas-
Gottschalk, G.; Eberhardt, U.; Schlegel, Mikrobiologie der eutropha - Alcaligenes Stämmen H1, H16 und
1362 H.G. Universität Göttingen Verwertung von Fructose durch Hydrogenomonas H 16(I.) Arch. Mikrobiol. 1964; 48:95-108 1964 eutrophus - Fructose H20 Glutami Strain - Metabolsim 163.
3-Hydroxybutyrate-3-
hydroxyvalerate (3HB-
3HV) as well as 3-
hydroxybutyrate-4-
hydroxybutyrate (3HB-
4HB)
copolyesters have been
investigated by differential
scanning calorimetry,
Centro di Studio per la thermogravimetric
Fisica delle analysis and dynamic
Macromolecole CNR, Viscoelastic relaxations and thermal properties of bacterial mechanical
Universita di Bologna, poly(3-hydroxybutyrate-co-3-hydroxyvalerate) and spectroscopy, over a wide
1363 Scandola M, Ceccorulli G, Doi Y Italy. poly(3-hydroxybutyrate-co-4-hydroxybutyrate). Int J Biol Macromol 1990 Apr;12(2):112-7 1990 ra 359.
1364 M.Zueger; D.Seebach Vorschrift zur Depolymerisation von PHB 205.
4.10 Literature on Polyhydroxyalkanoates.xls - page 327
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Küng; W.; Strempfl; F.; Korneti; L.; Wachstum und speicherung von poly-beta-
1365 Braunegg; G.; Lafferty; R.M. hydroxybuttersäure bei Alcaligenes latus Vortrag Millstadt 1982 1982 244.
Weitere Untersuchungen zur N-Verwertung des H2-
oxidierenden Bakterienstammes Alcaligenes eutrophus
und alimentärer Ribonukleinsäure durch wachsende
1366 Greife, H. A.; Molnar, S.; Günther, K.-D. Broiler Arch. Gefl gelk. 1981; 45:57-68 1981 187.
Shear piezoelectricity is
observed in uniaxially
oriented system of
optically active
biopolymers such as
poysaccharidesm
poypeptides and
poynucleotides. The
The Institute of magnitude of the
Physical and Chemical piezoelectric constant is
Research, Wako, Piezoelectricity - Biopolymers - proportional to the degree Physical properties -
1373 Fukada Eiichi Saitama 351, Japan Piezoelectricity of natural biomaterials Ferroelectrics 1984, Vol. 60: 285-296 1984 Crystallinity - Bone growth of crystallinity, the degree Applications 685 korr.
Synthesis and
accumulation of poly(beta-
hydroxyalkanoate) in
Rhizobium
leguminosarum, R.
leguminosarum biovar.
1 Biopolymers Trifolii, Thizobium
Laboratory, Research "galega", Thizobizum
Centre Poly-biòs, Area "hedysarum" and R.
di Ricerca, Trieste and meliloti were studied.
2 Dipartimento di Poly(beta-
Biotecnologie Agrarie, hydroxybutyrate) is
Università di Padova, Poly-beta-hydroxybutyrate (PHB) biosynthesis and Rhizobium sp. - Biosynthesis - accumulated up to 55 % of
1377 Tombolini R.1; Nuti M.P.2 Padova, Italy accumulation by different Rhizobium species Fems Microbiology Letters 1989, 60:299-304 1989 Accumulation the c Strain - Metabolsim kopiert
Polymer Chemistry
Laboratory, The Poly[(R)-3-hydroxybutyric
Institute of Physical acid] and its copolymers
and Chemical were prepared by
Research (RIKEN ), biosynthetic and
Hirosawa, Wako-shi, chemosynthetic methods.
Saitama 351- 0198, The films of
Japan * Corresponding polyesters were prepared
author. Tel.: ?81-48- by both the solution-cast
4679402; fax: ?81-48- Keywords : and melt-crystallized
4684667. Poly(hydroxyalkanoic acid)s; techniques. The
E-mail address : International Journal of Biological Enzymatic degradability; enzymatic degradation of
ydoi@postman.riken.g Structural effects on enzymatic degradabilities for Macromolecules Chemical structure; Solid-state polyester films
1379 Hideki Abe, Yoshiharu Doi * o.jp (Y. Doi) poly[(R)-3-hydroxybutyric acid] and its copolymers 25 (1999) 185–192 1999 structure w ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 330
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
a Polymer Chemistry
Laboratory, The
Institute of Physical
and Chemical
Research (RIKEN), Thin films with average
Hirosawa, Wako-shi, layer thickness 100 nm of
Saitama 351-0198, poly[(R)-3-hydroxybutyric
Japan acid] (P[(R)-3HB]) and
b Department of poly[(R)-3-hydroxybutyric
Industrial Chemistry, acid-co-10
Science University of mol% 6-hydroxyhexanoic
Tokyo, 1-3, acid] were isothermally
Kagurazaka, Shinjuku- Microscopic visualization on crystalline morphologies of Keywords: Poly[(R)-3- crystallized at a given
H. Abe a, * , Y. Kikkawa b , T. Iwata a , ku, Tokyo 162-8601, thin films for hydroxybutyric acid]; Thin film; crystallization temperature
1380 H. Aoki b , T. Akehata b , Y. Doi a Japan * poly[(R)-3-hydroxybutyric acid] and its copolymer Polymer 41 (2000) 867–874 2000 Lamellar morphology after melting at 20 ganze Artikel
Regulatory mechanism in
PHB [poly-
a National Institute of (hydroxybutyrate)]
Bioscience and Human- accumulation by
Technology, Higashi 1- cyanobacteria, especially
1, Tsukuba, Ibaraki, by a thermophilic isolate,
305- 8566 Japan Synechococcus MA19
b National Institute of was reviewed in
Ad6anced comparison with a
Interdisciplinary Keywords : Photosynthesis; genetically engineered
Yasuo Asada a, *, Masato Miyake a , Research, Higashi 1- 1- Photosynthetic accumulation of poly-(hydroxybutyrate) by International Journal of Biological Cyanobacteria; Biodegradable strain. The strain, MA19
Jun Miyake b , Ryuichiro Kurane a , 4, Tsukuba, Ibaraki, cyanobacteria—the metabolism and potential for CO2 Macromolecules plastics; accumulates PHB under
1383 Yutaka Tokiwa a 305- 8562 Japan recycling 25 (1999) 37–42 1999 Poly(hydroxyalkanoates) nitrogen ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 331
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
United States
Department of
Agriculture, Pseudomonas
Agricultural Research resino6orans produces a
Ser6ice, Eastern medium-chain-length
Regional * poly(hydroxyalkanoate)
Corresponding author. (MCL-PHA) copolymer
Tel.: ?1 215 2336483; when grown on
fax: ?1 215 tallow (PHA–tal). This
2336795; e-mail: polymer had a repeat unit
rashby@arserrc.govR composition ranging from
esearch Center, Keywords : Medium-chain- C4 to C14 with some
600East Mermaid International Journal of Biological length poly(hydroxyalkanoate); mono-unsaturation in the
Richard D. Ashby *, Anne-Marie Lane, Wyndmoor, Radiation crosslinking of a bacterial medium-chain-length Macromolecules Pseudomonas resino6orans; C12
1384 Cromwick 2 , Thomas A. Foglia PA 19038, USA poly(hydroxyalkanoate) elastomer from tallow 1 23 (1998) 61–72 1998 Radiation crosslinking and C14 alkyl sid ganze Artikel
Polyhydroxyalkanoate
a Department of (PHA) cellular inclusions
Biochemistry and consist of polyesters,
Molecular Biology, phospholipids, and
Uni6ersity of proteins. Both the
Massachusetts, polymerase and the
Amherst MA, USA depolymerase enzymes
b Department of Keywords : are active components of
Biological Sciences, Polyhydroxyalkanoate (PHA); the structure. Recently,
E.S. Stuart a, *, Ali Tehrani a , Henry E. James Madison Ultrastructural studies; Polymer proteins associated with
Valentin b,1 , Douglas Dennis b , Uni6ersity, Protein organization on the PHA inclusion cytoplasmic inclusion; Subcellular these inclusions have
1385 Robert W. Lenz c , R. Clinton Fuller a,c Harrisonburg VI, USA boundary Journal of Biotechnology 64 (1998) 137–144 1998 compartmentaliza-tion been des ganze Artikel
a Dipartimento di
Scienze Chimiche, The sequence
Uni6ersita ` di Catania, distributions of two
Viale A. Doria 6, microbial copolyesters
95125 Catania, Italy obtained by fermentation
b Istituto per la of Rhodospirillum rubrum,
Chimica e la grown with
Tecnologia dei 3-hydroxyhexanoic or 3-
Materiali Polimerici, hydroxyheptanoic acids,
Consiglio Nazionale Keywords : were determined by
Alberto Ballistreri a, *, Mario Giuffrida b delle Ricerche, Viale Characterization by mass spectrometry of Polyhydroxyalkanoates; analyzing the oligomers
, Giuseppe Impallomeni b , Robert W. A. Doria 6, 95125 poly(3-hydroxyalkanoates) produced by Rhodospirillum International Journal of Biological Sequence distribution of prepared by partial
Lenz c , Catania, Italy* rubrum Macromolecules copolymers; Mass spectrometry pyrolysis or
1386 R. Clinton Fuller c Correspond from 3-hydroxyacids 26 (1999) 201–211 1999 of PHAs partial met ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 332
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
a
Department of
Pharmaceutics and
Biopharmacy , Philipps-
University ,
Ketzerbach 63, D- The aerosol solvent
35037 Marburg , extraction system (ASES)
Germany is a method based on
b solvent extraction using
Schwarz Pharma AG , supercritical carbon
Monheim , dioxide
Germany*Correspondi for the preparation of
ng author. Tel.: 149- microspheres. The ASES
6421-285-880; fax: technology seems to be
149- Biodegradable semi-crystalline comb polyesters influence Keywords : ASES; Supercritical strongly affected by
6421-287-016. the carbon dioxide; Biodegradable physico-chemical
a ba, * Armin Breitenbach , Detlef Mohr E-mail address : microsphere production by means of a supercritical fluid branched polyesters; properties of
1387 , Thomas Kissel kissel@mail extraction technique (ASES) Journal of Controlled Release 63 (2000) 53–68 2000 Microspheres biodegradabl ganze Artikel
AbstractÐLignocellulosic
*Stazione materials treated by the
Sperimentale per la steam explosion technique
Cellulosa, Carta e alone, or in the presence
Fibre Tessili Vegetali of chemical reagents,
ed Arti®ciali, Piazza undergo remarkable
Leonardo modi®cations at the level
da Vinci 26, 20133 of both the chemical
Milano, Italy composition
}Author to whom STEAM EXPLODED BIOMASS FOR THE PREPARATION KeywordsÐSteam explosion and supramolecular
B. FOCHER*}, A. MARZETTI*, P. L. correspondence OF CONVENTIONAL AND ADVANCED BIOPOLYMER- Biomass and Bioenergy Vol. 14, No. 3, pp. process; lignocellulosics; chitin, structure, developing
1393 BELTRAME$ and M. AVELLA% should be addressed. BASED MATERIALS 187±194, 1998 1998 algae; composites features s ganze Artikel
Institut fuë r
Mikrobiologie der
Westfaë lischen Rhodococcus ruber and
Wilhems-Universitaë t related Gram-positive
Muënster, Corrensstra bacteria synthesized and
Me 3, D-48149 Muë accumulated novel
nster, Germany copolyesters containing 3-
* Corresponding hydroxypivalic acid as
author. Tel.: +49 (251) Keywords: Rhodococcus ruber; constituent if the cells
8339821; 3-Hydroxybutyric acid; 3- were cultivated in a
Fax: +49 (251) Biosynthesis of novel copolyesters containing 3- Hydroxypivalic acid; 2,2- mineral salts medium
Bernd Fuë chtenbusch, Dirk Fabritius, 8338388; E-mail: hydroxypivalic Dimethyl-3-hydroxypropionic containing 3-
Marc Waë ltermann, Alexander steinbu@uni- acid by Rhodococcus ruber NCIMB 40126 and related acid; Polyhydroxyalkanoic hydroxypivalic acid and
1394 Steinbuë chel * muenster.de bacteria FEMS Microbiology Letters 159 (1998) 85^92 1998 acid glucose as c ganze Artikel
Department of
Biochemistry and
Molecular Biology,
University of
Massachusetts Polyhydroxyalkanoates
Amherst, MA 01003, (PHAs), in the form of
USA metabolic storage
* Corresponding reserves, are assembled
author. Tel.: ?1-413- in intracellular cytoplasmic
545-0328; fax: ?1-413- inclusions,
545- often called granules. This
3291. review discusses both the
E-mail address : Microbial inclusions with special reference to PHA International Journal of Biological structure and function of
rcfuller@biochem.uma inclusions and Macromolecules this assembly. In addition
1395 R. Clinton Fuller * ss.edu (R.C. Fuller) intracellular boundary envelopes 25 (1999) 21–29 1999 an overview of othe ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 335
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
a Laboratory of
Polymers, Materials Some
and Reagents polyhydroxyalkanoates
Institute, Havana (PHA),
University, Havana polyhydroxybutyrate
City 10400, Cuba (PHB) and copolymers
b Advanced Material poly(hydroxybutyrate-co-
Laboratory, Polymer hydroxyvalerate) (P(HB-co-
Section, North HV)), were characterized
Fluminense State by different techniques
Norma Galego a,b,* , Chavati Rozsa a , University, Campos, (GPC, DSC, DMA, FTIR,
Rube´n Sa´nchez b , Juan Fung c , R.J., Brazil Characterization and application of poly(b- DRX) in order to be used
Anali´a Va´zquez d , Julio Santo * Corresponding hydroxyalkanoates) in hydroxyapatite (HA) Material
1396 Toma´s e author. family as composite biomaterials Polymer Testing 19 (2000) 485–492 2000 composit Characterisation ganze Artikel
a Department of
Chemical Engineering,
University of Waterloo, Batch culture of
Waterloo, Ontario, Alcaligenes latus,
Canada American Type Culture
b Department of Collection 29713, was
Chemical Engineering, investigated for producing
University of Almeri´a, the intracellular bioplastic
Almeri´a, Spain* Keywords: Poly( b- poly( b-hydroxybutyric
Corresponding author. hydroxybutyric acid); acid) (PHB). A central,
Tel.: 134-950-215-566; Polyhydroxybutyrate; composite experimental
fax: 134-950-215- Polyhydroxyalkanoate; design was used to
Enrico Grothe a , Murray Moo-Young a 484. Fermentation optimization for the production of Enzyme and Microbial Technology 25 (1999) Alcaligenes latus; Biopolymer; optimize the composition
1397 , Yusuf Chisti b, * E-mail: ychisti@u poly( b-hydroxybutyric acid) microbial thermoplastic 132–141 1999 Bioplastic of t ganze Artikel
¨ ¨ ¨ Institute of
Biotechnology , Swiss An improved activity assay
Federal Institute of for polyhydroxyalkanoate
Technology , ETH (PHA) polymerases from
Zurich , Honggerberg Pseudomonas oleovorans
HPT , CH- 8093 Zurich GPo1 was
, developed. The activity
Switzerland*Correspon assay is based on the
ding author. Tel.: 141- detection of released
1-633-3286; fax: 141-1- Development of an improved in vitro activity assay for Keywords : PHA polymerase; In Coenzyme A (CoA) using
633- 1051. E-mail medium vitro activity assay; Medium 5,59-dithiobis (2-
address : chain length PHA polymerases based on CoenzymeA chain length nitrobenzoic
1 * Guy de Roo, Qun Ren , Bernard bw@biotech.biol.ethz. release Journal of Microbiological Methods 41 (2000) polyhydroxyalkanoates; acid) (DTNB), a
1398 Witholt , Birgit Kessler ch (B. Witholt) measurements 1–8 2000 Pseudomonas oleovorans compound ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 336
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
The School of
Metallurgy and Poly(3-hydroxybutyrate)
Materials, The (PHB) has been blended
University of with poly(vinyl acetate)
Birmingham, (PVAc) and the system
Edgbaston, has been found to be
Birmingham B15 2TT, miscible over the
UK complete composition
* Corresponding range studied, i.e. 0–100
author. Tel.: 144-1214- Keywords: Poly(3- wt%. The blends exhibited
144544; fax: 144-1214- Crystallisation of poly(3-hydroxybutyrate)/polyvinyl acetate hydroxybutyrate); Polyvinyl a single glass transition
1399 J.N. Hay * , L. Sharma 145232. blends Polymer 41 (2000) 5749–5757 2000 acetate; Blends temperature, which var ganze Artikel
Institut fu «r
Mikrobiologie, We recently identified the
Westfa«lische phaGPp gene encoding
Wilhelms-Universita«t (R)-3-hydroxydecanoyl-
Mu«nster, Corrensstra ACP:CoA transacylase in
Me 3, D-48149 Pseudomonas putida,
Mu«nster, Germany Keywords: Pseudomonas which directly
* Corresponding aeruginosa; links the fatty acid de novo
author. Tel. : +49 (251) The Pseudomonas aeruginosa phaG gene product is Polyhydroxyalkanoic acid; Fatty biosynthesis and
833 9821;Fax: +49 involved in the acid biosynthesis; polyhydroxyalkanoate
(251) 833 8388; E- synthesis of polyhydroxyalkanoic acid consisting of Transacylase; (PHA) biosynthesis. An
Nils Hoffmann, Alexander Steinbu« chel mail: steinbu@uni- medium-chain-length constituents from non-related carbon Polyhydroxyalkanoate open reading frame (ORF)
1402 *, Bernd H.A. Rehm muenster.de sources FEMS Microbiology Letters 184 (2000) 253^259 2000 synthesis of which t ganze Artikel
a Institut fu«r
Mikrobiologie und
Genetik der
Universita«t
Go«ttingen, Sinorhizobium meliloti
Grisebachstr. 8, 37077 1021 responds to external
Go«ttingen, Germany biotin signals from alfalfa
b Department of plants through the bioS
Biology, University of regulatory locus.
Waterloo, Waterloo, Immunogold
Kai Hofmann a , Elke B. Heinz a , Ont., N2L 3G1, Keywords: Alfalfa; labeling and electron
Trevor C. Charles b , Michael Hoppert a Canada* Polyhydroxybutyrate; Biotin; microscopy revealed that
, Corresponding author. Sinorhizobium meliloti strain 1021 bioS and bdhA gene Rhizosphere; Root the BioS protein is located
Wolfgang Liebl a , Wolfgang R. Streit a; Tel. : +49 (551) transcriptions colonization; Sinorhizobium within the S. meliloti
1403 * 393775;Fax: +49 (55 are both affected by biotin available in de¢ned medium FEMS Microbiology Letters 182 (2000) 41^44 2000 meliloti cytoplasm. Under biotin-li ganze Artikel
Department of
Biomolecular
Engineering, Tokyo The crystallinity and the
Institute of pro®le of biodegradation
Technology, 4259 by environmental
Nagatsuta, Midori-Ku, microorganisms in river
Yokohama 226-8501, water were investigated
Japan* Corresponding for bacterial
author. Tel. : +81-45- poly(3-hydroxybutyric
924-5794; fax: +81-45- Influence of tacticity and molecular weight of poly(vinyl acid) [PHB] blend ®lms
924-5827.E-mail alcohol) on with stereoregular
address:yinoue@bio.tit crystallization and biodegradation of poly(3-hydroxybutyric poly(vinyl alcohol)s [PVA]
Tetsuya Ikejima, Naoko Yoshie, Yoshio ech.ac.jp (Y. Inoue), acid)/ Polymer Degradation and Stability 66 (1999) 263- and low-molecular weight
1404 Inoue* nyoshie@bio.t poly(vinyl alcohol) blend films 270 1999 atactic ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 338
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Crystallization behavior
and environmental
biodegradability were
investigated for the films
Department of of bacterial poly(3-
Biomolecular hydroxybutyric acid)
Engineering, Tokyo (PHB) blends with chitin
Institute of and chitosan. The blend
Technology, 4259 films showed X-ray
Nagatsuta, Midori-Ku, Crystallization behavior and environmental Poly(3-hydroxybutyric acid); diffractive peaks that
Yokohama 226-8501, biodegradability of the blend Crystallization behavior; arose from the PHB
1405 T. Ikejima, Y. Inoue * Japan films of poly(3-hydroxybutyric acid) with chitin and chitosan Carbohydrate Polymers 41 (2000) 351–356 2000 Environmental biodegradability crystalline ganze Artikel
Institut fuër
Mikrobiologie, Westfaë
lische Wilhelms- Purified recombinant
Universita ë t poly(hydroxyalkanoic
Muënster, Corrensstra acid), PHA, synthase from
Me 3, D-48149 Muë Keywords: Chromatium vinosum was
nster, Germany * Poly(hydroxyalkanoic acid); used to examine in vitro
Corresponding author. Poly(3-hydroxybutyric acid); poly(3-hydroxybutyric
Tel.: +49 (251) 833 Poly(hydroxyalkanoic acid) acid) (P(3HB)) formation.
9821;Fax: +49 (251) synthase; In vitro synthesis; In combination with
833 8388; E-mail: In vitro synthesis of poly(3-hydroxybutyric acid) by using Chromatium vinosum; purified propionyl-
steinbu@uni- an Propionyl-coenzyme A coenzyme A transferase of
1406 Ralf Jossek, Alexander Steinbuë chel * muenster.de enzymatic coenzyme A recycling system FEMS Microbiology Letters 168 (1998) 319^324 1998 transferase Clostridium propionicum ganze Artikel
natural abundance
solution 13C nuclear
magnetic resonance
Department of Polymer (n.m.r.) spectroscopy was
Science and used to monitor the
Engineering and intracellular production
Department of and degradation in vivo of
Biochemistry and two poly(3-
Molecular Biology, hydroxyalkanoates)
University of bacterial polyesters, (PHAs), produced by
Curley J.M., Lenz R.W., Fuller R.C., Massachusetts, intracellular PHA production Pseudomonas Oleovorans
Browne, S.E., Gabriel, C.B. and Amherst, MA 01003, 13C n.m.r. spectroscopy in living cells of Pseudomonas and degradation, 13C n.m.r. , poly(3-
1408 Panday, S. USA and oleovorans Polymer 1997, Vol. 38, No. 21 pp 5313-5319 1997 spectroscopy in vivo hydroxynonanoate) ganze Artikel
4.10 Literature on Polyhydroxyalkanoates.xls - page 339
Adress(es) /
ID Autor(s) / Inventor(s) Applicant(s) Title Source / Application Number Year Keyword(s) Abstract Objective Hardware Ablage
Unsaturated
Department of biopolyesters, (PHA-DB),
Chemistry, Zonguldak obtained from pure
Karaelmas University, anchovy (hamci),
67100, Zonguldak, hazelnut,
Turkey; and soybean oily acids and the
TU¬ BIú TAK, mixtures of octanoic acid
Marmara Research (in weight ratios of 50/50
Center, Food, Science and 70/30) were
and Technology chlorinated
Institute, Chlorination of Poly(3-hydroxy alkanoates) Containing up to 54 wt % Cl content.
Ali Hakan Arkin, † Baki Hazer,* ,†,‡ and Gebze, 41470, Unsaturated The molecular weights
1414 Mehlika Borcakli ‡ Kocaeli, Turkey Side Chains Macromolecules 2000, 33, 3219-3223 2000 (MW) of the ch
Centre de Recherches
sur les
Macromole´cules Blends of bacterial
Ve´ge´tales (CERMAV- poly(hydroxybutyrate)
CNRS), Universite´ (PHB) with
Joseph Fourier, poly(hydroxyoctanoate)
BP 53, 38041 (PHO) were
Grenoble Cedex 9, prepared by co-dissolving
France; and Institut the two polyesters in
Universitaire de chloroform and casting the
Technologie, mixture. To probe the
De´partement de question
Chimie-Mate´riaux, 39, Poly(3-hydroxybutyrate) and Poly(3-hydroxyoctanoate) of blend miscibility,
Bd Gambetta, 38000 Blends: scanning electron
1417 Alain Dufresne* ,† and Marc Vincendon Grenoble, Fra Morphology and Mechanical Behavior Macromolecules 2000, 33, 2998-3008 2000 microscopy (SEM) obs
4.11 Literatures on polysaccharides
342
343
4.11 Literatures on Polysaccharides.xls - page 344
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
1 A vortex-bowl disk atomizer system for Champagne CP, Blahuta N, Brion Biotechnol Bioeng 2000 Jun Food Research and Development 2000 production, alginate, beads, Using a model system, a concept for the immobilization of microbial
the production of alginate beads in a F, Gagnon C 20;68(6):681-8 Centre, Agriculture Canada, 3600 cultures within alginate beads directly in a 1500-L fermentor with a
1500-liter fermentor. Casavant Blvd., West, Saint- height to diameter ratio of 1.85 is described. The system is comprised
Hyacinthe, Quebec, Canada J2S 8E3. of a 60-cm diameter bowl fixed to the top of an agitation shaft, where
ChampagneC@em.agr.ca calcium-ion-rich media is continuously recirculated from the bulk
solution to the bowl. The rotation of the shaft and bowl creates a
climbing film (vortex) of solution. An atomizing disk centrally recessed
within the bowl sprays an alginate solution into the climbing film where
the droplets harden into beads. The effect of heat treatment on the
alginate solution on resulting bead properties was examined. The
sterilization operation did not appear to have a major effect on the
alginate bead mechanical properties of firmness and elasticity which
was much more a function of alginate concentration. Beads of various
sizes were produced by the unit. The system was characterized by the
dimensionless numbers Reomega = (omega x rho x D(2))/mu a
2 Production and characterization of a Bhushan B J Appl Microbiol 2000 May;88(5):800- MTCC & Gene Bank, Environmental 2000 production, chitinase, Bacillus sp., An alkalophilic, environmental micro-organism, Bacillus sp. BG-11,
thermostable chitinase from a new 8 Biotechnology Laboratory, Institute of has been isolated and characterized. It produced 76 U ml-1 of
alkalophilic Bacillus sp. BG-11. Microbial Technology, Chandigarh, chitinase in liquid batch fermentation after 72 h of incubation at 50
India. bharat@lion.imtech.ernet.in degrees C using chitin-enriched medium. The molecular weight of
purified chitinase was estimated to be 41 kDa by SDS-PAGE. The pH
and temperature optima of chitinase immobilized on chitosan and
calcium alginate were 8.5 and 50 degrees C, respectively, which were
same as that of free enzyme. The pH and thermostability of
immobilized chitinase were enhanced significantly. The chitinase
immobilized on chitosan was stable between pH 5.0 and 10.0, and the
half-life of chitosan-immobilized enzyme at 70, 80 and 90 degrees C
was 90, 70 and 60 min, respectively. The end-products formed during
the enzyme-substrate reaction were identified by 13C-NMR, and N-
acetyl-D-glucosamine was found to be the major end-product. GlcNAc
(GlcNAc)2 and (GlcNAc)3 inhibited the chitinase activity by 32, 25 and
18%, respectively, at a concentr
3 Alginate hydrogel microspheres and Senuma Y, Lowe C, Zweifel Y, Biotechnol Bioeng 2000 Mar Polymer Laboratory, Swiss Federal 2000 alginate, hydrospheres, production Our spinning disk atomization (SDA) can, relative to other existing
microcapsules prepared by spinning Hilborn JG, Marison I 5;67(5):616-22 Institute of Technology Lausanne, CH- techniques, produce micron-sized particles with very narrow size
disk atomization. 1015 Lausanne EPFL, Switzerland. distribution. The aim of this work is to present this technology for the
production of alginate microspheres and microcapsules. We atomized
and gelled aqueous alginate solutions into very narrowly dispersed
microspheres with sizes ranging from 300 to 600 microm. Here, the
interest is to produce, at high rate, particles of a given size with a
narrow size distribution and also to show a new method of
encapsulation using SDA. The viscosity and flow rate contributions in
the drop formation is qualitatively analyzed to show how they affect
droplet size. In addition, a technique for high degree of encapsulation
is presented in which yeast is used as a model system. The
production of yeast-loaded microspheres by SDA shows the potential
of the technique for biotechnology applications. Copyright 2000 John
Wiley & Sons, Inc.
4.11 Literatures on Polysaccharides.xls - page 345
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
4 Regulation of alginate biosynthesis in Fakhr MK, Penaloza-Vazquez A, J Bacteriol 1999 Jun;181(11):3478- Department of Microbiology and 1999 exopolysaccharide, alginate, Both Pseudomonas aeruginosa and the phytopathogen P. syringae
Pseudomonas syringae pv. syringae. Chakrabarty AM, Bender CL 85 Molecular Genetics, Oklahoma State regulation, production, gene, produce the exopolysaccharide alginate. However, the environmental
University, Stillwater, Oklahoma pseudomonas, aeruginosa, signals that trigger alginate gene expression in P. syringae are
74078, USA. syringae, different from those in P. aeruginosa with copper being a major signal
in P. syringae. In P. aeruginosa, the alternate sigma factor encoded
by algT (sigma22) and the response regulator AlgR1 are required for
transcription of algD, a gene which encodes a key enzyme in the
alginate biosynthetic pathway. In the present study, we cloned and
characterized the gene encoding AlgR1 from P. syringae. The
deduced amino acid sequence of AlgR1 from P. syringae showed 86%
identity to its P. aeruginosa counterpart. Sequence analysis of the
region flanking algR1 in P. syringae revealed the presence of argH,
algZ, and hemC in an arrangement virtually identical to that reported
in P. aeruginosa. An algR1 mutant, P. syringae FF5.32, was defective
in alginate production but could be complemented when algR1 was
expressed in trans. The alg
5 Synthesis of the A-band polysaccharide Rocchetta HL, Pacan JC, Lam JS Mol Microbiol 1998 Sep;29(6):1419- Department of Microbiology and 1998/99 pseudomonas, aeruginosa, Pseudomonas aeruginosa is capable of producing various cell-surface
sugar D-rhamnose requires Rmd and 34 Published erratum appears in Mol Canadian Bacterial Diseases polysaccharides, production, cell- polysaccharides including alginate, A-band and B-band
WbpW: identification of multiple AlgA Microbiol 1999 Jan;31(1):397-8 Network, University of Guelph, ON. surface, alginate, lipopolysaccharides (LPS). The D-mannuronic acid residues of
homologues, WbpW and ORF488, in lipopolysaccharides alginate and the D-rhamnose (D-Rha) residues of A-band
Pseudomonas aeruginosa. polysaccharide are both derived from the common sugar nucleotide
precursor GDP-D-mannose (D-Man). Three genes, rmd, gmd and
wbpW, which encode proteins involved in the synthesis of GDP-D-
Rha, have been localized to the 5' end of the A-band gene cluster. In
this study, WbpW was found to be homologous to phosphomannose
isomerases (PMIs) and GDP-mannose pyrophosphorylases (GMPs)
involved in GDP-D-Man biosynthesis. To confirm the enzymatic
activity of WbpW, Escherichia coli PMI and GMP mutants deficient in
the K30 capsule were complemented with wbpW, and restoration of
K30 capsule production was observed. This indicates that WbpW, like
AlgA, is a bifunctional enzyme that possesses both PMI and GMP
activities for the synthesis of GDP-D-Man. No gene encoding a
phosphomannose mutase
6 Effect of nutrients on alginate synthesis Sabry SA, Ghanem KM, Sabra Microbiologia 1996 Dec;12(4):593-8 Department of Botany and 1996 nutrient, alginate, production, The role of nutrients on alginate production by Azotobacter vinelandii
in Azotobacter vinelandii and WA Microbiology, Faculty of Science, Azotobacter vinelandii was studied in batch cultures. The largest amount of bacterial alginate
characterization of the produced Alexandria University, Egypt. was obtained in presence of: 0.3 g/l MgSO4.7H2O. 0.4 g/l NaCl, 42
alginate. mg/l CaCl2.2H2O,.4 mg/l KH2PO4, 16 mg/l K2HPO4, 2.5 mg/l
FeSO4.7H2O, 2.9 mg/l H3BO3, 2 mg/l ZnSO4.7H2O, 2 mg/l
Na2MoO4.2H2O, 0.3 mg/l CuSO4.5H2O, 0.2 mg/l MnCl2.4H2O.
Alginate production was not enhanced by natural additives or inducing
agents, except for acetate, which increased alginate yield. The pure
alginate contained 0.36% ash and 0.4% protein. It is similar to algal
alginate, but it has an extra acetyl group. It contains 69.5% M-M block,
27.5% M-G block and 3% G-G block.
7 Anaerobic production of alginate by Hassett DJ J Bacteriol 1996 Dec;178(24):7322-5 Department of Molecular Genetics, 1996 pseudomonas, aeruginosa, Pseudomonas aeruginosa produced alginate and elevated algD
Pseudomonas aeruginosa: alginate Biochemitsry and Microbiology, production, alginate, anaerob, (encoding GDPmannose 6-dehydrogenase) transcription under strict
restricts diffusion of oxygen. University of Cincinnati College of nitrate anaerobic conditions, especially when using nitrate as a terminal
Medicine, Ohio 45257-0524, USA. electron acceptor. Purified alginate added to bacterial suspensions
hassetdj@ucbeh.san.uc.edu caused a decrease in growth, suggesting that alginate contributes to
oxygen limitation for the organism and likely for patients afflicted with
the inherited autosomal disease cystic fibrosis.
4.11 Literatures on Polysaccharides.xls - page 346
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
8 Alginates of Pseudomonas aeruginosa: Schmitt-Andrieu L, Hulen C C R Acad Sci III 1996 Departement de biologie, universite 1996 Pseudomonas aeruginosa is an opportunistic pathogen causing
a complex regulation of the pathway of Mar;319(3):153-60 de Cergy-Pontoise, France. severe infections, especially in lungs of patients with cystic fibrosis.
biosynthesis.[Article in French] Environmental conditions induce the production by the bacteria of a
viscous mucoid exopolysaccharide, called alginate, which is one of
the most important factor of virulence of P. aeruginosa. Alginate is a
linear polymer of beta-1, 4-linked L-guluronic acid and D-mannuronic
acid. The alginate biosynthetic pathway involves genes called alg
which are clustered at the 34 min region of chromosomal DNA of P.
aeruginosa. The key enzyme of alginate biosynthesis, the GDP-
mannose dehydrogenase is encoded by the gene algD. Expression of
algD is positively controlled by several proteins, especially AlgU, a
putative sigma factor homologous to sigma E of E. coli, AlgR and
AlgP, a transactivator and an histone-like respectively. Here, a
scheme of alginate biosynthetic pathway and a model for the alg
genes regulation are described from results published in literature and
from our own interpret
9 Copper as a signal for alginate Kidambi SP, Sundin GW, Palmer Appl Environ Microbiol 1995 Department of Plant Pathology, 1995 copper, CuSO4, alginate Plant-associated pseudomonads are commonly exposed to copper
synthesis in Pseudomonas syringae pv. DA, Chakrabarty AM, Bender CL Jun;61(6):2172-9 Oklahoma State University, Stillwater bactericides, which are applied to reduce the disease incidence
syringae. 74078-9947, USA. caused by these bacteria. Consequently, many of these bacteria have
acquired resistance or tolerance to copper salts. We recently
conducted a survey of 37 copper-resistant (Cur) Pseudomonas spp.,
including P. cepacia, P. fluorescens, P. syringae, and P. viridiflava,
and found that a subset of the P. syringae strains showed a dramatic
increase in exopolysaccharide (EPS) production on mannitol-
glutamate medium containing CuSO4 at 250 micrograms/ml. A
modified carbazole assay indicated that the EPS produced on copper-
amended media contained high levels of uronic acids, suggesting that
the EPS was primarily alginic acid. Uronic acids extracted from
selected strains were further confirmed to be alginate by
demonstrating their sensitivity to alginate lyase and by descending
paper chromatography following acid hydrolysis. Subinhibitory levels
of arsenate, cobalt, lithium, rubidium, molybdenum,
10 Production of purified alginates suitable Klock G, Frank H, Houben R, Appl Microbiol Biotechnol 1994 Lehrstuhl fur Biotechnologie, 1994 production, alginates, purified Alginate is used as a matrix for immunoisolation of cells and tissues in
for use in immunoisolated Zekorn T, Horcher A, Siebers U, Jan;40(5):638-43 Biozentrum-Am Hubland, University of vivo. We have demonstrated previously that commercial alginates
transplantation. Wohrle M, Federlin K, Wurzburg, Germany. contain various fractions of mitogenic impurities and that they can be
Zimmermann U removed by free flow electrophoresis. The use of purified material is a
necessity in order to reveal the parameters that control
biocompatibility of the implanted material (such as stability, size,
surface charge and curvature, etc.). In this study, we present a
protocol for the chemical purification of alginates on a large-scale.
Beads made from alginates purified by this multi-step chemical
extraction procedure did not induce a significant foreign body reaction
when implanted for 3 weeks either intraperitoneally or beneath the
kidney capsule of Lewis or non-diabetic BB/Gi rats.
4.11 Literatures on Polysaccharides.xls - page 347
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
11 Synthesis of lipopolysaccharide O side Goldberg JB, Hatano K, Pier GB J Bacteriol 1993 Mar;175(6):1605-11 Channing Laboratory, Department of 1993 lipopolysaccharide, We have cloned a lipopolysaccharide (LPS) biosynthetic gene from
chains by Pseudomonas aeruginosa Medicine, Brigham and Women's phosphomanomutase, Pseudomonas aeruginosa PAO1 that complements the defect in the
PAO1 requires the enzyme Hospital, Harvard Medical School, production and incorporation of LPS O side chains in the LPS-rough
phosphomannomutase. Boston, Massachusetts 02115-5899. strain AK1012. This gene was characterized by pulsed-field gel
electrophoresis, deletion and restriction mapping of the cloned DNA,
and biochemical analysis of the protein product. The cloned DNA was
found to map to the 7-to-11-min region of the P. aeruginosa
chromosome, and the gene needed for complementation of the LPS-
rough phenotype was contained on a 2.6-kb HindIII-SacI fragment.
This same size restriction fragment contains the alginate gene algC,
which encodes the enzyme phosphomannomutase (PMM) and also
maps to this region of the P. aeruginosa chromosome. The LPS-rough
strain AK1012 was deficient in PMM activity, and this activity was
restored to parental levels when the cloned gene was transferred to
strain AK1012. In addition, the cloned gene could complement the
PMM deficiency in the algC mutant strain 8858,
12 Oxygen-dependent alginate synthesis Leitao JH, Sa-Correia I J Gen Microbiol 1993 Mar;139 ( Pt Laboratorio de Engenharia 1993 alginate, oxygen, production, Alginate production by the highly alginate-producing Pseudomonas
and enzymes in Pseudomonas 3):441-5 Bioquimica, Instituto Superior aeruginosa 8821M was maximal at a dissolved oxygen tension (DOT)
aeruginosa. Tecnico, Lisboa, Portugal. of 5% of air saturation. Lower DOT limited growth and alginate
synthesis. At higher DOT values up to 70% of air saturation, the
specific alginate production rate decreased. Nevertheless, the
molecular mass of the alginate increased at higher aerations, as
indicated by the viscosity of solutions of the isolated biopolymer. The
specific activity of the four enzymes leading to GDP-mannuronic acid
formation, phosphomannose isomerase (PMI), phosphomannomutase
(PMM), GDP-mannose pyrophosphorylase (GMP) and GDP-mannose
dehydrogenase (GMD), increased with DOT of up to 25%. At higher
DOT, however, only GMP and GMD maintained their maximum
values. Changes observed at high oxygen concentrations in the
relative activities of PMI and GMP, which are activities of the same
bifunctional protein, were attributed to the much higher sensitivity of
PMI activity to irreversible oxidative inactivation.
13 Continuous chitosan hydrolyzate Yamasaki Y, Fukumoto I, Biosci Biotechnol Biochem 1992 Applied Biological Sciences, Faculty 1992 chitosan, alginate, Enterobacter Chitosanolytic enzymes from Enterobacter sp. G-1 were immobilized
production by immobilized Kumagai N, Ohta Y, Nakagawa T, Oct;56(10):1546-51 of Agriculture, Shimane University, on various carriers to continuously hydrolyze chitosan. Four different
chitosanolytic enzyme from Kawamukai M, Matsuda H Matsue, Japan. carriers were tested: FE-3901 (strong basic anion exchange resin,
Enterobacter sp. G-1. ionic binding), glutaraldehyde-treated FE-4612 (weak basic anion
exchange resin, cross-linking), Chitopearl (chitosan beads), and
alginate calcium. Glutaraldehyde-treated FE-4612 and Chitopearl
immobilized more protein than the others. The enzyme immobilized on
FE-3901 had the greatest activity. The activity of enzyme immobilized
on FE-3901 decreased rapidly when exposed to a continuous flow of
1% chitosan. The enzyme immobilized with Chitopearl retained more
than 50% of its original activity after 17 days, and the activity was fully
restored by re-immobilization.
4.11 Literatures on Polysaccharides.xls - page 348
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
14 Production of alginate beads by Poncelet D, Lencki R, Beaulieu C, Appl Microbiol Biotechnol 1992 INRS-Sante, Universite du Quebec, 1992 alginate, microspheres, beads, Small diameter alginate beads (microspheres) were formed via
emulsification/internal gelation. I. Halle JP, Neufeld RJ, Fournier A Oct;38(1):39-45 Pointe-Claire, Canada. internal gelation of alginate solution emulsified within vegetable oil.
Methodology. Gelation was initiated by addition of an oil-soluble acid thereby
reducing the pH of the alginate solution and releasing soluble Ca2+
from the citrate complex. Smooth, spherical, micron-sized beads were
formed. The mean diameter ranged from 200 to 1000 microns,
controlled by the reactor impeller design and rotational speed. The
technique has potential for large-scale and continuous applications in
immobilization.
15 Production of exocellular De la Vega MG, Cejudo FJ, Appl Biochem Biotechnol 1991 Instituto de Bioquimica Vegetal y 1991 polysaccharide, Azotobacter Environmental conditions affect the production of extracellular
polysaccharide by Azotobacter Paneque A Sep;30(3):273-84 Fotosintesis, Universidad de Sevilla- chroococcum, production, polysaccharide by Azotobacter chroococcum ATCC 4412. Production
chroococcum. Consejo Superior de Investigaciones affection, environmental conditions of exocellular polymer from a variety of carbon sources depended on
Cientificas, Spain. the air flow rate. A high sucrose concentration in medium (8%)
markedly favored expopolysaccharide production, which reached 14
g/L in about 72 h. In cell suspensions incubated in the presence of 8%
sucrose in a nitrogen-free medium, biopolymer final concentration of 9
g/L corresponds to 68 g/g biomass. Maximum efficiency of sucrose
conversion into exopolysaccharide peaked at 70% for initial
disaccharide concentration of 6%. High performance liquid
chromatography and gas liquid chromatography of acid hydrolysates
of the exopolymer revealed the presence of mannuronosyl,
guluronosyl, and acetyl residues, but not neutral sugars. The infrared
spectrum corroborated the presence of carboxylate anions and O-
acetyl groups in the exopolymer. Though the presence of more than
one kind of polysaccharide cannot be ruled out, thes
16 Alginate biosynthesis in mucoid Martins LO, Sa-Correia I Enzyme Microb Technol 1991 Laboratorio de Engenharia 1991 alginate, biosynthesis, organisms The Pseudomonas aeruginosa algD gene, encoding GDP-mannose
recombinants of Pseudomonas May;13(5):385-9 Bioquimica, Instituto Superior dehydrogenase (GMD) and cloned at Chakrabarty's Laboratory in the
aeruginosa overproducing GDP- Tecnico, Lisboa, Portugal. expression vector pMMB24 (plasmid pVD211), was mobilized into
mannose dehydrogenase. P.aeruginosa strains 8821 and 8821M. Strain 8821M was a high-
alginate-producing variant, spontaneously obtained from mucoid
strain 8821, with derepressed levels of GMD, a key enzyme in the
regulation of alginate biosynthesis, leading to the irreversible
oxidation of GDP-mannose to GDP-mannuronic acid. A slight increase
in the level of GMD, in both strains harboring the plasmid pVD211 and
batch-grown at 37 degrees C without IPTG induction, led to the
increase of production rate and the final concentration of alginate
produced by control strains harboring the cloning vector. However, the
viscosity of the aqueous solutions prepared with the alginate (3 g l-1)
produced by mucoid strains harboring pVD211 was lower than those
with the alginate produced by the controls (shear rates in the range
0.6-12 s-1). The specific activity of
4.11 Literatures on Polysaccharides.xls - page 349
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
17 Oxygen-dependent up-regulation of Bayer AS, Eftekhar F, Tu J, Nast Infect Immun 1990 May;58(5):1344-9 Department of Medicine, Harbor- 1990 exopolysaccharide, Pseudomonas We previously showed substantial differences in Pseudomonas
mucoid exopolysaccharide (alginate) CC, Speert DP UCLA Medical Center, Torrance aeruginosa, alginate, regulation, aeruginosa exopolysaccharide production in vitro at oxygen tensions
production in Pseudomonas 90509. production, reflective of the right versus left cardiac circuits in vivo (40 versus 80
aeruginosa. mm Hg, respectively; A. S. Bayer, T. O'Brien, D. C. Norman, and C. C.
Nast, J. Antimicrob. Chemother. 23:21-35, 1989). However, those
studies did not specifically confirm this exopolysaccharide to be the
characteristic P. aeruginosa mucoid alginate seen in patients with
cystic fibrosis. With a murine monoclonal antibody prepared against
P. aeruginosa alginate, strongly positive immunofluorescence (IF)
staining of a nonmucoid P. aeruginosa strain (PA-96) was seen after
its exposure in vitro to oxygen tensions (pO2) of approximately 80 mm
Hg; the intensity of the IF staining under these conditions was similar
to that observed with a phenotypically mucoid P. aeruginosa strain
(C1712M) from a cystic fibrosis patient. In contrast, the same
nonmucoid strain (PA-96), after exposure to pO2 of approximately 40
mm Hg, s
18 Alginate production by clinical Anastassiou ED, Mintzas AC, J Clin Microbiol 1987 Apr;25(4):656- 1987 alginate, production, nonmucoid, The slime material from a revertant nonmucoid variant, derived by
nonmucoid Pseudomonas aeruginosa Kounavis C, Dimitracopoulos G 9 Pseudomonas serial passage of a heavily mucoid Pseudomonas aeruginosa strain
strains. isolated from a patient with bacteremia, was found to contain 16%
uronic acids, 48.5% carbohydrates, 11% protein, and 2% lipids.
Chromatographic analysis by ion exchange chromatography revealed
that this extracellular material consisted of three fractions, one uronic
acid fraction with properties similar to those of the alginate fraction of
the parental strain and two other fractions consisting of neutral sugars
and proteins in approximately a 5:1 ratio. In addition, the slime
material from six other clinical macroscopic nonmucoid P. aeruginosa
strains was found to contain alginate. These results demonstrate that
alginate production in various amounts is a property shared by all P.
aeruginosa strains.
19 Alginate biosynthesis by Pseudomonas Banerjee PC Arch Microbiol 1986 Sep;145(4):408- 1986 Biosynthesis, inhibitors, alginic Biosynthesis of alginic acid in presence of metabolic inhibitors by
aeruginosa: effect of arsenite and other 10 acid resting cells of mucoid Pseudomonas aeruginosa was studied. Among
metabolic inhibitors. the inhibitors tested, arsenite exhibited very interesting results, while
the others showed no remarkable effect. Firstly, arsenite stopped
alginate production from all the substrates during initial hours of
incubation; secondly, degradation of newly synthesized alginates to
smaller molecular weight fragments took place if it was added after a
few hours of incubation with the substrate; and thirdly, uncontrolled
synthesis of alginate started after several hours of inhibition.
Presence of arsenite was needed for the initial inhibitory phase of
alginate synthesis; but once the cells were capable of synthesizing
alginate after initial hours of inhibition, arsenite may be omitted from
the medium.
4.11 Literatures on Polysaccharides.xls - page 350
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
20 Polysaccharide production and the Couperwhite I, McCallum MF Antonie Van Leeuwenhoek 1975 Azotobacter vinelandii, During the growth of Azotobacter vinelandii in batch culture in Burk's
possible occurrence of GDP-D- 1975;41(1):25-32 polysaccharide, production, 2% glucose medium supplemented with 50 mg EDTA per litre, water-
mannose dehydrogenase in insoluble capsular polysaccaride material accumulated in cultures
Azotobacter vinelandii. prior to the appearance of water-soluble polysaccharide in the culture
medium. On isolation, hydrolysis and chromatography, both these
polysaccharides were observed to be composed of carbohydrate
monomers having the same chromatographic mobilities as glucose,
rhamnos, guluronic acid and mannuronic acid. The activity of GDP-D-
mannose dehydrogenase recorded in crude cell-free extracts from
Azotobacter vinelandii, when these polysaccharides were produced,
may indicate a close similarity between the biosynthetic pathway of
alginate synthesis in marine Phaeophyceae and this soil
microorganism.
21 A new process for the production of Kim D, Day DF Enzyme Microb Technol 1994 Department of Microbiology, 1994 dextran, fermentation, production A mixed-culture fermentation system was designed for the production
clinical dextran by mixed-culture Oct;16(10):844-8 Louisiana State University, Baton of size-limited dextrans. This process was simpler and more
fermentation of Lipomyces starkeyi and Rouge. economical than traditional methods. It required the establishment of
Leuconostoc mesenteroides. microbial consortia of Lipomyces starkeyi ATCC 74054 and
Leuconostoc mesenteroides ATCC 10830. Controlling initial
conditions, growth, and enzyme production by both organisms
controlled the product size. In this process, both strains were grown
separately and then mixed. Dextran fermentation was then allowed to
proceed. At the desired time (and molecular size), the fermentation
was harvested. The optimum pH and temperature for production of
clinical dextran (75,000 MW) were 5.2 (+/- 0.1) and 28 (+/- 0.5)
degrees C, respectively. Varying the ratio of L. mesenteroides to L.
starkeyi in the inoculum did not significantly affect either the final cell
ratios or dextran production.
22 Characterisation of and polysaccharide Marsh PD, West AA, Keevil CW J Med Microbiol 1987 Nov;24(3):259- Bacterial Metabolism Research 1987 glucosyltransferases, Small numbers of bacteria capable of growing on agar supplemented
production by amoxycillin-resistant 62 Laboratory, PHLS Centre for Applied polysaccharide production with amoxycillin 40 mg/L were isolated from the saliva of 9 out of 20
streptococci. Microbiology and Research, adult volunteers in a previous study. All the bacteria were identified as
Salisbury, Wiltshire. Streptococcus sanguis although no strains produced dextran in
conventional tests. However, using a specific assay, all the antibiotic-
resistant strains were found to secrete glucosyltransferases (GTF),
the enzymes that synthesise these extracellular polysaccharides; the
production of GTF-S, the enzyme that synthesizes dextran, was 22-
43% less than that of an antibiotic-sensitive control strain. Enzyme
production by both antibiotic-resistant and sensitive bacteria was
markedly inhibited by dextran primer. The amoxycillin-resistant
bacteria were resistant to other penicillins; their resistance to
erythromycin was variable but they were uniformly sensitive to
cephalothin and clindamycin. As dextran production has been
proposed as a key factor in the colonisation of damaged heart valves
by bacteria such as
23 Studies on production of pullulan by the Sun W, Zhou T, Xie H, Jiang N, Chin J Biotechnol 1999;15(2):121-8 State Key Laboratory of Microbial 1999 pullulan, production, fed-batch The feed-batch fermentaStudies on production of pullulan by the feed
feed batch fermentation. Ren Y Resources, Chinese Academy of batch fermentation. tion of pullulan was investigated based on the
Sciences, Beijing, China. conditions of batch fermentation. The optimal conditions of pullulan
fermentation were determined by the investigation on the effect of
feed mode, initial feed time, intermittent time, and composition of the
feed solution on parameters such as productivity, conversion yield,
biomass, dissolved oxygen (DO), pH of the fermentation broth,
viscosity of the fermentation broth and molecular weight of the
product. Above 70% of conversion yield and 100 kD of average
molecular weight of the product was obtained at the optimal
conditions.
4.11 Literatures on Polysaccharides.xls - page 351
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
24 Effect of nitrogen source on pullulan West TP, Strohfus B Microbios 1999;99(394):147-59 Olson Biochemistry Laboratories, 1999 pullulan, production, nitrogen Pullulan production by Aureobasidium pullulans ATCC 201253 using
production by Aureobasidium pullulans Department of Chemistry and selected nitrogen sources was studied in a medium using corn syrup
grown in a batch bioreactor. Biochemistry, South Dakota State as a carbon source. Independent of the corn syrup concentration
University, Brookings 57007, USA. present, the use of corn steep liquor or hydrolysed soy protein as a
nitrogen source instead of ammonium sulphate did not elevate
polysaccharide production by ATCC 201253 cells grown in an
aerated, batch bioreactor containing 4 litres of medium. Pullulan
production on corn steep liquor or hydrolysed soy protein as a
nitrogen source became more comparable as the concentration of
corn syrup was increased. Cell weights after 7 days of growth on any
of the nitrogen sources were similar. The viscosity of the
polysaccharide on day 7 was highest for cells grown on ammonium
sulphate and 12.5% corn syrup. The pullulan content of the
polysaccharide elaborated by ammonium sulphate-grown cells on day
7 decreased as the corn syrup level rose in the medium while the
pullulan content of polysaccharide produced by cells grown on cor
25 Pullulan production by Aureobasidium West TP, Strohfus B Microbios 1996;88(354):7-18 Olson Biochemistry Laboratories, 1996 pullulan production, Pullulan production by Aureobasidium pullulans strain RP-1 using thin
pullulans grown on ethanol stillage as a Department of Chemistry and stillage from fuel ethanol production as a nitrogen source was studied
nitrogen source. Biochemistry, South Dakota State in a medium using corn syrup as a carbon source. The use of 1% thin
University, Brookings 57007, USA. stillage as a nitrogen source instead of ammonium sulphate elevated
polysaccharide production by strain RP-1 cells when grown on a
concentration of up to 7.5% corn syrup, independent of yeast extract
supplementation. Dry weights of cells grown in medium containing
ammonium sulphate as the nitrogen source were higher than the
stillage-grown cells after 7 days of growth. The viscosity of the
polysaccharide on day 7 was higher for cells grown on thin stillage
rather than ammonium sulphate as a nitrogen source. The pullulan
content of the polysaccharide elaborated by ammonium sulphate-
grown cells on day 7 was higher than the pullulan content of
polysaccharide produced by stillage-grown cells regardless of whether
yeast extract was added to the culture medium.
26 Studies on the condition of fermentation Sun W, Zhou T, Xie H, Ren Y, Chin J Biotechnol 1994;10(4):283-90 Institute of Microbiology, Chinese 1994 pullulan production, Studies on optimal conditions for pullulan fermentation based on the
of pullulan by Aureobasidium pullulans. Jiang N Academy of Sciences, Beijing, China. results obtained from a shaking flask were carried out in a 16-L auto-
controlling fermentor. It found that the optimal DE value of starch
hydrolyzate was 40-50 when 10% starch hydrolysate was used as
carbon source. The optimal concentration of ammonium sulfate in the
medium for fermentation was different from that of the shaking flask.
The fermentation kinetics and effects of seed age, seed volume,
airflow rate, pressure of tank, agitation speed and number of vane
group on the production of pullulan were investigated.
27 Flow injection analysis with immobilized Englbrecht U, Schmidt HL J Chem Technol Biotechnol Lehrstuhl fur Allgemeine Chemie und 1992 flow injection system, pullulan A flow injection system is described for the parallel determination of
enzymes for process control of pullulan 1992;53(4):397-400 Biochemie, Technische Universitat production, pullulan and glucose during a fermentation of the fungus
production by fermentation. Munchen, Freising-Weihenstephan, Aureobasidium pullulans. The polysaccharide was hydrolyzed by
Germany. pullulanase and amyloglucosidase, immobilized to controlled-pore
glass (CPG). The glucose produced was oxidized by glucose
dehydrogenase and the NADH formed determined photometrically.
The pullulan concentration was calculated from the difference to the
response obtained for free glucose. The calibration curves for
monomer and polymer were both linear between 2 mg dm-3 and 20
mg dm-3. Analysis of one sample for the determination of glucose and
pullulan took about 10 min.
4.11 Literatures on Polysaccharides.xls - page 352
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
28 Production of pullulan [Article in Behrens U, Lohse R Nahrung 1977;21(3):199-204 1977 pullulan production, optimum Optimum conditions for the production of pullulan by Pullularia
German] conditions pullulans were elaborated by examinating growth and production with
different carbohydrates and mixtures of carbohydrates. With starch
hydrolysates or mixtures of starch and simple sugars, p.e. glucose or
saccharose, better results were achieved than with simple sugars
alone or with starch. Condtions for optimum pullulan production are
fast undisturbed growth, mediated by fast utilizable simple sugars like
glucose followed by a substantial decreased growth rate in which
production occurs, mediated by a sufficient supply of nutrite
substances and a slow utilizable carbohydrate like starch.
29 Production and purification of protease Yang J, Shih I, Tzeng Y, Wang S Enzyme Microb Technol 2000 Mar Department of Food Engineering, Da- 2000 Bacillus subtilis, crustacean waste, A protease-producing microorganism was isolated in northern Taiwan
from a Bacillus subtilis that can 1;26(5-6):406-413 Yeh University, Chang-Hwa, Taiwan chitin production, deproteinization and identified as a strain of Bacillus subtilis. B. subtilis Y-108 thus
deproteinize crustacean wastes*. isolated can be used for deproteinization of crustacean wastes in the
preparation of chitin. For deproteinization tests, liquid phase
fermentation of untreated shrimp shell, crab shell, and lobster shell
wastes with this microbe showed protein removal of 88, 67, and 83%,
respectively. In contrast, the protein removal of the acid treated
wastes was 76, 62, 56%, respectively. The optimized conditions for
protease production was found when the culture was shaken at 30
degrees C for 3 days in 100 ml of medium (phosphate buffer adjusted
to pH 6.0) containing 7% shrimp and crab shell powder (SCSP), 0.1%
K(2)HPO(4), 0.05% MgSO(4), 1.0% arabinose, 1.5% NaNO(3), and
1.5% CaCl(2). Under such conditions, the protease of B. subtilis Y-
108 attained the highest activity. It was as high as 20.2 U/ml. The
protease was purified in a three-step procedure involving ammonium
sulfate precipita
30 Production of a recombinant chitin Tokuyasu K, Kaneko S, Hayashi FEBS Lett 1999 Sep 10;458(1):23-6 National Food Research Institute, 1999 chitin, deacetylase, Escherichia With the aid of a signal sequence of a chitinase from Streptomyces
deacetylase in the culture medium of K, Mori Y Tsukuba, Japan. coli, lividans, a recombinant chitin deacetylase, whose gene originated
Escherichia coli cells. tokuyasu@nfri.affrc.go.jp from a Deuteromycete, Colletotrichum lindemuthianum, was produced
in the culture medium of Escherichia coli cells, existing as a highly
active form without the signal peptide. During the production of the
recombinant chitin deacetylase, both a slight increase in the value of
OD600 nm in the culture medium and a drastic decrease in viable cell
number were observed. When penta-N-acetyl-chitopentaose was
used as the substrate, the recombinant chitin deacetylase had
comparable kinetic parameters to those of the original enzyme from
the fungus. The addition of a C-terminal six histidine sequence to the
recombinant enzyme caused a slight decrease in the kcat value, and
the further addition of a 12 amino acid sequence at its N-terminus
caused a further decrease in the value. This production system
allowed us to easily produce in the culture media the recombinant
chitin deacetylases pos
4.11 Literatures on Polysaccharides.xls - page 353
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
31 Chitin biosynthesis during Selitrennikoff CP, Allin D, Proc Natl Acad Sci U S A 1976 1976 chitin, biosynthesis, Blastocladiella De novo construction of a chitinous cell wall accompanies
Blastocladiella zoospore germination: Sonneborn DR Feb;73(2):534-8 zoospore Blastocladiella emersonii zoospore germination. At least an order of
evidence that the hexosamine magnitude increase in total hexosamine occurs during germination.
biosynthetic pathway is post- This increase is into polymer (chitin) and occurs on schedule in the
translationally activated during cell presence of cycloheximide. Uridine-5'-diphospho-N-
differentiation. acetylglucosamine (UDPGlcNAc), both the end product of hexosamine
biosynthesis and a substrate for chitin biosynthesis, is a potent
inhibitor of the activity of the first pathway-specific enzyme of
hexosamine biosynthesis in zoospore extracts. Certain uridine
nucleotides, not perceptibly influencing the activity of the first enzyme
per se, counteract the inhibitory effects of UDPGlcNAc. The
concentration of UDPGlcNAc in the zoospore is sufficient to act as an
inhibitor of the enzyme, but the amount of UDPGlcNAc is sufficient, by
over an order of magnitude, to account for the chitin synthesized
during germination. Both the production of UDPGlcNAc and its
utilization for chitin synthesis appear to be post
32 Chitin synthase in Mortierella vinacea: Peberdy JF, Moore PM J Gen Microbiol 1975 Oct;90(2):228- 1975 chitin, synthase, Mortierella Chitin synthase of Mortierella vinacea was present in the "microsomal'
properties, cellular location and 36 vinacea fraction (100 000 g precipitate), the 'cell-wall' fraction (2000 g
synthesis in growing cultures. precipitate) and the 'mitochondrial' fraction (10 000 g precipitate). The
properties of the 'microsomal' enzyme were investigated. The pH
optimum was between 5-8 and 6-2, and the temperature optimum was
between 31 and 33 degrees C. The Km for UDP N-acetyl-D-
glucosamine was 1.8 mM. The enzyme was stimulated by Mg2+ and a
slight stimulation was also effected by N-acetyl-D-glucosamine.
Soluble chitodextrins were inhibitory. A pH-dependent, heat-stable
inhibitor of chitin synthase activity was present in the soluble
cytoplasm from the mycelium. The effects of aeration and glucose
concentration on enzyme production in growing cultures were also
investigated; maximum specific activity of chitin synthase was
associated with the cessation of exponential growth.
33 Production and isolation of chitosan White SA, Farina PR, Fulton I Appl Environ Microbiol 1979 1979 production, isolation, chitosan, A method for the lab-scale production and isolation of chitosan
from Mucor rouxii. Aug;38(2):323-8 Mucor rouxii (polyglucosamine) from hyphal walls of Mucor rouxii was developed.
Hyphal wall yields were generally 16 to 22% on a dry cell weight
basis, of which 35 to 40% was glucosamine. Chitosan was readily
extracted from purified, mycelial walls with acetic, formic, and
hydrochloric acids; the last named was the most efficient. The yield of
chitosan isolated ranged from 4 to 8% of the dry weight of the cell wall
material.
34 Theoretical maximum and observed Phillips KR, Lawford HG Can J Microbiol 1983 1983 curdlan, production, yields, As a guide to both strain and process improvement and based on
product yields associated with curdlan Oct;29(10):1270-6 Alcaligenes faecalis, review certain assumptions concerning both glucose and energy metabolism
production by Alcaligenes faecalis. of the process organism, Alcaligenes faecalis var. myxogenes, the
theoretical "maximum" carbon (glucose) substrate to product
conversion efficiency (i.e., product yield) has been estimated for
"curdlan-type" beta(1 leads to 3)-glucan exopolysaccharide production
in batch fermentations. Under nitrogen limitation, which promotes
curdlan biosynthesis (mu = 0), the rate of glucose consumption for
cellular maintenance energy (grams of glucose per gram of cells per
hour) was approximately five times higher than under carbon
limitation. The decrease in the theoretical "maximum" curdlan
conversion efficiency of 74% to the average value of 50-56% was due
primarily to the high maintenance coefficient of the nitrogen-starved
culture.
4.11 Literatures on Polysaccharides.xls - page 354
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
35 Production of curdlan-type Phillips KR, Pik J, Lawford HG, Can J Microbiol 1983 1983 curdlan, production, batch culture, The biosynthesis of a thermogelable, extracellular homo-beta-(1 leads
polysaccharide by Alcaligenes faecalis Lavers B, Kligerman A, Lawford Oct;29(10):1331-8 coninuous culture, Alcaligenes to 3)-glucan called "curdlan," has been studied in batch and
in batch and continuous culture. GR faecalis, review continuous cultures of Alcaligenes faecalis var. myxogenes. Curdlan
production is associated with the poststationary phase of a nitrogen-
depleted, aerobic batch culture. Exopolymer is not detected in single-
stage, carbon-limited continuous cultures but curdlan can be isolated
from the effluent of a nitrogen-limited chemostat operating at a dilution
rate (D) of less than 0.1 h-1. A spontaneous variant of strain ATCC
21680 was isolated and found to be compatible with long-term,
nitrogen-limited chemostat culture. The specific rate of curdlan
production is approximately four times higher in poststationary batch
cultures than in single-stage continuous fermentations. The product
yield (Yp/S) associated with batch processing (nongrowing cultures) is
approximately 0.5 g curdlan/g glucose, with CO2 being the only
detectable by-product.
36 Special bacterial polysaccharides and Harada T Biochem Soc Symp 1983;48:97-116 1983 bacterial polysaccharides, curdlan, Alcaligenes faecalis var. myxogenes 10C3, which we isolated from
polysaccharases. production, review, Alcaligenes soil, produces a water-soluble and an insoluble extracellular
faecalis polysaccharide. The former (succinoglycan) is composed of glucose,
galactose, pyruvic acid and succinic acid (molar proportions 7:1:1:1)
with (beta 1-3)-, (beta 1-4)- and (beta 1-6)-glucosidic linkages. The
latter (curdlan) is composed entirely of (beta 1-3)-linked D-glucose
and forms a resilient firm gel when heated in suspension. The
organism also produces extracellularly a repeating-unit
octasaccharide of succinoglycan and cyclic (beta 1-2)-D-glucan.
These polymers or oligomers are also produced by many strains of
Agrobacterium and Rhizobium. Spontaneous mutation in ability to
produce these polysaccharides or oligosaccharides occurs in these
strains. The structures of succinoglycan, and similar polymers
containing riburonic acid or galactose as the end residue of the side
chain, were elucidated by successive fragmentation with two special
enzymes obtained from Cytophaga arvensicola
37 Spontaneous mutation of Amemura A, Hisamatsu M, Appl Environ Microbiol 1977 1977 curdlan, production, Alcaligenes Alcaligenes faecalis var. myxogenes 10C3, which produces large
polysaccharide production in Harada T Dec;34(6):617-20 faecalis, spontaneous mutation amounts of succinoglucan and small amounts of curdlan, was
Alcaligenes faecalis var. myxogenes genetically unstable and mutated spontaneously to a form producing
10C3. more curdland than succinoglucan when stocked on nutrient agar
slants. The mutation occurred in the absence of cell division when the
cells were incubated in saline and was enhanced by treatment with N-
methyl-N'-nitro-N-nitrosoguanidine, ethyl methane sulfonate, or
ultraviolet light. Mutant strains were genetically stable and did not
revert spontaneously for at least 1 year when stocked on nutrient agar
slants.
38 Ability of casamino acids to support West TP, Fullenkamp NA Microbios 2000;102(402):89-101 Department of Chemistry and 2000
gellan production by Sphingomonas Biochemistry, South Dakota State
paucimobilis ATCC 31461. University, Brookings 57007, USA.
4.11 Literatures on Polysaccharides.xls - page 355
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
39 Structures and properties of gellan Fialho AM, Martins LO, Donval Appl Environ Microbiol 1999 Centro de Engenharia Biologica e 1999 sphingomonas, gellan The dairy industry produces large quantities of whey as a by-product
polymers produced by sphingomonas ML, Leitao JH, Ridout MJ, Jay AJ, Jun;65(6):2485-91 Quimica, Instituto Superior Tecnico, of cheese production and is increasingly looking for new ways to
paucimobilis ATCC 31461 from lactose Morris VJ, Sa-Correia I 1049-001 Lisbon, Portugal. utilize this waste product. Gellan gum is reliably produced by
compared with those produced from Sphingomonas paucimobilis in growth media containing lactose, a
glucose and from cheese whey. significant component of cheese whey, as a carbon source. We
studied and compared polysaccharide biosynthesis by S. paucimobilis
ATCC 31461 in media containing glucose, lactose (5 to 30 g/liter), and
sweet cheese whey. We found that altering the growth medium can
markedly affect the polysaccharide yield, acyl substitution level,
polymer rheological properties, and susceptibility to degradation.
Depression of gellan production from lactose compared with gellan
production from glucose (approximately 30%) did not appear to occur
at the level of synthesis of sugar nucleotides, which are the donors of
monomers used for biosynthesis of the repetitive tetrasaccharide unit
of gellan. The lactose-derived biopolymer had the highest total acyl
content; the glucose
40 Exopolysaccharides produced by Kleerebezem M, van Kranenburg Antonie Van Leeuwenhoek 1999 Jul- Wageningen Centre for Food 1999 review, polysaccharides, Over the last years, important advances have been made in the study
Lactococcus lactis: from genetic R, Tuinier R, Boels IC, Zoon P, Nov;76(1-4):357-65 Sciences, NIZO food research, Ede, production of the production of exopolysaccharides (EPS) by several lactic acid
engineering to improved rheological Looijesteijn E, Hugenholtz J, de The Netherlands. bacteria, including Lactococcus lactis. From different EPS-producing
properties? Vos WM lactococcal strains the specific eps gene clusters have been
characterised. They contain eps genes, which are involved in EPS
repeating unit synthesis, export, polymerisation, and chain length
determination. The function of the glycosyltransferase genes has been
established and the availability of these genes opened the way to EPS
engineering. In addition to the eps genes, biosynthesis of EPS
requires a number of housekeeping genes that are involved in the
metabolic pathways leading to the EPS-building blocks, the nucleotide
sugars. The identification and characterisation of several of these
housekeeping genes (galE, galU, rfbABCD) allows the design of
metabolic engineering strategies that should lead to increased EPS
production levels by L. lactis. Finally, model development has been
initiated in order to
41 Heteropolysaccharides from lactic acid De Vuyst L, Degeest B FEMS Microbiol Rev 1999 Division of Industrial Microbiology, 1999 review, polysaccharides, Microbial exopolysaccharides are biothickeners that can be added to
bacteria. Apr;23(2):153-77 Fermentation Technology and production, lactic acid, bacteria a wide variety of food products, where they serve as viscosifying,
Downstream Processing (IMDO), stabilizing, emulsifying or gelling agents. Numerous
Faculty of Sciences, Vrije Universiteit exopolysaccharides with different composition, size and structure are
Brussel (VUB), Belgium. synthesized by lactic acid bacteria. The heteropolysaccharides from
ldvuyst@vub.ac.be both mesophilic and thermophilic lactic acid bacteria have received
renewed interest recently. Structural analysis combined with
rheological studies revealed that there is considerable variation
among the different exopolysaccharides; some of them exhibit
remarkable thickening and shear-thinning properties and display high
intrinsic viscosities. Hence, several slime-producing lactic acid
bacterium strains and their biopolymers have interesting functional
and technological properties, which may be exploited towards different
products, in particular, natural fermented milks. However, information
on the biosynthesis, molecular organization and fermentation
conditions is rather scarce, and the
4.11 Literatures on Polysaccharides.xls - page 356
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
42 Alginate production by Azotobacter Clementi F Crit Rev Biotechnol 1997;17(4):327- Dipartimento di Biologia, Difesa e 1997 review, alginates, production Although all commercial alginates are today of algal origin, there is
vinelandii. 61 Biotecnologie Agroforestali, interest in the production of alginate-like polymers from bacteria. The
Universita della Basilicata, Potenza, species Azotobacter vinelandii seems to be the best candidate for the
Italy. industrial production of alginate molecules characterized by a
chemical composition, molecular mass and molecular mass
distribution suited to a well defined application, especially required in
the biotechnological, biomedical and pharmaceutical fields. The
production of alginate by A. vinelandii has been to date widely
investigated both in batch (mainly in the shaken flask scale) and in
continuous cultures. This article summarizes current knowledge on
the structure and properties of alginates and their applications and
presents an overview of up-dated research on the physiology,
genetics and kinetics of the production of alginate by Azotobacter
vinelandii and its rheology, including the results of our recent studies.
43 Bacterial exopolysaccharides--their Sutherland IW Antibiot Chemother 1989;42:50-5 Department of Microbiology, 1989 review, exopolysaccharides, [No abstract available]
nature and production. Edinburgh University, UK polysaccharides, production
44 Special bacterial polysaccharides and Harada T Biochem Soc Symp 1983;48:97-116 1983 review, polysaccharides, bacterial Alcaligenes faecalis var. myxogenes 10C3, which we isolated from
polysaccharases. soil, produces a water-soluble and an insoluble extracellular
polysaccharide. The former (succinoglycan) is composed of glucose,
galactose, pyruvic acid and succinic acid (molar proportions 7:1:1:1)
with (beta 1-3)-, (beta 1-4)- and (beta 1-6)-glucosidic linkages. The
latter (curdlan) is composed entirely of (beta 1-3)-linked D-glucose
and forms a resilient firm gel when heated in suspension. The
organism also produces extracellularly a repeating-unit
octasaccharide of succinoglycan and cyclic (beta 1-2)-D-glucan.
These polymers or oligomers are also produced by many strains of
Agrobacterium and Rhizobium. Spontaneous mutation in ability to
produce these polysaccharides or oligosaccharides occurs in these
strains. The structures of succinoglycan, and similar polymers
containing riburonic acid or galactose as the end residue of the side
chain, were elucidated by successive fragmentation with two special
enzymes obtained from Cytophaga arvensicola
45 Production of microbial Slodki ME, Cadmus MC Adv Appl Microbiol 1978;23:19-54 1978 review, microbial, polysaccharides
polysaccharides.
46 Influence of Zn2+ and Fe3+ on M. Reeslev, B. Jensen Applied Microbiology and Department of General Microbiology, 1995 cultivation aureobasidium Cultivation of Aureobasidium pullulans in medium with a low
polysaccharide production and Biotechnology ISSN: 0175-7598 University of Copenhagen, Solvgade pullulans, pullulan, production concentration of yeast extract (0.4 g/l) led to a decrease in the growth
mycelium/yeast dimorphism of (printed version) ISSN: 1432-0614 83H, 1307 Copenhagen K, Denmark. rate early in the fermentation as compared to cultivations in medium
Aureobasidium pullulans in batch (electronic version) Abstract Volume Fax:+45-35-322040 with high concentration of yeast extract. When this medium was
cultivations 42 Issue 6 (1995) pp 910-915 supplemented with zinc and iron the cultivation closely resembled that
obtained in medium with high concentration of yeast extract (4.0 g/l).
The culture retained a high growth rate throughout the fermentation
and the initiation of the mycelial to yeast (M-Y) transition and the
exopolysaccharide production was delayed. In a defined medium or in
defined medium without iron only a little exopolysaccharide was
produced and the yeast fraction of the total biomass at the onset of
the stationary phase was 22%-25%. However, cultivation in the
defined medium without zinc resulted in a high production of
exopolysaccharide and an increased intensity of the M-Y transition,
which led to a yeast fraction of 41%.
4.11 Literatures on Polysaccharides.xls - page 357
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
47 Enhanced production of pigment-free Y. Shabtai, I. Mukmenev Applied Microbiology and Program for Biotechnology, Ben- 1995 pullulan, production A two-stage fermentation process was established for the production
pullulan by a morphogenetically Biotechnology ISSN: 0175-7598 Gurion University of the Negev, P.O.B of pigment-free pullulan by the yeast-like fungus Aureobasidium
arrested Aureobasidium pullulans (printed version) ISSN: 1432-0614 653, Beer-Sheva 84105, Israel. Fax: pullulans (ATCC 42023). In the first stage, starting at pH 4.5 with soy
(ATCC 42023) in a two-stage (electronic version) Abstract Volume 972-7-472916 bean oil as the carbon source and glutamate as the nitrogen source, a
fermentation with shift from soy bean oil 43 Issue 4 (1995) pp 595-603 cell mass of about 15 g l-1 dry cell weight was obtained, the
to sucrose population being restricted mainly to the yeast form of the
microorganism (yeast form more than 90% of total cells) and the
formation of pigment in the culture being prevented. Small amounts of
pullulan (less than 2 g l-1) are produced at this phase, and the
viscosity remained low throughout the entire growth stage. When the
oil and glutamate source were nearly exhausted (below 5% of initial
amounts), the cells were shifted to a production stage with sucrose as
the carbon source with continued nitrogen depletion. Production of
pullulan started immediately with no lag period. During 50 h of the
production phase more than 35 g l-1 of pullulan was produced
(productivity approx. 0.7
48 Pullulan fermentation in a reciprocating J. Audet, M. Lounes, J. Thibault Bioprocess Engineering ISSN: 0178- Department of Chemical Engineering, 1996 pullulan, production Abstract Reciprocating plate bioreactors are particularly well suited for
plate bioreactor 515X (printed version) ISSN: 1432- Laval University, Sainte-Foy conducting fermentations which give rise to highly viscous broth. To
0797 (electronic version) Abstract (Quebec), Canada, G1K 7P4 evaluate their performance for polysaccharide fermentations, a series
Volume 15 Issue 4 (1996) pp 209- of pullulan fermentations were performed with a particular emphasis
214 placed on the influence of aeration on both the quantity and quality of
the product. Two experiments were conducted at constant aeration
rates and two others with constant dissolved oxygen concentrations.
For the latter two experiments, the dissolved oxygen concentration
was controlled by manipulating either the aeration flow rate or the
reciprocating frequency of the perforated plates. It was found that, in
general, a higher dissolved oxygen concentration leads to a higher
productivity but the quality of the product, expressed in terms of the
viscosity of the fermentation broth, was nevertheless reduced. It
appears that the optimum yield, in terms of both quantity and quality,
would be achieved at an intermediate dissolved oxygen co
49 The production of exopolysaccharides P. A. Gibbs, R. J. Seviour Applied Microbiology and Biotechnology Research Centre, La 1998 pullulan, production No increases in exopolysaccharide (EPS) yields in Aureobasidium
by Aureobasidium pullulans in Biotechnology ISSN: 0175-7598 Trobe University, PO Box 199, pullulans were observed when grown with reduced-shear impellers
fermenters with low-shear (printed version) ISSN: 1432-0614 Bendigo, Victoria, Australia, 3550 instead of standard Rushton turbines in the same vessel. However,
configurations (electronic version) Abstract Volume yields were dramatically reduced when the organism was grown in an
49 Issue 2 (1998) pp 168-174 airlift reactor. This fall in production could be counteracted by
improving fluid circulation through the placement of impellers within
the draught tube, a strategy that resulted in the highest EPS
concentration (approx. 13 g l-1) of all the fermenter configurations
tested.
4.11 Literatures on Polysaccharides.xls - page 358
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
50 Polysaccharide production: J. Audet, H. Gagnon, M. Lounes, Bioprocess Engineering ISSN: 0178- Department of Chemical Engineering, 1998 Polysaccharide Production, mixing This investigation was undertaken with the objective to compare
Experimental comparison of the J. Thibault 515X (printed version) ISSN: 1432- Laval University, Sainte-Foy devices experimentally the performance of four different mixing devices for the
performance of four mixing devices 0797 (electronic version) Abstract (Quebec), Canada, G1K 7P4 production of the polysaccharide pullulan with Aureobasidium
Volume 19 Issue 1 (1998) pp 45-52 pullulans (2552). Fermentations were performed using identical
bioreactors with respectively an assembly of three Rushton turbines
(RTB), a helical ribbon impeller (HR) and two different reciprocating
plates (RPB1, RPB2). Each mixing vessel had identical geometry and
working volume (18 L). These four fermentations were performed with
an equal level of power input per unit volume (1000 W/m3) and gas
flow rate (0.5 vvm, 9 L/min). For each system, the evolution of
biomass, polysaccharide concentration, dissolved oxygen and
agitation speed or frequency were recorded as a function of time
along with the rheological properties of the culture broths. The type of
mixing device used had a significant impact on the rate of biomass
production and on polysaccharide physical properties. However, the
rate of polysaccharide produc
51 Does the agitation rate and/or oxygen P. A. Gibbs, R. J. Seviour Applied Microbiology and Biotechnology Research Centre, La 1996 agitation rate, oxygen saturation, When Aureobasidium pullulans was grown at a number of agitation
saturation influence exopolysaccharide Biotechnology ISSN: 0175-7598 Trobe University, PO Box 199, exopolysaccharide, production, rates under batch conditions, exopolysaccharide yields were
production by Aureobasidium pullulans (printed version) ISSN: 1432-0614 Bendigo, Victoria, 3550, Australia. Aureobasidium pullulans dramatically reduced at high rates i.e. at least 750 rpm. Investigations
in batch culture? (electronic version) Abstract Volume Fax: 61 54 447 476 e-mail: R. with gas blending, which allowed pO2 manipulation and control
46 Issue 5/6 (1996) pp 503-510 Seviour@latrobe.edu.au independently of the agitation rate, showed that this yield reduction
was due solely to the high pO2 levels that occurred at these agitation
rates. Thus, polysaccharide production at 1000 rpm could be elevated
by maintaining the pO2 at a low level during the initial phase of the
fermentation. However, both the timing of the pO2 decrease and the
level at which it was maintained were crucial for obtaining yields at
1000 rpm, similar to those observed at low agitation rates.
52 Bacterial alginates: biosynthesis and B. H. A. Rehm (1), S. Valla (2) Applied Microbiology and (1) Institut fuer Mikrobiologie der 1997 alginate, production, biosynthesis, Alginate is a copolymer of -d-mannuronic acid and -l-guluronic acid
applications Biotechnology ISSN: 0175-7598 Westfaelischen Wilhelms-Universitaet bacterial (GulA), linked together by 1-4 linkages. The polymer is a well-
(printed version) ISSN: 1432-0614 Muenster, Corrensstr. 3, D-48149 established industrial product obtained commercially by harvesting
(electronic version) Abstract Volume Muenster, Germany Tel.: +49 251 833 brown seaweeds. Some bacteria, mostly derived from the genus
48 Issue 3 (1997) pp 281-288 9848 Fax: +49 251 833 8388 e-mail: Pseudomonas and belonging to the RNA superfamily I, are also
Rehm@uni-muenster.de (2) UNIGEN, capable of producing copious amounts of this polymer as an
Center for Molecular Biology, exopolysaccharide. The molecular genetics, regulation and
Norwegian University of Science and biochemistry of alginate biosynthesis have been particularly well
Technology, 7005 Trondheim, Norway characterized in the opportunistic human pathogen Pseudomonas
aeruginosa, although the biochemistry of the polymerization process
is still poorly understood. In the last 3 years major aspects of the
molecular genetics of alginate biosynthesis in Azotobacter vinelandii
have also been reported. In both organisms the immediate precursor
of polymerization is GDP-mannuronic acid, and the sugar residues in
this compound are polymerized into mannuronan. This uniform
polymer is then further modified by acetylation.
4.11 Literatures on Polysaccharides.xls - page 359
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
53 Effect of phosphate and oxygen W. Sabra, A. -P. Zeng, S. Sabry, Applied Microbiology and Gesellschaft fuer Biotechnologische alginate, production, Alginate production by Azotobacter vinelandii was studied in batch
concentrations on alginate production S. Omar, W. -D. Deckwer Biotechnology ISSN: 0175-7598 Forschung mbH, Biochemical and continuous cultures under microaerobic conditions. In batch
and stoichiometry of metabolism of (printed version) ISSN: 1432-0614 Engineering Division, Mascheroder culture at a pO2 of 2-3% (air saturation) alginate production was
Azotobacter vinelandii under (electronic version) Abstract Volume Weg 1, D-38124 Braunschweig, enhanced by decreasing the PO3-4 level in the medium. Alginate yield
microaerobic conditions 52 Issue 6 (1999) pp 773-780 Germany e-mail: WDD@GBF.de Fax: from biomass (YP/X) reached the highest value of 0.66 g/g at the
+49-531-6181111 (2) Microbiology lowest phosphate level (100 mg/l), compared to 0.40 g/g and 0.25 g/g
Department, Faculty of Science, at higher phosphate levels (200 mg/l and 400 mg/l, respectively). In
University of Alexandria, Alexandria, contrast, biomass formation behaved differently and the growth yield
Egypt (YX/S) decreased with decreasing PO43- concentrations. Moreover,
the respiratory quotient (RQ) of the culture was dependent on the
initial phosphate concentration, especially in the phosphate-limited
phase of growth. As the initial phosphate level decreased from 400
mg/l to 100 mg/l, the average RQ value of the culture declined from
1.46 to 0.89. The low RQ value is very close to the theoretical
optimum RQ, calculated to be 0.8 on the basis of the stoichiometry of
the metabolic pat
54 Development of a fermentation process N. Dyrset, K. Q. Lystad, D. W. Applied Microbiology and SINTEF Applied Chemistry, N-7034 1994 alginate, production, lyase A high-cell-density fermentation process for production of an
for production of an alginate G-lyase Levine Biotechnology ISSN: 0175-7598 Trondheim, Norway, Fax-no.: 47-7- extracellular alginate lyase from Klebsiella pneumoniae on a defined
from Klebsiella pneumoniae (printed version) ISSN: 1432-0614 596995 medium has been developed. The process employs a strategy using
(electronic version) Abstract Volume two carbon sources. One low-molecular-mass, low-viscosity carbon
41 Issue 5 (1994) pp 523-530 source (sucrose) with high water solubility is used as the main carbon
source for growth, while the high-molecular-mass and viscous alginate
in low concentration is used as an inducer for enzyme synthesis. The
repression of alginate lyase production by sucrose and the growth
inhibition that we observed at increased levels of ammonia were
circumvented by a computer-assisted fed-batch addition of the carbon
sources (sucrose and alginate) and by supplying nitrogen sources as
ammonia in the pH control. No enzyme production was observed
when dissolved oxygen limited growth at an oxygen uptake rate of
40%-50% of the maximum uptake rate. An optimal composition of the
feeding solution (12.5 g alginate and 587.5 g sucrose l-1) was found
both for the maximu
55 Utilization of a cell-bound Jai-Yul Kong, Hang-Woo Lee, J Mar Biotechnol 6:99-103 (1998) © unknown 1998 A cell-bound polysaccharide (CBP) produced by the marine bacterium
polysaccharide produced by the marine Jong-Wook Hong, Yang-Soon 1998 by Springer-Verlag New York, Zoogloea sp. (KCCM 10036) was used as the adsorbent of metal ions
bacterium Zoogloea sp.: New Kang, Jong-Deog Kim, Myung- Inc. and as a new support for enzyme immobilization. The CBP gel beads
biomaterial for metal adsorption and Woong Chang, Seoung-Kwon showed highly effective adsorbing in Cr, Pb, and Fe ion in solutions.
enzyme immobilization Bae The adsorption rates were above 95% at pH 5.0, 25°C, in 10 mg/liter
of each metal solution. The gel beads formed by the CBP were stable
within the range of pH 4.0-7.0 and at a temperature of 40-55°C. The
optimum pH and temperature of the immobilized glucoamylase by the
CBP gel beads (poly-G) were 5.0 and 45°C, respectively. The
immobilized glucoamylase produced 10.5 mg/liter of glucose from 10
mg/ml of soluble starch.
4.11 Literatures on Polysaccharides.xls - page 360
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
56 MICROBIAL STRAINS AND HUISMAN, Gjalt, W. , 3370 Brittan Patent, Application METABOLIX, INC., 303 Third Street, 1999 Polysaccharides, production DNA constructs and genetically engineered microbial strains
PROCESSES FOR THE Avenue #18, San Carlos, CA Number:WO1999US0006878 Cambridge, MA 02142-1196, United constructed using these DNA constructs, which produce a nuclease
MANUFACTURE OF BIOMATERIALS 94070-3419, United States of States of America enzyme with specificity for DNA and/or RNA, are provided. These
America BOYNTON, Laura , 5843 strains secrete nuclease into the periplasm or growth medium in an
Darlington Road #3, Pittsburgh, amount effective to enhance productivity and/or recovery of polymer,
PA 15217, United States of and are particularly suited for use in high cell density fermentation
America HOROWITZ, Daniel, M. , processes. These constructs are useful for modifying microbial strains
Apartment No. 206, 435 to improve production and recovery processes for polymers such as
Washington Street, Somerville, intracellular proteins, such as enzymes, growth factors, and cytokines;
MA 02143, United States of for producing polyhydroxyalkanoates; and for producing extracellular
America GERNGROSS, Tillman, polysaccharides, such as xanthan gum, alginates, gellan gum,
U. , 6 Dorrance Place, Hanover, zooglan, hyaluronic acid and microbial cellulose.
NH 03755, United States of
America PEOPLES, Oliver, P. , 27
Radcliffe Road, Arlington, MA
02174, United States of America
57 Sulfated extracellular polysaccharide T. Matsunaga (1), H. Sudo (2), H. (1) Department of Biotechnology, Applied Microbiology and 1996 polysaccharide, production The cyanobacterium, Aphanocapsa halo-phytia MN-11, was
production by the halophilic Takemasa (1), Y. Wachi (1), N. Tokyo University of Agriculture and Biotechnology ISSN: 0175-7598 immobilized in calcium alginate gel and coated on light-diffusing
cyanobacterium Aphanocapsa Nakamura (1) Technology, Koganei, Tokyo 184, (printed version) ISSN: 1432-0614 optical fibers (LDOF) for sulfated extracellular polysaccharide
halophytia immobilized on light- Japan (2) Thermal and Chemical (electronic version) Abstract Volume production. Results indicated that sulfated extracellular
diffusing optical fibers Laboratory, Mitsubishi Heavy 45 Issue 1/2 (1996) pp 24-27 polysaccharide production depends on the number of immobilized
Industries Ltd., 1-8-1, Sachiura, cells and the light intensity. In addition, the production rate reached
Kanazawa-ku Yokohama, Kanagawa 116.0 mg (mg dry cells)-1 day-1 when the cells that were immobilized
236, Japan on LDOF were incubated under a light intensity of 1380 cd sr m-2 at a
cell concentration of 1.0×108 cells/cm3 gel. Cells immobilized on
LDOF produced about ten times more sulfated extracellular
polysaccharide than those immobilized in calcium alginate beads only
(11.7 mg(mg dry cells)-1 day-1).
58 Bacterial alginates: biosynthesis and B. H. A. Rehm (1), S. Valla (2) (1) Institut fuer Mikrobiologie der Applied Microbiology and 1997 alginate Alginate is a copolymer of -d-mannuronic acid and -l-guluronic acid
applications Westfaelischen Wilhelms- Biotechnology ISSN: 0175-7598 (GulA), linked together by 1-4 linkages. The polymer is a well-
Universitaet Muenster, Corrensstr. 3, (printed version) ISSN: 1432-0614 established industrial product obtained commercially by harvesting
D-48149 Muenster, Germany Tel.: (electronic version) Abstract Volume brown seaweeds. Some bacteria, mostly derived from the genus
+49 251 833 9848 Fax: +49 251 833 48 Issue 3 (1997) pp 281-288 Pseudomonas and belonging to the RNA superfamily I, are also
8388 e-mail: Rehm@uni- capable of producing copious amounts of this polymer as an
muenster.de (2) UNIGEN, Center for exopolysaccharide. The molecular genetics, regulation and
Molecular Biology, Norwegian biochemistry of alginate biosynthesis have been particularly well
University of Science and characterized in the opportunistic human pathogen Pseudomonas
Technology, 7005 Trondheim, aeruginosa, although the biochemistry of the polymerization process
Norway is still poorly understood. In the last 3 years major aspects of the
molecular genetics of alginate biosynthesis in Azotobacter vinelandii
have also been reported. In both organisms the immediate precursor
of polymerization is GDP-mannuronic acid, and the sugar residues in
this compound are polymerized into mannuronan. This uniform
polymer is then further modified by acetylation at posit
4.11 Literatures on Polysaccharides.xls - page 361
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
59 Effect of phosphate and oxygen W. Sabra, A. -P. Zeng, S. Sabry, Gesellschaft fuer Biotechnologische Applied Microbiology and 1999 alginate, phosphate, oxygen, Alginate production by Azotobacter vinelandii was studied in batch
concentrations on alginate production S. Omar, W. -D. Deckwer Forschung mbH, Biochemical Biotechnology ISSN: 0175-7598 Azotobacter vinelandii and continuous cultures under microaerobic conditions. In batch
and stoichiometry of metabolism of Engineering Division, Mascheroder (printed version) ISSN: 1432-0614 culture at a pO2 of 2-3% (air saturation) alginate production was
Azotobacter vinelandii under Weg 1, D-38124 Braunschweig, (electronic version) Abstract Volume enhanced by decreasing the PO3-4 level in the medium. Alginate yield
microaerobic conditions Germany e-mail: WDD@GBF.de 52 Issue 6 (1999) pp 773-780 from biomass (YP/X) reached the highest value of 0.66 g/g at the
Fax: +49-531-6181111 (2) lowest phosphate level (100 mg/l), compared to 0.40 g/g and 0.25 g/g
Microbiology Department, Faculty of at higher phosphate levels (200 mg/l and 400 mg/l, respectively). In
Science, University of Alexandria, contrast, biomass formation behaved differently and the growth yield
Alexandria, Egypt (YX/S) decreased with decreasing PO43- concentrations. Moreover,
the respiratory quotient (RQ) of the culture was dependent on the
initial phosphate concentration, especially in the phosphate-limited
phase of growth. As the initial phosphate level decreased from 400
mg/l to 100 mg/l, the average RQ value of the culture declined from
1.46 to 0.89. The low RQ value is very close to the theoretical
optimum RQ, calculated to be 0.8 on the basis of the stoichiometry of
the metabolic pa
60 Production of a polysaccharide under RIGHELATO RENTON CLIVE; Pats. Nr. US4110162,BE855083, Tate & Lyle Ltd 1978 polysaccharide Production, Polysaccharide is produced in good yields with good control by
carbon limiting conditions JARMAN TREVOR RODNEY CA1086671, DE2723166, carbon, limitation continuous culture of a polysaccharide-producing strain of
DK235377, FI771705, FR2352880, Azotobacter vinelandii under carbon-limited conditions, preferably with
GB1513061, IT1083007, restricted oxygen uptake, with the advantage that the effluents
JP52145596, JP55042839B, produced are non-polluting having a low biological oxygen demand
LU77433, NL7705898, NO771843, (B.O.D.).
SE7706261
61 Microbiological process for the Pat. Nr. GB2026515 Tate & Lyle Ltd 1980 Polysaccharides, production, A process for the production of polysaccharide consisting of a
production of alginate type alginate, Pseudomonas partially acetylated variable block copolymer of D-mannuronic and L-
polysaccharide guluronic acid residues, comprises cultivating in a nutrient medium
therefor a strain of Pseudomonas, which is non- pathogenic to
humans, and which has been obtained by treating a non- mucoid
species of Pseudomonas, which is non-pathogenic to humans, with a
beta -lactam or aminoglycoside antibiotic whereby a mucoid strain
tolerant to said antibiotic as selected, and isolating from the medium
the polysaccharide produced. Particularly suitable strains may be
derived from P. mendocina, P. tabaci or P. putida. Suitable antibiotics
include the penicillins, eg carboxyalkyl or carboxyaralkyl derivatives of
penicillins, or esters thereof, or 3-halophenyl penicillins. A preferred
antibiotic is carbenicillin (disodium alpha - carboxybenzyl penicillin).
62 Continuous process for the production RIGHELATO RENTON C; Pats. Nr. US4130461, BE855084, Tate & Lyle Ltd 1978 polysaccharides, production, Polysaccharide is produced in high yields by continuous culture of a
of polysaccharide under phosphate DEAVIN LYNDA CA1087123, DE2723165, continuous culture polysaccharide-producing strain of Azotobacter vinelandii under
limiting conditions DK235277, FI771704, FR2352879, phosphate-limited conditions, preferably with restricted oxygen
GB1513104, IT1083006, uptake.
JP1038813C, JP52145595,
JP55030360B, LU77431,
NL7705897, NO771842, SE7706260
4.11 Literatures on Polysaccharides.xls - page 362
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
63 PROCESS FOR THE PRODUCTION Imrie, F Pat. Nr. US3856625, BE800878, Tate & Lyle Ltd 1974 alginate, polysaccharide, An alginate-type polysaccharide is obtained by the aerobic cultivation
OF POLYSACCHARIDE CA986444, CH591559, DE2329808, production of a bacterium of the species Azotobacter vinelandii in an aqueous
FR2233397, JP49102891, nutrient medium containing sources of carbon, molybdenum, iron,
JP53007519B, JP928683C, mangesium, potassium, sodium, sulfate, calcium and phosphate. The
NL7308158 carbon source comprises at least one monosaccharide or
disaccharide. Contrary to normal culture conditions for this bacterium,
for good Polysaccharide production, the phosphate concentration in
the nutrient medium must be 0.1-0.8 millimolar, preferably 0.2-0.6
millimolar; and the pH of the medium must be maintained within the
range of from 7.0 to 8.2, preferably 7.3 to 7.9.
64 Production of high-purity alginate useful ZIMMERMANN ULRICH (DE); Pats. Nr. DE19836960, WO0009566 2000 Production, alginate, algae Production of high-purity alginate comprises: (a) extracting algal
for making capsules of encapsulating BEHRINGER MARCUS (DE) material or crude alginate with a solution of a complexing agent; (b)
implants comprises extraction, sedimenting cell components and particles from the solution with a
sedimentation, filtration and porous binder, (c) filtering the solution; (d) precipitating alginate from
precipitation the solution; and (e) collecting the precipitate. An Independent claim
is also included for an alginate composition consisting of a copolymer
of mannuronic acid (MA) and guluronic acid (GA) with a MA:GA ratio
of 1-90:100 and a molecular weight above 1000 kD.
65 Leuconostoc strains for biosynthesis of NEESER JEAN-RICHARD (CH); Pats. Nr US6004800, AU6901598, Nestec SA (CH) 1999 dextran, strains, production Strains of Leuconostoc mesenteroides ssp. cremoris which provide,
dextran EYER KURT (CH); SCHMID BR9801736, CA2233411, upon culturing, dextran, and the strains include deposited strains
DANIEL (CH); AEBISCHER CN1201039, CZ9801669, CNCM I-1692 and CNCM I-1693.
JUERG (CH); D AMICO NICOLA EP0881283, HU9801263,
(CH); RENIERO ROBERTO (CH); NO982004, NZ330239, PL326483
DE MALEPRADE DOMINIQUE
(CH); LESENS CORINNE (FR)
66 Process for the production of dextran DAY DONAL F (US); KIM DOMAN Pat. Nr. US5229277 UNIV LOUISIANA STATE (US) 1993 dextran, production, polymer A process for the production of dextran polymers of controlled
polymers of controlled molecular size (US) average number molecular weight sizes, and molecular weight size
and molecular size distributions distributions via the mixed culture fermentation of Leuconostoc
mesenteroides and a constitutive mutant microorganism capable of
elaborating the enzyme dextranase, particularly Lipomyces starkeyi
ATCC 74054, in the presence of sucrose. The Leuconostoc
mesenteroides produces the dextran polymer, and the mutant
Lipomyces starkeyi ATCC 74054 concurrently produces dextranase,
an enzyme whose activity reduces the size of the dextran polymers
and permits their growth or reduction in molecular weight size in direct
relation to the temperature and time period regimen imposed as
conditions for the reactions.
67 No title available. Pat.Nr GB634129 0 Dextran, sucrose, fermentation, Dextran for use in pharmaceutical preparations, especially for
degradation to a blood plasma substitute, is made by growing
Leuconostoc meserentoides in refined sucrose media containing as a
growth factor for the micro-organisms the liquid obtained by boiling a
suspension in water of fresh yeast free from autolyzed products, e.g. a
20 per cent w/v suspension, at pH7.5-8 and separating off the cell
residues. The Leuconostoc is preferably a strain obtained by
continuous subculture on a solid sucrose-peptone-agar medium
followed by sub culture in pure sucrose media containing the yeast
extract and ammonium, potassium, magnesium and phosphate ions.
An example of the bulk medium for dextran production is: the
acqueous yeast extract 250ml., microcosmic salt 5g., potassium
dihydrogen phosphate 1g., magnesium sulphate 0.5g., sucrose 100g.,
tap water to 1000ml.
4.11 Literatures on Polysaccharides.xls - page 363
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
68 A process for the production of dextran. JARL KURT; ENGBLOM CURT Pat. Nr. EP0087404, JP58155097, SORIGONA AB (SE) 1983 dextrane, saccharose, production A process for preparing by means of microorganisms or enzymes,
SE439647, SE8201021 dextrane having a molecular weight suitable for clinical use starting
from a saccharose-containing substrate, wherein it is carried out
continuously with continuous supply of substrate and microorganisms
or enzymes and continuous discharge of dextran-containing reaction
mixture from which the dextran is then recovered.
69 PRODUCTION OF DEXTRAN YAMADA MASAHIKO; INOUE Pat.Nr. JP8173178, JP2933842B2 SHIKISHIMA SEIPAN KK 1996 dextrane, culture conditions, PURPOSE: To obtain dextran useful for a blood plasma substitute,
TOSHIYASU; HARA MASATO; fermentation etc., without being greatly affected by culture conditions by culturing a
TAKAYAMA KENICHIRO variant strain capable of producing a dextransucrase in a culture
medium containing sucrose without using the induction of the sucrose
in the culture medium. CONSTITUTION: A dextransucrase
constituent variant strain of Leuconostoc mesenteroides for producing
dextran is cultured in a culture medium containing sucrose.
Leuconostoc mesenteroides M209 strain (FERM BP-4903) or
Leuconostoc mesenteroides M898 strain (FERM BP-4904) can be
exemplified as the dextransucrase constituent variant strain.
70 PRODUCTION OF DEXTRAN SHIBATA TAKASHI; others: 01 Pat.Nr. JP7274991 FUJISAWA PHARMACEUT CO LTD 1995 dextran, production, synthase PURPOSE:To directly obtain a dextran having a weight-average
molecular weight higher than that of a starting raw material, useful as
a plasma extender and a raw material for a food in high yield, by
continuously adding a solution of sucrose to a dextran precursor in the
presence of a dextran synthase. CONSTITUTION:A dextran synthase
such as dextransucrase prepared by culturing Leuconostoc
mesenteroides NRRL-B-512 strain in a medium is added to a solution
of sucrose and allowed to stand at pH5.2 at 30 deg.C for 24 hours to
synthesize a dextran precursor comprising a low-molecular dextran
which is an oligosaccharide having 2-10 glycosyl residues. The
dextran synthase is further added to the solution, the solution is
reacted for five hours with a solution of sucrose which is continuously
added. After the completion of the reaction, the reaction solution is
heated to deactivate the enzyme, a low-molecular substance is
removed by an ultrafilter having 10,000 fractionated molecular weight
to give the objective dex
71 PRODUCTION OF DEXTRAN UNNO TAKEHIRO; others: 01 Pat.Nr. JP7289277 NIPPON SHOKUHIN KAKO CO LTD 1995 dextran, inoculation PURPOSE:To efficiently. obtain the subject compound useful for a
blood extender, a plasma substitute, a gel filtering agent, etc., by
culturing a microorganism, belonging to the genus Gluconobacter and
capable of producing dextran in a culture medium containing a starch
partial hydrolyzate, etc., and CaCO3 and then collecting the resultant
product. CONSTITUTION:This method for efficiently producing
dextran is to inoculate a microorganism, belonging to the genus
Gluconobacter and capable of producing the dextran (e.g.
Gluconobacter oxydans ATCC11894 strain) into a culture medium,
containing a starch partial hydrolyzate or its reduced substance as a
carbon source and having a calcium carbonate content within the
range of 0.01-10wt.%, culture the microorganism at 25 deg.C for 4
days under shaking, centrifuge the resultant culture solution, remove
the microbial cell, add 0.1% active carbon to the supernatant, allow
the obtained mixture to stand at 50 deg.C for 30min, carry out the
decoloring treatment, then pas
4.11 Literatures on Polysaccharides.xls - page 364
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
72 Microbial enhancement of polymer ANTLOGA KATHLEEN MARIE; Pat. Nr. GB2153834,CA1271150, STANDARD OIL CO OHIO 1985 polymer, viscosity A method for increasing the viscosity of a solution of a preformed
viscosity BALL LAWRENCE ERNEST; NO162522B, NO162522C polymer which comprises combining, under conditions favourable to
GRIFFIN WILLIAM MICHAEL microbial growth, (a) an aqueous solution of the preformed polymer;
and (b) a microorganism incapable of de novo synthesis of the
polymer, but capable of increasing the viscosity of the polymer
solution is disclosed. The present invention may be applied, for
example, to oil recovery, water clarification and paper production.
Polymers which may be treated by this method include guar gum,
hydroxypropyl guar gum, sodium carboxymethyl cellulose,
hydroxyethyl cellulose, carboxymethyl hydexyethyl cellulose, xanthan
gum, scleroglucan, locust bean gum, polyacrylamide, hydrolyzed
polyacrylamide, poly (acrylic acid) and its salts, poly (2-acrylamido-2-
methyl propane sulphuric acid (2 salt, ANPS), poly (acrylic acid-co-
acrylate ester), poly (vinyl pyrrolidane), cellulose sulphate esters, poly
(ethylene oxide), poly (vinyl alcohol), polyamine, poly (vinyl acetate-co-
maleic anhydride) and po
73 High molecular weight pullulan and THORNE LINDA P (US); Pat.Nr. US6010899 SHINETSU CHEMICAL CO (JP); 2000 pullulan, production A method for obtaining a substantially biologically pure culture strain
method for its production ARMENTROUT RICHARD W SHINETSU BIO INC (US) of Aureobasidium pullulans from a wild type strain by enriching the
(US); POLLOCK THOMAS J (US) collected strain for organisms which grow as fungal yeastlike cells,
growing colonies from isolated yeastlike cells and selecting those
yeastlike cells which exhibit reduced pigmentation. Biologically pure
culture strains obtained by the invention as well as methods for
producing pullulan having decreased pigmentation and/or increased
molecular weight are disclosed.
74 Method for producing pullulan from SUN WANRU (CN); JIANG NING Pat.Nr. CN1216781 INST OF MICROBIOLOGY CHINESE 1999 pullulan, production, fermentation The present invention relates to a new production method of pullulan
fermentation liquor (CN); REN YONG-E (CN) A (CN by using fermentation process. It is characterized by that in the course
of fermentation said method adopts discontinuous or continuous flow
addition of solution containing carbon source and nitrogen source to
produce pullulan, in which the carbon source can use cane sugar or
starch hydrolysate, and the nitrogen source is inorganic nitrogen salt,
etc. The fermentative conversion rate of pullulan produced by said
invented method can be up to above 70% in general, highest is up to
76%, and the mean molecular weight is one hundred thousand
Daltons.
75 Process for the production of pullulan KATO KOSO; SHIOSAKA Pat. Nr. US3912591 HAYASHIBARA BIOCHEM LAB 1975 pullulan, production, saccharides, In the production of pullulan by aerobic, microbial fermentation of
MAKOTO fermentation saccharides, the degree of polymerization, the yield and the culture
period are controlled by adjusting the pH value and the concentration
of phosphate ion in the culture medium.
76 Method for purifying pullulan KATO KOSO; NOMURA TATSUO Pat. Nr. US4004977 HAYASHIBARA BIOCHEM LAB 1977 pullulan, production A method for purifying pullulan which comprises cultivating a strain of
Aureobasidium pullulans in a liquid medium, removing the cells from
the culture broth, precipitating pullulan present in said broth with at
least one solvent selected from the group consisting of alcohols,
esters and ethers respectively with three or more carbon atoms and
ketones with four or more carbon atoms to recover, and then
dehydrating and/or drying the recovered pullulan.
4.11 Literatures on Polysaccharides.xls - page 365
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
77 High pullulan content product, and its MIYAKE TOSHIO (JP); NOMURA Pat. Nr. EP0586034, A3 HAYASHIBARA BIOCHEM LAB 1994 pullulan, production, Disclosed is a novel high pullulan content product containing pullulan
preparation and uses. TATSUO (JP); OZAKI having an average molecular weight less than 250,000, said product
YOSHIHIDE (JP) being prepared by continuously cultivating a microorganism capable
of producing pullulan in a nutrient culture medium containing a 10-20
w/v % saccharide while controlling the viscosity of the nutrient culture
medium to a level below 30cp. The product can be advantageously
used in a variety of fields such as a viscosity-imparting agent, coating
agent, adhesive, formed product, food product, cosmetic,
pharmaceutical, and material for agriculture, forestry, stock raising
and paper processings, as well as for mining and manufacturing
industries.
78 PRODUCTION OF HIGH-MOLECULAR- NAGURA SHIGEHIRO; others: 01 Pat.Nr. JP5328988 SHIN ETSU CHEM CO LTD 1993 Production, pullulan, molecular PURPOSE:To provide a process for producing pullulan which can
WEIGHT PULLULAN weight give pullulan of high molecular weight and prevent the culture medium
from blackening due to production of black pigments.
CONSTITUTION:In the production of pullulan by culturing a
microorganism capable of producing pullulan, Aureobasidium
pullulans, the culture mixture is heat-treated at 50 to 75 deg.C for 0.3
to 3hrs. The heat treatment inhibits the medium for producing pullulan
from blackening.
79 PRODUCTION OF PULLULAN WITH YOSHIDA MIKIHIKO Pat. Nr. JP57141401 HAYASHIBARA SEIBUTSU KAGAKU 1982 Production, pullulan, molecular PURPOSE:To obtain high-purity pullulan with a narrowed MW
NARROWED MOLECULAR KENKYUSHO KK weight distribution in high yields, by partially decomposing raw pullulan,
WEIGHTDISTRIBUTION fractionating the decomposition product and collecting the fractions
having a weight-average MW/number- average MW ratio of below a
specified value. CONSTITUTION:Raw pullulan is partially
decomposed, the decomposition product is fractionated and the
fractions having a weight-average MW/number-average MW ratio of
below 1.5 are collected. The resulting pullulan fractions ar usually
decolorized and desalted by active carbon, an ion exchange resin,
etc., to obtain the purpose pullulan product. USE:This pullulan
product is used advantageously as a water-soluble high-molecular
standard reagent. For example, in case where it is used in gel filtration
or liquid chromatography, it is suitable to use pullulan with a MW
distribution which is narrowed to such an extent that the reversed
Mw/reversed Mn ratio is about 1.3-1.1. Moreover, the product is useful
as a plasma expander, a blood flow impr
80 Production of xanthan gum by emulsion MAURY LUCIEN G Pat. Nr. US4352882 KELCO BIOSPECIALTIES LTD 1982 xanthan, production, emulsion, Preparation of xanthan gum is effected by dispersing the aqueous
fermentation fermentation xanthamonas culture medium in a water insoluble oil such as a
hydrocarbon or vegetable oil. Such dispersions generate substantially
less viscosity and as a result, fermentation can be carried out to a
higher polymer content with less energy input.
4.11 Literatures on Polysaccharides.xls - page 366
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
81 PRODUCTION OF XANTHAN GUM NISHI HISAMITSU Pat. Nr. JP58165798 ASAHI DOW KK 1983 xanthan, production, fermentation PURPOSE:Specific compounds such as organic acids, organic bases,
vitamins and others are added to the fermentation medium containing
a carbon source to produce xanthan gum with good viscosity
properties, high heat stability and salt resistance.
CONSTITUTION:The fermentation culture medium containing a
carbon source used in the cultivation of Xanthomonas campestris
NRRL. B-1459 in an aqueous solution containing at least one of
carbon sources, nitrogen sources, phosphate salts, and magnesium
salts along with at least one selected from organic acids, inorganic
bases or vitamins. The culture medium is adjusted in pH to 6.8-7.2,
sterilized and cooled. The cultivation is carried out at 25-30 deg.C
with aeration for 70-95hr and, after completion of fermentation, a small
amount of methanol and water in an amout of 2-5 times the volume of
methanol are added to effect dilution. Then, the mixture is subjected to
centrifugation to remove cell bodies. Xanthan gum is obtained as a
precipitate by adding alcohol and a salt
82 PRODUCTION OF XANTHAN GUM HISAYOSHI KEISUKE; others: 01 Pat. Nr. JP58165797 KOJIN KK 1983 XANTHAN, production, enzyme, PURPOSE:A xanthan gum solution is treated with a small amount of a
WITH HIGH CLARITY specific enzyme to remove cell bodies as contaminants efficiently to
increase the clarity of the product. CONSTITUTION:Lysozyme as an
enzyme is added to a xanthan gum solution of 1-10% gun
concentration by 1-500ppm and the reaction is effected at a pH of 4.0-
9.0 and 25-60 deg.C. At this time, a combination thereof with N-
acetylmuramyl-L-alanine amidase and peptidase may be allowed and
slow agitation is preferred so that the high-viscosity solution is made
uniform during the reaction.
83 IMPROVED PRODUCTION OF NISHI HISAMITSU Pat. Nr. JP61173796 ASAHI CHEM IND CO LTD 1986 xanthan, production PURPOSE:To form xantham gum useful as foods, etc., in an
XANTHAN GUM aggregated state, to carry out its production and recovery efficiently,
by fermenting aerobically Xanthomonas campestris in an aqueous
medium containing both an inorganic salt and an aqueous solvent.
CONSTITUTION:Xanthomonas campestris IFO 13303 is aerobically
fermented in an aqueous medium containing preferably 0.25-0.75wt%
inorganic salt (e.g., CaCl2, etc.) and preferably 15-30vol.% aqueous
organic solvent (e.g., acetone, etc.).
84 Production of xanthan having a low JARMAN TREVOR RODNEY; Pat. Nr. EP0066961 KELCO BIOSPECIALTIES LTD (GB) 1982 xanthan, low, pyruvate Low pyruvate xanthan gum comprising 0.1-1% by weight pyruvate
pyruvate content. PACE GARY WILLIAM (FCC Method) has useful properties for secondary oil recovery. It is
produced by aerobically fermenting an organism of the genus
Xanthomonas in a broth comprising: 1) a chemically defined simple
salts medium comprising sources of nitrogen, sulphur, potassium,
phosphorus, magnesium, calcium, and (optionally) iron, said simple
salts medium being substantially free of cobalt, copper, manganese,
zinc and boron; 2) an assimilable carbon source, and 3) a complex
organic material which is a nitrogen source.
85 Inoculation procedure for xanthan gum JARMAN TREVOR RODNEY Pat. Nr. EP0066957 KELCO BIOSPECIALTIES LTD (GB) 1982 Inoculation, xanthan, production, Inoculation of the nutrient medium for production of xanthan gum by
production. fermentation aerobic fermentation is effected at a dilution of 0.5-0.01% using an
inoculum comprising an organism of the genus Xanthomonas, wherein
the total levels of iron, manganese, and zinc in said nutrient medium
are limited such that there is no more than 10 ppm iron, no more than
3 ppm zinc and the ppm ratio of iron : manganese is from 40 : 1 to 2 :
1.
4.11 Literatures on Polysaccharides.xls - page 367
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
86 Process for xanthan gum production. JARMAN TREVOR RODNEY Pat. Nr. EP0066377 KELCO BIOSPECIALTIES LTD (GB) 1982 Xanthan, production Xanthan gum is produced by an improved process of fermenting an
assimilable carbon source by an organism of the genus Xanthomonas
comprising limiting the trace elements Fe, Mn, Zn, Cu, Co and B as
follows:(.) with the proviso that the ratio Re: Mn ranges from 40: 1 to
2: 1.
87 High phosphate process for making low EMPEY RICHARD A; DOMINIK Pat.Nr. US4263399 MERCK & CO INC 1981 xanthan, production A novel process is described for making a low calcium xanthan gum
calcium, smooth flow xanthan gum JURGEN G exhibiting smooth flow properties which comprises the use of high
levels of phosphate in the fermentation medium.
88 No title available. QUINN FRANCIS X (FR); Pat. Nr. DE19547748 INST FRANCAIS DU PETROL (FR) 1996 xanthan, gellan, welan, rhamsan, A method for treating a fermentation must intended for the production
MONOT FREDERIC (FR) scleroglucan, production of exopolysaccharides of microbial origin comprises adding a
surfactant drop by drop, without stirring, to an aqueous solution of the
fermentation must containing the polysaccharide. The polysaccharide
separates into a supernatant phase. It may be, for example, gellan,
welan, rhamsan, scleroglucan or xanthan.
89 PRODUCTION OF XANTHAN GUM WEISROCK WILLIAM P; KLEIN Pat. Nr. CA1153970 STANDARD OIL CO 1983 No abstract available.
FROM A CHEMICALLY DEFINED HARRIET S
MEDIUM
90 Xanthan gum from dairy permeates and POLLOCK THOMAS J (US); Pat. Nr. EP0624651 SHINETSU BIO INC (US); SHINETSU 1994 xanthan, production, dairy, The present invention relates to the unexpected discovery that
other filtered dairy products. ARMENTROUT RICHARD W CHEMICAL CO (JP) permeates xanthan gum can be produced from filtered whey or milk products,
(US) including whey permeates and milk permeates, by a fermentation
process which uses organisms which are capable of converting
lactose to xanthan gum.
91 Process for making cellulase-free KANG KENNETH S Pat. Nr. US4259477 MERCK & CO INC 1981 xanthan, cellulase Cellulase in xanthan gum can be completely destroyed by treating
xanthan gum xanthan gum beer with about 0.08 to 0.1% alkali metal hypochlorite
followed by heat treatment.
92 RECOMBINANT - DNA MEDIATED CAPAGE MICHAEL A; Pat. Nr. EP0326544 (WO8705938) GETTY SCIENT DEV CO (US) 1989 xanthan No abstract available.
PRODUCTION OF XANTHAN GUM. DOHERTY DANIEL H; BETLACH
MICHAEL R; VANDERSLICE
REBECCA W
93 Process for the production of CROS PATRICK Pat.Nr. EP0319372 RHONE POULENC CHIMIE (FR) 1989 Process for the production of biopolymers by fermentation of
polysaccharides. carbohydrates by means of microorganisms. The process consists in
performing the fermentation in an aqueous nutrient medium containing
starch as source of assimilable carbon in the presence of a
saccharification enzyme. Application to the manufacture of xanthan
gum in particular.
94 Preparation of xanthan gum. POLLOCK THOMAS J; THORNE Pat. Nr. EP0287363 SYNTRO CORP (US) 1988 xanthan A method of increasing xanthan gum production, comprising culturing
LINDA a Xanthomonas campestris strain having a xanthan-increasing
modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing
rifampicinresistance; (2) a mutation causing bacitracin-resistance; or
(3) exogenous genetic information controlling the synthesis of
xanthan; and separating xanthan from the culture medium, is provided
along with specific DNA sequences and Xanthomonas campestris
strains showing increased xanthan gum production.
95 Process for the fermentative production DEMAIN ARNOLD L; SOUW Pat. Nr. US4245046 MASSACHUSETTS INST 1981 Xanthan, organic acid Xanthan gum is produced by fermentation with the bacterium,
of xanthan gum with organic acids PETER TECHNOLOGY Xanthomonas campestris NRRL B-1459, of a nutrient medium
containing a sugar and a stimulatory organic acid which stimulates the
production of xanthan gum. The stimulatory organic acid can be a
source of pyruvic acid, alpha-keto-glutaric acid, succinic acid or
mixtures thereof.
96 Fermentation process for production of WERNAU WILLIAM C Pat. Nr. US4282321 PFIZER 1981 xanthan Increased xanthan concentrations are obtained in Xanthomonas
xanthan fermentations by the gradual addition of a source of assimilable
carbon, preferably glucose, to the aqueous nitrient medium during the
course of the fermentation cycle.
4.11 Literatures on Polysaccharides.xls - page 368
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
97 Process for the production of xanthan Pat. Nr. GB2008138 Tate & Lyle Ltd 1979 xanthan The conversion efficiency in a continuous fermentation of a strain of
gum, the genus Xanthomonas to produce a polysaccharide is enhanced by
the choice of the carbohydrate carbon source as the growth-limiting
substrate. The process is applied to the production of xanthan gums
by fermentation of x campestris.
98 Method for fermentation production of HONMA TAIRA (JP); NAGURA Pat. Nr. US5580763 SHINETSU CHEMICAL CO (JP); 1996 xanthan, nitrogen A method for the fermentation production of xanthan gum which
xanthan gum SHIGEHIRO (JP); MUROFUSHI SHINETSU BIO INC (US) comprises the step of carrying out culture by using a water-soluble
KANJI (JP) inorganic nitrogen component alone as the nitrogen source of a
production medium, and by mixing and using the water-soluble
inorganic nitrogen component and a water-insoluble organic nitrogen
component as the nitrogen sources of a seed fermentation medium.
99 Process for the production of a xanthan EYSSAUTIER BRUNO Pat. Nr. FR2606423 SANOFI ELF BIO IND (FR) 1988 xanthan This process for the production of a xanthan gum with high capacity
with high thickening capacity, and for thickening aqueous media consists in rapidly heating the final
applications of this xanthan. broth from carbohydrate fermentation by a bacterium of the genus
Xanthomonas. The heating of the medium is carried out at close to
neutral pH, at a temperature of between 105 DEG C and 120 DEG C
for 30 seconds to 8 minutes before isolating the xanthan.
100 PROCESS FOR PRODUCING PEREIRA ROSEIRO JOSE Pat. Nr. WO9505476 NERA ASSOCIACAO EMPRESARIAL 1995 xanthan, pseudoplastic, organic A process for the activation of the production of xanthan, to give
XANTHAN USING NON- CARLOS (PT); AMARAL DA (PT); AIDA ASSOCIACAO acid pseudoplastic characteristics to solutions and suspensions, through
METABOLIZABLE ORGANIC ACIDS COLACO MARIA TERESA (PT) INTERPROFISSIO (PT); PEREIRA the growth of Xanthomonas bacteria genus in a solution of mineral
ROSEIRO JOSE CARLOS (PT); salts and one or more carbohydrates, by adding linear or branched
AMARAL COLACO MARIA TERESA chained, saturated or unsaturated non-metabolizable organic acids
(PT) (e.g. isobutyric acid, carob extract). This process results in improved
yields up to 25 % higher, and a final product with fewer impurities.
101 Process for production of saline- MUROFUSHI KANJI (JP); Pat Nr. EP0718311 SHINETSU CHEMICAL CO (JP); 1996 xanthan, A process for saline-solution soluble xanthan gum which comprises
solution soluble xanthan gum NAGURA SHIGEHIRO (JP) SHINETSU BIO INC (US) the steps of precipitating xanthan gum by mixing, with stirring, an
aqueous solution of xanthan gum with an organic solvent which is a
non-solvent to xanthan gum but is hydrophilic, removing liquid from
the precipitated xanthan gum to a liquid content of at most 50%,
disintegrating the cake of xanthan gum after the liquid removal to an
average grain size of from 0.3 to 2 cm in diameter, and drying the
disintegrated xanthan gum by fluidizing the same at a temperature not
exceeding 80 DEG C
102 MICROBIAL STRAINS AND GERNGROSS TILLMAN U; Pat. Nr.WO9950389 METABOLIX INC (US) 1999 biomaterials, production, DNA constructs and genetically engineered microbial strains
PROCESSES FOR THE HOROWITZ DANIEL M; alginates, gellan gum, zooglan, constructed using these DNA constructs, which produce a nuclease
MANUFACTURE OF BIOMATERIALS BOYNTON LAURA; HUISMAN hyaluronic acid, xanthan, microbial enzyme with specificity for DNA and/or RNA, are provided. These
GJALT W; PEOPLES OLIVER P cellulose strains secrete nuclease into the periplasm or growth medium in an
amount effective to enhance productivity and/or recovery of polymer,
and are particularly suited for use in high cell density fermentation
processes. These constructs are useful for modifying microbial strains
to improve production and recovery processes for polymers such as
intracellular proteins, such as enzymes, growth factors, and cytokines;
for producing polyhydroxyalkanoates; and for producing extracellular
polysaccharides, such as xanthan gum, alginates, gellan gum,
zooglan, hyaluronic acid and microbial cellulose.
4.11 Literatures on Polysaccharides.xls - page 369
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
103 Fermentation process for the BANKS GEOFFREY T (GB); Pat. Nr. US4692408 IMP BIOTECHNOLOGY (GB) 1987 polysaccharide, production, Polysaccharides, such as xanthan gum, are produced by culturing
production of polysaccharides BROWNING PAUL D (GB) xanthan, fermentation microorganisms, e.g. of the Xanthomonas genus, in a two stage
process. In the first stage, growth of the microorganism is favored, e.g.
by using a predetermined quantity of a carbon-containing nutrient
which does not support biosynthesis of the polysaccharide. In the
second stage, the conditions are such that biosynthesis of the
polysaccharide takes place with substantially no growth of the
microorganism, e.g. by adding carbohydrate in the absence of nutrient
required for polysaccharide growth. By this process, the requirement
for oxygen is greatly reduced at the time when the culture medium has
its highest viscosity, thereby minimizing problems of low oxygen
transfer capability in viscous media.
104 Process of using xanthomonas BAUER KEITH A (US); Pat. Nr. US4400467 STANDARD OIL CO INDIANA (US) 1983 heteropolysaccharide, xanthan This invention involves the production of heteropolysaccharides such
campestris NRRL B-12075 and NRRL B-KHOSROVI BEHZAD (US) as xanthan gum by the continuous fermentation of suitable nutrient
12074 for making heteropolysaccharide media with new degenerative resistant variants of Xanthomanas
campestris. Fermentation is conducted in a nitrogen, sulfur or
phosphorous limited nutrient medium containing glucose or a minimal
medium plus yeast extract and glutamic acid, in a first fermenter to
enhance cultural growth. After the limiting growth element (nitrogen,
sulfur or phosphorous) has been essentially consumed, the medium
is then transferred to a second fermenter and fermentation continued
while adding a suitable carbohydrate which the bacteria convert into
the heteropolysaccharide product. The process may be modified by
carrying out cultural growth and production of the polysaccharide in
the same fermenter. The bacteria employed were cultured from a
glucose-mineral salts medium fortified with yeast extract or a glucose-
defined minimal medium in which ammonium chloride served as the
sole assimilable n
105 Production of high-pyruvate xanthan CADMUS MARTIN C; KNUTSON Pat. Nr. US4394447 US AGRICULTURE 1983 high pyruvate, xanthan A high-pyruvate xanthan gum, substantially free of insolubles and
gum on synthetic medium JR CLARENCE A undesirable coloration, is produced by fermentation of Xanthomonas
campestris on a carbohydrate-containing nutrient medium having
(NH4)2HPO4 at a level of at least 0.15% as the primary nitrogen
source, and having a total phosphate level of at least about 0.25%.
106 Method for producing a low viscosity WEISROCK WILLIAM P Pat.Nr. US4377637 STANDARD OIL CO INDIANA (US) 1983 xanthan, low viscosity In the production of xanthan gum by action of the Xanthomonas
xanthan gum bacteria on a nutrient medium, a low viscosity xanthan gum is
produced by adding sulfate anions in a concentration ranging from
about 0.2 to about 0.5 wt % of the nutrient medium during the culture
of the Xanthomonas bacteria in the nutrient medium. A reduced
viscosity xanthan gum is produced which can be converted to the
normal viscosity xanthan gum.
107 Production of xanthan gum from a WEISROCK WILLIAM P; KLEIN Pat. Nr. US4374929 STANDARD OIL CO INDIANA (US) 1983 Xanthan, production, continuous A process is described for the continuous manufacture of xanthan
chemically defined medium introduction HARRIET S culture gum in which continuous culture is conducted under conditions of
nutrient limited growth using relatively inexpensive chemically defined
media containing certain vitamins with or without amino acids. The
process is directed broadly to use of bacteria of the genus
Xanthomonas to produce xanthan gum from the aforesaid media.
4.11 Literatures on Polysaccharides.xls - page 370
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
108 Semi-continuous method for production WEISROCK WILLIAM P Pat. Nr. US4328308 STANDARD OIL CO INDIANA 1982 xanthan, semi-continuous, Xanthan gum is produced by means of semi-continuous fermentation
of xanthan gum using Xanthomanas fermentation using a culture of either Xanthomonas campestris XCP-1 ATCC 31600
campestris ATCC 31600 and or Xanthomonas campestris P-107 ATCC 31602, in a minimal
Xanthomanas campestris ATCC 31602 medium, allowing the system to ferment for a period of about 24
hours, withdrawing a portion of the fermented medium, recovering
xanthan from the withdrawn portion, adding fresh, sterile medium to
the residual medium and repeating the above cycle.
109 Production of polysaccharides of high CROS PATRICK (FR) Pat. Nr. US5610037 RHONE POULENC CHIMIE (FR) 1997 polysaccharide, xanthan, Polysaccharide biopolymers, e.g., xanthan gum, are produced by the
viscosity using xanthomonas fermentation aerobic microbial fermentation of a carbohydrate in an aqueous
campestris and glycoamylase with nutrient medium containing starch as a source of carbon, and wherein
fluidized starch the fermentation is carried out in the presence of a saccharide-
specific amylolytic enzyme.
110 Method for improving specific xanthan WEISROCK WILLIAM P Pat. Nr. US4311796 STANDARD OIL CO INDIANA 1982 xanthan In the production of xanthan gum by the action of Xanthomonas
productivity during continuous bacteria on a nutrient medium, the specific productivity of the
fermentation organism employed can be improved by the increase in average cell
concentration through the stepwise increase of growth limiting
nutrients in the medium.
111 Method for improving xanthan yield WEISROCK WILLIAM P Pat. Nr. US4301247 STANDARD OIL CO INDIANA 1981 xanthan, cholate, deoxycholate In the production of xanthan gum by action of Xanthomonas bacteria
on a nutrient medium, the yield of xanthan gum can be improved by
the addition of deoxycholate or cholate to the nutrient medium at the
time of inoculation of the bacteria on the nutrient medium.
112 Process for the fermentative production DEMAIN ARNOLD L; SOUW Pat. Nr. US4245046 MASSACHUSETTS INST 1981 Xanthan, organic acid Xanthan gum is produced by fermentation with the bacterium,
of xanthan gum with organic acids PETER TECHNOLOGY Xanthomonas campestris NRRL B-1459, of a nutrient medium
containing a sugar and a stimulatory organic acid which stimulates the
production of xanthan gum. The stimulatory organic acid can be a
source of pyruvic acid, alpha-keto-glutaric acid, succinic acid or
mixtures thereof.
113 Apparatus and method for the HOMMA TAIRA (JP); Pat. Nr. US5972695 SHINETSU CHEMICAL CO (JP); 1999 fermenter, xanthan A fermenter for the production of xanthan gum is provided with an
production of xanthan gum MUROFUSHI KANJI (JP); SHINETSU BIO INC (US) upper helical impeller and a lower turbine impeller which are
NAGURA SHIGEHIRO (JP) positioned therewithin, and an agitator shaft for driving these helical
impeller and turbine impeller. The helical impeller consists of a pair of
vertically spaced arms extending from the agitator shaft in opposite
directions and arranged in twisted relationship, and at least one
shearing paddle bridging these arms, and the turbine impeller consists
of a rotating disc having at least one turbine blade attached thereto.
114 Fermentation feedstock DE TROOSTEMBERGH JEAN- )Pat. Nr. EP0609995 CERESTAR HOLDING BV (NL 1994 fermentation, xanthan, mannose, A fermentation process for the production of a product comprising
CLAUDE M (NL); BECK ROLAND feedstock mannose units eg. xanthan gum in which a simple sugar is a
H F DR (BE); DE component of the fermentation feedstock and a part of that sugar is
WANNEMAEKER BENEDICTE L mannose. Preferably the sugar is a mixture of mannose and glucose
T (BE) optionally containing minor amounts of other sugars, the mixture of
mannose and glucose suitably being produced by the epimerisation of
glucose.
115 Method for fermentation production of HONMA TAIRA (JP); NAGURA Pat. Nr. US5580763 SHINETSU CHEMICAL CO (JP); 1996 xanthan, nitrogen A method for the fermentation production of xanthan gum which
xanthan gum SHIGEHIRO (JP); MUROFUSHI SHINETSU BIO INC (US) comprises the step of carrying out culture by using a water-soluble
KANJI (JP) inorganic nitrogen component alone as the nitrogen source of a
production medium, and by mixing and using the water-soluble
inorganic nitrogen component and a water-insoluble organic nitrogen
component as the nitrogen sources of a seed fermentation medium.
4.11 Literatures on Polysaccharides.xls - page 371
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
116 Xanthan gum-producing strain of POLLOCK THOMAS J (US); Pat. Nr. US5340743 SHINETSU CHEMICAL CO (US); 1994 xanthan A method of increasing xanthan gum production, comprising culturing
xanthomonas THORNE LINDA (US) SHINETSU BIO INC (US) a Xanthomonas campestris strain having a xanthan-increasing
modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing rifampicin-
resistance; (2) a mutation causing bacitracin-resistance; or (3)
exogenous genetic information controlling the synthesis of xanthan;
and separating xanthan from the culture medium, is provided along
with specific DNA sequences and Xanthomonas campestris strains
showing increased xanthan gum production.
117 Xanthomonas campestris strain for POLLOCK THOMAS J (US); Pat. Nr. US5279961 SHINETSU CHEMICAL CO (US); 1994 xanthan, xanthomonas, resistance A method of increasing xanthan gum production, comprising culturing
production of Xanthan gum THORNE LINDA (US) SHINETSU BIO INC (US) a Xanthomonas campestris strain having a xanthan-increasing
modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing rifampicin-
resistance; (2) a mutation causing bacitracin-resistance; or (3)
exogenous genetic information controlling the synthesis of xanthan;
and separating xanthan from the culture medium, is provided along
with specific DNA sequences and Xanthomonas campestris strains
showing increased xanthan gum production.
118 Process for the production of WILKE MICHAELA (DE); Pat. Nr. US4978750 WOLFF WALSRODE AG (DE) 1990 heteropolysaccharide, xanthan, pH Cellulase-free heteropolysaccharides, more especially xanthan, are
heteropolysaccharides having improved SZABLIKOWSKI KLAUS (DE); obtainable by treatment at special pH values, heat treatment,
properties, more especially xanthan BALSER KLAUS (DE) optionally cooling, neutralization and, optionally, subsequent
precipitation in a high-turbulence precipitation bath.
119 Continuous process for the production LAWFORD HUGH G Pat. Nr. US4355106 WESTON GEORGE LTD 1982 The present invention is directed to a two-stage continuous process
of gelable exopolysaccharide for the production of a gelable curdlan-type exopolysaccharide. In the
first stage a stable, curdlan-producing strain of microorganism such as
Alcaligenes faecalis var. myxogenes ATCC 31749 and ATCC 31750,
is grown aerobically in an aerated, agitated culture medium containing
assimilable carbon, nutrients and organic salts. The amount of
nitrogen in the first stage is so limited that the effluent therefrom
contains substantially no inorganic nitrogen. The effluent is introduced
into a second stage in a constant volume fermenter wherein it is mixed
with a nitrogen-free carbohydrate. The resultant mixture is aerated
and mixed at pH 5.5 to 6.5 at a temperature of from 25 DEG to 35
DEG C., the volume and dilution rate in the reactor being selected so
that the residence time of the microorganism in the fermenter does not
exceed an equivalent to the maximum length of time during which the
activity of a batch culture of the microorganism with respec
4.11 Literatures on Polysaccharides.xls - page 372
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
120 METHOD OF BROWN ALGAE KURNYGINA V T; NEKRASOVA Pat. Nr. RU2132622 FITOLON; TOVARISHCHESTVO S 1999 FIELD: biotechnology. SUBSTANCE: invention relates to processing
PROCESSING V B; NIKITINA T V; OGRANICHENNO of brown algae, namely, laminaria and bady wrack (Fucus vesiculosis)
BELOZERSKIKH O A for preparing lipid concentrates and water-soluble concentrates
enriched with iodine. Milled algae are extracted with an organic
solvent containing 1-6 carbon atoms at ratio raw : extractant = 1:(1-
20). After distillation of solvent lipid and aqueous concentrates are
obtained and separated their. An aqueous extract is dried to obtain
water-soluble concentrate. Method provides the most effectiveness of
extraction of lipid-soluble component of brown algae which are rich
with nonsaturated substances and to use its as a substance for
production of curative-prophylactic additions "Clamin" and "Phytolon".
The powder obtained from water-soluble substances of brown algae
extract is the complex of polysaccharides, mannitol, vitamins, mineral
substances (including that enriched with iodine)that can be used as
the food and prophylactic addition in medicinal, food and chemical-
pharmaceutic
121 PROCESS FOR THE PRODUCTION SANTOS PATRICK FERREIRA Pat. Nr. AU616683 COMMISSARIAT ENERGIE 1991 Polysaccharides, production, No abstract available.
AND EXTRACTION OF DOS; THEPENIER CATHERINE; ATOMIQUE extraction
POLYSACCHARIDES FROM A BARNIER HENRI; GUDIN
PORPHYRIDIUM CRUENTUM CLAUDE
CULTURE AND APPARATUS FOR
PERFORMING THE PROCESS
122 The production of polysaccharides from CASH HOWARD A; JOHAL Pat. Nr. EP0347236, A3 STANDARD OIL CO OHIO (US) 1989 polysaccharides, fungus, A process to produce products, in particular polysaccharides, from
filamentous fungi. SARJIT S filamentous fungi, in an immobilized cell bioreactor wherein the fungus
is fixed and adheres to the surface of a porous, non-particulate
support and aqueous liquid medium is passed through the
immobilized system and product containing medium is recycled or
withdrawn from the system.
123 Water-soluble polysaccharides, CAREL SERGE; PAGE YVES- Pat. Nr. EP0308279 LIPHA (FR) 1989 polysaccharides, water-soluble New water-soluble polysaccharides. These polysaccharides extracted
process for obtaining them, their use as MARIE; VANDERHOVEN from Escherichia coli and from Klebsiella pneumoniae contain less
medicaments and a preparation CHRISTINE; MURRAY NORMAN; than 1% of proteins, less than 0.5% of osamines, from 65 to 75% of
containing them. MONSIGNY MICHEL; neutral oses, from 18 to 27% of uronic acids, from 5 to 9% of pyruvic
DELMOTTE FRANCIS; ROCHE acid in the form of pyruvilidene, and have a molecular mass greater
ANNE-CLAUDE; PETIT CLAIRE than 50,000. They have an immunomodulating activity which makes
them useful in the field of therapeutics.
124 Process for the production of BOUNIOT ALBERT Pat. Nr. US3988313 RHONE POULENC SA 1976 polysaccharides, non-fibrous Polysaccharides produced by fermentation are obtained in a non-
fermentation polysaccharides having a fibrous form by washing the product produced by precipitation from
non-fibrous structure the fermentation medium with an aqueous organic liquid in which the
proportion of organic liquid is high enough to give a washed product
which is not soft, difficult to dry and with a tendency to agglomerate,
but not so high that the washed product, after drying and grinding, has
a fibrous structure, and then drying and grinding the washed
polysaccharide.
4.11 Literatures on Polysaccharides.xls - page 373
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
125 CULTIVATION OF PHOTOSYNTHETIC MATSUMOTO KAZUNORI; Pat. Nr. JP11196858 RESEARCH INSTITUTE OF 1999 polysaccharide, photosynthetic, PROBLEM TO BE SOLVED: To provide a method for culturing a
MICROORGANISM AND SUDO HIROAKI INNOVATIVE TECHNOLOGY FOR extracellular photosynthetic microorganism high in utility, generating efficiency of a
PRODUCTION OF EXTRACELLULAR THE EARTH; MITSUBISHI HEAVY polysaccharide and utilizing efficiency of a light, and a method for
POLYSACCHARIDE IND LTD producing an extracellular polysaccharide. SOLUTION: This method
for culturing a photosynthetic microorganism comprises using agar-
agar as a comprehensive immobilizing carrier and culturing it to obtain
an N/P ratio in a culturing solution of >=3. In the method for producing
a polysaccharide derived from a microorganism by culturing the
photosynthetic microorganism generating an extracellular
polysaccharide using an immobilizing carrier, agar-agar is used as the
comprehensive immobilizing carrier and the photosynthetic
microorganism is cultured to cause the N/P ratio in the culturing
solution of >=3 to generate the objective extracellular polysaccharide.
126 PRODUCTION OF YUMOTO ISAO Pat. Nr. JP11113591 AGENCY OF IND SCIENCE & 1999 Polysaccharide, Deleya, phb, PROBLEM TO BE SOLVED: To efficiently obtain a polysaccharide
POLYSACCHARIDE TECHNOL polyhydroxybutyric acid useful as e.g. a food thickening agent, soil modifier such as water-
holding agent, flocculant for e.g. wastewater treatment, by culturing a
strain belonging to the genus Deleya and capable of producing the
aimed polysaccharide followed by collecting the aimed product from
the cultured product. SOLUTION: A strain belonging to the genus
Deleya and capable of producing the aimed polysaccharide (e.g.
Deleya marina L-2 strain: FERM P-16406) is cultured, and the aimed
polysaccharide, along with &beta -polyhydroxybutyric acid produced
by the strain, is collected to obtain the objective polysaccharide useful
as e.g. a food thickening agent, a soil modifier as a water-holding
agent, a flocculant used in wastewater treatment, and at the same
time, obtain &beta - polyhydroxybutyric acid useful for e.g. soft drink
bottles made of a hard and brittle biodegradable polymeric material
having a high melting point (170 deg.C) known as a biodegradable
plastic.
127 Polysaccharide producing process RIGHELATO RENTON C; Pat. Nr. US4234688 Tate & Lyle Ltd 1980 polysaccharide, production, The solution viscosity of a polysaccharide, microbial alginate,
using protease and Azotobacter JARMAN TREVOR R Azotobacter produced by culturing strains of Azotobacter vinelandii, is controlled
by addition of a protease to the culture broth. The protease can be
added during the culture, to obtain a polysaccharide of increased
viscosity. Alternatively or additionally protease can also be added
after culture but before the polysaccharide is isolated from the broth,
for example, to prevent reduction of viscosity during storage. Neutral
and alkaline proteases having activity at around pH 7 are particularly
suitable.
128 Strain of Klebsiella pneumoniae, subsp. PAUL FRANCOIS MARIE Pat. Nr. US5876982 BIOEUROPE (FR) 1999 polysaccharide, L-fucose PCT No. PCT/FR96/00127 Sec. 371 Date Jul. 25, 1997 Sec. 102(e)
pneumoniae, and a process for the BERNARD (FR); PERRY DAVID Date Jul. 25, 1997 PCT Filed Jan. 25, 1996 PCT Pub. No.
production of a polysaccharide FRANK (FR); MONSAN PIERRE WO96/23057 PCT Pub. Date Aug. 1, 1996The present invention
containing L-fucose FREDERIC (FR) discloses a new strain of Klebsiella pneumoniae subsp. pneumoniae
BEC1000 CNCMI-1507 which produces industrially useful quantities
of a polysaccharide containing L-fucose. Also disclosed is a process
of producing the polysaccharide using this strain and mutants thereof.
The polysaccharide has properties which are particularly useful to the
cosmetics industry.
4.11 Literatures on Polysaccharides.xls - page 374
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
129 NOVEL CELLULOSE-PRODUCING TSUCHIDA TAKAYASU (JP); Pat. Nr. EP0831101 BIO POLYMER RES CO LTD (JP) 1998 cellulose, bacteria Novel cellulose-producing bacteria including one capable of
BACTERIA WATANABE KUNIHIKO (JP); producing of a bacterial cellulose having a weight-average degree of
YANO HISATO (JP); TABUCHI polymerization in terms of polystyrene of 1.6 x 10<4> or above, one
MARI (JP); TAHARA NAOKI (JP); capable of producing a bacterial cellulose containing a small amount
MORINAGA YASUSHI (JP); of the fraction with low degrees of polymerization, one producing a
TAKEMURA HIROSHI (JP); Bingham polysaccharide as a by-product, and one producing a small
TOYOSAKI HIROSHI (JP); amount of water-soluble polysaccharide; a method for the production
YOSHINAGA FUMIHIRO (JP) of bacterial cellulose, which comprises culturing these cellulose-
producing bacteria; and bacterial cellulose thus obtained.
130 PRODUCTION OF EXTRACELLULAR UEHARA AKIYOSHI; Pat. Nr. JP9131199 AJINOMOTO CO INC 1997 Lipomyces, Polysaccharide, PROBLEM TO BE SOLVED: To profitably produce the subject
POLYSACCHARIDE PRODUCED KAWAHARA YOSHIO; SHIMIZU mannose, glucuronic acid, polysaccharide useful as a soil conditioner, a paper-strengthening
WITH MICROORGANISM OF GENUS SHIGEATSU galactose, trisaccharide agent, etc., by culturing a microorganism belonging to the genus
LIPOMYCES Lipomyces and having an extracellular polysaccharide- producing
ability in a culture medium, maintaining the viscosity of the culture
solution at a specific value or smaller, and (semi)continuously
culturing the microorganism. SOLUTION: This method for producing
the extracellular polysaccharide comprises culturing and multiplying a
microorganism (e.g. Lipomyces starkyi- CBS 1807) belonging to the
genus Lipomyces and having an ability to produce the extracellular
polysaccharide, maintaining the viscosity of the culture solution at
<=150 centipoises, continuously or semi-continuously culturing the
microorganism to produce and accumulate the extracellular
polysaccharide in the culture solution, centrifugally removing the cells
from the culture solution, concentrating the filtrate and subsequently
drying the concentrated filtra
131 Polysaccharide products derived from ABBOTT THOMAS P (US); Pat. Nr. US5567812 US ARMY (US) 1996 Lesquerella fendleri, Previously unrecognized polysaccharide products are extracted from
lesquerella fendleri and methods of CARLSON KENNETH D (US); polysaccharide either whole Lesquerella fendleri seed or commercially processed and
their production KLEIMAN ROBERT (US) oil-extracted seed meal or presscake or other seed material.
Processes used include the steps of: (1) combining the seed material
with an aqueous solution; (2) high speed stirring or sonification of the
resultant seed material for the separation of the polysaccharide from
the seed; and (3) isolation of the polysaccharide from the aqueous
filtrate. The resultant polysaccharides are highly polymeric and
enhance solution viscosities over a wide range of pH, bleaching and
salt conditions.
132 Production of fructan (levan) HAN YOUN W (US); CLARKE Pat. Nr. US5547863 US ARMY (US) 1996 fructan, levan, bacillus polymyxa Soil isolates, identified as strains of Bacillus polymyxa, NRRL B-
polyfructose polymers using bacillus MARGARET A (US) 18475 and NRRL B-18476, produce large quantities of a pure and
polymyxa uniform extracellular polysaccharide fructan (levan), in a sucrose
medium. The levan consists entirely of fructose and the residues
linked by beta , 2-6 fructofuranoside linkage.
133 Polysaccharide, its applications, ist FONTAINE THIERRY (FR); Pat. Nr. US5455343 SANOFI ELF (FR) 1995 pseudomonas, polysaccharide This polysaccharide consists of repeating units which are composed
production by fermentation and the FOURNET BERNARD of a backbone, comprising 2 radicals of D-mannose, 2 of D-glucose, 1
pseudomonas strain which produces it (FR);PLANARD MARIE FRANCE of D-galactose, 1 of D-glucuronic acid, 1 of D-xylose, 1 of L-lyxose
(FR) and 1 of L-fucose, on which pyruvic acid groups may be grafted and of
which certain of the saccharide hydroxyl groups are esterified as
acetate. It can be employed as a viscosity agent for thickening and
gelling.
4.11 Literatures on Polysaccharides.xls - page 375
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
134 Microbial cellulose modified during BROWN JR R MALCOLM (US) Pat. Nr. US4942128 UNIV TEXAS (US) 1990 microbial cellulose The present invention involves a method of producing cellulose. This
synthesis method comprises inoculating a quantity of nutrient medium
comprising a polysaccharide derivative such as
carboxymethylcellulose (CMC) with a cellulose-producing
microorganism. The inoculated medium is then aerobically incubated
to facilitate the production of cellulose. The step of substantially
drying the cellulose may be added for certain products. Substantially
dried cellulose resulting from this procedure is highly absorbent,
tending to retain its absorbent properties during repeated wetting and
drying, and is usable where such absorbency is desired. A subject of
the present invention is a composition of matter consisting essentially
of such cellulose in a native or substantially dried form. Microbial
cellulose produced in the presence of carboxymethyl cellulose may be
substantially dried by many means known to those skilled in the art.
This drying may be, for example, by washing with a non-aqueous
hydrophilic solvent or by air-drying.
135 Process for multiplication of EYSSAUTIER BRUNO Pat. Nr. US5017479 SANOFI SA (FR) 1991 microorganisms, growth, Process for obtaining a mass of polysaccharide-producing
polysaccharide-producing polysaccharide microorganisms, consisting in conducting the growth of the
microorganisms and use thereof in a microorganisms in a medium containing an enzyme which hydrolyzes
polysaccharide production process the formed polysaccharide. Application in a process for the production
of polysaccharide in two stages, in which the growth stage takes place
in the presence of an enzyme, particularly for the production of
scleroglucane using sclerotium type fungi.
136 Fermentation process for the EYSSAUTIER BRUNO Pat. Nr. US4940663 SANOFI SA (FR) 1990 xanthan, fermentation process The invention relates to a process for the fermentation of
production of xanthane carbohydrates by bacteria of the genus Xanthomonas for the
production of a polysaccharide of the xanthane type, in which the
source of nitrogen consists of a gelatin with a molecular weight of less
than 5000. Application: preparation of xanthane.
137 Process for the production and BARNIER HENRI (FR); Pat: Nr. US4906746 COMMISSARIAT ENERGIE 1990 porphyridium cruentum, Process for the production and extraction of polysaccharides from a
extraction of polysaccharides from a FERREIRA DOS SANTOS ATOMIQUE polysaccharide, extraction porphyridium cruentum culture and apparatus for performing the
porphyridium cruentum culture and PATRICK F (FR); GUDIN process. This production and extraction process comprises a stage of
apparatus for performing the process CLAUDE (FR); THEPENIER concentrating the polysaccharides consisting of leaving the culture
CATHERINE (FR) medium (1) in a photoreactor (22) exposed to sunlight under stagnant
conditions and at ambient temperature, leading to the formation of a
polysaccharide-rich cream (23) and recovering said cream by
skimming, a stage (24) of heating the concentrate obtained at a
temperature between 60 DEG and 100 DEG C., a stage of separating
the solid and liquid phases formed (26), a stage (30) of precipitating
the polysaccharides contained in the liquid phase and a stage (16) of
drying the precipitate obtained.
138 Production of bacterial polysaccharides ELLWOOD DEREK C (GB); )Pat. Nr. US4696900 SECR DEFENCE BRIT (GB 1987 Xanthomonas, polysaccharide, Polysaccharides are produced by single stage continuous culture of
EVANS CHARLES G T (GB); Xanthomonas bacteria, especially of the Xanthomonas campestris
YEO RICHARD G (GB) group in a chemically-defined culture medium. Cultures have been run
for over 2,000 hours without reduction in the polysaccharide yield. The
physical and chemical properties of the product can be controlled by
selection of the growth limiting substrate (limiting nutrilite) in the
culture medium to give a range of polysaccharides suitable for various
applications.
4.11 Literatures on Polysaccharides.xls - page 376
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
139 Microbial polysaccharide articles and RING DAVID F (US); NASHED Pat. Nr. US4655758 JOHNSON & JOHNSON PROD INC 1987 polysaccharide, microbial cellulose Laminar polysaccharide structures, e.g., laminar microbial
methods of production WILSON (US); DOW THURMAN (US) cellulosestructures, are disclosed. These structures comprise
(US) densified planiform sheets or laminae that merge into one another and
together define plural regions having reduced polysaccharide
microfibril density. The disclosed laminar polysaccharide structures
are derived by manipulating fibrous polysaccharide pellicles produced
by microorganisms such as those of the genere Acetobacter,
Rhizobium, Agrobacterium, Pseudomonas, Sphaerotilus, and the like.
140 Polysaccharide production using novel JARMAN TREVOR R (GB); Pat: Nr. US4490467 KELCO BIOSPECIALTIES LTD (GB) 1984 Pseudomonas mendocina, A process for producing polysaccharide consisting of a partially
strains of Pseudomonas mendocina HACKING ANDREW J GB) polysaccharide acetylated variable block copolymer of D-mannuronic and L-guluronic
acid residues comprises growing a biologically pure culture of a
Pseudomonas mendocina microorganism selected from the group
consisting of NCIB 11687, 11688, and 11689 in an aqueous nutrient
medium by submerged aerobic fermentation of an assimilable carbon
source and recovering the polysaccharide. Biologically pure cultures
of the organisms are another feature of the invention.
141 Production of an allose-containing TAKEMOTO HISAO (JP); Pat. Nr. US4425431 TOYO SODA MFG CO LTD (JP) 1984 allose, polysaccharide, galactose, A new polysaccharide including allose as a constituent sugar and
polysaccharide IGARASHI TATSUO (JP) Pseudomonas viscogena further characterized by galactose as a major constituent sugar is
described. The polysaccharide is produced extracellularly by
cultivation of Pseudomonas viscogena strains in nutrient medium.
142 Process for culturing a microalga, and CYSEWSKI GERRY R Pat. Nr. US4417415 BATTELLE DEVELOPMENT CORP 1983 Porphyridium cruentum, Porphyridium cruentum is cultured in an enriched seawater medium
extracting a polysaccharide therefrom (US);ANDERSON DANIEL B (US) (US) polysaccharide, extraction, algae using a high initial cell concentration until the productivity of
polysaccharide production by the alga is maximized. The whole
culture is then extracted by making the culture strongly alkaline, and
heat treating it. The culture is cooled, acidified and the polysaccharide
precipitated by addition of a water-miscible organic solvent such as
ethanol. Very high yields of polysaccharide are obtained, in excess of
4.5 grams per liter of culture.
143 Production of microbial polysaccharides KIM LEO (US); ASH STUART G Pat. Nr. US4384044 SHELL OIL CO 1983 polysaccharide, production This invention relates to a process for the production of a
(GB) polysaccharide wherein a microorganism species which produces
polysaccharide (preferably in the stationary phase of the growth cycle)
is supported on a porous, particulate inert support, the pore size being
greater than about 0.5 mu m, to form an immobilized cell system,
aqueous nutrient medium is passed through the immobilized system,
and polysaccharide-containing medium is withdrawn from the system.
The invention provides also for the use of the polysaccharide in the
displacement of fluid from subsurface formations, and an immobilized
cell system for use in the foregoing process.
144 Process for the production of GOVAN JOHN R (GB); JARMAN Pat. Nr. US4235966 TALRES DEV (NL) 1980 Polysaccharide, production A process for the production of polysaccharide consisting of a partially
polysaccharide TREVOR R (GB) acetylated variable block copolymer of D-mannuronic and L-guluronic
acid residues, comprises cultivating in a nutrient medium therefore a
strain of Pseudomonas, which is non-pathogenic to humans, and
which has been obtained by treating a non-mucoid species of
Pseudomonas, which is non-pathogenic to humans, with a beta -
lactam or aminoglycoside antibiotic whereby a mucoid strain tolerant
to said antibiotic was selected, and isolating from the medium the
polysaccharide produced.
145 Process for the production of novel HISATSUKA KENICHI; ISHIYAMA Pat: Nr. US4153508 IDEMITSU KOSAN CO 1979 Polysaccharide, production Polysaccharides forming gels are produced by cultivating a
polysaccharide SABURO; INOUE microorganism such as Arthrobacter carbazolum FERM 2574 in a
AKIRA;TSUMURA OSAMU; suitable medium.
SATO MIKIO
4.11 Literatures on Polysaccharides.xls - page 377
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
146 Continuous process for the production RIGHELATO RENTON C; Pat: Nr. US4130461 Tate & Lyle Ltd 1978 Azotobacter vinelandii, Polysaccharide is produced in high yields by continuous culture of a
of polysaccharide under phosphate DEAVIN LYNDA Polysaccharide, phosphate- polysaccharide-producing strain of Azotobacter vinelandii under
limiting conditions limitation phosphate-limited conditions, preferably with restricted oxygen
uptake.
147 Production of polysaccharides of high CROS PATRICK (FR) Pat. Nr. US5610037 RHONE POULENC CHIMIE (FR) 1997 xanthan, polysaccharide, Polysaccharide biopolymers, e.g., xanthan gum, are produced by the
viscosity using xanthomonas aerobic microbial fermentation of a carbohydrate in an aqueous
campestris and glycoamylase with nutrient medium containing starch as a source of carbon, and wherein
fluidized starch the fermentation is carried out in the presence of a saccharide-specific
amylolytic enzyme.
148 Microbiological process for the Pat. Nr. GB2026515 TATE & LYLE LTD 1980 polysaccharide, penicillin A process for the production of polysaccharide consisting of a partially
production of alginate type acetylated variable block copolymer of D-mannuronic and L-guluronic
polysaccharide acid residues, comprises cultivating in a nutrient medium therefor a
strain of Pseudomonas, which is non- pathogenic to humans, and
which has been obtained by treating a non- mucoid species of
Pseudomonas, which is non-pathogenic to humans, with a beta -
lactam or aminoglycoside antibiotic whereby a mucoid strain tolerant
to said antibiotic was selected, and isolating from the medium the
polysaccharide produced. Particularly suitable strains may be derived
from P. mendocina, P. tabaci or P. putida. Suitable antibiotics include
the penicillins, eg carboxyalkyl or carboxyaralkyl derivatives of
penicillins, or esters thereof, or 3-halophenyl penicillins. A preferred
antibiotic is carbenicillin (disodium alpha - carboxybenzyl penicillin).
149 NOVEL CELLULOSE-PRODUCING MATSUOKA MASANOBU (JP); Pat. Nr. EP0834555 BIOPOLYMER RES CO LTD (JP) 1998 cellulose, bacteria This invention relates to a microorganism that is capable of producing
BACTERIA TSUCHIDA TAKAYASU (JP); a cellulosic product (referred to hereinafter as a "cellulose-producing
KOJIMA YUKIKO (JP); SETO bacterium") and belongs to a novel subspecies which is substantialy
AKIRA (JP); TONOUCHI NAOTO negative or very slightly positive in oxidation of acetates and lactates.
(JP); YOSHINAGA FUMIHIRO This invention also relates to novel saccharide analog-resistant
(JP) strains, amino acid analog-resistant strains and levan sucrase-
defective strains. Further, this invention relates to a method for the
production of cellulosic material (bacterial cellulose:"BC"), which
comprises culturing these novel bactria and to bacterial cellulose
which may be thus obtained. A larger amount of bacterial cellulose
may be produced by culturing Acetobacter xylinum subsp.
nonacetoxidans, the present resistant strains and the levan sucrase-
defective strains, which have been derived and bred from the
cellulose-producing bacteria, than by culturing the BPR 2001 strain in
the medium containing especially sucrose or glucose as carbon
sources.
4.11 Literatures on Polysaccharides.xls - page 378
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
150 Microbial production of polyfructose MAYS THOMAS D (US); DALLY Pat. Nr. US4879228 IGI BIOTECHNOLOGY INC (US) 1989 polyfructose, production A water-soluble levan having a weight average molecular weight of
ELLEN L (US) about 10,0000-40 million, preferably about 5-25 million and especially
about 10-20 million which stabilizes a bovine serum albumin colloid
having index (EAI) of about 3-100 determined according to the formula
EAI=2T/OC wherein T is turbidity measured at 500 nm, C is the weight
of emulsified protein per unit volume of the aqueous phase, and O is
the volume fraction of a dispersed oil phase is produced by fermenting
a nutrient growth medium feedstock having a carbon source
consisting essentially of an assimilable sugar selected from the group
consisting of sucrose, raffinose, or a mixture thereof with a
Zymomonas mobilis microorganism capable of converting at least
50% of the fructose value of the sugar to said levan under nutrient
growth conditions which enhance levan production while suppressing
ethanol production. It is useful as a colloid stabilizing agent,
particularly with foods, beverages pharmaceuticals, dentrifices, and
cosmetics.
151 PRODUCTION OF LEVAN KOJIMA ICHIRO; others: 01 Pat. Nr. JP3219889 NIPPON OIL CO LTD 1991 levan, production, Serratia PURPOSE:To obtain the subject substance at an excellent production
rate by culturing a levan-producing bacillus belonging to Serratia
genus. CONSTITUTION:By separation from the soil, a levan-
producing bacillus, Serratia levanicum [Serratia sp.NOC 1219
(FERMP-11171)] having the following mycological properties is
obtained; Shape: rod bacillus having (0.6-0.8)X(1.0-2.0)mu; no
mobility; growth temperature: 8-41 deg.C; growth pH: 4.0-11.5; H2S
production: negative; gas production from glucose: negative, etc. The
obtained bacillus is then inoculated into a culture medium containing a
hydrocarbon source such as an alcohol, a nitrogen source such as
urea, an inorganic salt, etc., such as an Mg salt and aerobically
cultured under aeration-agitation, etc., at pH3.5-9.5, at 20-40 deg.C
for 1-5 days to obtain a cultured material. The resultant cultured
material is diluted using about double amount of water and centrifuged
at about 10000G for about 10min. To the separated supernatant,
isopropanol, etc., is added to obta
152 Increased cellulose production from Tonouchi N, Yanase H, Kojima Y, Biosci Biotechnol Biochem 1998 Bio-Polymer Research Co., Ltd., 1998 levan, production, acetobacter Cellulose production from sucrose by Acetobacter strains is
sucrose with reduced levan Tsuchida T, Yoshinaga F, May;62(5):833-6 Kanagawa, Japan. accompanied by the accumulation of a water-soluble polysaccharide,
accumulation by an Acetobacter strain Horinouchi S called levan. To improve cellulose productivity, a levansucrase-
harboring a recombinant plasmid. deficient mutant, LD-2, was derived from Acetobacter strain 757 and
used as a host for the construction of recombinant strains. An LD-2
mutant harboring a plasmid containing the sucrase gene, sucZE3,
from Zymomonas mobilis together with zliS, a gene that encodes a
secretion-activating factor under the control of the Escherichia coli lac
promoter, had sucrase activity and produced much cellulose and little
levan in a medium containing sucrose. In addition, a mutant
levansucrase gene, mutant sacB, from Bacillus subtilis, which
encodes a protein with little levan-forming activity, was generated by
site-directed mutagenesis and introduced into the LD-2 mutant. This
introduction also resulted in the higher cellulose productivity and little
levan.
153 Fructan from Erwinia herbicola. Blake JD, Clarke ML, Jansson PE, J Bacteriol 1982 Sep;151(3):1595-7 1982 levan, fructan, Erwinia Levan production by strains of Erwinia herbicola is common, and this
McNeil KE property has some taxonomic significance for species differentiation
within the "herbicola" group. The extracellular polysaccharide
elaborated by strain 403 was characterized by nuclear magnetic
resonance spectroscopy and methylation analysis. Results showed it
to be a typical bacterial levan.
4.11 Literatures on Polysaccharides.xls - page 379
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
154 Production of an extracellular levan by Howell A Jr, Jordan HV Arch Oral Biol 1967 Apr;12(4):571-3 1976 extracellular, levan, Odontomyces
Odontomyces viscosus.
155 Ability of casamino acids to support West TP, Fullenkamp NA Microbios 2000;102(402):89-101 Department of Chemistry and 2000 casamino acid, gellan, production, The ability of casamino acids and vitamin-assay casamino acids to
gellan production by Sphingomonas Biochemistry, South Dakota State Sphingomonas support gellan production by Sphingomonas paucimobilis ATCC
paucimobilis ATCC 31461. University, Brookings 57007, USA. 31461 was examined in a medium containing glucose or corn syrup as
the carbon source relative to yeast extract supplementation. When
glucose or corn syrup served as the carbon source, the presence of
yeast extract in the growth medium stimulated gellan production by
strain ATCC 31461 on casamino acids. Using vitamin-assay casamino
acids as the nitrogen source, the addition of vitamins lowered gellan
synthesis by glucose-grown cells regardless of yeast extract
supplementation while gellan elaboration by corn syrup-grown strain
ATCC 31461 cells could only be increased by supplementing vitamins
into medium lacking yeast extract. Independent of carbon source, the
absence of yeast extract in the medium reduced biomass production.
Biomass production by the strain grown on either carbon source was
increased by supplementing vitamins in the medium containing yeast
extract.
156 Structures and properties of gellan Fialho AM, Martins LO, Donval Appl Environ Microbiol 1999 Centro de Engenharia Biologica e 1999 gellan, structure, cheese whey, The dairy industry produces large quantities of whey as a by-product
polymers produced by sphingomonas ML, Leitao JH, Ridout MJ, Jay AJ, Jun;65(6):2485-91 Quimica, Instituto Superior Tecnico, lactose, Sphingomonas of cheese production and is increasingly looking for new ways to
paucimobilis ATCC 31461 from lactose Morris VJ, Sa-Correia I 1049-001 Lisbon, Portugal. utilize this waste product. Gellan gum is reliably produced by
compared with those produced from Sphingomonas paucimobilis in growth media containing lactose, a
glucose and from cheese whey. significant component of cheese whey, as a carbon source. We
studied and compared polysaccharide biosynthesis by S. paucimobilis
ATCC 31461 in media containing glucose, lactose (5 to 30 g/liter), and
sweet cheese whey. We found that altering the growth medium can
markedly affect the polysaccharide yield, acyl substitution level,
polymer rheological properties, and susceptibility to degradation.
Depression of gellan production from lactose compared with gellan
production from glucose (approximately 30%) did not appear to occur
at the level of synthesis of sugar nucleotides, which are the donors of
monomers used for biosynthesis of the repetitive tetrasaccharide unit
of gellan. The lactose-derived biopolymer had the highest total acyl
content; the glu
157 Xanthan gum production under several Casas JA, Santos VE, Garcia- Enzyme Microb Technol 2000 Feb Dpt. Ing. Quimica, Fac. CC. Quimicas, 2000 xanthan, molecular structure, Xanthan gum production under several operational conditions has
operational conditions: molecular Ochoa F 1;26(2-4):282-291 Universidad Complutense, Madrid, rheological properties been studied. Temperature, initial nitrogen concentration and oxygen
structure and rheological properties*. Spain mass transfer rate have been changed and average molecular weight,
pyruvilation and acetylation degree of xanthan produced have been
measured in order to know the influence of these variables on the
synthesised xanthan molecular structure. Also, xanthan gum solution
viscosity has been measured, and rheological properties of the
solutions have been related to molecular structure and operational
conditions. The Casson model has been employed to describe the
rheological behaviour. The parameter values of the Casson model,
tau(0) and K(c), have been obtained for each polysaccharide
synthesised under different operational conditions. Both pyruvilation
and acetylation degrees and average molecular weight of xanthan
increase with fermentation time at any operating conditions. Xanthan
molecules with the highest average molecular weight have been
obtained at 25 degrees C. Nevertheless, a
4.11 Literatures on Polysaccharides.xls - page 380
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
158 Agitator speed and dissolved oxygen Amanullah A, Tuttiett B, Nienow Biotechnol Bioeng 1998 Jan Centre for Bioprocess Engineering, 1998 xanthan fermentations, agitator Agitation speed affects both the extent of motion in Xanthan
effects in xanthan fermentations AW 20;57(2):198-210 School of Chemical Engineering, The speed, oxygen, method fermentation broths because of their rheological complexity and the
University of Birmingham, Edgbaston, rate of oxygen transfer. The combination of these two effects causes
Birmingham B15 2TT, UK. the dissolved oxygen concentration and its spatial uniformity also to
change with agitator speed. Separating these complex interactions
has been achieved in this study in the following way. First, the
influence of agitation speeds of 500 and 1000 rpm has been
investigated at a constant nonlimiting dissolved oxygen concentration
of 20% of air saturation using gas blending. Under these controlled
dissolved oxygen conditions, the results demonstrate that the
biological performance of the culture was independent of agitation
speed as long as broth homogeneity could be ensured. With the
development of increasing rheological complexity lending to stagnant
regions at Xanthan concentrations >20 g/L, it is shown that the
superior bulk mixing achieved at 1000 rpm, compared with 500 rpm,
leading to an increased proport
159 Intracellular compounds quantification Garcia-Ochoa F, Santos VE, Biotechnol Bioeng 1998 Jan Departamento de Ingenieria Quimica, 1998 xanthan, flow cytometry The use of flow cytometry (FCM) to quantitatively analyze intracellular
by means of flow cytometry in bacteria: Alcon A 5;57(1):87-94 Facultad de Ciencias Quimicas, compounds is studied. FCM is a very useful technique for individual
application to xanthan production by Universidad Complutense, 28040 cell studies in microbial systems, and gives access to information
Xanthomonas campestris. Madrid, Spain. which cannot be obtained in any other way. Nevertheless, it provides
chapu@encmax.sim.ucm.es data in arbitrary units, that is, relative data. This analytical technique
could be employed for kinetic modeling of microbial systems and even
for internal phenomena analysis, but for this purpose, absolute data-
that is concentration of intracellular compounds-must be used. In this
work, relative flow cytometry data are transformed into absolute data
by means of calibrations employing the same fluorochromes with
another technique: spectrofluorymetry. Calibrations of DNA, RNA, and
protein intracellular concentrations are presented for the bacteria,
Xanthomonas campestris. Other analytical methods, based on
biochemical determinations, were also employed to quantify
intracellular compounds, but the results obtained are very poor
compared wi
160 Xanthan gum biosynthesis and Becker A, Katzen F, Puhler A, Appl Microbiol Biotechnol 1998 Lehrstuhl fur Genetik, Universitat 1998 xanthan, biosynthesis Xanthan gum is a complex exopolysaccharide produced by the plant-
application: a biochemical/genetic Ielpi L Aug;50(2):145-52 Bielefeld, Germany. pathogenic bacterium Xanthomonas campestris pv. campestris. It
perspective. consists of D-glucosyl, D-mannosyl, and D-glucuronyl acid residues in
a molar ratio of 2:2:1 and variable proportions of O-acetyl and pyruvyl
residues. Because of its physical properties, it is widely used as a
thickener or viscosifier in both food and non-food industries. Xanthan
gum is also used as a stabilizer for a wide variety of suspensions,
emulsions, and foams. This article outlines aspects of the biochemical
assembly and genetic loci involved in its biosynthesis, including the
synthesis of the sugar nucleotide substrates, the building and
decoration of the pentasaccharide subunit, and the polymerization
and secretion of the polymer. An overview of the applications and
industrial production of xanthan is also covered.
4.11 Literatures on Polysaccharides.xls - page 381
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
161 Enhancing xanthan fermentations by Amanullah A, Satti S, Nienow AW Biotechnol Prog 1998 Mar- Centre for Bioprocess Engineering, 1998 xanthan, fermentation process, This paper is the fourth in a series aimed at improving the
different modes of glucose feeding. Apr;14(2):265-9 School of Chemical Engineering, The feeding understanding and operation of conventional agitated fermenters for
University of Birmingham, Edgbaston, the production of the commercially important gum, Xanthan. In the
Birmingham B15 2TT, U.K. first, reproducible fermentations were established and this protocol
was used in studies of different agitator types and of bulk mixing and
dissolved oxygen concentration in the next two. Here, building on the
previous work, the influence of different glucose feeding strategies on
Xanthan production in a 20-L agitated fermenter under equivalent
conditions of agitation and dissolved oxygen is reported. The
biological performances in three types of fed-batch cultures (a two-
step glucose addition, multiple glucose-pulse feeding and continuous
feeding of glucose) are compared to two batch fermentations with
different initial glucose concentrations. The work confirmed that
improved performance cannot be achieved by increasing the initial
glucose concentration above 50 g/L nor by a single 10 g/L pulse
addition (initial gluco
162 Production and rheological properties Meade MJ, Tanenbaum SW, Can J Microbiol 1995 Department of Environmental and 1995 succinoglycan, Pseudomonas sp., Pseudomonas sp. ATCC 31260 produced substantial amounts of
of a succinoglycan from Pseudomonas Nakas JP Dec;41(12):1147-52 Forest Biology, State University of wood, production, rehological anionic extracellular polysaccharide (EPS) from a mineral acid
sp. 31260 grown on wood hydrolysates. New York College of Environmental properties hydrolysate of wood, prepared using the "Tennessee Valley
Science and Forestry, Syracuse Authority" process. Partially purified EPS production approached 16.5
13210, USA. g/L (as hexadecyltrimethylammonium bromide precipitate) when the
pH of the hydrolysate was initially adjusted to 7.5 and amended with
0.05% each of peptone and yeast extract. This EPS, now
characterized as a succinoglycan, is composed of glucose, galactose,
succinate, pyruvate, and acetate. Solutions of this EPS are
pseudoplastic, and under specified conditions, are rheologically
comparable with commercially available xanthan.
163 [Isolation of xanthan from Xanthomonas Lorda GS, Pastor MD, Balatti AP Rev Argent Microbiol 1995 Jul- Dpto. de Quimica, Facultad de 1995 xanthan, Xanthomonas Xanthan production from Xanthomonas campestris was studied by a
campesteris B-1459 in mechanically Sep;27(3):146-55 Ciencias Exactas y Naturales, campesteris B-1459, mechanically mechanically shaken fermentor. Influence of glucose concentration,
agitated fermentors]. [Article in Universidad Nacional de La Pampa, agitated fermentors aeration of culture media, rheology of broths and pH control was
Spanish] Argentina. evaluated. Different aeration conditions based on variation of stirring
rates were assayed. Substrate concentration was determined
according to the Miller method, and polymer production was
performed by the Cadmus method. The higher xanthan levels (i.e.
2.3%) were obtained at 750 rpm, with 1 v/v. min. In such conditions,
viscosity ranges about 7000 cPoise and a low level of dissolved
oxygen were detected in the culture medium. Xanthan production was
influenced by the glucose concentration and the presence of
amaranth within the culture medium. In the processes wherein an
automatic control of pH was performed, the polymer concentration did
not increase regarding to processes involving regular pH evolution.
164 [Xanthan production by Xanthomonas Lorda GS, Pastor MD, Balatti AP Rev Argent Microbiol 1994 Jan- Dpto. de Quimica, Facultad de 1994 xanthan, Xanthomonas The production of xantano from Xanthomonas campestris B-1459 was
campestris B-1459]. [Article in Spanish] Mar;26(1):9-20 Ciencias Exactas y Naturales, campesteris B-1459 analyzed. The experiments were performed in shaked flasks at 250
Universidad Nacional de La Pampa, rpm and 2.5 cm eccentricity. Using a base modified medium it was
Argentina. possible to achieve xantano concentration of 35 g/l in 72 h of process.
The modified medium contained glucose as carbon source, and yeast
extract, meat peptone, malt extract and amaranth meal as growth
factors and nitrogen sources, in a KH2PO4/K2HPO4 buffer.
4.11 Literatures on Polysaccharides.xls - page 382
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
165 Genetic stability and xanthan gum Martinez-Salazar JM, Palacios Mol Microbiol 1993 Jun;8(6):1053-61 Departamento de Bioingenieria, 1993 xanthan, Xanthomonas, genetic A transposon (Tn5-SC) was constructed that can be used to quantify
production in Xanthomonas campestris AN, Sanchez R, Caro AD, Universidad Nacional Autonoma de stability genetic deletions or amplifications. This transposon was used to
pv. campestris NRRL B1459. Soberon-Chavez G Mexico, Cuernavaca, Morelos. evaluate the genomic stability of Xanthomonas campestris pv.
campestris NRRL B1459 and we found that the genome of this
bacterium is as stable as other Gram-negative bacteria or even more
stable. Homologous recombination between plasmid sequences was
determined in strain NRRL B1459 and was found to occur at a similar
level to that reported for other Gram-negative bacteria. We report
here that in X.c.c. NRRL B1459 there is no straightforward correlation
between the occurrence of genetic rearrangements and frequency of
homologous recombination. These data are discussed with respect to
the reported instability of strain NRRL B1459 for xanthan gum
production.
166 [Production of xanthan gum in Anselmo RJ, Viora S, Carletti S Rev Argent Microbiol 1992 Apr- Universidad Nacional de Lujan, 1992 xanthan production, immobilized The efficiency of xanthan production through surface processes was
immobilized cultures ofXanthomonas Jun;24(2):86-90 Argentina. cultures evaluated. The best porous material was selected first. Thereafter, a
campestris]. [Article in Spanish] comparative study was performed using submerged agitated process
vs other without agitation but containing the selected porous material.
The culture medium used was white potatoes infusion, buffered with
K2HPO4 and supplemented with glucose in diverse concentrations.
Besides, to evaluate a different type of surface process, three
vegetables were valued: Ipomaea batatus, Solanum tuberosum and
Daucus carota, with an without glucose supplement. Larger xanthan
production was achieved with immobilization of X. campestris vs the
conventional method, when the liquid culture medium was used. The
highest yield was obtained when the white potatoes infusion was
supplemented with glucose 2.5%, yielding a conversion of this
saccharide to xanthan up to 58%. When X. campestris was cultured
on fragmented vegetables, the highest xanthan gum yield (5.6g) was
obtained with Solanum tuberosum
167 [Production of xanthan gums]. [Article in Pares EP, Anselmo RJ Rev Argent Microbiol 1991 Apr- Universidad Nacional de Lujan, 1991 xanthan production, xanthomonas Xanthomonas campestris was investigated in 70 samples of infected
Spanish] Jun;23(2):97-100 Argentina. campestris plants in the neighbourhood of Lujan, province of Buenos Aires,
between February and August, 1990. The production of xanthan gum
was determined from 50 strains of Xanthomonas campestris, as well
as the conversion efficiency of substrate concentration into gum and
the number of colony forming units (CFU) of Xanthomonas
campestris/ml of broth culture. The highest number of strains
producing extracellular polysaccharide was obtained from alfalfa.
Xanthomonas campestris pv. alfalfa gave elevated cell concentration
and conversion efficiency of glucose in xanthan gum.
168 A novel bioreactor system for Robinson DK, Wang DI Ann N Y Acad Sci 1987;506:229-41 Department of Chemical Engineering, 1987 bioreactor, method, biopolymer, No abstract available.
biopolymer production. Massachusetts Institute of polysaccharide, polyalcanoate
Technology, Cambridge 02139.
169 [Nitrogen utilization and xanthan Behrens U, Makarskij A, Z Allg Mikrobiol 1977;17(5):339-45 1977 xanthan, xanthomonas campestris, In media with mixed nitrogen sources (nitrate plus yeast extract) a
production by Xanthomonas Ambrosius J, Franke R nitrogen three auxic growth is observed. The first growth phase is
campestris]. [Article in German] characterized by preferential utilization of the amino acids of the yeast
autolysate and the utilization of only small amounts of nitrate. During
the second growth phase nitrate is preferentially utilized. In the third
phase there is only growth without dividing of cells and the
accumulation of xanthan takes place. The change from growth by
dividing to growth without dividing means a change from balanced to
unbalanced growth. It is proposed that xanthan production is
connected with unbalanced growth.
4.11 Literatures on Polysaccharides.xls - page 383
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
170 Studies on production of pullulan by the Sun W, Zhou T, Xie H, Jiang N, Chin J Biotechnol 1999;15(2):121-8 State Key Laboratory of Microbial 1999 pullulan, fed-bach, production The feed-batch fermentation of pullulan was investigated based on the
feed batch fermentation. Ren Y Resources, Chinese Academy of conditions of batch fermentation. The optimal conditions of pullulan
Sciences, Beijing, China. fermentation were determined by the investigation on the effect of
feed mode, initial feed time, intermittent time, and composition of the
feed solution on parameters such as productivity, conversion yield,
biomass, dissolved oxygen (DO), pH of the fermentation broth,
viscosity of the fermentation broth and molecular weight of the
product. Above 70% of conversion yield and 100 kD of average
molecular weight of the product was obtained at the optimal
conditions.
171 Effect of nitrogen source on pullulan West TP, Strohfus B Microbios 1999;99(394):147-59 Olson Biochemistry Laboratories, 1999 pullulan, production, nitrogen, Pullulan production by Aureobasidium pullulans ATCC 201253 using
production by Aureobasidium pullulans Department of Chemistry and bioreactor selected nitrogen sources was studied in a medium using corn syrup
grown in a batch bioreactor. Biochemistry, South Dakota State as a carbon source. Independent of the corn syrup concentration
University, Brookings 57007, USA present, the use of corn steep liquor or hydrolysed soy protein as a
nitrogen source instead of ammonium sulphate did not elevate
polysaccharide production by ATCC 201253 cells grown in an
aerated, batch bioreactor containing 4 litres of medium. Pullulan
production on corn steep liquor or hydrolysed soy protein as a
nitrogen source became more comparable as the concentration of
corn syrup was increased. Cell weights after 7 days of growth on any
of the nitrogen sources were similar. The viscosity of the
polysaccharide on day 7 was highest for cells grown on ammonium
sulphate and 12.5% corn syrup. The pullulan content of the
polysaccharide elaborated by ammonium sulphate-grown cells on day
7 decreased as the corn syrup level rose in the medium while the
pullulan content of polysaccharide produced by cells grown on
172 Pullulan production by Aureobasidium West TP, Strohfus B Microbios 1996;88(354):7-18 Olson Biochemistry Laboratories, 1996 Pullulan, production , Pullulan production by Aureobasidium pullulans strain RP-1 using thin
pullulans grown on ethanol stillage as a Department of Chemistry and Aureobasidium pullulans, ethanol stillage from fuel ethanol production as a nitrogen source was studied
nitrogen source. Biochemistry, South Dakota State stillage, nitrogen source. in a medium using corn syrup as a carbon source. The use of 1% thin
University, Brookings 57007, USA stillage as a nitrogen source instead of ammonium sulphate elevated
polysaccharide production by strain RP-1 cells when grown on a
concentration of up to 7.5% corn syrup, independent of yeast extract
supplementation. Dry weights of cells grown in medium containing
ammonium sulphate as the nitrogen source were higher than the
stillage-grown cells after 7 days of growth. The viscosity of the
polysaccharide on day 7 was higher for cells grown on thin stillage
rather than ammonium sulphate as a nitrogen source. The pullulan
content of the polysaccharide elaborated by ammonium sulphate-
grown cells on day 7 was higher than the pullulan content of
polysaccharide produced by stillage-grown cells regardless of whether
yeast extract was added to the culture medium.
173 Studies on the condition of fermentation Sun W, Zhou T, Xie H, Ren Y, Chin J Biotechnol 1994;10(4):283-90 Institute of Microbiology, Chinese 1994 pullulan, fermentation, optimal Studies on optimal conditions for pullulan fermentation based on the
of pullulan by Aureobasidium pullulans. Jiang N Academy of Sciences, Beijing, China. conditions, Aureobasidium results obtained from a shaking flask were carried out in a 16-L auto-
pullulans controlling fermentor. It found that the optimal DE value of starch
hydrolyzate was 40-50 when 10% starch hydrolysate was used as
carbon source. The optimal concentration of ammonium sulfate in the
medium for fermentation was different from that of the shaking flask.
The fermentation kinetics and effects of seed age, seed volume,
airflow rate, pressure of tank, agitation speed and number of vane
group on the production of pullulan were investigated.
4.11 Literatures on Polysaccharides.xls - page 384
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
174 [Production of pullulan]. [Article in Behrens U, Lohse R Nahrung 1977;21(3):199-204 1977 Optimum conditions, production, Optimum conditions for the production of pullulan by Pullularia
German] pullulan, Pullularia pullulans pullulans were elaborated by examinating growth and production with
different carbohydrates and mixtures of carbohydrates. With starch
hydrolysates or mixtures of starch and simple sugars, p.e. glucose or
saccharose, better results were achieved than with simple sugars
alone or with starch. Condtions for optimum pullulan production are
fast undisturbed growth, mediated by fast utilizable simple sugars like
glucose followed by a substantial decreased growth rate in which
production occurs, mediated by a sufficient supply of nutrite
substances and a slow utilizable carbohydrate like starch.
175 Process for the production of TANNAHILL ALEX L; FINN Pat. Nr. US3878045 CORNELL RES FOUNDATION INC 1975 methylomonas, Disclosed is an improved process for the preparation of a new
heteropolysaccharide by fermentation ROBERT K heteropolysaccharide, methanol heteropolysaccharide by a fermentation process comprising culturing
of methanol a heteropolysaccharide-producing strain of a microorganism of the
genus Methylomonas on an aqueous culture medium containing
methanol as the sole source of assimilable carbon. The concentration
of the product polysaccharide in the fermentation broth is increased,
the fermentation time is shortened, and the properties of the
polysaccharide are improved by the controlled addition of methanol to
the fermentation process near the end of the logarithmic phase of
growth of the bacteria.
176 Algal polysaccharide production CHEN LAWRENCE C M; Pat. Nr. US3879890 CANADIAN PATENTS DEV 1975 alga, polysaccharide production Selected polysaccharides are produced from algal plant tissue by (a)
CRAIGIE JAMES S; separating vegetative parts or spores into (i) gametophytes, or (ii)
MCCANDLESS ESTHER L; tetrasporophytes; (b) vegetatively propagating the separated plant
MCLACHLAN JACK L; NEISH material; (c) harvesting the resulting plant growth; and (d) recovering
DECEASED ARTHUR C; the desired polysaccharides from the harvested material. Different
SHACKLOCK PETER F; specific polysaccharides (e.g., kappa- or lambda-carrageenan) have
WALTER JOHN A been found to be produced by (i) or (ii) above. This method avoids
difficult post-harvest separations and is amenable to controlled
vegetative propagation of the separated plant material under optimum
conditions.
177 PROCESS FOR THE PRODUCTION IMRIE F Pat. Nr. US3856625 Tate & Lyle Ltd 1974 alginate, sulfate, calcium, An alginate-type polysaccharide is obtained by the aerobic cultivation
OF POLYSACCHARIDE phostphate,carbon, molybdenum, of a bacterium of the species Azotobacter vinelandii in an aqueous
iron, mangesium, potassium, nutrient medium containing sources of carbon, molybdenum, iron,
sodium mangesium, potassium, sodium, sulfate, calcium and phosphate. The
carbon source comprises at least one monosaccharide or
disaccharide. Contrary to normal culture conditions for this bacterium,
for good polysaccharide production, the phosphate concentration in
the nutrient medium must be 0.1-0.8 millimolar, preferably 0.2-0.6
millimolar; and the pH of the medium must be maintained within the
range of from 7.0 to 8.2, preferably 7.3 to 7.9.
4.11 Literatures on Polysaccharides.xls - page 385
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
178 POLYSACCHARIDE AND MURATA HIDEKI (JP); SHIOMI Pat. Nr. EP0569591, A4, B1, B1 STATE OF JAPAN AS 1993 alcaligenes, rhamnose, fucose, The invention provides a polymer comprising a polysaccharide
PRODUCTION THEREOF. MICHIO (JP); YOTSUJI AKIRA REPRESENTED (JP); HAKUTO KK glucose, glucuronic acid, excellent in water absorbency, moisture absorbency, moisture
(JP); ISHINO SHUICHI (JP); (JP); KYOWA HAKKO KOGYO KK rfermentation retentivity and thickening function. The polysaccharide is produced by
NOHATA YASUHIRO (JP); (JP) the fermentation in a natural or synthetic medium using alcaligenes,
SUGIMOTO SEIJI (JP); KURANE and has the following characteristics: (a) it is mainly constituted of
RYUICHIRO (JP) rhamnose, fucose, glucose and glucuronic acid in a molar ratio of (1-
4):2(1-8):(1-4); (b) its elementary analysis gives a carbon content of
36 +/- 3 wt %, a hydrogen content of 7 +/- 1 wt %, an oxygen content
of 56 +/- 4 wt %, and a content of water of crystallization of 9 - 13 %;
(c) it is difficultly soluble in water, soluble in alkali, and insoluble in
methanol, ethanol and acetone; (d) its UV absorption spectrum has
neither an absorption (near 280 nm) characteristic of a protein
(peptide) nor an absorption (near 260nm) characteristic of a nucleic
acid; and (e) its IR absorption spectrum has an absorption pattern
(around 800 -1200 cm<-><1>) characteristic of a polysaccharide.
179 NOVEL POLYSACCHARIDE, NAKAGAWA MASAHIRA (JP); Pat. Nr. WO9533066 NAKAGAWA MASAHIRA (JP); 1995
PROCESS FOR PRODUCTION KAWASHIMA KAORU (JP); KAWASHIMA KAORU (JP); MISAKI
THEREOF, USE THEREOF, AND MISAKI AKIRA (JP); NAKANISHI AKIRA (JP); NAKANISHI OSAMU
AGROBACTERIUM RADIOBACTER OSAMU (JP); OKUMIYA (JP); OKUMIYA TAKESHI (JP);
TNM2 STRAIN TAKESHI (JP); OOISO YOICHI OOISO YOICHI (JP); TAYCA CORP
(JP); SUGIHARA RYOSUKE (JP) (JP); SUGIHARA RYOSUKE (JP)
180 METHOD TO CONTROL AND SINSKEY ANTHONY J (US); Pat. Nr. WO8800948 MASSACHUSETTS INST 1988 Genes, polysaccharide A method for identifying, characterizing, utilizing and modifying a set
PRODUCE NOVEL BIOPOLYMERS EASSON DONALD DAVIDSON TECHNOLOGY of genes which interact to produce a specific polymer. The method is
JR (US); RHA CHOKYUN (US) demonstrated for production of an exocellular polysaccharide
produced by the bacteria Zoogloea ramigera. The isolated
polysaccharide is useful as a viscosity modifier, oil field chemical,
drag reducing agent, dispersant or flocculant. Modification of the
isolated genes, for example, by insertion of a regulatable promoter,
provides a means for alteration of the enzymes responsible for
synthesis of the polysaccharide and its resulting structure.
181 CONTINUOUS PRODUCTION OF ELLWOOD DEREK CLIFFORD Pat. Nr. WO8601830 SECR DEFENCE BRIT (GB) 1986 nitrogen, Xanthomonas Polysaccharide is produced by a single stage continuous culture of
BACTERIAL POLYSACCHARIDE (GB); EVANS CHARLES campestris Xanthomonas bacteria, especially of the Xanthomonas campestris
GERVASE THORNGAT (GB); group, in a chemically defined culture medium having a growth limiting
YEO RICHARD GRENVILLE (GB) nutrilite which is a nitrogen source selected from glutamic acid,
asparagine, a glutamate salt or an asparagine salt. During the
continuous process the culture has a mean residence time in the
culture vessel of 16 hr 2/3 or less, preferably between 9 and 16 hr
2/3. The use of glutamic acid, asparagine, glutamate salt or
asparagine salt as the limiting nitrogen nutrilite increases the output of
polysaccharide at mean residence times of 16 hr 2/3 and below, when
compared with the outputs achieved using inorganic nitrogen sources
at the same mean residence times.
4.11 Literatures on Polysaccharides.xls - page 386
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
182 Water shield polysaccharide gum GUANGHUI XU (CN); WENJUN Pat. Nr. CN1118810 XU WEIJIA (CN) 1996 water shield, bacteria The production technology includes separating bacillus from viscose
producing bacteria and producing SUN (CN) substance on leaf, stem and bud of water shield by using a special
technology for water shield culture medium, and breeding strains having strong ability to produce
polysaccharide gum water shield polysaccharide gum through a series of microbiological
breeding such as purification, rejuvenation, activation, selection and
taming, and cultivating in air-lift fermenting reactor for 28-46 h. to
obtain a large amount of water shield polysaccharide gum whose
viscosity reaches 1000 mpa. S at 20 deg.C. Such product can be used
in medicine, foodstuff additive, suspending agent and sticking agent.
183 POLYSACCHARIDE SOLUTION YINHE WANG XIUYUAN CUI Pat. Nr. CN1051935 MICROORGANISM RESEARCH 1991 bacillus 74-230, yellow monobleb The invention relates to the production method of polysaccharide by
PRODUCTION BY FERMENTATION WENHUA (CN) INSTI C (CN) bacillus, petroleum micro-organism fermentation. It uses the mixed strain of the produced
OF MICROORGANISM vicous short bacillus 74-230 and the wild rape yellow monobleb
bacillus, hydro-carbon kind and carbonhydrate mixed carbon base,
then the micro-organism outside balb polysaccharide are produced by
fermentation. The invented method can reduce the quantity of
carbonhydrate needed and cost. The viscosity of fermentation liquid
reaches more than 10000 centipoise, the transformation rate of
residue is more than 50%. The obtained polysaccharide fermentation
liquid can be directly used in petroleum exploitation. The said
invention provides a micro-organism polysaccharide fermentation
technology for concerned industries of production and application on
the spot, reducing the carbonhydrate comsumption, rapid starting the
fermentation process, and high viscosity fermentation liquid.
184 FERMENTATIVE PRODUCTION OF KURANE RYUICHIRO; others: 03 Pat. Nr. JP4200389 AGENCY OF IND SCIENCE & 1992 PURPOSE:To easily obtain a polysaccharide having stable
POLYSACCHARIDE HAVING WATER- TECHNOL; others: 02 constituent component ratio at a low cost by culturing a bacterial
ABSORPTIVITY, MOISTURE- strain of genus Alcaligenes on a synthetic medium.
ABSORPTIVITY, MOISTURE- CONSTITUTION:A synthetic medium (A) is produced by compounding
RETENTION AND VISCOSITY 1-4wt.% of one or more sugars selected from glucose, fructose,
maltose, etc., 0.01-0.1wt.% of one or more inorganic salts selected
from K or Na phosphate, sodium chloride, ammonium chloride, etc.,
10-1,000mg/l of one or more amino acids selected from Arg, Cit, Orn,
Vat, etc., and 0.03-10mg/l of one or more minor metal salts selected
from sulfate, chloride, etc., of Fe, Ca, Mn, etc. Alcaligenes latus B-16
strain (FERM BP-2015) (B) is inoculated to the medium A and
aerobically cultured at 15-40 deg.C and pH4-10 for 1-10 days under
aeration and agitation in deep tank to obtain a cultured product (C).
The objective polysaccharide having water-absorptivity, moisture-
absorptivity, moisture retention and viscosity is produced by treating
the component C by ethanol precipitation proc
4.11 Literatures on Polysaccharides.xls - page 387
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
185 PRODUCTION OF WATER-SOLUBLE FURUTA HITOSHI; others: 03 Pat. Nr. JP7188301 FUJI OIL CO LTD 1995 water-soluble, polysaccharide, PURPOSE:To efficiently and easily obtain a polysaccharide to be
POLYSACCHARIDE beans suitably formulated in e.g. beverages of low turbidity with no
deterioration over time, by adjusting the pH level of an aqueous
solution of a water-soluble polysaccharide extracted from beans
under an acidic state followed by heat treatment and then separating
and removing the precipitate. CONSTITUTION:An aqueous solution
of a water-soluble polysaccharide extracted from beans under an
acidic state is adjusted to pH6 to <9 and then heat treated, and the
precipitate ' is separated and removed. The beans to be used is
soybean, and cotyledons of their seeds are used. The heat treatment
is conducted by adding a reducing agent or oxidizing agent to the
system; during or prior to the heat treatment, a treatment using a
protease (e.g. pepsin, subtilisin, bromelain, papain) is carried out. A
high-molecular flocculant may be added to the system in separating
and removing the precipitate. The reducing agent is one selected from
sodium hyposulfite, pota
186 PRODUCTION OF HARDLY YOSHIDA TSUKASA; others: 03 Pat. Nr. JP2163101 SANMATSU KOGYO KK 1990 polysaccharide, digestion, low- PURPOSE:To obtain the subject polysaccharide having low calorific
DIGESTIBLE POLYSACCHARIDE calorie value from a sugar which is a hydrolyzed product of starch by heating
and polymerizing the sugar in the presence of a sugar alcohol and a
weak inorganic acid under anhydrous condition and removing bitter-
taste substances and digestible substances from the product.
CONSTITUTION:A sugar (preferably glucose or maltose) produced by
the hydrolysis of starch is polymerized by heating at 150-200 deg.C in
the presence of a sugar alcohol (preferably sorbitol) and a weak
inorganic acid (preferably phosphoric acid) under anhydrous condition
as far as possible and preferably under normal or reduced pressure.
The objective polysaccharide is obtained by removing bitter-taste
substances and digestible substances from the obtained reaction
mixture. The polymerization reaction is carried out preferably in the
presence of 0.1-1wt.% of the weak inorganic acid and >=10wt.% of the
sugar alcohol.
187 Novel polysaccharides, process for NAKAGAWA MASAHIRA (JP); Pat. Nr. EP0613951, A3 TAYCA CORP (JP) 1994 polysaccharides, Azotobacter Disclosed are novel polysaccharides having the following
producing polysaccharides, uses of MISAKI AKIRA (JP); NAKANISHI beijerinckii TNM1, method physicochemical properties: (1) a molecular weight determined by gel
polysaccharides and Azotobacter OSAMU (JP); OKUMIYA filtration chromatography is about 5 x 10<3> to 10 x 10<6>, (2) the
beijerinckii TNM1. TAKESHI (JP); OOISO YOICHI constituent glycoses are D-galacturonic acid, L-rhamnose and D-
(JP); SUGIHARA RYOSUKE (JP) glucose, (3) the constituent glycoses are joined substantially by 1,3-
linkages, and (4) a configuration of D-galacturonic acid is alpha , that
of L-rhamnose is beta and that of D-glucose is alpha . A process for
producing polysaccharides composed of D-galacturonic acid, L-
rhamnose and D-glucose, use of the polysaccharides and a strain for
producing the polysaccharides are also disclosed.
4.11 Literatures on Polysaccharides.xls - page 388
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
188 PRODUCTION OF TAKIMURA YASUSHI; TAKEI Pat. Nr, JP8131160 Kao Corp 1996 microbial strain, polysaccharide PURPOSE:To obtain the titled compound useful as antitumor agent,
POLYSACCHARIDE HIGHLY AKIRA; HAMA MASAKATSU; NSG-1 etc., in high purity, by culturing a microbial strain capable of producing
PRODUCING CELL AND IKUGA YUTAKA polysaccharide NSG-1, incubating the proliferated cell in a liquid
POLYSACCHARIDE PRODUCING containing a carbohydrate to produce polysaccharide NSG-1 and
CELL separating the product from the reaction liquid. CONSTITUTION:A
microbial strain capable of producing polysaccharide NSG-1 [e.g.
Sclerotinia sclerotiorum (IFO 9353), etc.] is cultured in a medium and
the obtained primary seed strain is inoculated and cultured in a
medium to obtain secondary seed strain. The strain is added to a jar
fermenter, cultured in a mass and filtered to obtain cultured cells. The
cell is filled together with a liquid containing a carbohydrate such as
glucose, etc., into a jar fermenter and incubated. The objective
polysaccharide NSG-1 produced in the reaction liquid is separated
therefrom.
189 MUCILAGINOUS POLYSACCHARIDE MURATA TATSUO; others: 02 Pat. Nr. JP1121302 HIGASHIMARU SHOYU KK 1989 Ganoderma, beta-1,4-bonds, PURPOSE:To obtain novel polysaccharides, produced by cultivating a
SUBSTANCE AND PRODUCTION glucide, viscosity, emulsifying, strain of the genus Ganoderma and having beta-1,4-bonds in the
THEREOF humecting glucide part and characteristics of increasing viscosity, emulsifying
and humecting, etc. CONSTITUTION:A fungus, belonging to the
genus Ganoderma and capable of producing mucilaginous
polysaccharide substances [Ganoderma.lucidum ITM052 strain
(FERM-P No.9660)] is cultivated in a liquid culture medium consisting
essentially of glucose and yeast extract or glutamine or glutamic acid
and the mucilaginous polysaccharide substance is separated and
collected from the culture fluid. The above-mentioned polysaccharide
substance has a structure of glucide part having at least beta-1,4-
bonds and exhibits the following properties. That is appearance; white
substance exhibiting high viscosity. Solubility; double in warm water
and insoluble in ethanol, methanol and acetone. pH=6.1 in 1%
aqueous solution. Constituent saccharide; glucose and fructose.
Constituent amino acid; serine, glycine, al
190 NEW POLYSACCHARIDE ISHIGAMI YUTAKA; others: 03 Pat. Nr. JP3047801 AGENCY OF IND SCIENCE & 1991 NEW MATERIAL:The compound of formula I [R<1> is acyl; R<2> is -
DERIVATIVE AND PRODUCTION TECHNOL; others: 01 OH, -OM (M is alkali metal), -NH2 or -OR<1>; n is >=2]. USE:Coating
THEREOF material for microcapsule of liposome, etc. PREPARATION:A
polysaccharide of formula II (R<3> is -OH or -OM) [preferably
hyaluronic acid (derivative)] is made to react with a fatty acid of
formula HO-R<1> or its halide.
191 PRODUCTION OF FIBER OR SHEET KOBAYASHI YOSHIO; FUKUOKA Pat. Nr. JP63243399 AGENCY IND SCIENCE TECHN;
EXCELLENT IN WATER RESISTANCE SATOSHI; MATSUO RYUKICHI; NIPPON SYNTHETIC CHEM IND
BASED ON WATER-SOLUBLE KAGEYAMA SATORU;
MARINE ALGAE TYPE TSUTSUMI SHUJI
POLYSACCHARIDE
4.11 Literatures on Polysaccharides.xls - page 389
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
192 WATER-SOLUBLE HIGHLY VISCOUS OKURA TAKESHI; others: 01 Pat. Nr. JP3124701 POLA CHEM IND INC 1991 stable, water-soluble, PURPOSE:To obtain a stable water-soluble polysaccharide mainly
POLYSACCHARIDE AND IST polysaccharide, glucose, viscous, constituted of glucose, being highly viscous and having an ability to
PRODUCTION gel, Pestalotiopsis, liquid medium form a gel, by culturing a polysaccharide-producing strain of the
genus Pestalotiopsis in a liquid medium and collecting the
polysaccharide from the culture. CONSTITUTION:A polysaccharide-
producing strain belonging to the genus Pestalotiopsis (e.g.
Pestalotiopsis sp. P-104 strain, FERM-P10792) is cultured in a liquid
medium containing 0.1-3wt.% acetate. A water-soluble highly viscous
polysaccharide is obtained by collecting it from the culture. This
polysaccharide is a white fibrous powder, is tasteless and odorless,
has a viscosity of 10000-30000cp when measured in a 1% aqueous
solution, a composition comprising 94-98% glucose and 6-2%
galactose, is insoluble in a general organic solvent, is soluble in
water, a dilute acid and a dilute alkali, shows such color reactions that
it is positive to the anthrone-sulfuric acid reaction, positive to the
Fehling reaction and negative to
193 PRODUCTION OF SONODA YORIKAZU; others: 02 Pat. Nr. JP6078781 KUMAMOTO MARINE BIO KENKYU 1994 sulfuric acid- acidic polysaccharide PURPOSE:To obtain the polysaccharide hydrolysate by treating
POLYSACCHARIDE HYDROLYSATE KAIHATSU KYODO KUMIAI porphyran, Acinetobacter. sulfuric acid- acidic polysaccharide porphyran with a porphyran-
WITH MICROORGANISM assimilating microorganism belonging to the genus Acinetobacter.
ASSIMILATING SULFURIC ACID- CONSTITUTION:Sulfuric acid acidic polysaccharide porphyran is
ACIDIC POLYSACCHARIDE treated with a porphyran-assimilating microorganism (e.g.
PORPHYRAN Acinetobacter SP.KP-47 strain) assimilating and hydrolyzing the
sulfuric acid-acidic porphyran to produce oligosaccharides. The
sulfuric acid-acidic polysaccharide porphyran is rapidly hydrolyzed to
provide the polysaccharide hydrolysates.
194 NEW FRUCTAN AND ITS FUKAYA MASAHIRO; TAKEUCHI Pat. Nr. JP11046786 NAKANO VINEGAR CO LTD 1999 fructan, sucrose, Acetobacter. PROBLEM TO BE SOLVED: To obtain a new fructan having an
PRODUCTION TOSHIHARU; TSUKAMOTO intestinal metabolism-regulating action, a lipid metabolism-improving
YOSHINORI action, a mineral absorption-stimulating action, etc., and useful for
medicines, functional foods, etc. by treating sucrose with the culture
product or cells of a microorganism belonging to the genus
Acetobacter. SOLUTION: A new fructan of the formula. The new
fructan of the formula is an undecasaccharide capable of exhibiting an
intestinal function-regulating action, a lipid metabolism-improving
action, a mineral absorption-stimulating action, etc., and enables to
expect the application of the fructan to medicines, functional foods,
etc. The sugar compound is obtained by treating sucrose with the
culture product, cells or cell treated product of a microorganism
belonging to the genus Acetobacter or Gluconobacter [e.g.
Gluconobacter albidus IFO 3250).
195 Production of fructan (levan) HAN YOUN W (US); CLARKE Pat. Nr. US5547863 US ARMY (US) 1996 Soil isolates, Bacillus polymyxa, Soil isolates, identified as strains of Bacillus polymyxa, NRRL B-
polyfructose polymers using bacillus MARGARET A (US) NRRL B-18475, NRRL B-18476, 18475 and NRRL B-18476, produce large quantities of a pure and
polymyxa extracellular, fructan uniform extracellular polysaccharide fructan (levan), in a sucrose
(levan),sucrose medium medium. The levan consists entirely of fructose and the residues
linked by beta , 2-6 fructofuranoside linkage.
4.11 Literatures on Polysaccharides.xls - page 390
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
196 Production of fructan NAKAKUKI TERUO; others: 02 Pat. Nr. JP61187797 NIPPON SHOKUHIN KAKO KK 1986 Sucrose, Aspergillus, bifidus PURPOSE:Sucrose is treated with cell bodies of an Aspergillus to
bacteria enable practical production with diversification of products which can
be used in proliferation of bifidus bacteria. CONSTITUTION:Cell
bodies of Aspergillus sidwii such as IAM2544 strain which is prepared
by liquid cultivation are added to 10-40wt% sucrose solution in an
amount of 5-20wt% based on the sucrose and the culture is carried
out at a pH of 5.0-6.5 at 60-65 deg.C for production of oligofructan
and at 45 deg.C for high-polymeric fructan as an optimal temperature.
The reaction mixture is filtered with a membrane filter, then,
oligofructan is fractionated by means of a reverse-osmotic membrane.
The fractionated oligofructan is deionized, decolored, concentrated
into a fine powder, while the other high-polymer fructan fractions are
concentrated, precipitated with acetone to give the fructan with a
structure of the formula (n is 1-5 in oligofructan, while n is more than
1,000 in high-polymeric fructan).
197 PRODUCTION OF CARRAGEENAN SUZUKI SHOJI; others: 02 Pat. Nr. JP62153301 MITSUBISHI ACETATE CO LTD 1987 carrageenan, polyphosphate PURPOSE:To obtain carrageenan of excellent clarity without
detriment to its gel properties, by adding a polyphosphate to the
system in any one of the production steps of extracting carrageenan
from red algae, filtering the extract and drying it or after the drying
step. CONSTITUTION:Carrageenan which gives a solution of
excellent clarity is obtained by adding a polyphosphate to the system
n any one of the production steps of extracting carrageenan from red
algae with warm water or the like, filtering the extract and drying it or
after the drying step. The amount of the polyphosphate added is
suitably 0.001-50% based on carrageenan. As the polyphosphate, a
linear polyphosphate having at least two phosphorus atoms in the
molecule or a cyclic polymetaphosphate having at least three
phosphorus atoms in the molecule (e.g., sodium hexametaphosphate
or sodium tetrapholyphosphate) is suitable.
198 PRODUCTION OF CARRAGEENAN SUZUKI SHOJI; others: 02 Pat. Nr. JP62149703 Mitsubishi Acetate Co LTD 1987 organic acid (salt), carrageenan PURPOSE:To produce carrageenan excellent in clarity of its solution,
by adding an organic acid (salt) to the carrageenan.
CONSTITUTION:0.001-10%, based on carrageenan, organic acid
(e.g., adipic acid) and/or its salt are added to the system in any one of
the steps of adding warm water to red algae, filtration, drying, grinding
and mixing.
199 CARRAGEENAN GEL AND KATO TAKENORI; others: 01 Pat. Nr. JP1240154 1989 carrageenan, potassium alginate PURPOSE:To produce carrageenan gel having excellent melting in
PRODUCTION THEREOF the mouth free from water release at all, by using potassium alginate
in gel production. CONSTITUTION:In production carrageenan gel by
a conventional procedure, >=0.01wt.% potassium alginate is added to
gel mix.
4.11 Literatures on Polysaccharides.xls - page 391
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
200 PRODUCTION OF CARRAGEENAN ITOU HAJIME; others: 02 Pat. Nr. JP59113001 MITSUBISHI ACETATE KK 1984 Chondrus ocellatus Holmes f. PURPOSE:To obtain carrageenan, having good thermal stability, and
crispus, carrageenan capable of giving a transparent solution and gel with a high efficiency,
by adding ammonium chloride to the carrageenan in any stage of
production thereof to give a specific proportion of the ammonium
chloride in the dried carrageenan which is the final product.
CONSTITUTION:A raw material alga, e.g. Chondrus ocellatus Holmes
f. crispus, is extracted at 5-8pH to give a carrageenan extract solution,
which is filtered to adjust the filtrate to 9-12pH. The resultant adjusted
extract solution is if necessary refiltered and dehydrated. Ammonium
chloride is then added to the carrageenan in any above-mentioned
stage to give 0.1-3wt%, based on the dried carrageenan which is the
final product, ammonium chloride. Thus, the aimed carrageenan is
obtained.
201 PRODUCTION OF CARRAGEENAN ITOU HAJIME; others: 02 Pat. Nr. JP59113002 MITSUBISHI ACETATE KK 1984 alga, carrageenan PURPOSE:To obtain carrageenan, having good thermal stability, and
capable of giving a gel having improved sense of eating with a high
efficiency, by extracting a raw material alga with warm water, adding a
hydrous water-miscible organic solvent containing an alkali in a
specific concentration to the resultant extract, and precipitating the
aimed carrageenan. CONSTITUTION:A raw material alga, e.g.
Chondrus ocellatus Holmes f. crispus, is extracted with warm water at
5-8pH, and a hydrous water-miscible organic solvent containing 0.01-
1g equivalent/l alkali is added to the resultant aqueous solution of the
carrageenan preferably at 1:(1-2) mixing ratio between the former
aqueous solution and the latter hydrous organic solvent to precipitate
the carrageenan. The resultant precipitate is usually dried to afford
the aimed product.
202 PRODUCTION OF MATSUNAGA TADASHI; others: Pat. Nr. JP6098786 1994 alginate PURPOSE:To efficiently produce a polysaccharide useful as a food
POLYSACCHARIDE FROM FINE 01 additive, a base material of a medicine, etc., with a high productivity
ALGA while reducing the cost by fixing a fine alga secreting the
polysaccharide outside the body to the surface of a luminous material,
culturing it and collecting the product. CONSTITUTION:A fine alga
secreting a polysaccharide outside the body, e.g. a blue- green algae
Aphanocapsa halophytia is cultured till the stationary phase in a
culture solution prepared by adding Na2HPO4, NaNO3, etc., as a
nutritive salt to a sterilized natural sea water. After collecting the
cultured algae by centrifugation, the concentrated algae are
suspended in a buffer solution and 4wt.% sodium alginate solution is
mixed therewith in a volume ratio of 1:1. A luminous material, e.g. an
optical fiber from which the clad layer is removed is immersed in the
mixture solution and taken out therefrom after about 10sec.
Immediately after take-out, the luminous material is immersed in 0.5N
CaCl2 solution and
4.11 Literatures on Polysaccharides.xls - page 392
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
203 PRODUCTION OF ITOU HAJIME; others: 02 at. Nr. JP58103502 MITSUBISHI ACETATE KK 1983 PURPOSE:To effect efficient and smooth production of a
POLYSACCHARIDE FROM FINE polysaccharide from its solution with the aid of a hydrophilic organic
ALGA solvent and, to enhance the efficiency of purification and dewatering
of polysaccharide. CONSTITUTION:In the first stage, a hydrophilic
organic solvent (e.g. isopropyl alcohol) is added to an aqueous
polysaccharide solution agitated under high shear conditions in an
amount corresponding to 50-80% of the amount necessary to
precipitate the polysaccharide (e.g., carrageenan, furcellaran, agar).
Thus, there is obtained a uniform solution of a polysaccharide in a
mixed solvent containing the hydrophilic organic solvent and water.
This makes it possible to avoid disadvantages, such as formation of
crumbs due to non-uniformity of the system caused by the addition of
a water-soluble organic solvent in the subsequent stage. Then, in the
second stage, the above solvent is added to said solution, with
agitation, so as to provide the amount of the hydrophilic organic
solvent necessary to precipi
204 CONTINUOUS PRODUCTION OF KOBAYASHI SHOICHI; others: 03 Pat. Nr. JP4370098 NATL FOOD RES INST; others: 01 1992 PURPOSE:To efficiently produce polysaccharide owing to continuous
POLYSACCHARIDE utilization of algae by culturing algae to produce polysaccharide and
then separating polysaccharide and simultaneously repeatedly
culturing these algae. CONSTITUTION:Algae (preferably fine algae of
the genus Spirulina, the genus Nostoc, etc.) having polysaccharide
producing ability are cultured and polysaccharide is produced and
then separated or produced and simultaneously separated. Further,
these algae are repeatedly cultured to continuously produce
polysaccharide. For example, when polysaccharide is produced by
algae of the genus Spirulina, gel-like polysaccharide is attached to
wire net by passing a alga- culturing liquid through wire net having 30
mesh to separate polysaccharide.
205 PRODUCTION OF VISCOUS UOZUMI TAKESHI;others: 03 Pat. Nr. JP4053495 1992 PURPOSE:To improve the production of a viscous polysaccharide
POLYSACCHARIDE useful as a raw material for drugs, foods, etc., by culturing a plant
tissue as a callus thereof in a liquid medium. CONSTITUTION:A part
of the tissue, e.g. leaf, cotyledon or seed, of the Malvaceae plant such
as Hibiscus or Abelmoschus is cultured in a basic medium containing
1-10muM of auxin and 0.01-1muM of cytokinin at 25-30 deg.C to
induce the callus thereof. The callus is subjected to a subculture in an
agar medium containing 1-10muM of auxin and 0.01-5muM of
cytokinin for 2-4 months and the multiplied callus is subjected to a
shaking culture in a liquid medium containing the same concentrations
of the auxin and cytokinin in a dark atmosphere to produce the
objective viscous polysaccharide.
4.11 Literatures on Polysaccharides.xls - page 393
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
206 PRODUCTION OF SHIMIZU MASAKI;others: 03 JP60042331 TERUMO KK 1985 PURPOSE:To obtain a polysaccharide N9GI having low toxicity and
POLYSACCHARIDE N9GI useful as an antineoplastic agent, by ecoloring and purifying the
colored polysaccharide N9GI obtained from the hot-water extract of
the bark of Melia azadirachta, with a hypohalous acid salt without
lowering the pharmacological activity of the polysaccharide.
CONSTITUTION:The polysaccharide N9GI obtained from the hot-
water extract of the bark of Melia azadirachta has brown color
originated from the bark, and cannot be decolored even by activated
carbon treatment. The polysaccharide is dissolved in water, added
with an aqueous solution of a hypohalous acid salt in an amount of
preferably 0.2-1%, and stirred at room temperature for 2-15min. The
reaction liquid is treated with a dialyzing membrane, etc. to remove
excess hypohalous acid salt, and freeze-dried to obtain white
polysaccharide N9GI. The hypohalous acid salt is preferably
thehypochlorite, hypobromite or hypoiodite of Na or K. The
pharmacological acitivity remains unchanged by the decol
207 Process of producing a {37 DUC NGUYEN- Pat. Nr. US4104123 SANTERRE ORSAN 1978 The method of the invention, to produce a polysaccharide of the
xanthemonas-type{38 {0 CONG;BREHANTJEAN-LOUIS xanthane type, makes use of a strain of Xanthemonas, notably of the
polysaccharide MARIE;PONS BENOIT-JOSEPH; strain no. ATCC 31 176 deposited on Oct. 14, 1975, which is
SECHET MAURICE HENRI cultivated on a medium with 5 to 55 g/l or more of carbohydrates and
comprising at least one amino-acid selected from glutamic acid,
glutamine, arginine, tyrosine, threonine, aspartic acid, asparagine,
proline, leucine tryptophane and other amino-acids giving a
production of polysaccharide at least equal to 50% of that yielded by
corn steep liquor, the total nitrogen of said medium being 0.1 g/l to 5
g/1; the fermentation is carried out at 25 DEG -35 DEG C under
aerobiosis.
208 PRODUCTION OF TAKAHASHI HIROFUMI Pat. Nr. JP53044693 1978 PURPOSE:A specific lactic bacterium is cultured under specified
POLYSACCHARIDE conditions to produce glucan that can be used as starting material for
artificial serum and carcinostatice agent. CONSTITUTION:A
bacterium mold selected from Bacillus leaevolacticus M-4
(ATCC23549), the same M-1(ATCC23493) and the same M-91(FERM-
544) is cultured in a medium containing 1-10wt/v% of sucrose as the
carbon source, nitrogen source and other nutritions at 20-40 deg.C
and a pH4-8 under standing or slight aeration to form and accumulate
a polysaccharide that is of glucose polymer and entirely insoluble in
water together with or solely a fructose polymer that has a molecular
weight of over 20,000,000 and is soluble in water. They are, as it is or
after slightly hydrolyzed with a mineral acid, isolated and purified.
209 PRODUCTION OF AMAMIYA YUMIKO;others: 01 Pat. Nr. JP55037189 SANRAKU INC 1980
POLYSACCHARIDE USING
MICROORGANISM
4.11 Literatures on Polysaccharides.xls - page 394
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
210 PRODUCTION OF NAKANISHI OSAMU; OISO Pat. Nr. JP8256787 Teika Corp 1996 PURPOSE: To obtain a polysaccharide having good humectancy
POLYSACCHARIDE AND KLEBSIELLA YOICHI; OKUMIYA TAKESHI; unaffected by humidity and film formability, by culturing a
OXYTOCA TNM3 STRAIN SUGIHARA RYOSUKE; polysaccharide-productive Klebsiella oxytoca TNM3 strain or a mutant
KAWASHIMA KAORU thereof and taking the product from the resultant cultured product.
CONSTITUTION: The polysaccharide-productive Klebsiella oxytoca
TNM3 strain (FERM BP-4669) (or a mutant thereof), which has been
found by screening microbes capable of extracellularly producing
polysaccharides in high efficiency and was named so as a new
microbe, is inoculated into a medium and then subjected to
reciprocatingly shaking culture at 28 deg.C for one day, and the
resultant culture fluid is inoculated upon a jar fermenter and cultured
under aerating agitation at 28 deg.C for 86h while keeping the fluid at
pH7, thus obtaining the objective polysaccharide made up of a main
recurring unit having structure expressed by the formula and having
the above advantages.
211 PRODUCTION OF SUGISAWA AKIRA;others: 04 Pat. Nr. JP61239897 HOUSE FOOD IND CO LTD 1986 PURPOSE:To produce a polysaccharide which is dissolved under
POLYSACCHARIDE heating at low concentration, forms gel at normal temperature and
usable in a wide range, obtained by cultivating a specific bacterium
belonging to the genus Bacillus in a given medium.
CONSTITUTION:A bacterium (e.g., Bacillus SP-1) belonging to the
genus Bacillus separated from soil is inoculated into a medium
consisting of a carbon source (e.g., starch), a nitrogen source (e.g.,
urea), an inorganic substance (e.g., NaCl), etc., and cultivated at 5.5-
0.5pH at 15-45 deg.C for several days to form a polysaccharide
having main constituent components consisting of mannose, glucose,
xylose and glucuronic acid. Then, a mold and other solid contents in
the culture mixture are removed and a polysaccharide is separated
and purified.
212 PRODUCTION OF TANAKA MINORU;others: 04 Pat. Nr. JP57194799 SHIYOUWA SANGYO KK 1982 PURPOSE:Bacillus polymyxa is cultured in a medium containing salts
POLYSACCHARIDE and a polysaccharide salt with a specific substitution degree is
collected to obtain a polysaccharide having strong activities of
inhibiting the increase in serum cholesterol and reducing the
atherogenic index. CONSTITUTION:Bacillus polymyxa 271 is
cultured in a medium which is preapred by adding a nitrogen source
such as pepton, corn-steep liquor, yeast extract or urea and salts such
as phosphate or magnesium sulfate to a solution containing 3-5% of
glucose, galactose, lactose or molasses as a carbon source. Then,
the resultant saccharide is substituted with at least one of cations of
alkali metal, alkaline earth metal, transition metal, manganese,
aluminum, zinc or copper and of ammonium by more than 0.2
substitution degree to give the objective polysaccharide.
4.11 Literatures on Polysaccharides.xls - page 395
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
213 PRODUCTION OF TANAKA MINORU;others: 04 Pat. Nr. JP57194798 SHIYOUWA SANGYO KK 1982 PURPOSE:Bacillus polymyxa 271 is cultured in a medium and
POLYSACCHARIDE saccharide of a specific molecular weight is coolected whereby a
polysaccharide is obtained, which has a strong activity of reducing
atherogenic index and inhibiting the increase in serum cholesterol.
CONSTITUTION:Bacillus polymyxa 271 is inoculated in a medium that
is prepared by adding pepton, corn-steep liquor, yeast extract, urea or
other nitrogen sources and salts such as magnesium sulfate to a
solution containing about 3- 5% of glucose, sucrose, lactose or
molasses as a carbon source and cultured aerobically. The resultant
high-viscosity polysaccharide is precipitated with methanol, subjected
to ultrafiltration to effect the purification and give the objective
polysaccharide of more than 200,000mol.wt. The molecular weight of
the above polysaccharide is required to be more than 200,000 so that
the polysaccharide may have activities of strongly inhibiting the
increase in the serum cholesterol and remarkably reducing the
atherogenic index.
214 MICROBIOLOGICAL PRODUCTION BENGUTO ANDERUSU Pat. Nr. JP60002195 PERSTORP AB 1985
OF POLYSACCHARIDE NOORUBERI; NIRUSU
RUUDOBIGU MORIN; RAARUSU
INGUBAARU BIIBERIERU
215 Microbial polysaccharides, process for VOELSKOW HARTMUT (DE); Pat. Nr. US4567140 Hoechst AG (DE) 1986 Polysaccharides are obtained by fermentation using a mixed culture of
their preparation, microorganisms SCHLINGMANN MERTEN (DE) several microorganisms, of which at least one also produces a
suitable for this and use of the polysaccharide in pure culture, which polysaccharides are suitable as
polysaccharides viscosity regulators. A mixed culture of the strains Pseudomonas
maltophilia DSM 2130 and Agrobacterium tumefaciens DSM 2128 is
particularly suitable.
216 POLYSACCHARIDE AND ITS NODA KIYOSHI; others: 06 Pat. Nr. JP6248003 KURORERA KOGYO KK 1994 PURPOSE:To obtain a polysaccharide produced extracellularly by a
PRODUCTION specific kind of green alga, containing a specific amount or more of
galactose, excellent in separability, purification easiness and
producibility, useful as an antineoplastic agent, etc.
CONSTITUTION:This polysaccharide produced extracellularly by a
monocytic green alga belonging to Chlorella contains >=80wt.%,
based on the whole neutral saccharide, o galactose as its purified
state. It is preferable that the objective saccharide corresponding to a
fraction of15000-25000 molecular weight be obtained by culturing this
green alga in a culture fluid and purifying the supernatant of the
resultant culture fluid through ultrafiltration of dialysis.
217 POLYSACCHARIDE A - 1845, Endo Akira, others:01 Pat Nr. JP 4278095 Japan steel works ltd:the 1992 PURPOSE:To provide the subject polysaccharide useful as low
PRODUCTION THEREOF AND calorie dietary fibers for foods, drugs, cosme+G30tics, etc., by
MICROORGANISM PRODUCING THE culturing a polysaccharide A-1845- producing bacterium belonging to
SAME the Streptomyces and subsequently collecting the product from the
cultured solution. CONSTITUTION:A polysaccharide A-1845-
producing bacterium belong to the Strepomyces [e.g. Streptomyces
Sp-A-1854(FERM 12043)] is cultured, and the resultant
polysaccharide A-1846 is collected from the cultured product. The
polysaccharide A-1845 is white, has hexose, uronic acid, pentose,
methylpentose, amino sugar and phosphorus as constituents, has
mannose, galactose, galactwronic acid, xylose, rhamnose, glucose,
fucose, and ribose as constituting saccharides, is soluble in water, is
insoluble in methanol, ethanol, phopanol and acetone, is positive to
an anothrone reaction, negative to a ninhydrin reaction, is acidic, does
not accept the action of amylase, and has a specific rotation power
[alpha]D<24> of +57.0 deg.
4.11 Literatures on Polysaccharides.xls - page 396
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
218 POLYSACCHARIDE MH-2 AND Minoda Taiji, others: 01 Pat. Nr. JP55120601 Ajinomoto Co inc 1980 PURPOSE:To obtain novel polysaccharide MH-2 useful for food as a
PRODUCTION THEREOF thickener by a method wherein polysaccharide MH-2 is recovered
from culture products of a methane-utilizing polysaccharide MH-2
producing strain. CONSTITUTION:A methane-utilizing
polysaccharide MH-2 producing strain is cultured in the presence of
methane and a produced polysaccharide MH-2 is recovered from the
culture products. As the microorganisum used grows in the presence
of methane as a sole carbon source, methane is used as a carbon
source. But, the growth of the microoranism is promoted by the
presence of carbon dioxide. Hence, a vapor phase consisting of
methane, carbon dioxide and oxygen or air is used. Preferred pH of
the medium is 4.5-8.0. Preferred culture temp. is 35-55 deg.C. A static
culture, a shaking culture or an aeration-stirring culture can be used.
The aeration-strring culture is preferred for the mass production of the
polysaccharide. The concentration of the polysaccharide MH-2 in the
medium is 1-2g/l.
219 Continuous process for the production Lawford Hugh G Pat. Nr. US4355106 Weston George Ltd 1982 The present invention is directed to a two-stage continuous process
of gelable exopolysaccharide for the production of a gelable curdlan-type exopolysaccharide. In the
first stage a stable, curdlan-producing strain of microorganism such as
Alcaligenes faecalis var. myxogenes ATCC 31749 and ATCC 31750,
is grown aerobically in an aerated, agitated culture medium containing
assimilable carbon, nutrients and organic salts. The amount of
nitrogen in the first stage is so limited that the effluent therefrom
contains substantially no inorganic nitrogen. The effluent is introduced
into a second stage in a constant volume fermenter wherein it is mixed
with a nitrogen-free carbohydrate. The resultant mixture is aerated
and mixed at pH 5.5 to 6.5 at a temperature of from 25 DEG to 35
DEG C., the volume and dilution rate in the reactor being selected so
that the residence time of the microorganism in the fermenter does not
exceed an equivalent to the maximum length of time during which the
activity of a batch culture of the microorganism with respec
220 Effects of yeast extract on the S. Guillouet (1), J. H. Choi (2), C. Applied Microbiology and (1) Massachusetts Institute of 1999 zooglan, Zoogloea ramigera Although many studies have examined the influence of culture
production and the quality of the K. Rha (2), A. J. Sinskey (1) Biotechnology ISSN: 0175-7598 Technology, Department of Biology, 115SLR, yeast extract conditions on the production and composition of polysaccharides, little
exopolysaccharide, zooglan, produced (printed version) ISSN: 1432-0614 Room68-370, 31 Ames Street, is known about the factors influencing the quality of
by Zoogloea ramigera 115SLR (electronic version) Abstract Volume Cambridge, MA 02139, USA e-mail: exopolysaccharides (EPS). In this work we studied the effect of yeast
51 Issue 2 (1999) pp 235-240 asinskey@mit.edu (2) Massachusetts extract on the production, composition and molecular weight of the
Institute of Technology, Biomaterials EPS zooglan produced by Zoogloea ramigera 115SLR. This
Science and Engineering Laboratory, bacterium was grown on a new completely defined synthetic medium
Room 56-265, 77 Massachusetts and on a medium containing yeast extract. Growth and polysaccharide
Avenue, Cambridge, MA 02139, USA production performances were comparable on the two media with a
glucose to exopolysaccharide conversion yield of 35% (g/g). The
polysaccharides produced on these two media have an identical
composition but a different molecular weight and molecular weight
distribution. The yeast extract medium leads to a more homogeneous
polysaccharide solution.
4.11 Literatures on Polysaccharides.xls - page 397
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
221 Kinetics of Thermoascus aurantiacus N. Roche, A. Durand Applied Microbiology and Plate-forme de predeveloppement en 1996 during solid-state fermentation, The fungal solubilization of cell wall components of sugar-beet pulp,
solid-state fermentation on sugar-beet Biotechnology ISSN: 0175-7598 biotechnologie, Institut National de la fungus, enzymes during solid-state fermentation of Thermoascus aurantiacus, is
pulp - polysaccharide alteration and (printed version) ISSN: 1432-0614 Recherche Agronomique, 17, rue reported here. The extracellular fungal enzyme activities related to the
production of related enzymatic activitie (electronic version) Abstract Volume Sully, 21034, Dijon cedex, France substrate degradation were also studied. In 120 h, more than 60% of
45 Issue 5 (1996) pp 584-588 the main sugar-beet pulp polysaccharides, i.e. pectins, arabinose- and
glucose-containing polysaccharides, were rapidly brought into solution
by the fungus. The slow accumulation of monosaccharides compared
to the fast degradation of the polysaccharides suggested that most of
the released sugars were consumed by the fungus. The analysis of
the enzymes present in the water extracts of the solid-state cultures
proved that the fungus was able to synthesize a complete enzymatic
system required for the hydrolysis of the main sugar-beet pulp
polysaccharides. The highest enzyme activities measured were -
glucosidase and -L-arabinofuranosidase.
222 Production and purification of rhamnose J. M. Serrat (1) (1), G. Caminal Bioprocess Engineering ISSN: 0178- (1) Unitat d'Enginyeria Quimica. 1994 rhamnose, Klebsiella sp. I-714 A rhamnose-containing microbial polysaccharide has been produced
from microbial polysaccharide produced (1), F. Godia (1), C. Sola (1), J. 515X (printed version) ISSN: 1432- Institut d'Enginyeria Bioquimica. by Klebsiella sp. I-714. strain. The polysaccharide has been used as a
by Klebsiella sp. I-714 Lopez-Santin (1), D. F. Perry (2), 0797 (electronic version) Abstract Universitat Autonoma de Barcelona. source for the obtention of L-rhamnose. A biotechnological process
P. Monsan (2) Volume 12 Issue 6 (1995) pp 287- 08193-Bellaterra, Spain (1) Present has been developed to purify the hydrolyzed polysaccharide (EPSH),
291 address: XAM, European Space which contains rhamnose, galactose and glucuronic acid. Microbial
Research and Technology Centre, removal of galactose is followed by a continuous chromatographic
Keplerlaan 1. Post Hous 299.2200 separation of glucuronic acid to render pure rhamnose. The technical
Noordwijk, The Netherlands (2) feasibility of the process has been studied, with special emphasis on
BioEurope. 4 Impasse Didier Daurat, microbial inhibitor's removal.
31031 Tolouse, France
223 Amylose-like polysaccharide K. Kirimura (1), S. Yusa (1), S. Applied Microbiology and (1) Department of Applied Chemistry, 1998 Aspergillus niger Yang no. 2 , When 120 mg glucose/ml was used as a carbon source, in shake
accumulation and hyphal cell-surface Rugsaseel (1), H. Nakagawa (1), Biotechnology ISSN: 0175-7598 School of Science and Engineering, shake culture culture Aspergillus niger Yang no. 2 maximally produced only 15.4 mg
structure in relation to citric acid M. Osumi (2), S. Usami (1) (printed version) ISSN: 1432-0614 Waseda University, Ohkubo 3-4-1, citric acid/ml but accumulated 3.0 mg extracellular polysaccharide/ml.
production by Aspergillus niger in (electronic version) Abstract Volume Shinjuku-ku, Tokyo 169-8555, Japan The polysaccharide secreted by mycelia of Yang no. 2 in shake
shake culture 52 Issue 3 (1999) pp 421-428 Fax: +81-3-3232-3889 (2) Department culture was confirmed to be an amylose-like -1,4-glucan by hydrolysis
of Chemical and Biological Sciences, analysis with acid, amylase and glucoamylase. However, in static
Faculty of Science, Japan Women's cultures, such as semi-solid and surface cultures free from physical
University, 2-8-1 Mejiro-dai, Bunkyo- stresses caused by shaking damage, Yang no. 2 produced more citric
ku Tokyo, 112-8681, Japan acid but did not accumulate the polysaccharide. With cultivation time
in shake culture, the amount of extracellular polysaccharide and the
viscosity of the culture broth increased. The increase of shaking
speed caused a remarkable increase in the accumulation of
extracellular polysaccharide, e.g. 11.2 mg extracellular
polysaccharide/ml was accumulated in the medium at a shaking speed
of 200 rpm. The addition of 2.0 mg carboxymethylcellulose (CMC)/ml
as a viscous additive to the medium
4.11 Literatures on Polysaccharides.xls - page 398
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
224 Effects of yeast extract and glucose on Yang-Ming Lo (1)(2)(3), Shang- Applied Microbiology and (1) Department of Chemical 1997 xanthan, xanthomonas, Although available kinetic data provide a useful insight into the effects
xanthan production and cell growth in Tian Yang (1), David B. Min (2) Biotechnology ISSN: 0175-7598 Engineering, The Ohio State campestris, carbon, glucose, of medium composition on xanthan production by Xanthomonas
batch culture of Xanthomonas (printed version) ISSN: 1432-0614 University, Columbus, Ohio, USA (2) nitrogen, yeast extract campestris, they cannot account for the synergetic effects of carbon
campestris (electronic version) Abstract Volume Department of Food Science and (glucose) and nitrogen (yeast extract) substrates on cell growth and
47 Issue 6 (1997) pp 689-694 Technology, The Ohio State xanthan production. In this work, we studied the effects of the
University, Columbus, Ohio, USA (3) glucose/yeast-extract ratio (G/YE) in the medium on cell growth and
Department of Animal and Food xanthan production in various operating modes, including batch, two-
Sciences, 037 Townsend Hall, stage batch, and fed-batch fermentations. In general, both the xanthan
University of Delaware, Newark, DE yield and specific production rate increased with increasing G/YE in
19717, USA Tel.: (302) 831 1045 Fax: the medium, but the cell yield and specific growth rate decreased as
(302) 831 2822; e-mail: G/YE increased. A two-stage batch fermentation with a G/YE shift
ymlo@udel.edu from an initial low level (2.5% glucose/0.3% yeast extract) to a high
level (5.0% glucose/0.3% yeast extract) at the end of the exponential
growth phase was found to be preferable for xanthan production. This
two-stage fermentation design both provided fast cell growth and gave
225 Xanthan production - effect of agitation H. Umasankar, G. Annadurai, M. Bioprocess Engineering ISSN: 0178- Department of Chemical Engineering, 1995 glucose, xanthan, xanthomonas, Glucose fermentation by Xanthomonas campestris to xanthan was
Chellapandian, M. R. V. Krishnan 515X (printed version) ISSN: 1432- Anna University, Madras 600 025, campestris, fermenter, agitation investigated in a stirred tank fermenter for the effect of agitation on
0797 (electronic version) Abstract India cell growth and product synthesis. In the range investigated for speed
Volume 15 Issue 1 (1996) pp 35-37 between 300 to 500 rpm, these factors registered a rise with
increasing degrees of turbulence, the experiments being carried out
over a span of two days.
226 Influence of nutrients on cell growth and H. Umashankar, G. Annadurai, M. Bioprocess Engineering ISSN: 0178- Department of Chemical Engineering, 1995 Xanthan, xanthomonas, Xanthan production by Xanthomonas campestris was performed in a
xanthan production by Xanthomonas Chellapandian, M. R. V. Krishnan 515X (printed version) ISSN: 1432- Anna University, Madras 600 025, campestris, nutrients, batch batch fermentation study with a view to achieving maximum yields.
campestris 0797 (electronic version) Abstract India fermentation The factors influencing the production - mainly the nutrients, were
Volume 14 Issue 6 (1996) pp 307- investigated. Trace elements such as phosphate and magnesium at
309 6.0 g/l and 0.2 g/l enhanced the yields.
227 Growth and xanthan production of A. Prell, J. Lasik, J. Konic\uek, M. Bioprocess Engineering ISSN: 0178- Institute of Microbiology, Academy of 1995 xanthan, xanthomonas, Growth of X. campestris and production of xanthan were studied in
Xanthomonas campestris depending on Sobotka, J. Sys 515X (printed version) ISSN: 1432- Sciences of the Czech Republic, campestris, Nitrogen several batch fermentations with different starting concentrations of N-
the N-source concentration 0797 (electronic version) Abstract Viden\uska 1083, 142 20 Praha 4, source. The dependencies of growth, productivity and yields on initial
Volume 13 Issue 6 (1995) pp 289- Czech Republic E-mail: N-source concentration were observed. The maximum yields in the
292 prell@biomed.cas.cz course of cultivations were identified.
228 Use of industrial medium components L. De Vuyst, A. Vermeire Applied Microbiology and Department of Chemical Engineering, 1994 xanthan, carbon, nitrogen, Xanthan production is influenced by the type and initial concentration
for xanthan production by Xanthomonas Biotechnology ISSN: 0175-7598 Free University of Brussels, Pleinlaan phosphate, citrate, medium, of the carbon and nitrogen source as well as by the phosphate and
campestris NRRL-B-1459 (printed version) ISSN: 1432-0614 2, B-1050 Brussels, Belgium method citrate concentrations added. An optimal and industrially useful
(electronic version) Abstract Volume fermentation medium has been devised. It consists of either glucose
42 Issue 2/3 (1994) pp 187-191 (4.0%), sucrose (4.0%) or sirodex A (2.8%) as a sole carbon source,
corn steep liquor (2.0%) as a combined nitrogen-phosphate source
and additional phosphate (0.1%) and citrate (0.1%) depending on the
application of the xanthan formed.
4.11 Literatures on Polysaccharides.xls - page 399
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
229 Pullulan content of the ethanol C. J. Israilides (1), A. Smith (2), J. Applied Microbiology and (1) Institute of Technology of 1998 pullulan, agro-industrial waste, Ethanol-precipitated substances after fermentation of various agro-
precipitate from fermented agro- E. Harthill (2), C. Barnett (2), G. Biotechnology ISSN: 0175-7598 Agricultural Products, National fermentation, waste industrial wastes by Aureobasidium pullulans were examined for their
industrial wastes Bambalov (3), B. Scanlon (2) (printed version) ISSN: 1432-0614 Agriculture Research Foundation, 1 pullulan content. Grape skin pulp extract, starch waste, olive oil waste
(electronic version) Abstract Volume Sof Venizelou St., Lycovrissi 14123, effluents and molasses served as substrates for the fermentation. A
49 Issue 5 (1998) pp 613-617 Athens, Greece (2) Department of Life glucose-based defined medium was used for comparison purposes.
Sciences, The Nottingham Trent Samples were analysed by an enzyme-coupled assay method and by
University, Clifton Lane, Nottingham, high-performance anion-exchange chromatography with pulsed
NG11 8NS, UK (3) Higher Institute of amperometric detection after enzymic hydrolysis with pullulanase.
Food and Flavour Industries, 26 Fermentation of grape skin pulp extract gave 22.3 g l-1 ethanol
Maritza Blvd, 4000 Plovdiv, Bulgaria precipitate, which was relatively pure pullulan (97.4% w/w) as
assessed by the coupled-enzyme assay. Hydrolysed starch gave only
12.9 g l-1 ethanol precipitate, which increased to 30.8 g l-1 when the
medium was supplemented with NH4NO3 and K2HPO4; this again
was relatively pure pullulan (88.6% w/w). Molasses and olive oil
wastes produced heterogeneous ethanol-precipitated substances
containing small amounts of pullulan, even whe
230 Optimization of batch fermentation R. S. Karthikeyan, S. K. Rakshit, Bioprocess Engineering ISSN: 0178- Biotechnology Research Center, 1995 batchfermentation, dextran, The nutrient medium (containing sucrose, yeast extract and K2HPO4),
conditions for dextran production A. Baradarajan 515X (printed version) ISSN: 1432- Department of Chemical Engineering, conditions, optimum, method temperature and initial pH conditions were optimised for batch dextran
0797 (electronic version) Abstract Indian Institute of Technology, production in shake flask fermentations using a strain of Leuconostoc
Volume 15 Issue 5 (1996) pp 247- Madras 600 036, India mesenteroides NRRL B 512 (F). A 25-1 fractional factorial central
251 composite experimental design was attempted. Multistage Monte
Carlo optimization program was used to maximize the multiple
regression equation obtained. The optimal values of tested variables
for maximal dextran production were found to be: sucrose, 300 g/l;
yeast extract, 10 g/l; K2HPO4, 30 g/l; temperature, 23 °C and initial
pH 8.3 with a predicted dextran yield of 154 g/l.
231 Heteropolysaccharide S-130 Kang; Kenneth S., Veeder; Pat. Nr. US4342866 Merck & Co., Inc., Rahway, NJ 1982 heteropolysaccharide, S-130, The new heteropolysaccharide S-130, prepared by fermentation of an
George T. Alcaligenes, ATCC 31555 unnamed Alcaligenes species, ATCC 31555 has valuable properties
as a thickening, suspending and stabilizing agent in aqueous
systems. It is especially useful in formulating oil well drilling fluids and
muds. Its chemical composition is 2.8-7.5% acyl groups, 11.6-14.9%
glucuronic acid; and the neutral sugars mannose, glucose and
rhamnose, in the approximate molar ratio 1:2:2.
232 Deacetylated polysaccharide S-60 Kang; Kenneth S., Colegrove; Pat. Nr. US4326052 Merck & Co., Inc., Rahway, NJ 1980 Deacetylated, Polysaccharide, S- Deacetylated Polysaccharide S-60, prepared by deacetylating the
George T., Veeder; George T. 60, Pseudomonas elodea, ATCC polysaccharide S-60 produced by fermentation of Pseudomonas
31461 elodea, ATCC 31461, has valuable properties in both the clarified and
non-clarified form, and is useful as an agar substitute or a shapeable
room deodorant. The non-clarified deacetylated gum contains about
17% protein and principally carbohydrate, which comprises glucuronic
acid (~13% based on wt. gum) and the neutral sugars rhamnose and
glucose in the approximate molar ratio 3:2. The clarified, deacetylated
gum contains mostly carbohydrate and no more than about 2%
protein.
233 Polysaccharide S-60 and bacterial Kang; Kenneth S., Veeder; Pat. Nr. US4326053 Merck & Co., Inc., Rahway, NJ 1982 Polysaccharide, S-60, A novel polysaccharide S-60 is disclosed composed of principally
fermentation process for its preparation George T. Pseudomonas elodea carbohydrate, 10-15% protein, and 3-4.5% acetyl groups as the O-
glycosidically linked ester. The carbohydrate portion contains about
11% glucuronic acid (based on wt. gum) and the neutral sugars
rhamnose and glucose, the latter having an approximate molar ratio of
3 to 2. This polysaccharide is produced by a new Pseudomonas
species, P. elodea, in a suitable fermentation medium.
4.11 Literatures on Polysaccharides.xls - page 400
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
234 Production of heteropolysaccharide by Finn; Robert K. ,Tannahill; Alex L. Pat. Nr.US3923782 Cornell Research Foundation, Inc., 1975 heteropolysaccharide, Disclosed is a new heteropolysaccharide polymer and a method for
fermentation of methanol ,Laptewicz, Jr.; Joseph E. Ithaca, NY Methylomonas producing this polymer by a fermentation process comprising culturing
a heteropolysaccharide-producing strain of a micro-organism of the
genus Methylomonas on an aqueous culture medium containing
methanol as the sole source of assimilable carbon. Several uses for
the heteropolysaccharide are also disclosed such as its use as a drag
reducing agent, a thickening agent, an emulsifier, a soil suspending
agent and a flocculant or deflocculant.
235 Polysaccharide and bacterial Kang; Kenneth Suk , Veeder, III; Pat. Nr. US3933788 Kelco Company, San Diego, CA 1976 heteropolysaccharide, bacteria A process for producing a heteropolysaccharide by a bacterial
fermentation process for ist preparation George T. , Richey; Danny D. fermentation procedure in which a new species of bacteria is
incubated in a fermentation medium which contains a carbon source,
preferably a hydrolyzed starch, a source of magnesium ions, a source
of phosphorous, a source of nitrogen and water with the incubation
taking place at a temperature of about 28° to about 35°C. The
heteropolysaccharide produced by the above fermentation process. A
thickened aqueous media containing an effective quantity of the
heteropolysaccharide to thicken the media.
236 Polysaccharide and bacterial Kang; Kenneth Suk , McNeely; Pat. Nr. US3960832 1976 heteropolysaccharide, bacteria, A process for producing a novel heteropolysaccharide by a bacterial
fermentation process for its preparation William H. carbohydrate, magnesium, fermentation in which a new bacteria is incubated in a final
phosphorus, nitrogen, water fermentation medium containing a suitable carbohydrate source, a
source of magnesium ions, a source of phosphorus and nitrogen, and
water, the incubation taking place at a temperature of about 25 to
35°C. for about 35 to 60 hours. The heteropolysaccharide produced
by the above process are used to thicken aqueous media.
Compositions containing the above polysaccharide in combination
with certain salts containing di- and trivalent metal ions are useful for
example, in drilling fluids, paint compositions, polishes and as
additives for foods.
237 Polysaccharide and bacterial Kang; Kenneth Suk , McNeely; Pat. Nr. US3915800 Kelco Company, San Diego, CA 1975 heteropolysaccharide, bacteria, A process for producing a novel heteropolysaccharide by a bacterial
fermentation process for its preparation William H. carbohydrate, magnesium, fermentation in which a new bacteria is incubated in a final
phosphorus, nitrogen, water fermentation medium containing a suitable carbohydrate source, a
source of magnesium ions, a source of phosphorus and nitrogen, and
water, the incubation taking place at a temperature of about 25° to
35°C. for about 35 to 60 hours. The heteropolysaccharide produced
by the above process. Thickened aqueous medium containing an
effective quantity of the above polysaccharide to thicken the media.
Thickened aqueous medium containing an effective quantity of the
above polysaccharide in combination with certain salts containing di-
and trivalent metal ions. Aqueous gels having specified alkaline pH
and containing the above polysaccharide in combination with certain
salts containing di- and trivalent metal ions. Compositions containing
the above polysaccharide in combination with certain salts containing
di- and trivalent metal ions.
238 Polysaccharide S-60 and bacterial Kang; Kenneth S., Veeder; Pat. Nr. US4377636 Merck & Co., Inc., Rahway, NJ 1983 polysaccharide s-60, A novel polysaccharide S-60 is disclosed composed of principally
fermentation process for its preparation George T pseudomonas elodea carbohydrate, 10-15% protein, and 3-4.5% acetyl groups as the O-
glycosidically linked ester. The carbohydrate portion contains about
11% glucuronic acid (based on wt. gum) and the neutral sugars
rhamnose and glucose, the latter having an approximate molar ratio of
3 to 2. This polysaccharide is produced by a new Pseudomonas
species, P. elodea, in a suitable fermentation medium.
4.11 Literatures on Polysaccharides.xls - page 401
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
239 Bacterial polysaccharide Kang; Kenneth S. , Veeder, III; Pat. Nr. US4247639 Merck & Co., Inc., Rahway, NJ 1981 heteropolysaccharide, mannose, A high-viscosity heteropolysaccharide composed of 33% mannose,
George T. glucose, galactose, glucuronic 29% glucose, 21% galactose and 17% glucuronic acid, and containing
acid, acetyl, pyruvate 5.7% acetyl and 4.9% pyruvate.
240 Process for the preparation of Williams; Alan G. Lawson; Pat. Nr. US4298725 Tate & Lyle Limited, United Kingdom 1981 Pseudomonas sp NCIB 11264 A polysaccharide processing useful flow and gel-forming properties is
polysaccharide 9 Christopher J. Wimpenny; Julian (ATCC 31260) prepared by cultivation of Pseudomonas sp NCIB 11264 (ATCC
W. T. 31260). The polysaccharide, which readily can be produced in up to
75% yield by continuous culture, possesses properties which are
similar to those of xanthan and other gums.
241 Deacetylated polysaccharide S-60 Kang; Kenneth S., Colegrove; Pat. Nr. US4385123 Merck & Co., Inc., Rahway, NJ 1983 Deacetylated, Polysaccharide S- Deacetylated Polysaccharide S-60, prepared by deacetylating the
George T., Veeder; George T. 60, Pseudomonas elodea, ATCC polysaccharide S-60 produced by fermentation of Pseudomonas
31461 elodea, ATCC 31461, has valuable properties in both the clarified and
non-clarified form, and is useful as an agar substitute or a shapeable
room deodorant. The non-clarified deacetylated gum contains about
17% protein and principally carbohydrate, which comprises glucuronic
acid (~13% based on wt. gum) and the neutral sugars rhamnose and
glucose in the approximate molar ratio 3:2. The clarified, deacetylated
gum contains mostly carbohydrate and no more than about 2%
protein.
242 Microbial heteropolysaccharide Cox; Roger B. , Steer; David C. Pat. Nr. US4329448 Lever Brothers Company, New York, 1982 heteropolysaccharide, Biopolymer An heteropolysaccharide known as Biopolymer PS 87 comprises
NY PS 87, glucose, galactose, glucose, galactose, mannose, glucuronic acid and fucose. Biopolymer
mannose, glucuronic acid, fucose PS 87 is pseudoplastic, has a consistency at 20° C. of at least 150
poise and a yield stress value at 20° C. of at least 30 dynes/cm2.
Biopolymer PS 87 is synthesised by a strain of Bacillus polymyxa or a
genetically similar micro-organism and has many domestic and
industrial uses as a suspending agent or thickener.
243 Microbial production of polyfructose Mays; Thomas D. , Dally; Ellen L. Pat. Nr. US4769254 Igene Biotechnology, Inc., Columbia, 1988 levan, microbial production A water-soluble levan having a weight average molecular weight of
MD about 10,000-40 million, preferably about 5-25 million and especially
about 10-20 million which stabilizes a bovine serum albumin colloid
having index (EAI) of about 3-100 determined according to the formula
EAI=2T/OC wherein T is turbidity measured at 500 nm, C is the
weight of emulsified protein per unit volume of the aqueous phase,
and O is the volume fraction of a dispersed oil phase is produced by
fermenting a nutrient growth medium feedstock having a carbon
source consisting essentially of an assimilable sugar selected from
the group consisting of sucrose, raffinose, or a mixture thereof with a
microorganism capable of converting at least 50%. of the fructose
value of the sugar to said levan under nutrient growth conditions
which enhance levan production while suppressing ethanol
production. It is useful as a colloid stabilizing agent, particularly with
foods, beverages, pharmaceuticals, dentifrices, and cosmetics.
244 Rifampicin resistant xanthan Pollock; Thomas J. , Thorne; Pat. Nr. US5310677 Shin-Etsu Chemical Co., Ltd., Tokyo, 1994 xanthan, xanthomonas campestris, A method of increasing xanthan gum production, comprising culturing
hyperproducing Xanthomonas Linda Japan Shin-Etsu Bio, Inc., San Diego, rifampicin, bacitracin, resistance a Xanthomonas campestris strain having a xanthan-increasing
campestris strain CA modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing rifampicin-
resistance; (2) a mutation causing bacitracin-resistance; or (3)
exogenous genetic information controlling the synthesis of xanthan;
and separating xanthan from the culture medium, is provided along
with specific DNA sequences and Xanthomonas campestris strains
showing increased xanthan gum production.
4.11 Literatures on Polysaccharides.xls - page 402
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
245 Xanthomonas campestris strain Pollock; Thomas J. , Thorne; Pat. Nr. US5194386 Shin-Etsu Chemical Co., Ltd., Tokyo, 1993 xanthan, xanthomonas campestris, A method of increasing xanthan gum production, comprising culturing
expressing xanthan gum Linda Japan Shin-Etsu Bio, Inc., San Diego, rifampicin, bacitracin, resistance a Xanthomonas campestris strain having a xanthan-increasing
CA modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing rifampicin-
resistance; (2) a mutation causing bacitracin-resistance; or (3)
exogQenous genetic information controlling the synthesis of xanthan;
and separating xanthan from the culture medium, is provided along
with specific DNA sequences and Xanthomonas campestris strains
showing increased xanthan gum production.
246 Preparation of xanthan gum Pollock; Thomas J. , Thorne; Pat. Nr. US5912151 Shin-Etsu Chemical Co., Ltd., Tokyo, 1999 xanthan, xanthomonas campestris, A method of increasing xanthan gum production, comprising culturing
Linda Japan Shin-Etsu Bio, Inc., San Diego, rifampicin, bacitracin, resistance a Xanthomonas campestris strain having a xanthan-increasing
CA modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing rifampicin-
resistance; (2) a mutation causing bacitracin-resistance; or (3)
exogenous genetic information controlling the synthesis of xanthan;
and separating xanthan from the culture medium, is provided along
with specific DNA sequences and Xanthomonas campestris strains
showing increased xanthan gum production.
247 Biologically pure culture of a strain of Pollock; Thomas J. , Thorne; Pat. Nr. US5472870 Shin-Etsu Chemical Co., Ltd., Tokyo, 1995 xanthan, xanthomonas campestris, A method of increasing xanthan gum production, comprising culturing
Xanthomonas compestris ATCC 55429 Linda Japan Shin-Etsu Bio, Inc., San Diego, rifampicin, bacitracin, resistance, a Xanthomonas campestris strain having a xanthan-increasing
CA ATCC 55429 modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing rifampicin-
resistance; (2) a mutation causing bacitracin-resistance; or (3)
exogenous genetic information controlling the synthesis of xanthan;
and separating xanthan from the culture medium, is provided along
with specific DNA sequences and Xanthomonas campestris strains
showing increased xanthan gum production. The strain is preferably
ATCC 55429.
248 Xanthan gum-producing strain of Pollock; Thomas J. , Thorne; Pat. Nr. US5340743 Shin-Etsu Chemical Co., Ltd., Tokyo, 1994 xanthan, xanthomonas campestris, A method of increasing xanthan gum production, comprising culturing
xanthomonas Linda Japan Shin-Etsu Bio, Inc., San Diego, rifampicin, bacitracin, resistance a Xanthomonas campestris strain having a xanthan-increasing
CA modification in a culture medium, wherein the modification is selected
from the group consisting of (1) a mutation causing rifampicin-
resistance; (2) a mutation causing bacitracin-resistance; or (3)
exogenous genetic information controlling the synthesis of xanthan;
and separating xanthan from the culture medium, is provided along
with specific DNA sequences and Xanthomonas campestris strains
showing increased xanthan gum production.
249 XANTHAN GUM USING MILK AS TOOMASU JIEI PORATSUKU, Pat. Nr. JP6319577A2 SHIN ETSU CHEM CO LTD 1994
MATERIAL, PRODUCTION THEREOF RICHIYAADO DABURIYUU
AND FERMENTATION CULTURE AAMENTOROOTO
SOLUTION
250 Leuconostoc strains for biosynthesis of Aebischer; Jurg , Niederscharli, Pat. Nr. US6004800 Nestec S.A., Vevey, Switzerland 1999 dextran, leuconostoc, Strains of Leuconostoc mesenteroides ssp. cremoris which provide,
dextran Switzerland D'Amico; Nicola , mesenteroide upon culturing, dextran, and the strains include deposited strains
Treycovagnes, Switzerland De CNCM I-1692 and CNCM I-1693.
Maleprade; Dominique , Vevey,
Switzerland Eyer; Kurt , Thun,
Switzerland Lesens; Corinne ,
Beauvais, France Neeser; Jean-
Richard , Savigny, Switzerland
Reniero; Roberto , Le Mont-
Pelerin, Switzerland Schmid;
Daniel , Lausanne, Switzerland
4.11 Literatures on Polysaccharides.xls - page 403
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
251 MICROBIAL CHITOSAN AND ITS ONO SUKEJI TOMOMATSU Pat. Nr. JP10316702A2 RENGO CO LTD 1998 chitosan, bacteria, microbial Problem to be solved: To obtain a microbial chitosan having a high
PRODUCTION AKIO SUZUKI JUNICHI molecular weight and conforming to the Food Standards at high
production efficiency by culturing mold belonging to the genus Absidia
in a culture medium under aerobic conditions in which the minimum
dissolved oxygen concentration in the medium in the phase of the
logarithmic growth of the microbes is specified and causticizing the
cultured microbes under heating. Solution: The chitosan-producing
bacteria are those containing a considerable amount of chitosan as a
constituent of cell walls and are desirably mold belonging to the genus
Absidia particularly Absidia coerlea. The carbon source of the medium
is glucose, starch, molasses or the like, and the nitrogen source is
yeast extract, gluten flour, urea an ammonium salt or the like. To
perform the culture, the medium is relatively densely inoculated with
spores or mycelia, and the DO value in the medium in the phase of
the logarithmic growth of the microbes under aerobic conditions under
high
252 Production of xanthan gum and ice- H. Kawahara, H. Obata Applied Microbiology and Department of Biotechnology, Faculty 1997 Xanthomonas, campestris, pv. Xanthomonas campestris pv. translucens IFO13599 could produce
nucleating material from whey by Biotechnology ISSN: 0175-7598 of Engineering, Kansai University, 3-3- Translucens, IFO13599, xanthan xanthan gum (18.5 mg/100 mg, lactose) with lactose as the growth
Xanthomonas campestris pv. (printed version) ISSN: 1432-0614 35 Yamate-cho, Suita-shi, Osaka 564- gum substrate in spite of a low level of -galactosidase. This productivity
translucens (electronic version) Abstract Volume 8680, Japan Tel.: +81 6 368 0832 corresponded to one-fifth that with glucose. This strain could also
49 Issue 4 (1998) pp 353-358 Fax: +81 6 388 8609 e-mail: produce ice-nucleating material having an ice-nucleating temperature,
kawahara@ipcku.kansai-u.ac.jp T50, of -2.8 °C with xanthan gum in the culture broth. We found that
this strain produced both materials in whey medium from which the
insoluble components had been removed. The production of xanthan
with ice-nucleating material reached a maximum after cultivation for
168 h under optimum conditions. Furthermore, the xanthan obtained
had a low viscosity because of its variant structure revealed, by TLC
and HPLC analyses, to be lacking pyruvic acid. Furthermore, we
concluded that this mixture had considerable potential as a
regeneratic agent, when compared to other regeneratic agents such
as carboxymethylcellulose.
253 Variations in xanthan production by H. Rodriguez (1), L. Aguilar (2), Applied Microbiology and (1) Department of Microbiology, 1997 streptomycin, tetracycline, Mutants resistant to different antibiotics (streptomycin, tetracycline,
antibiotic-resistant mutants of M. LaO (1) Biotechnology ISSN: 0175-7598 Cuban Research Institute on ampicillin, penicillin, Xanthomonas ampicillin and penicillin) were obtained from several strains of
Xanthomonas campestris (printed version) ISSN: 1432-0614 Sugarcane By-Products (ICIDCA), campestris, xanthan production Xanthomonas campestris and evaluated for xanthan production. Most
(electronic version) Abstract Volume P.O. Box 4026, CP 11 000, Ciudad of the mutants showed alterations in their polysaccharide production,
48 Issue 5 (1997) pp 626-629 Habana, Cuba Fax: 53 7 338236 e- either increasing, decreasing or totally losing their polymer-production
mail: icidca@ceniai.inf.cu (2) capacity. The existence of two types of antibiotic-resistance
Department of Biochemistry, Cuban mechanisms for the assayed drugs is suggested: one that affects
Research Institute on Sugarcane By- xanthan production and another that does not. Differences in outer-
Products (ICIDCA), Ciudad Habana, membrane protein patterns of mutants that were simultaneously
Cuba altered in antibiotic resistance and xanthan production were found, in
comparison with their parental strains. These findings suggest the
existence of a genetic relationship between antibiotic-resistance
mechanisms and xanthan production. Some of the mutants obtained
showed significant increases in broth viscosity and xanthan
concentration. These results suggest that resistance to streptomycin
and ampicillin can be use
4.11 Literatures on Polysaccharides.xls - page 404
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
254 Modeling and control of batch O. Georgieva (1), T. Patarinska Bioprocess Engineering ISSN: 0178- (1) Institute of Control and System 1995 batch fermentation, xanthan gum, An approach of model-based control design of batch biotechnological
fermentation processes under (2) 515X (printed version) ISSN: 1432- Research-Bulgarian Academy of Xanthomonas campestris ITS-342, processes combining the advantages of two different analytical
conditions of uncertainty 0797 (electronic version) Abstract Sciences, Acad. G. Bonchev St., bl.2, Method descriptions (deterministic and fuzzy model) is proposed. The
Volume 14 Issue 6 (1996) pp 299- Sofia 1113, Bulgaria (2) Center of approach uses the kinetic unstructured model accounting for the basic
306 Systems Engineering and Applied process dependencies. Using the fuzzy optimal decomposition of the
Mechanics Faculty of Applied physiological space into fuzzy regions, a new model is derived as a
Sciences, University Catholic of fuzzy weighted sum of distinct subsystems with unstructured models
Louvain, Batiment Euler, 4-6, describing the process dynamics in the respective region. The
Georges Lemaitre Str., B-1348, proposed model can be considered as a compromise between the
Louvain-la-Neuve, Belgium simple fuzzy model (input-output process description) which does not
take into account the analytical process characteristics and the
unstructured deterministic model that is not suitable for the control
design purpose. On-line linearizing control law on the basis of the
developed model is also proposed. The theoretical results are
illustrated for the example of batch xanthan gum fermentation of strain
Xanthomonas campestris ITS-342
255 Effects of substrate limitation on B. O. Solomon (1) (1), A.-P. Zeng Applied Microbiology and (1) Gesellschaft fuer 1994 klebsiella, pneumoniae, substrate Product formation during anaerobic degradation of glycerol by
product distribution and H2/CO2 ratio in (1), H. Biebl (1), A. Okechukwu Biotechnology ISSN: 0175-7598 Biotechnologische Forschung mbH, limitation, effect Klebsiella pneumoniae DSM 2026, under glycerol limitation and
Klebsiella pneumoniae during Ejiofor (1) (2), C. Posten (1), W. (printed version) ISSN: 1432-0614 Biochemical Engineering Division, D- glycerol excess in continuous cultures, has been investigated. Major
anaerobic fermentation of Glycerol D. Deckwer (1) (electronic version) Abstract Volume 38124 Braunschweig, Germany (1) and minor products and by-products as well as gaseous products
42 Issue 2/3 (1994) pp 222-226 Chemical Engineering Department, were measured. The results indicated a positive correlation between
Obafemi Awolowo University, Ile-Ife, specific glycerol uptake and most product formation rates under
Osun State, Nigeria (2) Department of glycerol limitation. The production of 1,3-propanediol, lactate, formate,
Applied Microbiology and Brewing, acetate, succinate and the by-products of anaerobic glycerol
Nnamdi Azikwe University, Awka, degradation by K. pneumoniae, acetoin and 2,3-butanediol, was
Anambra State, Nigeria favoured by glycerol excess, while hydrogen generation and ethanol
formation were best under glycerol limitation. It was also found that
under glycerol limitation the rate of hydrogen evolution was generally
higher than the CO2 production rate while under excess glycerol the
reverse was true. Hence, on the basis of the ratio of the specific rates
of evolution of H2 and CO2 (qH2/qCO2), it is possible to infer the
existence of glycerol l
256 Influence of phosphate on rhamnose- J. Farres, G. Caminal, J. Lopez- Applied Microbiology and Departament d'Enginyeria Quimica, 1997 rhamnose, polysaccharide Physiological conditions enhancing rhamnose-containing
containing exopolysaccharide rheology Santin Biotechnology ISSN: 0175-7598 Universitat Autonoma de Barcelona, synthesis, Klebsiella I-714 polysaccharide synthesis by Klebsiella I-714 were studied in batch
and production by Klebsiella I-714 (printed version) ISSN: 1432-0614 08193 Bellaterra, Spain Fax: 34 3 culture (0.3-l and 2-l bioreactors). The four carbon sources tested,
(electronic version) Abstract Volume 5812013 e-mail: Lopez@uab- sucrose, sorbitol, Neosorb and Cerelose, allowed exopolysaccharide
48 Issue 4 (1997) pp 522-527 eq.uab.es production. Larger amounts of polymer were produced when high
carbon/nitrogen ratios and complex nitrogen sources were used.
Exopolysaccharide synthesis was greatest at 30 °C, which was a
suboptimal growth temperature. A reduction in the phosphate content
of the medium enhanced rhamnose-containing polysaccharide
production. When the initial carbon source concentration was
augmented, byproducts other than exopolysaccharide were formed.
Rhamnose-containing polysaccharide rheology can be modulated by
changing the phosphate content of the medium.
4.11 Literatures on Polysaccharides.xls - page 405
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
257 Properties of levansucrase from M. A. Perez Oseguera, L. Applied Microbiology and Departamento de Bioingenieria, 1995 levan, sucrase, Bacillus circulans A polysaccharide-producing bacterium was isolated from cane sugar.
Bacillus circulans Guereca, A. Lopez-Munguia Biotechnology SSN: 0175-7598 Instituto de Biotecnologia, It was identified as Bacillus circulans and produced levansucrase at
(printed version) ISSN: 1432-0614 Universidad Nacional Autonoma de pH and temperature optima of 5-7 and 40°C respectively. The enzyme
(electronic version) Abstract Volume Mexico, Apartado Postal 510-3, is extracellular and inducible with sucrose. It possesses initial
45 Issue 4 (1996) pp 465-471 Cuernavaca Morelos 62271, Mexico. hydrolytic and transferase activities that can be altered by modifying
Fax: 52 73 172388 reaction conditions. Levansucrase was recovered from the
fermentation broth by extraction with polyethylene glycol (1500 Da).
Further purification resulted in an enzyme with a molecular mass of 52
kDa and a pI of 4.7. At high sucrose concentration (300 mM), the
transferase activity but not the hydrolase activity were inhibited. Levan
increased the transferase activity but had no effect on the hydrolytic
activity. The levansucrase had high transferase activity with maltose,
galactose and lactose and moderate activity towards sorbitol and
glycerol.
258 Fermenteurs agites sans organes C. G. Dussap; J. B. Gros Bull.Soc.Chim.Fr. 1985, 6 1075- 1985 pneumatical, agitated, gas-liquid, In this work, the possibilities of use of pneumatically agitated gas-
d'agitation mecanique. Application a la 1082. fermentors, method liquid fermentors -bubbles columns and air-lift fermentors- are
production de polysaccharides considered from the following data: power input, mixing time and
exocellulaires hydrodynamics of the liquid phase, aeration (k1a values and
equilibrium oxygen concentrations in the fermentation broth).Two
examples are examinated: the former deals with the comparison
between a stirred tank fermentor and a bubble column filled with
xanthan solutions.The latter concerns alginate production by
Azotobacter vinelandii : a kinetic model is proposed and emphasis is
laid on the fermentors characteristics influence on alginate
productivity.
259 Production of an extracellular Nakata K, Kurane R Biosci Biotechnol Biochem 1999 Central Research Laboratories, 1999 Ethanol; Flocculation Tests; Klebsiella pneumoniae H12 produced a newly identified extracellular
polysaccharide bioflocculant by Dec, 63:12:2064-8 Mercian Corporation, Fujisawa, Klebsiella pneumoniae; polysaccharide in an ethanol medium with a yield of 3.0 g/l. The molar
Klebsiella pneumoniae. Japan. knakata@mb.infoweb.ne.jp Polysaccharides, composition of the polysaccharide was 56.04% galactose, 25.92%
Bacterial glucose, 10.92% galacturonic acid, 3.71% mannose, and 3.37%
glucuronic acid. The addition of 0.5%-1.5% NaCl increased
production. The polysaccharide flocculated with kaolin clay in
suspension at the concentration of 1 ppm in a 300-ppm solution of
CaCl2. Almost all bacterial species cells aggregated in the
polysaccharide solution. The ability to flocculate with kaolin clay
changed with the pH and with the concentrations of coexisting cation
and anion species. The polysaccharide flocculant may participate in in
vivo bacterial aggregation or adherence to host organisms.
260 Preparation and preliminary Grigorova D, Pavlova K, Panchev Appl Biochem Biotechnol 1999 Sep, Laboratory of Applied Microbiology, 1999 Culture Media; Fermentation; The effects of various carbon and nitrogen sources on the synthesis of
characterization of exopolysaccharides I 81:3:181-91 Bulgarian Academy of Sciences, Hydrogen-Ion Concentration; exopolysaccharides by Rhodotorula acheniorum MC were studied.
by yeast Rhodotorula acheniorum MC. Plovdiv, Bulgaria. Nitrogen; The dynamic viscosity of cell-free culture broths during
Polysaccharides; Rhodotorula exopolysaccharide synthesis were measured. The highest values for
the viscosity (10.14 MPa.s) and crude polysaccharide productivity (6.6
g/L) were obtained in a medium supplied with 5% sucrose. Ammonium
sulfate was the most favorable nitrogen source for exopolysaccharide
synthesis. The value of pH played a determinant role, and the
obligatory condition for exopolysaccharide production was low (pH 1.7-
2.0) during the fermentation. The chemical composition and sugar
constituents of the crude exopolysaccharides were determined.
Mannose was the main monosaccharide component, and its
concentration was the highest (69.13%) in the crude
exopolysaccharide synthesized in the medium that included 5%
sucrose as a carbon source.
4.11 Literatures on Polysaccharides.xls - page 406
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
261 Environmental regulation of Mendrygal KE, González JE J Bacteriol 2000 Feb, 182:3:599-606 Department of Molecular and Cell 2000 Bacterial Proteins; Gene Exopolysaccharide production by Sinorhizobium meliloti is required for
exopolysaccharide production in Biology, University of Texas at Dallas, Expression Regulation, Bacterial; invasion of root nodules on alfalfa and successful establishment of a
Sinorhizobium meliloti. Richardson, Texas 75083-0688, USA. Molecular Weight; nitrogen-fixing symbiosis between the two partners. S. meliloti wild-
Phosphoric Acid Esters; type strain Rm1021 requires production of either succinoglycan, a
Polysaccharides, Bacterial ; polymer of repeating octasaccharide subunits, or EPS II, an
Sinorhizobium exopolysaccharide of repeating dimer subunits. The reason for the
meliloti production of two functional exopolysaccharides is not clear. Earlier
reports suggested that low-phosphate conditions stimulate the
production of EPS II in Rm1021. We found that phosphate
concentrations determine which exopolysaccharide is produced by S.
meliloti. The low-phosphate conditions normally found in the soil (1 to
10 microM) stimulate EPS II production, while the high-phosphate
conditions inside the nodule (20 to 100 mM) block EPS II synthesis
and induce the production of succinoglycan. Interestingly, the EPS II
produced by S. meliloti in low-phosphate conditions does not allow the
invasion of alfalfa no
262 Regulation of alginate biosynthesis in Fakhr MK, Peñaloza-Vázquez A, J Bacteriol 1999 Jun, 181:11:3478- Department of Microbiology and 1999 Alginates; Bacterial Proteins ; Both Pseudomonas aeruginosa and the phytopathogen P. syringae
Pseudomonas syringae pv. syringae. Chakrabarty AM, Bender CL 85 Molecular Genetics, Oklahoma State Base Sequence; Binding produce the exopolysaccharide alginate. However, the environmental
University, Stillwater, Oklahoma Sites;Carbohydrate signals that trigger alginate gene expression in P. syringae are
74078, USA. Dehydrogenases;Cloning, different from those in P. aeruginosa with copper being a major signal
Molecular; Comparative Study; in P. syringae. In P. aeruginosa, the alternate sigma factor encoded
Consensus Sequence ; DNA by algT (sigma22) and the response regulator AlgR1 are required for
Transposable Elements ; DNA- transcription of algD, a gene which encodes a key enzyme in the
Binding proteins; Gene Expression alginate biosynthetic pathway. In the present study, we cloned and
Regulation, Bacterial ; Gene characterized the gene encoding AlgR1 from P. syringae. The
Expression deduced amino acid sequence of AlgR1 from P. syringae showed 86%
Regulation,Enzymologic; Genetic identity to its P. aeruginosa counterpart. Sequence analysis of the
Complementation Test; Molecular region flanking algR1 in P. syringae revealed the presence of argH,
Sequence Data; algZ, and hemC in an arrangement virtually identical to that reported
Mutagenesis,Insertional; Mutation; in P. aeruginosa. An algR1 mutant, P. syringae FF5.32, was defective
Promoter Regions (Genetics) ; in alginate production but could be complemented when algR1 was
Pseudomonas expressed in trans. The alg
263 Alginate production by Azotobacter Clementi F Crit Rev Biotechnol 1997, 17:4:327- Dipartimento di Biologia, Difesa e 1997 Alginates; Azotobacter vinelandii; Although all commercial alginates are today of algal origin, there is
vinelandii. 61 Biotecnologie Agroforestali, Bacterial Proteins; interest in the production of alginate-like polymers from bacteria. The
Università della Basilicata, Potenza, Biocompatible Materials species Azotobacter vinelandii seems to be the best candidate for the
Italy. industrial production of alginate molecules characterized by a
chemical composition, molecular mass and molecular mass
distribution suited to a well defined application, especially required in
the biotechnological, biomedical and pharmaceutical fields. The
production of alginate by A. vinelandii has been to date widely
investigated both in batch (mainly in the shaken flask scale) and in
continuous cultures. This article summarizes current knowledge on
the structure and properties of alginates and their applications and
presents an overview of up-dated research on the physiology,
genetics and kinetics of the production of alginate by Azotobacter
vinelandii and its rheology, including the results of our recent studies.
4.11 Literatures on Polysaccharides.xls - page 407
ID Title Author(s) / Inventor(s) Source / Application Number Address(es) / Applicant(s) Year Keyword(s) Abstract
264 PRODUCTION OF SHIMIZU MASAKI YAMAMOTO Pat. Nr. JP60042330A2 Terumo corp 1985 Melia azadirachta, Purpose: To produce the titled substance useful as an antineoplastic
POLYSACCHARIDE N9GI SHIGEHIRO TAMURA YASUKO POLYSACCHARIDE N9GI agent, in an industrial scale, by extracting the bark of Melia
NOMURA TAKEO azadirachta with hot water, purifying the extract, contacting with a
lectin-immobilized carrier, eluting with methyl-α-D-glucoside,
etc., and dialyzing the eluted solution. Constitution: The bark of Melia
azadirachta is extracted with hot water, and purified by dialysis,
alcohol precipitation, etc. The purified extract liquid is made to contact
with a lactin-immobilized carrier [e.g. ConA-Sepharose (product of
Pharmacia Labs., Inc.)] to adsorb the polysaccharide. The adsorbed
fraction is eluted with methyl-α-D-glucoside or mannoside, and
the eluted solution is dialyzed by water with a membrane having a
fractionation molecular weight of ≤50,000 to obtain the
polysaccharide N9GI from the residual solution. The polysaccharide
N9GI is composed of N9GIa and N9GIb, both of which contain
α- (1,4)-glucan as main chain, and accordingly, the
polysaccharide bonds speci
Appendix 5. EDPs Website Directory
1. www.ics.trieste.it/
2. www.polystyrene.org
Polystyrene packaging council of America is the trade association representing major resin suppliers and
the manufacturers of polystyrene products in US. The website offered online information about the
environment including PS Recycling Program, The Economic Realities of Recycling, Degradability and
Compostability of Packaging Materials (Their opinion is against EDPs).
3. www.polyfoam.com/recycling-news
A Canada based website provides information for polyform manufacturers. Most of the site is under
construction thus can not be read. Main contents include: Historic data and quality policy, Manufacturing
process, Raws materials and Recycling program. Seems no information on EDPs.
Other items are : Packaging, Insulation, Automotive and Tooling .
4. www.unep.or.jp/OGT_DATA/WRAT
To further strengthen UNEP's role in sustainable urban and freshwater basin management, International
Environmental Technology Centre (IETC) was inaugurated in October 1992 in Japan and its offices in
Osaka and Shiga officially opened in April 1994. IETC's main role is to promote the application of
Environmentally Sound Technologies (ESTs) to address urban environmental problems, such as sewage,
air pollution, solid waste and noise, and the management of freshwater basins to developing countries and
countries with economies in transition. Substantial information, indirectly related to EDPs, can be found in
the International Source Book of ESTs for SWM (http://www.unep.or.jp/ietc/ESTdir/pub/MSW/index.html).
5. www.ciwmb.ca.gov/plastics
The website of Integrated Waste Management Board, which is one of six agencies under the umbrella of
the California Environmental Protection Agency responsible for managing California's solid waste.
408
http://www.agriholland.nl/proterra/about.html
Proterra is an International Centre which develops the market for Agro-based Materials such as
biodegradable polymers, natural cellulose fibers and composites. Proterra's main goal is to stimulate the
application of renewable raw materials in durable goods, packaging and disposables.
15. The Basel Convention on the Control of Trans-boundary Movements of Hazardous Wastes and their
Disposal (http://www.basel.int/)
It contains online detained and comprehensive information about environmentally sound waste
management, technical, legal and trade issues.
http://uncweb.carl.org
http://www.amazon.co.uk
http://www.wiley-vch.de
http://www.vsppub.com/
http://www.patent-info.ch/en/default.htm
Information search in all fields of patents, patent statistics, patent analysis, trademarks, technology
monitoring, and competitive intelligence
http://www.european-patent-office.org/tws/twsindex.htm
409
5.4 Degradable Polymers
Associations, Companies, Financial/Business, Research (USA)
http://www.ia-usa.org/peudegra.htm , Last update: 02. Dec. 1998,
http://www.devicelink.com/mpb/archive/97/11/003.html
Polymers in Controlled Drug Delivery (by Lisa Brannon-Peppas)
Delivery systems, mechanisms, references
http://www.staehelin.ch/biomat/biomat.html
Biodegradable Implants in Sports Medicine: The Biological Base Sections
Abstract/ In Vivo Degradation/ Osseous Replacement/ Biocompatibility and Clinical Classification of
Tissue Response/ Conclusion/ References/ Publishing and Reprint Information
http://www.mli.kvl.dk/foodchem/special/biopack/
Production and application of Biobased Packaging Materials for the food industry
http://www.biomat.net/
Selected internet links related to Biomaterials and some relevant links to biomedical engineering, biology,
medicine and health sciences in general. This Website intends to become a major tool in linking the
biomaterials community worldwide. WWW resources, organizations, research centers, education, meetings,
articles, journals, books, publishers, industry, scientific links
http://dcwww.epfl.ch/igc1/poly-hp.htm
WWW links for polysaccharide
http://www.agriholland.nl/proterra/links.html
For some technical information on materials have a look at: IDEMAT.
http://www.labmed.umn.edu/umbbd/index.html
The University of Minnesota Biocatalysis/Biodegradation Database
This database contains information on microbial biocatalytic reactions and biodegradation pathways for
primarily xenobiotic, chemical compounds. The goal of the UM-BBD is to provide information on
microbial enzyme-catalyzed reactions that are important for biotechnology.
http://www.agnic.org/agdb/biodeg.html (chargeable)
The BIODEG database contains 5,000 data-value records from experiments testing the biodegradable
properties of more than 700 chemicals. It covers screening studies, biological treatment studies, grab
sample studies, and field experiments. The compiler/provider is Syracuse Research Corporation (SRC),
Environmental Science Center, Merrill Lane, Syracuse, NY 13210.
http://www.aist.go.jp/RIODB/dbefc/index_E.html
National Institute for Resources and Environment is responsible for this page
List of informations
Biodegradationtion of chemicals in sediments -(Updated on '97, July 15.)
Decomposition reaction of chemicals in ambient air -(Opened on '98, August 31.)
Distribution of chemicals in coastal sediment -(Updated on '97, May 21.)
Concentration of chemicals in ambient air -(Opened on '96, October 21.)
Composition of chemicals or isomers at their sources -(Updated on '98, August 24.)
410
Appendix 6. Inventory of Patents
1984 US4476255 Photoreactive plastic composition and BAILEY W. J. (US); OWENS ILLINOIS INC (US)
articles degradable by ultraviolet TAYLOR L. J. (US)
radiation and a process for their
manufacture
1985 US4495311 Degradable hydrocarbon polymers HUDGIN D. (US); PRINCETON POLYMER LAB
ZAWADZKI T.(US) (US)
1985 US4519161 Agricultural process using GILEAD D. (IL); GILEAD D. (IL); SCOTT G.
controllably degradable polymer SCOTT G. (GB) (GB)
composition film
1986 EP0181473 Components for cartridge for hunting, FIOCCHI G. FIOCCHI MUNIZIONI SPA (IT)
shooting purposes and the like of
photodegradable synthetic plastic
material.
1987 US4709808 Degradable polymer composition and BALDUFF D. C. OWENS ILLINOIS PLASTIC
articles prepared from same (US); JABARIN S. PROD (US)
A (US)
411
1987 EP0216412 Photodegradant compositions and COORAY B. B. AKZO NV (NL)
photdegradable polymer compositions
made therefrom.
1989 JP1014243 Photodegradable film or type YAMAGUCHI M. DENKI KAGAKU KOGYO KK;
1991 US4983651 Degradable plastics GRIFFIN G. J.L. EPRON IND LTD (GB)
(GB)
1992 GB2247681 A Photo-degradable plastics material HANCOCK M. ECC INT LTD (GB)
1994 GB2272902 Photodegradable polyolefin YOUN S. J. JEONG DAELIM IND CO LTD (KR)
composition H. G., KANG T. G.,
SONG B. K.
1994 US5281681 Photodegradable and biodegradable AUSTIN R. (US) EXXON CHEMICAL PATENTS
polyethylene INC (US)
1994 US5334700 Photodegradable and biodegradable AUSTIN R. (US) EXXON CHEMICAL PATENTS
polyethylene INC (US)
2000 CN1240803 Degradable and combustible QIAN Q., CHEN UNIV F. (CN)
polyethylene plastics Q., LI N.
2000 CN1242390 PE raw material with photo LIU X. (CN); LIU JINYING IND CO LTD JILIN
degradable and biodegradable C. (CN) (CN)
properties
1977 US4021388 Synthetic resin sheet material GRIFFIN G. J.L. COLOROLL LTD
412
1980 US4207221 Degradable plastic composition TAYLOR L. J. (US); OWENS ILLINOIS INC (US)
containing unsaturated wax TOBIAS J. W. (US)
1980 JP55085496 Manufacture of decomposable plant NAKAMURA M., NAKAMURA M., YOSHINO T.,
cultural pot made of structural YOSHINO T., KATSURAI T.
ingredient of organic fertilizer OGAWA I.,
KATSURAI T.
1982 US4337181 Biodegradable starch-based blown OTEY F.; US AGRICULTURE
films WESTHOFF R.
1991 EP0430641 Disposable diaper having fastening SIPINEN ALLAN MINNESOTA MINNING &
means that are degradable JCO MINNESOTA MFG (US)
M (US)
1992 US5091262 Starch filled coextruded degradable KNOTT J. E., REXENE PROD CO (US)
polyethylene film GAGE P.D
1998 US5811161 Package of paper or paperboard having NICKEL J. L., KORSNAES AB (SE)
a thin extruded polyethylene coating JOEVES H.,
NORDIN R.,
NORDIN B.
2000 CN1242390 Polyethylene raw material with photo LIU X., LIU C. JINYING IND CO LTD JILIN
degradable and biodegradable (CN)
properties
2000 CN1242390 PE raw material with photo LIU X. (CN); LIU C. JINYING IND CO LTD JILIN
degradable and biodegradable (CN) (CN)
properties
413
6.3 Patents on Packaging, Hygine and Non-pharmaceutical Applications
414
1994 94-338742 Biodegradable multifilament used for fishery material--- Zeneca KK
composed of multifilament comprising poly(beta-
hydroxyalkanoate), having good heat resistance
1995 95-067312 Bonding articles together using poly(hydroxyalkanoate)s---which Kemmish, D.J.
are biodegradable, useful in packaging, carton sealing, sanitary Zeneca Ltd; Monsanto Co.
towels, disposable nappies, hospital equipment, etc.
1995 95-092171 Laminate manufactured by vacuum deposition of functional Utz, H
layer between two films---using non-metallic transparent material Fraunhofer Ges Foerderung
acting as a barrier and bonding layer, eliminating need for Angewandten
laminating adhesive and allowing recycling
1995 95-117776 Toilet material for pets, giving good biodegrdability---including Suzuki Sogyo KK
deodorant and/or antibacterial agent, biodegradable resin and
optional aromatic materials
1995 95-215202 Manufacturing biodegradable cellulose and/or cellulose acetate Kemmish, J.D., Montador, J.H. &
film having good water barrier properties---comprises applying Kemmist, D.J.
acquieos suspension of at least partly amorphous particles of Zeneca Ltd; Monsanto Co.
poly(hydroxyalkanoate) to cellulose and/or cellulose acetate film
and heating
1995 95-162679 Increasing transparency of moulded articles or sheets of Bueler, F.S., Fanelli, R., Treutlein, R.
thermoplatic starch or starch-polymer blend---by treating & Zechner, T.
granulate, articles or sheets with silicone oil, animal or plant fat EMS Inventa AG
or oils or solution of synthetic or natural polymer
415
1989 89-146427 Microcapsule production containing soluble protein or Sandow, J.K. & Schmeidel, R.
peptide---using mixure of poly(hydroxybutyric acid) and Hoechst AG
poly(lactide-co-glycolide)
1991 91-324928 Biocompatible microspheres for parenteral Spenlehauer, G. Veillard M. &
administration ---containing biodegradable and Verrechia, T.
biocompatible polymer and surfactant, used for treating Rhone Pulenc Rorer SA
inflammation, infections and cancer
1992 92-060919 Auxiliary material for fixing artificial joint or filling bone Terumo Corp.
defects---comprises biodegradable or bio-absorbable
material and leaves structure to allow formation of fresh
bone
1992 92-176586 Controlled release microparticles containing Canal, T., Carli, F., Lovrecich, M.
polysaccharide gelling agent, etc.---comprising & Lourecich, M.L.
biodegradable polymer, interfacial agent, amphiphilic Vectorpharma Int. SpA
polymer and active substance, especially calcitonin, etc.
1992 92-391146 Synthetic bone-tooth filler for artificial limb and Fuse, T., Machino, H., Matuura,
denture material---comprises water- K., Nijima, K., Otani, S. &
insoluble,biodegradable coating applied to substrate Yanagisawa, S.
with porous surface layer Mitsubishi Kasei Corp.; Res. Dev.
Corp. Japan
1993 93-153559 Dispenser, especially for controlled release of sexual Buschmann, E., Kiessling, U.,
pheromone(s)---used in plant protection, comprises Neumann, U. & Renz, G.
pheromone-impermeable container sealed with BASF AG
pheromone-permeable foil
1993 93-164265 Slow release fertiliser---has multiple alternate coatings of a Nippon Steel Chem. Co.;
biodegradable polymer (I) and a water-soluble polymer (II) Nippon Steel Corp.
1994 94-135531 Particles of crystallizable polymer coated with surfactant of Clauss, J., Goerge, N., Horowitz,
phospholipid to maintain amorphous state---for making D.M., Hunter, B.K. & Sanders,
shaped articles e.g. fibres, for controlled release of J.K.M.
pharmaceutical or agrochemical or for removal of solvent, etc. Zeneca Ltd; Monsanto Co.
1994 94-183125 Sustained release microspheres requiring no surgical implant-- Kino, S., Mizuta, H. & Osajima, T.
-contain hydrophobic antipsychotic encapsulated in Yoshimoto Pharm.. Ind. KK
biodegradable polymer, allowing prolonged therapeutic effect
by infrequent administration
1994 94-193872 Preparation of drug-releasing biodegradable compositions Miettinen-Laehde, S.S. & Toermaelae,
used for antibiotics, etc.---by ultrasonically melting P.O.
biodegradable polymer matrix and pharmaceutical substance Oriion-Yhtymae OY
1995 95-041205 Sustained release preparation of water-soluble peptide Kirin Brewery KK
hormone---comprising fine tube with specified diameter made
of waster-insoluble biodegradable, high-Mwt substance,
containing core
1995 95-044929 Biodegradable urethral stent---substantially shorter than the Viherksoski, E.
urethra in which it is totally installed
1995 95-351303 Polymer microspheres useful for drug delivery and targeting, Coombes, A.G., Davis, S.S. &
etc---prepared by mixing solution of water-soluble polymer Schacht, E.
and solution of conjugate of poly(ethylene glycol) and Univ. Ghent
evaporating first solvent
Univ. Nottingham
1995 95-122881 Absorbable polymer composition for surgical and medical Arnold, S.C. Reilly, E.P. &
devices, e.g. sutures---comprises absorbable poly(ester Scopelianos, A.G.
anhydride), polylactone or poly(iminocarbonate) and Ethicon Inc.; Johnson & Johnson
polysuccinimide as bio-absorbable reinforcing filler)
416
1996 96-040269 Degradable multilayer melt-blown microfibre webs used for Joseph, E.G. & Rutherford, D.R.
surgical dressings, etc.---comrpise layers of polyolefin, PCL Minnesota Mining & MFG Co.
and degradable resins
1996 96-201507 Long-term fertiliser rods---consist of a shell made of segments Pluder, K.
of polymer material which biodegrade at different rates and Buna GMBH
are filled with plant nutrients
1996 96-267854 Surgical device, e.g. stample or ligating clip----comprising Arnold, S.C., Reilly, E.P. &
polysuccinimide to increase stiffness of polymer and device Scopelianos, A.G.
can withstand heavy loads. Ethicon Inc.
1996 96-350294 Biodegradable resin composites used as containers for medical Mitsubishi Gas Chem. Co. Ltd
products---comprise poly(3-hydroxybutyric acid) and
poly(caprolactone) with specified capillary size
1997 97-044600 Expandable intra-luminal stent----made from sheet materials Willams, M.S.
curled into cylinder having over lapping edges, and Advanced Cardiovascular Systems
incorporating external protrusions which engage apertures to
hold the stent in the expanded condition
1997 97-459058 Membrane for tissue or bone regeneration---contains at least Hutmacher, D. & Kirsch, A.
three layers and is flexible and biocompatible Kirsch, A.
417
1994 94-199818 New fibre-producing plants expressing heterologous Maliyakal, J. & John, M.
bioplastic, especially poly(hydroxyalkanoate)---contain Monsanto Co.
enzymes involved in bioplastic synthesis under control of
fibre-specific cotton promoter
1994 94-265917 Poly(3-hydroxybutyric acid) production by ring-opening Hori, Y. Nishishita, T. & Yamaguchi,
polymerization---if beta-butyrolactone in presence of tin A.
compound catalyst Tagasago Int. Corp.;
Takasago Perfumery Co. Ltd
1994 94-545260 Polyester compostion Hammond, T., Liggat, J.J., Montador,
J.H. & Webb, A. Zeneca Ltd
1995 95-012035 Biodegradable resin composition preparation for films or Sumitomo Seika Chem. Co. Ltd
sheets---by blending biodegradable plastic with water-soluble
thermoplastic resin.
1995 95-075207 New block copolymers with hydrophilic and hydrophobic Domb, A.J., Gref, R., Langer, R.,
blocks----covalently bonded to multifunctional compound, Minamitake, Y. & Peracchia, M.T.
used to make particles for controlled and optimal targeted Massachusetts Inst. Technology
delivery of therapeutic or diagnostic agens
1995 95-162982 Genetically modified micro-organism producing Buttcher, V., Kossman, J. & Wesh, T.
poly(hydroxyalkanoate)---includes foreign gene for hexosyl Inst. Genbiologische Forschung
transferase to allow use of in expensive sugar substrates, also
producing specific polysaccharide Hoechst-Schering
1995 95-311553 Production of biodegradable, e.g. poly(hydroxy butyrate), Lampe, R.A., Noda, I. & Satkowski,
fibrils for non-wovens---by contacting melted or solvated M.M.
liquid resing mixture with gas low Procter and Gamble Co.
1995 95-367684 Degradation of waste polymers, especially poly(hydroxy fatty Batz, H., Jendrossek, D., Sluka, P. &
acid)s---by incubating in aqueous medium in presence of Steinbuechel, A.
micro-organisms; especially isloate SK37, and/or heating in Boehringer Mannheim GMBH
aqueous alkaline medium
1996 96-160943 Poly(hydroxy acid) production using recombinant bacteria; Liebergesell, M., Pries, A.,
especially Pseudomonas or Alcaligenes spp, containing Thiocapsa Steinbuchel, A. & Valentin, H.
poly(hydroxy acid) synthesase gene) Monsanto Co.
1996 96-486372 Thermoplastic biodegradable ether ester direct production Engelhardt, J., Koch, W., Kramer, H.,
from cellulose----uses quaternary ammonium base in Meister, F. & Michels, C.
etherification with oxiran before esterification with Wolff Walsrode AG
monocarboxylic acid, useful for moulding, film or fibre
1997 97-120248 Thermoplstic biodegradable poly(saccharide ester ester) for Engelhardt, J., Fink, H., Kalbe, J.,
fibres---prepared by esterification of the polysaccharide with Koch, R., Koch, W., Mueller, H.P.,
anhydride and reaction of free carboxyl groups with an Szablikowski, L., Weber, G., Weigel,
epoxide, for heat-sable products P. & Mueller, H.
Wolff Walsrode AG
1997 97-226171 Surface-modified cellulose micro-fibrils for filler in Cavaille, J.Y.N., Chanzy, H.D.,
composite---have hydroxyl functions on surface esterified by Fleury, E. & Sassi, J.F.
at least one organic ompound, containing at least one function Rhone Pulenc Rhodia AG
capable of reacting with hydroxyl groups
418
6.6 Blending, Composition and Plasticizer Patents
Year Ref. Title Author(s)/organization(s)
1991 91-001725 Destructurized starch and hydrophobic, thermo-plastic Lentz, D.J., Sachetto, J. & Silbiger, J.
polymer blends---have improved dimensional stability, Warner Lambert Co.
humidity resistance and toughness, are biodegradable and
used in capsules, foams, films, etc.
1992 92-024382 Hydroxyalkanoate polymer composition---contains Barham, P.J., Organ, S.J. & Webb, A.
ammonium chloride as nucleating agent, avoiding problems Zeneca Ltd; Monsanto Co.
with opacity and improving biodegradability
1992 92-064909 Biodegradable plastic composition---containing Carlson, A., Galvin, T.J. & Webb, A.
microbiologically produced copolymer of 3-hydroxybutyrate Zeneca Ltd; Monsanto Co.
and 3-hydroxyvalerate
1993 93-093341 Biodegradable blend of microbiologically produced Doi, Y. & Kumagai, Y.
poly(hydroxybutyric acid)---with chemically synthesized Sumitomo Metal Ind. Ltd
random compolymer of hydroxybutyric acid optical isomers,
for production of flexible film, sheet, etc.
1993 93-200640 Biodegradable polymer composition---contains PVA and Denki Kagaku Kogyo KK
poly(3-hydroxybutyric acid)
1993 93-288377 Compatible for polymer blends---comprises A-B block Ballard, D.G.H. & Buckmann, A.J.P.
copolymer where A is at least 50% alkylene side chains and Zeneca Ltd; Monsanto Co.
B is at least 70% hydroxybutyric acid residue side chains
1994 94-083141 Plasticizer for biodegradable, highly crystalline polyester(s)--- Montador, J.H. & Webb. A.
comprising an esterified hydroxy carboxylic acid with Zeneca Ltd; Monsanto Co.
multiple ester groups in the molecule
1994 94-183458 Polymer composition---containing an oligomer of a polymer Bal, J.S. & Hammond, T.
selected from poly(hydroxyalkanoate), polylactide, Zeneca Ltd; Monsanto Co.
poly(caprolactone) and copolymers
1994 121:135566 Polyesters, e.g. PLA or 3-hydroxybutyric acid/3-valeric acid Montador, J.H. & Webb, A.
copolymer, are plasticized with an ester such as Ac tri-Bu Zeneca Ltd; Monsanto Co.
citrate
1995 95-022746 Polyester composition with improved impact strength and Hammond, T., Liggatt, J.J., Montador,
elongation---comprises a biodegradable polyester and a J.H. & Webb, A.
specific plasticizer Zeneca Ltd; Monsanto Co.
1995 95-022752 Polyester composition comprising two Liggatt, J.J.
poly(hydroxyalkanoate) compounds---including one in (semi) Zeneca Ltd; Monsanto Co.
crystalline form, as a nucleant, for paper, fabric, hygiene
articles, sustained drug or agrochemical release system,
adhesive, etc.
1995 95-024214 Resin composition used to produce porous biodegradable Hisanaka, T. Kuwaki, T., Matsumura,
film---comprising resin mixture of copolymer of D- H., Muta, Y., Ochi, Y. & Shimada, T.
hydroxybuthyrate and D-hydroxy valerate, poly(epsilon- Zeneca Ltd
caprolactone) and inorganic filer
1995 95-027727 Starch composition for biodegradable sheet--includes Tsutsunaka Plastic Ind. Co. Ltd
biodegradable aliphatic polyester, low-Mwt aliphatic
polyester and reinforcing additives
1995 95-076327 Biodegradable thermoplastic mixture of starch ester and Kakushike, R., Rapthel, I., Reichwald,
poly(alkylene glycol)---using low-Mwt polyether(s) and K., Hermann, C. & Runge, J.
polyester(s) derived from amylopectin starch Buna GMBH
1996 96-343504 Biodegradable composition used as plasticizing or Hagiwara, T., Hongo, H., Hori, Y.,
compatibilizing compound----containing poly(3- Takahashi, Y. & Yamaguchi, A.
hydroxybutyric acid) or copolymer and block copolymer Takasago Int. Corp.; Takasago
having a stereospecifically regular structure Perfumery Co. Ltd
1997 97-414566 Biodegradable emulsion binder for non-woven fibre stock--- Iovine, C.P. & Walton, J.H.
97-70811 containing poly(hydroxybutyrate/ hydroxyvalerate) Nat. Starch & Chem. Investment
copolymer, imparts good mechanical properties and is
readily biodegradable Holding Corp.
419
6.7 Patents on Polyhydroxyalkanoates in Chronological Order
US3036959, 29.05.62, James Noel Baptist, Process for preparating poly-ß-hydroxybutyric acid
US3044942, 17.07.62, James Noel Baptist, W.R.Grace & Co, Process for preparating poly-ß-
hydroxybutyric acid
US3107172, 15.10.63, James Noel Baptist, Molded product containig poly-ß-hydroxybutyric acid and
method of making
US3121669, 18.02.64, James Noel Baptist, Process for preparating poly-ß-hydroxybutyric acid
US3182036, 04.05.65, James Noel Baptist, Plastized poly-beta-hydroxybutyric acid and process
US3553081, 05.01.71, Charles T. Goodbue and James R. Schaeffer, Eastman Kodak Company, Process of
microbiological oxidation
US4101533, 18.07.78, Lafferty Robert(AT); Heinzle Elmar, Agroferm AG, Cyclic carbonic acid esters as
solvents for poly-[{β-hydroxybutyric acid
GB2089823, 30.06.82, ICI PLC (GB), Extraction of poly( beta- hydroxybutyric acid)
US4324907, 13.04.82, Senior Peter James; Wright Leonard F; Alderson Barry, ICI PLC (GB), Extraction
process
US4358583, 09.11.82, Walker John; Whitton Jonathan R, ICI PLC (GB), Extraction of poly( beta -hydroxy
butyric acid)
US4433053, 21.02.84, Hughes Lorenzo (GB); Richardson Kenneth R (GB), ICI PLC (GB), Fermentation
process for the production of poly(beta- hydroxy-butyric acid)
US4786598, 22.11.88, Lafferty Robert(AT); Braunegg Gerhart (AT), Danubia Petrochem Polymere (AT),
Process for the biotechnological preparation of poly-D-(-)3-hydroxybutyric acid
EP0015123, 03.09.80, Holmes Paul Arthur; Wright Leopold Frederick; Alderson Barry; Senoir Peter
James, ICI PLC (GB), A process for the extraction of poly-3-hydroxy-butyric acid from microbial cells
EP0015669, 17.09.80, Powel Keith Adrian; Collonson Barbara Ann; Richardson Kenneth Raymond, ICI
PLC (GB), Microbial process for the production of poly(beta-hydroxybutyric acid) and micro-organisms
for use therein.
EP0024810, 11.03.81, Barham Peter John; Selwood Alan, ICI PLC (GB), Production of sharped articles by
removal of solvents from gel of high molecular weight crystalline polymers
EP0046017, 17.02.82, Walker John; Whitton Jonathan Richard; Alderson Barry, ICI PLC(GB), Extraction
of poly(beta-hydroxybutyric acid)
EP0046335, 24.02.82, Holmes Paul Arthur; Jones Eric, ICI PLC(GB), Extraction of poly(beta-
hydroxybutyric acid)
EP0052459, 26.10.82, Holmes Paul Arthur; Wright Leopold Frederick;Collins Stephan Hugh, ICI
PLC(GB), Beta-hydroxybutyrate polymers
420
EP0052460, 26.05.82, Holmes Paul Arthur; Wright Leopold Frederick;Collins Stephan Hugh, ICI PLC
(GB), Polymer blends
US4324907, 13.04.82, Senior Peter James; Wright Leonard F; Alderson Barry, ICI PLC (GB), Extraction
process
EP0052946, 02.06.82, Herman Terence John; Holmes Paul Arthur, ICI PLC (GB), Stabilised polyester
compositions
US4358583, 09.11.82, Walker John; Whitton Jonathan R, ICI PLC (GB), Extraction of poly( beta -hydroxy
butyric acid)
EP0069497, 12.01.83, Holmes Paul Arthur; Wright Leopold Frederick;Collins Stephan Hugh, ICI
PLC(GB), Copolyesters and process for their production
US4393167, 12.07.83, Holmes Paul A (GB); LIM Guan B (GB), ICI PLC (GB), Polymer blends containing
polymer of beta-hydroxybutiric acid and chlorine or nitrile group containig polymer
US4433053, 21.02.84, Hughes Lorenzo (GB); Richardson Kenneth R (GB), ICI PLC (GB), Fermentation
process for the production of poly(beta- hydroxy-butyric acid)
EP0114086, 25.07.84, Richardson Kenneth Raymond, ICI PLC (GB), Production of beta-hydroxybutyrate
polymers
EP0204442, 10.12.86, Senior Peter James; Collins Stephn HUGH; Richardson Kenneth Raymond, ICI
PLC(GB), Copolymer production
EP0274151, 13.07.88, Witholt Bernard;Lageveen Roland, Univ Groningen (NL), A process for producing
polyesters by fermentation.
EP0288908, 02.11.88, Doi Yoshiharu, Mitsubishi Gas Chemical Co (Jp), Process for production of a
random vopolymer comprising D-(-)-3-hydroxybutirate units and D-(-)-3-hydroxyvalerate
US4786598, 22.11.88, Lafferty Robert(AT); Braunegg Gerhart (AT), Danubia Petrochem Polymere (AT),
Process for the biotechnological preparation of poly-D-(-)3-hydroxybutiric acid
EP0304293, 22.02.89, Doi Yoshiharu, Mitsubishi Chrm. Ind (JP), Copolyester and process for production
the same
WO8900202, 12.01.89, Peoples Oliver P (US) , Massachusetts Inst Technology (US), Method for
producing novel polyester biopolymers
EP0315875, 17.05.89, Schmiedel Rainer Dr; Sandow Jurgen Kurt DR, Hoechst AG (DE), Process for
prepring biodegradable microcapsules containing peptides and proteins soluble in water and microcapsules
obtained by said process
US4910145, 20.03.90., Holmes Paul A (GB); LIM Guan B (GB), ICI PLC (GB), Separation process
US4957861, 18.09.90, Lafferty Robert(AT); Braunegg Gerhart (AT), Danubia Petrochem Polymere (AT),
Process for the biotechnological preparation of poly-D-(-)3-hydroxybutiric acid
EP0396289, 07.11.90, Anderson Alistar James (GB); Byrom David (GB); Dawes Edwin Alfred (GB);
Haywood Geoffrey William (GB), ICI PLC(GB), Copolymer production
EP0400855, 05.12.90, Herring John Michael (GB); Webb Andrew (GB), ICI PLC(GB), 3-hydroxybutyrate
polymer composition
421
DE4013293, 07.11.91, Wiethaup Wolfgang ipl Phys Dr; Moeller Knut; Hauser Bernard , Bat cigarettenfab
gmbh (DE), Cigarette filter contg. Irregularly oriented fibres-comprises spun poly-hydroxybutyric acid or
copolymer of hydroxybutyric acid
EP0454075, 30.10.91, Wiethaup Wolfgang ipl Phys Dr; Moeller Knut; Hauser Bernard , Bat cigarettenfab
gmbh (DE), Process for manufacturing cigarette filters
WO9100917, 24.01.91, Peoples Oliver P (US); Sinskey Anthony j (US), Massachusetts Inst Technology
(US), Method for producing novel polyester biopolymers
US5110980, 05.05.92, Ramsay Bruce A (CA); Ramsay Juliana (CA); Berger Eric (FR); Chavarie Claude
(CA); Braunegg Gerhart (AT), Ecole Polytechn (CA), Separation of poly-hydroxyalkanoic acid from
microbial biomass
JP4131196, 01.05.92, Saito Yuji, Taisei Corp (JP), Increase of share of PHb producing microorganisms in
active sludge
JP4156998, 29.05.92, Saito Yuji, Taisei Corp (JP), Method for monitoring PHB storage change of activated
sludge
DE4036067, 14.05.92, Blauhut Wilfred Dipl Ing (AT) Gierlinger Wolfgang (AT); Strempfl Friedrich Dipl
Ing DR (AT), Isolation of poly-hydroxy-alkanoate from fermentation broth - by conc., solvent extn. and
spraying into hot water
DE4040158, 17.06.92, Haeubl Georg Dr (AT); Scheuchenstuhl Willibald (AT); Estermann Robert (AT);
Hrabak Otto DR; Kroath Hans, Danubia Petrochem Deutschland, Coated flat articles useful in
pharmaceutical and foodstuff industries - obtd. by coating carrier sheet with aq. dispersion of poly hydroxy
alkanoate
DE4102170, 06.08.92, Kleinke Andreas Dipl Chem; Reichert Karl-Heinz prof Dr (DE) Bradel Roman
Dipl.Chem (DE), Danubia Petrochem Deutschland, Poly-hydroxy-alkanoate contg. Mixt. For heat stable
polymer prepn. Additionally comprises cpd. With reactive gps. Forming ester bonds wit
DE4212801, 19.11.92, Otanio Sugio(JP); Mitsubishi Chem. Ind (JP), Synthetic bone-tooth filler for
artificial limb and denture material-comprises water insoluble, biodegradable coating applied to substrate
WO9204410, 19.03.92, Bellis Harold Edward (US); Lin Kang (US), Du Pont (US), Films containing
polyhydroxy acids and a compatibilizer
WO9218553, 29.10.92, Lee Yang Gul (KR); Yim Guhn Been (KR), Kohap LTD (KR), Poly-beta-hydroxy
alkanoate (PHA) copolymer, method of its production, the microbe which produces it, and PHA copolymer
blend
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6.8 Other Relevant Patents
Title Patent Organization/Author Year Material Application
Soybean protein-based thermoplastic composites for moulded articles US5523293 Iowa State University 1996 soybean protein, packaging
Research Foundation Inc. vegetal protein
Biodegradable compostable plastic and method of making the same US5505830 Planet Polymer Technologies 1996 Cellulose acetate packaging
Inc.
Expanded starch-based products and method of preparation of thereof EP-712883 National Starch & Chemical 1996 starch packaging
Investment Holding Corp.
Incorporated Melt-stable lactide polymer composition and process for manufacture thereof US5981694 Cargill 1999 poly(L-lactide) packaging
Polylactic acid-based implant susceptible of bioresorption containing and antibiotic US05567431 CNRS 1996 poly(L-lactide) implant
Aliphatic polyester polymer blends based on polylactic acid, methods for manufacturing the same, EP-753539 Mitsubishi Gas Chemical Co. 1997 poly(L-lactide) moulding
and methods for moulding the same Inc., Shimadzu Corp. article
Plasticized polyhydroxyalkanoate compositions and methods for their use in the production of US06127512 Monsanto 2000 PHA packaging
shaped polymeric articles
L,D-polylactide copolymers with controlled morphology US5346966 DuPont 1994 poly(DL-lactide)
copolymer
Composition for sustained release of non-aggregated erythropoietin US5716644 Alkermes, Inc., 1998 poly(glycolide-co- drug delivery
lactide) system
Catalyst-free resorbable homopolymers and copolymers US4960866 Boehringer Ingelheim 1990 polyglycolide, medical
Zentrale polylactide, poly
(glycolide-co-lactide)
Blended polycaprolactone thermoplastic molding composition US05753781 Minnesota Mining and 1998 polycaprolacton packaging
Manufacturing Company
Biodegradable (3-Hydroxyalkanoate) compositions and blends US5625029 Eastman Chemical Company 1997 poly(3- packaging
hydroxybutyrate-co-
3-hydroxyvalerate)
Mixture of predominantly one polyhydroxyalkanoate and a compound which contains at least two US5231148 PCD Polymere G.m.b.H. 1993 PHAs packaging
reactive groups, such as acid and/or alcohol groups, and a polymer prepared by melting the mixture
Biodegradable copolymers USRE036548 The Procter & Gamble 2000 PHAs hygiene
Company products
Molding process for polydioxanone polymers US04490326 Ethicon, Inc. 1984 poly(p-dioxanone)
Surgical suture material and method of making and using same US05695879 B. Braun Surgical GmbH 1997 poly(glycolide-co- medical
trimethylene
carbonate)
Malic acid polymers US04320753 Research Corp. 1982 poly(b-malic acid) medical
Biodegradable polymers, the production thereof and use thereof for producing biodegradable US6114042 BASF Aktiengesellschaft 2000 Ecoflex packaging
moldings
Biodegradable foamable co-polyester compositions US06020393 Eastman Chemical Company 2000 Eastar Bio packaging
435
Degradable polyesters, a mixed culture of microorganisms for degrading these polyesters, and US6121033 University of Nebraska 2000 polyester based on packaging
methods for making these substances glutamic acid
Biodegradable poly (amino acid)s, derivatized amino acid polymers and methods for making same US5929198 Nalco Chemical Company 1999 poly(aspartic acid), preventing
poly(glutamic acid) scale
formation
High molecular weight polyanhydride and preparation there of US04757128 Massachusetts Institute of 1988 polyanhydride, drug delivery
Technology polyorthoester system
Bioerodible polymers for drug delivery in bone US5286763 Massachusetts Institute of 1994 polyanhydride, medical
Technology polyorthoester
Mehtod of producing plasticised polyvinyl alcohol and its use for the preparation of starch-based, US5462981 Novamont SpA 1995 polyvinylalcohol, packaging
biodegradable thermoplastic composition starch
Process for manufacturing solid compositions containing polyethylene oxide and an active US6048547 Seth P., Stamm A. 2000 poly(ethyleneoxide), pharmaceuti
ingredient poly(ethyleneglycol), cal
Acidic amino acid resin EP683177 Mitsubishi Chemical Corp. 1995 protein, lysine and packaging
poly(asparaginic
acid)
Fibers comprising water soluble polyamides and articles constructed therefrom US5869596 Fuller Licensing & Financing, 1999 polyamide diapers
Inc.
Biodegradable, anionic polymers derived from the amino acid L-tyrosine US6120491 The State University Rutgers 2000 polypeptides, L- medical
tyrosine
Decomposable packing material US5512339 Bayer AG 1996 BAK, copolyester packaging
amide
Bioabsorbable triglycolic acid poly(ester-amide)s US6120788 BioAmide Inc. 2000 polyester amide packaging,
medical
Biodegradable mixtures of polyphoshazene and other polymers US6077916 University Park 2000 polyphosphazene drug delivery
system
Polyurethane molding compound and biodegradable filaments manufactured from such molding US5496909 Firma Carl Freudenberg 1996 polyurethane packaging
compound
Lignin-containing polyols and their manufacture and use in the production of polyurethanes DE19545550 BASF AG 1997 polyurethane packaging
436
6.9 Patents in Medical and Pharmaceutical Applications
437
6.9 Patents in medical and pharmaceutical applications.xls - page 439
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9847496 : A2 : 19981029
WO 9847496 : A3 : 19990211
Diamido-diamine polymer-platinum compounds for tumor treatment, and AU 9871245 : A1 : 19981113
preparation thereof US 5985916 : A : 19991116 Access Pharmaceuticals, Inc., USA DD
WO 9900149 : A1 : 19990107
US 6045777 : A : 20000404
Method for enhancing the echogenicity and decreasing the attenuation of AU 9882731 : A1 : 19990119
microencapsulated gases EP 996470 : A1 : 20000503 Acusphere, Inc., USA EM microcapsules
WO 9804292 : A2 : 19980205
WO 9804292 : A3 : 19980514
US 5837221 : A : 19981117
CA 2260938 : AA : 19980205
AU 9733672 : A1 : 19980220
AU 720727 : B2 : 20000608
JP 11505272 : T2 : 19990518
JP 2987212 : B2 : 19991206
BR 9711109 : A : 19990817
CN 1226836 : A : 19990825
EP 957942 : A2 : 19991124 EM microcapsule
Polymer-lipid microencapsulated gases for use as imaging agents NO 9900402 : A : 19990322 Acusphere, Inc., USA (imaging)
WO 9966903 : A2 : 19991229
WO 9966903 : A3 : 20000203
Large porous particles emitted from an inhaler AU 9947068 : A1 : 20000110 Advanced Inhalation Research, Inc., USA DD microcapsule
Diketene acetal-polyol polymers with controlled physical state and
bioerodibility US 5968543 : A : 19991019 Advanced Polymer Systems, Inc., USA EM
US 5939453 : A : 19990817
PEG-poly(ortho ester), PEG-poly(ortho ester)-PEG, and poly(ortho ester)- WO 9962983 : A1 : 19991209
PEG-poly(ortho ester) block copolymers AU 9942204 : A1 : 19991220 Advanced Polymer Systems, Inc., USA EM
WO 9725366 : A1 : 19970717
CA 2242631 : AA : 19970717
AU 9715270 : A1 : 19970801
EP 869986 : A1 : 19981014
BR 9706960 : A : 19991228
Polymers with controlled physical state and bioerodibility JP 2000512322 : T2 : 20000919 Advanced Polymers Systems, Inc., USA EM
EP 911355 : A2 : 19990428
EP 911355 : A3 : 20000301
Resorbable polyesters with reduced hydrolysis time DE 19746403 : A1 : 19990429 Aesculap A.-G. + Co. K.-G., Germany EM
JP 11268116 : A2 : 19991005
JP 2990278 : B2 : 19991213
JP 11320674 : A2 : 19991124
Stretching of aliphatic polyester sheets JP 2990277 : B2 : 19991213 Agency of Industrial Sciences and Technology, Japan EM
WO 9741837 : A2 : 19971113
WO 9741837 : A3 : 19980226
CA 2251987 : AA : 19971113
AU 9728972 : A1 : 19971126
EP 904063 : A2 : 19990331
BR 9709217 : A : 19990810
CN 1226821 : A : 19990825
JP 2000503663 : T2 : 20000328 Alkermes Controlled Therapeutics Inc., USA
Manufacture of microparticles for the controlled-release dosage forms NO 9804808 : A : 19990106 Janssen Pharmaceutica N.V. DD microcapsule EM
US 5792477 : A : 19980811
Preparation of extended shelf-life biodegradable, biocompatible US 5916598 : A : 19990629 Alkermes Controlled Therapeutics, Inc. II, USA
microparticles containing a biologically active agent US 6110503 : A : 20000829 Janssen Pharmaceutica DD microcapsule
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
US 5656297 : A : 19970812
AT 154240 : E : 19970615
US 5413797 : A : 19950509
WO 9529664 : A1 : 19951109
CA 2189254 : AA : 19951109
AU 9524674 : A1 : 19951129
AU 688506 : B2 : 19980312
EP 758227 : A1 : 19970219
JP 10504017 : T2 : 19980414
US 5912015 : A : 19990615
AU 9871878 : A1 : 19980730
Modulated release from biocompatible polymers AU 704647 : B2 : 19990429 Alkermes Controlled Therapeutics, Inc., USA DD
WO 9907418 : A2 : 19990218
WO 9907418 : A3 : 19990603
AU 9887777 : A1 : 19990301
EP 1003569 : A2 : 20000531
Sterile bioerodible implant device containing a retinoid with improved US 6074661 : A : 20000613
biocompatibility US 6110485 : A : 20000829 Allergan Sales, Inc., USA EM
WO 9814168 : A2 : 19980409
US 6034101 : A : 20000307
AU 9748014 : A1 : 19980424
EP 932388 : A2 : 19990804
Dosage form and method for administering drug CN 1231603 : A : 19991013 Alza Corp., USA DD
WO 9736553 : A1 : 19971009
CA 2250760 : AA : 19971009
AU 9726004 : A1 : 19971022
EP 907338 : A1 : 19990414 American Cyanamid Co., USA
BR 9710651 : A : 19990817 Lichkus, Andrew M.
Crystalline copolymers their preparation and their use JP 2000508017 : T2 : 20000627 Kramer, Hildegard I. EM
Biodegradable pH/thermosensitive hydrogels for sustained delivery of
biologically active agents WO 2000038651 : A1 : 20000706 Amgen Inc., USA EM
Thermosensitive biodegradable hydrogels for sustained delivery of WO 2000000222 : A1 : 20000106
biologically active agents AU 9949599 : A1 : 20000117 Amgen Inc., USA DD
WO 9846212 : A1 : 19981022
US 6020004 : A : 20000201
Biodegradable microparticles for for the sustained delivery of therapeutic AU 9871348 : A1 : 19981111
drugs EP 975334 : A1 : 20000202 Amgen Inc., USA DD
WO 9953943 : A2 : 19991028
Therapeutic angiogenic factors, such as a pleitrophin or midkine protein, WO 9953943 : A3 : 20000120
formulations and methods for their use AU 9934955 : A1 : 19991108 Angiogenix, Incorporated, USA TE
WO 9921908 : A1 : 19990506 Angiotech Pharmaceuticals, Inc., Can.
Polymeric systems for drug delivery and uses thereof AU 9896176 : A1 : 19990517 University of British Columbia DD EM
US 5788978 : A : 19980804
Injectable pulsatile ivermectin composition BR 9706094 : A : 19990427 Argent. DD microcapsule
Asahi Optical Co., Ltd., Japan
Bone prosthetic sheets and their manufacture JP 2000126280 : A2 : 20000509 Gunze, Ltd. EM
WO 9729145 : A1 : 19970814
AU 9716011 : A1 : 19970828 Asta Medica A.-G., Germany
Copolymers with polyester-polycarbonate blocks containing EP 879258 : A1 : 19981125 Ferruti, Paolo
poly(caprolactone) segments, and use thereof for the preparation of JP 2000505831 : T2 : 20000516 Penco, Maurizio
biodegradable matrixes US 5916998 : A : 19990629 Ranucci, Elisabetta EM
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WO 9746265 : A1 : 19971211
AU 9731128 : A1 : 19980105
AU 719419 : B2 : 20000511
EP 906126 : A1 : 19990407
BR 9709639 : A : 19990810
CN 1226178 : A : 19990818
JP 2000511446 : T2 : 20000905
ZA 9704846 : A : 19981202 Astra Aktiebolag, Swed.
NO 9805628 : A : 19990203 Bowald, Staffan
Wound dressing comprising bioresorbable polymers SE 9804184 : A : 19990202 Dvarsater, Gudmund EM
Controlled release liquid delivery compositions with low initial drug burst WO 2000024374 : A1 : 20000504 Atrix Laboratories, Inc., USA DD
EP 950403 : A2 : 19991020
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Emulsions for in-situ delivery systems JP 11343228 : A2 : 19991214 Atrix Laboratories, Inc., USA DD
Polymer formulation for prevention of surgical adhesions US 5962006 : A : 19991005 Atrix Laboratories, Inc., USA EM
Biodegradable polymer encapsulated serotonin receptor antagonist and
method for preparing the same WO 2000035423 : A1 : 20000622 Aventis Pharmaceuticals Inc., USA DD
Ben-Gurion University of the Negev, Israel
Composition and method for forming biodegradable implants in situ and Eliaz, Rom
uses of these implants WO 9742987 : A1 : 19971120 Kost, Joseph EM
WO 9920253 : A1 : 19990429
SE 9703874 : A : 19990424
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AU 9894670 : A1 : 19990510
EP 1033973 : A1 : 20000913
ZA 9809199 : A : 19990415
Encapsulation method using biodegradable polymers NO 2000002039 : A : 20000613 Bioglan Therapeutics AB, Swed. DD microcapsule
WO 2000004916 : A1 : 20000203
Encapsulation of water soluble peptides AU 9949646 : A1 : 20000214 Biomeasure Incorporated, USA DD microcapsule
Preparation of ionic molecular conjugates of biodegradable polyesters and Biomeasure Incorporated, USA
bioactive peptides WO 2000043435 : A1 : 20000727 Poly-Med DD
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Bioactive and biodegradable composites of polymers and ceramics or AU 9896228 : A1 : 19990322
glasses and method to manufacture such composites EP 1009448 : A2 : 20000621 Bionix Implants Oy, Finland EM
WO 2000048573 : A1 : 20000824
Biodegradable composite material for the production of microcapsules DE 10008880 : A1 : 20000824 Bioserv A.-G., Germany DD microcapsule EM
DE 19614421 : A1 : 19971016
DE 19614421 : C2 : 19991216
Biodegradable bone substitute and implant material and parts manufactured WO 9738741 : A1 : 19971023
therewith AU 9726921 : A1 : 19971107 Biovision Gmbh, Germany TE
Biodegradable polymer material bearing biologically active agents and their
preparation WO 2000050497 : A1 : 20000831 Bioxid Oy, Finland DD
JP 11226110 : A2 : 19990824
Surgical adhesive compositions containing cyanoacrylates and EP 937468 : A2 : 19990825
biodegradable and bioabsorbable polymers US 6103778 : A : 20000815 BMG Co, Ltd., Japan EM
Biodegradable and bioabsorbable bone fixation materials and their JP 11206871 : A2 : 19990803
manufacture EP 933089 : A2 : 19990804 BMG Co, Ltd., Japan EM
WO 9925391 : A2 : 19990527
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Biodegradable polymer scaffold EP 1030697 : A2 : 20000830 Bonetec Corporation, Can. EM
Biodegradable, biopolymeric bioelectret implant for tissue regeneration WO 9918892 : A1 : 19990422 Cambridge Scientific, Inc., USA TE
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WO 9847445 : A1 : 19981029
Bioerodible polymeric semi-interpenetrating network alloys for surgical US 6071982 : A : 20000606
plates and bone cements EP 1003441 : A1 : 20000531 Cambridge Scientific, Inc., USA EM
US 5817328 : A : 19981006
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Material for buffered resorbable internal fixation devices and method for CA 2251472 : AA : 19971009
making it EP 915684 : A1 : 19990519 Cambridge Scientific, Inc., USA EM
WO 9736555 : A1 : 19971009
Material for buffered resorbable internal fixation devices and method for US 5817328 : A : 19981006
making same EP 915684 : A1 : 19990519 Cambridge Scientific, Inc., USA EM
Buffered resorbable internal fixation devices for repair of bone fractures WO 9725936 : A1 : 19970724 Cambridge Scientific, Inc., USA TE
WO 9850018 : A1 : 19981112
Preparation of microsphere drug delivery systems AU 9872019 : A1 : 19981127 Can. DD microcapsules
Method for preparation of polymer microcapsule of insulin, 5- Fu and Chemical Inst., Chinese Academy of Sciences, Peop. Rep.
streptomycin CN 1229646 : A : 19990929 China DD microcapsule
Chengdu Institute of Organic Chemistry, Chinese Academy of
Preparation of sustained-release microcapsule injections of hormones CN 1126589 : A : 19960717 Sciences, Peop. Rep. China DD microcapsule
Chengdu Institute of Organic Chemistry, Chinese Academy of
Release-controlled hormone microsphere injection and its preparation CN 1127634 : A : 19960731 Sciences, Peop. Rep. China DD microcapsule
US 5700485 : A : 19971223
US 5618563 : A : 19970408
CA 2220180 : AA : 19961107
WO 9634599 : A1 : 19961107
AU 9657207 : A1 : 19961121
AU 705737 : B2 : 19990603
EP 825853 : A1 : 19980304
Prolonged nerve blockade by the combination of local anesthetic and JP 11504634 : T2 : 19990427
glucocorticoid US 5922340 : A : 19990713 Children's Medical Center Corp., USA DD microcapsule
WO 9922781 : A2 : 19990514
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AU 9911259 : A1 : 19990524
Biocompatible biodegradable polymers for use as artificial tissue or organ EP 1032435 : A2 : 20000906 Children's Medical Center Corporation, USA TE
WO 9851290 : A2 : 19981119
WO 9851290 : A3 : 19990211 Children's Medical Center Corporation, USA
Local anesthetic formulations AU 9873890 : A1 : 19981208 Brigham and Women's Hospital, Inc. DD
Microparticles with adsorbent surfaces, methods of making same, and uses WO 2000006123 : A1 : 20000210
thereof AU 9952452 : A1 : 20000221 Chiron Corporation, USA DD microcapsule
WO 9930737 : A1 : 19990624
Polymeric microparticles combined with submicron oil-in-water emulsions for AU 9862538 : A1 : 19990705
vaccines US 6086901 : A : 20000711 Chiron Corporation, USA DD microcapsule
WO 9924061 : A1 : 19990520
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Method for producing IGF-1 sustained-release formulations EP 1028746 : A1 : 20000823 Chiron Corporation, USA DD microcapsule
DE 19932216 : A1 : 20000127
Particles, in particular micro- or nanoparticles, of crosslinked mono- and FR 2780901 : A1 : 20000114
oligosaccharides, their production, and cosmetic, pharmaceutical, or food NL 1012517 : C2 : 20000111
compositions containing them JP 2000038402 : A2 : 20000208 Coletica, Fr. DD microcapsule
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Biodegradable targetable microparticle delivery system JP 2000509428 : T2 : 20000725 Connaught Laboratories Ltd., Can. DD microcapsule
CA 2199890 : AA : 19970926
Stents and stent-grafts having enhanced hoop strength and methods of AU 9716507 : A1 : 19971002
making the same EP 797963 : A3 : 19980114 Corvita Corporation, USA EM coating
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Biodegradable gas-barrier multilayer poly(vinyl alcohol) film useful for EP 1022127 : A2 : 20000726
ostomy/urostomy bags or pouches JP 2000211075 : A2 : 20000802 Cryovac, Inc., USA EM
Laminates of lactic acid polymers containing biodegradation accelerators,
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Biodegradable products, biodegradable materials and their manufacture JP 10298435 : A2 : 19981110 Dainippon Ink and Chemicals, Inc., Japan EM
Sustained-release implants for treatment of dementia, and their manufacture JP 10120553 : A2 : 19980512 Eisai Co., Ltd., Japan DD
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Oral vaccine compositions AU 9954411 : A1 : 20000321 Elan Corporation, PLC, Ire. DD
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Ovulation-triggering drugs comprising LH JP 11503466 : T2 : 19990326 Emperaire, Jean-Claude, Fr. DD
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Hemostatic implant and its production JP 11070128 : A2 : 19990316 Ethicon G.m.b.H. und Co. K.-G., Germany EM
Gas sterilization and degassing of bioabsorbable medical goods JP 2000237289 : A2 : 20000905 Ethicon Inc., Japan EM
EP 841359 : A1 : 19980513
CA 2220351 : AA : 19980506
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Hydrogels of crosslinked absorbable polyoxaesters, their blends, and JP 10158375 : A2 : 19980616
devices BR 9705441 : A : 19990629 Ethicon, Inc., USA EM
US 5700583 : A : 19971223
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Hydrogels of absorbable polyoxaesters containing amines or amido groups US 5844017 : A : 19981201 Ethicon, Inc., USA EM
WO 9901114 : A1 : 19990114
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Prolonged anesthesia in joints and body spaces NO 992373 : A : 20000222 Euro-Celtique, S.A., Luxembourg DD
Positively-charged poly[.alpha.-(.omega.-aminoalkyl)glycolic acid] for the WO 9929758 : A1 : 19990617
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Biodegradable mixed polymeric micelles for gene delivery EP 1037611 : A1 : 20000927 Expression Genetics, Inc., USA DD EM
Polymerizable biodegradable polymers including carbonate or dioxanone US 6083524 : A : 20000704
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Polymer-based compliant tissue sealants US 6051248 : A : 20000418 Focal, Inc., USA EM
Focal, Inc., USA
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CN 1154385 : A : 19970716
Polymer blends containing bio absorbable polyoxaesters for use in the JP 9188806 : A2 : 19970722
medical field BR 9605439 : A : 19980804 Ethicon, Inc., USA EM
WO 9715389 : A1 : 19970501
US 5665428 : A : 19970909
CA 2235602 : AA : 19970501
AU 9674797 : A1 : 19970515
Preparation of peptide containing biodegradable microspheres by melt EP 857081 : A1 : 19980812
process JP 11515016 : T2 : 19991221 Macromed, Inc., USA EM
WO 9715287 : A1 : 19970501
US 5702717 : A : 19971230
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Thermosensitive biodegradable polymers based on poly(ether-ester) block EP 863745 : A1 : 19980916
copolymers JP 11513985 : T2 : 19991130 Macromed, Inc., USA DD EM
US 5626861 : A : 19970506
Polymeric-hydroxyapatite bone composite US 5766618 : A : 19980616 Massachusetts Institute of Technology, USA EM composite
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 771832 : A2 : 19970507
EP 771832 : A3 : 19980121
AU 9670534 : A1 : 19970515
AU 720550 : B2 : 20000601
CA 2189520 : AA : 19970507
Biologically absorbable aliphatic polyether-polyesters and their blends for CN 1154385 : A : 19970716
surgical devices JP 9194579 : A2 : 19970729 Ethicon, Inc., USA EM
WO 9713533 : A1 : 19970417
CA 2234612 : AA : 19970417
EP 880368 : A1 : 19981202
Moldable, hand-shapable biodegradable implant material AU 9672591 : A1 : 19970430 Osteobiologics, Inc., USA EM
WO 9713502 : A2 : 19970417
WO 9713502 : A3 : 19971002
US 5942253 : A : 19990824
AU 9674384 : A1 : 19970430
AU 714074 : B2 : 19991216
EP 859601 : A2 : 19980826
JP 11513667 : T2 : 19991124
US 6120807 : A : 20000919 Immunex Corporation, USA
Prolonged release of GM-CSF AU 9954017 : A1 : 19991223 American Cyanamid Company DD
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Biodegradable polymer matrixes for sustained delivery of local anesthetic US 5700485 : A : 19971223
agents US 5922340 : A : 19990713 Children's Medical Center Corporation, USA DD
WO 9711725 : A1 : 19970403
FI 98136 : B : 19970115
FI 98136 : C : 19970425
CA 2239776 : AA : 19970403
AU 9670870 : A1 : 19970417 Biocon Oy, Finland
Under tissue conditions degradable material and a method for its EP 854734 : A1 : 19980729 Pohjonen, Timo
manufacturing JP 11512626 : T2 : 19991102 Toermaelae, Pertti EM
WO 9711724 : A1 : 19970403
AU 9670869 : A1 : 19970417 Biocon Oy, Finland
Biodegradable implant manufacture of polymer-based material and a EP 861097 : A1 : 19980902 Toermaelae, Pertti
method for manufacturing JP 11511039 : T2 : 19990928 Vaelimaa, Tero EM
3-Phenylthiomethylstyrene derivative-coated polymer stents for endarterial
hypertrophy JP 9056807 : A2 : 19970304 Kanegafuchi Chemical Ind, Japan DD
WO 9710849 : A1 : 19970327
CA 2231886 : AA : 19970327
AU 9670980 : A1 : 19970409 Sam Yang Co., Ltd., S. Korea
AU 699988 : B2 : 19981217 Kim, Sung Chul
EP 854731 : A1 : 19980729 Chang, Eun Ok
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Copolymeric micelle drug compositions for delivery of hydrophobic drugs JP 10512287 : T2 : 19981124 Pai, Chaul Min DD
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JP 9135892 : A2 : 19970527
JP 9234242 : A2 : 19970909
JP 9234243 : A2 : 19970909
JP 11226111 : A2 : 19990824
CA 2205231 : AA : 19970320
AU 9669453 : A1 : 19970401
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EP 795336 : A1 : 19970917
CN 1168105 : A : 19971217 Takiron Co., Ltd., Japan
Osteosynthetic material, composited implant material, and process for NO 9702191 : A : 19970714 Shikinami, Yasuo
preparing the same US 5981619 : A : 19991109 Okuno, Masaki TE
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 761213 : A2 : 19970312
EP 761213 : A3 : 19980401
US 6045830 : A : 20000404
JP 9132524 : A2 : 19970520
CA 2184654 : AA : 19970305
Sustained-release pharmaceutical microcapsules comprising peptides and NO 9603678 : A : 19970305
biodegradable polymers CN 1148956 : A : 19970507 Takeda Chemical Industries, Ltd., Japan DD microcapsule
US 5610241 : A : 19970311
WO 9742249 : A1 : 19971113
Reactive polymer with biodegradable backbone and its preparation EP 898590 : A1 : 19990303 Cornell Research Foundation, Inc., USA EM
Method and means for cartilage repair CA 2178243 : AA : 19961208 Halpern, Alan A., USA TE
Biodegradable polymer needles for embedding sutures JP 9047457 : A2 : 19970218 Koseki Tomoaki, Japan EM
WO 9705185 : A2 : 19970213
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Multiblock biodegradable hydrogels for use as controlled release agents for EP 842209 : A2 : 19980520
drugs delivery and tissue treatment agents JP 11510837 : T2 : 19990921 Focal, Inc., USA DD
Introgene B.V., Neth.
Octoplus B.V.
Universiteit Utrecht
A transfection system using poly(organo)phosphazenes complexes with Hennink, Wilhelmus Everhardus
nucleic acids WO 9707226 : A1 : 19970227 Bout, Abraham DD
Drug delivery systems for macromolecular drugs WO 9704747 : A1 : 19970213 Dunn, James M., USA DD
Bioresorbable polycarbonate random copolymer-based fibers, method of
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Chikyu Kankyo Sangyo Gijutsu K, Japan
Biodegradable, flexible polymer compositions JP 9020857 : A2 : 19970121 Rikagaku Kenkyusho
Lactic acid-based resin compositions with good hydrolysis resistance JP 9012688 : A2 : 19970114 Toyo Boseki, Japan EM
WO 9702810 : A2 : 19970130
WO 9702810 : A3 : 19970220
CA 2223884 : AA : 19970130
AU 9664665 : A1 : 19970210
AU 709031 : B2 : 19990819
GB 2317340 : A1 : 19980325
GB 2317340 : B2 : 19981223 University of Nottingham, UK
EP 837673 : A2 : 19980429 Coombes, Allan Gerald Arthur
JP 11508912 : T2 : 19990803 Davis, Stanley Stewart
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Polymeric lamellar substrate particles for drug delivery US 6001395 : A : 19991214 Wood, John Michael DD
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Biocompatible and biodegradable nanoparticles designed for proteinaceous JP 11504655 : T2 : 19990427
drug absorption and delivery US 5962566 : A : 19991005 University of Liege, Belg. DD microcapsule
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AU 9661705 : A1 : 19961230
Krebs cycle acid polyesters and use thereof EP 830407 : A1 : 19980325 Dynagen, Inc., USA EM
WO 9701331 : A2 : 19970116
WO 9701331 : A3 : 19970227 Takeda Chemical Industries, Ltd., Japan
CA 2224381 : AA : 19970116 Okamoto, Kayoko
AU 9662420 : A1 : 19970130 Yamagata, Yutaka
EP 835101 : A2 : 19980415 Igari, Yasutaka
Method of producing sustained-release preparation JP 10007583 : A2 : 19980113 Misaki, Masafumi DD
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Spray-dried polymeric microparticles containing imaging agents AU 9663780 : A1 : 19961230 Brown University Research Foundation, USA EM imaging
6.9 Patents in medical and pharmaceutical applications.xls - page 456
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
Heat-sealable, multilayer, biodegradable polymer films including poly(lactic Mitsubishi Plastics Ind, Japan
acid) JP 8323946 : A2 : 19961210 Shimadzu Corp EM
EP 748634 : A2 : 19961218
EP 748634 : A3 : 19970730
DE 19521642 : A1 : 19961219
Surgical implant with infection-resistant surface of resorbable material JP 9024093 : A2 : 19970128 B. Braun Surgical Gmbh, Germany DD
WO 9639134 : A1 : 19961212
CA 2221784 : AA : 19961212
AU 9658457 : A1 : 19961224
AU 717260 : B2 : 20000323
JP 9263545 : A2 : 19971007
JP 2992677 : B2 : 19991220
EP 831808 : A1 : 19980401 Takeda Chemical Industries, Ltd., Japan
BR 9602633 : A : 19980422 Hoshino, Tetsuo
CN 1187122 : A : 19980708 Muranishi, Hiroya
US 5910492 : A : 19990608 Taketomi, Shigehisa
Osteogenetic promoting pharmaceutical composition NO 9705636 : A : 19980128 Iwasa, Susumu DD
EP 747072 : A2 : 19961211
EP 747072 : A3 : 19990303
US 5641502 : A : 19970624
Biodegradable moldable surgical material CA 2175285 : AA : 19961208 United States Surgical Corporation, USA EM
WO 9639095 : A1 : 19961212 Yissum Research Development Company of the Hebrew
Preparation of polymeric ocular inserts AU 9657757 : A1 : 19961224 University of Jerusalem, Israel DD
WO 9638133 : A1 : 19961205
US 5718922 : A : 19980217
Intravitreal microsphere drug delivery and method of preparation AU 9659545 : A1 : 19961218 Schepens Eye Research Institute, Inc., USA DD microcapsule
WO 9631202 : A1 : 19961010
US 5641745 : A : 19970624
CA 2217462 : AA : 19961010
AU 9652866 : A1 : 19961023
AU 700612 : B2 : 19990107
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Controlled release biodegradable micro- and nanospheres containing JP 11503147 : T2 : 19990323
cyclosporin ZA 9602670 : A : 19961009 Elan Corp Plc, Ire. DD microcapsule
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AU 9657409 : A1 : 19961129
Method for drug delivery to the pulmonary system US 6071497 : A : 20000606 Pharmaceutical Discovery Corporation, USA DD microcapsule
Sam Yang Co. Ltd., S. Korea
Yoon, Seok, Joon
Yeo, Guw, Dong
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CA 2219995 : AA : 19961107 Seo, Min, Hyo
CN 1183051 : A : 19980527 Pai, Chaul, Min
Implantable bioresorbable membrane and method for the preparation EP 857072 : A1 : 19980812 Jung, Jong, Pyoung
thereof JP 11504341 : T2 : 19990420 Lee, Seung, Jin EM
Preparation of cellular materials by the solution-precipitating technique for
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WO 9630060 : A1 : 19961003
CA 2216639 : AA : 19961003
AU 9651544 : A1 : 19961016
AU 712268 : B2 : 19991104
EP 817652 : A1 : 19980114
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Medical device treated with a hydrophilic polymer composition JP 11502734 : T2 : 19990309 Aortech Europe Ltd., UK
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9632951 : A1 : 19961024
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CA 2216417 : AA : 19961024
AU 9655557 : A1 : 19961107
AU 707013 : B2 : 19990701
EP 822822 : A1 : 19980211
CN 1181703 : A : 19980513
JP 10510293 : T2 : 19981006
BR 9608441 : A : 19990217
US 5766580 : A : 19980616 Galin, Miles A., USA
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Controlled release of miotic and mydriatic drugs in the anterior chamber NO 9704808 : A : 19971215 Israel, Stanley C. DD microcapsules
WO 9628143 : A1 : 19960919
DE 19513659 : A1 : 19960912
DE 19542837 : A1 : 19970522
AU 9650041 : A1 : 19961002
Polypeptide-containing pharmaceutical forms of administration in the form of EP 814778 : A1 : 19980107
microparticles JP 11501642 : T2 : 19990209 Boehringer Mannheim Gmbh, Germany DD microcapsules
US 5565215 : A : 19961015
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WO 9503356 : A1 : 19950202
WO 9503357 : A1 : 19950202
CA 2167920 : AA : 19950202
CA 2167921 : AA : 19950202
EP 710261 : A1 : 19960508
EP 712421 : A1 : 19960522
JP 9504042 : T2 : 19970422
Biodegradable injectable particles for imaging JP 9504308 : T2 : 19970428 Massachusetts Institute of Technology, USA EM imaging
Lactic acid polymer fibers and their preparation JP 8226016 : A2 : 19960903 Mitsubishi Rayon Co, Japan EM
WO 9628117 : A1 : 19960919
Biodegradable polymer implant for fracture nonunions AU 9647574 : A1 : 19961002 Board of Regents, the University of Texas System, USA EM
WO 9622786 : A1 : 19960801
Preparation of sustained-release emulsions containing LH-RH-antagonizing AU 9644591 : A1 : 19960814
bioactive peptides and biodegradable polymers JP 8259460 : A2 : 19961008 Takeda Chemical Industries, Ltd., Japan DD microcapsule
Manufacture of lactic acid-based polymers by ring-opening polymerization of
lactides JP 8193127 : A2 : 19960730 Daisow Co Ltd, Japan EM
EP 722966 : A2 : 19960724
EP 722966 : A3 : 19961023
CA 2167455 : AA : 19960720
AU 9642076 : A1 : 19960725
AU 708116 : B2 : 19990729
JP 8295730 : A2 : 19961112
BR 9600160 : A : 19980106
US 5644002 : A : 19970701
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Bioabsorbable polyalkylene diglycolates CN 1169440 : A : 19980107 Ethicon Inc., USA EM
Liquid polymer delivery system comprising biodegradable, water-insoluble WO 9621427 : A1 : 19960718
polymer AU 9646525 : A1 : 19960731 Atrix Laboratories, Inc., USA DD
CA 2160314 : AA : 19960413
FR 2725732 : A1 : 19960419
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Composite sheet materials comprising films and nonwoven fabrics of JP 9169082 : A2 : 19970630
polymers of lactic acid US 5702826 : A : 19971230 Fiberweb Sodoca Sarl, Fr. EM
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9620698 : A2 : 19960711
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CA 2207961 : AA : 19960711
AU 9647556 : A1 : 19960724
EP 805678 : A1 : 19971112
Surface-modified nanoparticles and method of making and using them JP 10511957 : T2 : 19981117 USA DD microcapsule
Biodegradable and injectable polymers as sustained-release drug carriers JP 8176016 : A2 : 19960709 University of Miami, USA DD
WO 9619248 : A2 : 19960627
Method of controlling pH in the vicinity of biodegradable implants, and WO 9619248 : A3 : 19961114
method of increasing surface porosity AU 9644241 : A1 : 19960710 Board of Regents, the University of Texas System, USA EM
WO 9615815 : A1 : 19960530
CA 2178602 : AA : 19960530
AU 9538144 : A1 : 19960617
AU 709240 : B2 : 19990826
CN 1139386 : A : 19970101
EP 755270 : A1 : 19970129
HU 74912 : A2 : 19970328
JP 9511762 : T2 : 19971125
RU 2139046 : C1 : 19991010
ZA 9509941 : A : 19960610
NO 9602843 : A : 19960705
Microcapsules having a biodegradable membrane encapsulating a gas core. FI 9602917 : A : 19960719 Bracco Research S.A., Switz. EM imaging
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CA 2205347 : AA : 19960530
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Compositions containing lazaroids and their use for preventing adhesions JP 10511645 : T2 : 19981110 University of Southern California, USA DD
WO 9612466 : A1 : 19960502
CA 2202510 : AA : 19960502
AU 9537379 : A1 : 19960515
AU 710749 : B2 : 19990930
ZA 9509041 : A : 19960717
Controlled-release container with core and outer shell EP 788340 : A1 : 19970813 Daratech Pty. Ltd., Australia DD
WO 9611720 : A1 : 19960425
AU 9536742 : A1 : 19960506
AU 699821 : B2 : 19981217
Drug-releasing stent EP 761251 : A1 : 19970312 Kabushikikaisha Igaki Iryo Sekkei, Japan DD
Aminoxyl-containing radical spin labeling in polymers and copolymers US 5516881 : A : 19960514 Cornell Research Foundation, Inc., USA DD
EP 710684 : A2 : 19960508
EP 710684 : A3 : 19960605
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JP 8225638 : A2 : 19960903
Preparation process of polyhydroxycarboxylic acid FI 9505175 : A : 19960503 Mitsui Toatsu Chemicals, Inc., Japan EM
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9607434 : A1 : 19960314
CA 2199047 : AA : 19960314
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AU 701907 : B2 : 19990211
ZA 9507471 : A : 19960708
EP 779821 : A1 : 19970625
CN 1157573 : A : 19970820
BR 9508888 : A : 19971230
HU 77368 : A2 : 19980330
JP 10505082 : T2 : 19980519
Contrast agents comprising gas-containing polymer microparticles and/or US 5990263 : A : 19991123 Marsden, John Christopher, UK
microballoons for diagnostic applications NO 9700995 : A : 19970506 Nycomed Imaging AS EM imaging
EP 707044 : A2 : 19960417
EP 707044 : A3 : 19960605
EP 707044 : B1 : 20000315
US 5641501 : A : 19970624
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JP 8208966 : A2 : 19960813
CA 2160207 : AA : 19960412
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Absorbable lactide polymer blends US 5705181 : A : 19980106 Ethicon, Inc., USA EM
WO 9610374 : A1 : 19960411
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CA 2201526 : AA : 19960411
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EP 784490 : A1 : 19970723
Differentially biodegradable biomedical implants JP 10506811 : T2 : 19980707 Otogen Corporation, USA EM
EP 711567 : A1 : 19960515
DE 4440095 : A1 : 19960515
JP 8206189 : A2 : 19960813
Surgical suture material comprising glycolide/trimethylene carbonate BR 9505138 : A : 19971021
copolymer US 6011121 : A : 20000104 B. Braun Surgical Gmbh, Germany EM
WO 9607399 : A1 : 19960314
CA 2196184 : AA : 19960314
AU 9533990 : A1 : 19960327
AU 695323 : B2 : 19980813
EP 779806 : A1 : 19970625
CN 1157562 : A : 19970820
BR 9509201 : A : 19971230
EP 1002529 : A1 : 20000524
JP 8217691 : A2 : 19960827
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Sustained-release preparation containing metal salt of a peptide NO 9701030 : A : 19970306 Takeda Chemical Industries, Ltd., Japan DD
WO 9603984 : A1 : 19960215
US 5626862 : A : 19970506
CA 2196304 : AA : 19960215
EP 774964 : A1 : 19970528
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Controlled local delivery of chemotherapeutic agents for treating solid US 5651986 : A : 19970729 Massachusetts Institute of Technology, USA
tumors US 5846565 : A : 19981208 Johns Hopkins Univ. DD
Lactic acid polymer-based compositions for injection molding JP 8027363 : A2 : 19960130 Mitsui Toatsu Chemicals, Japan EM
JP 8027255 : A2 : 19960130
Manufacture of poly(lactic acid) JP 3024907 : B2 : 20000327 Japan Steel Works Ltd, Japan EM
Biodegradable aliphatic polyesters and their manufacture JP 8003296 : A2 : 19960109 Mitsubishi Kagaku Kk, Japan EM
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
Poly(lactic acid) compositions JP 8003432 : A2 : 19960109 Mitsubishi Kagaku Kk, Japan EM
WO 9600592 : A2 : 19960111
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Biodegradable fracture fixation plates and their uses AU 9529521 : A1 : 19960125 Board of Regents, University of Texas System, USA EM
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CA 2193203 : AA : 19951228
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GB 2303551 : A1 : 19970226
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EP 766554 : A1 : 19970409
JP 9510477 : T2 : 19971021
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NO 9605403 : A : 19961216
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Polymer microparticles for drug delivery US 5869103 : A : 19990209 University of Nottingham, UK DD microcapsule
Immobilization of biologically active materials and diagnostic agents in cross- WO 9532736 : A1 : 19951207
linked poly(organophosphazenes) AU 9526581 : A1 : 19951221 Penn State Research Foundation, USA EM
EP 689807 : A2 : 19960103
Biodegradable mesh-and-film stent EP 689807 : A3 : 19960807 Advanced Cardiovascular Systems, Inc., USA EM
Production of high-molecular-weight poly(lactic acid) US 5470944 : A : 19951128 ARCH Development Corp., USA EM
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CA 2178487 : AA : 19950615
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EP 732915 : A1 : 19960925
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Pharmaceutical gels local delivery of fibrinolysis enhancing agents AT 195250 : E : 20000815 University of Texas System, USA DD
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CA 2187153 : AA : 19951019
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Effervescent pharmaceutical formulations containing controlled-release EP 754034 : A1 : 19970122
biodegradable microcapsules JP 9511517 : T2 : 19971118 Elan Corp., PLC, Ire. DD microcapsule
Bioerodible polymers for solid controlled release pharmaceutical
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Porous prosthetics with biodegradable material-impregnated interstitial WO 9528973 : A1 : 19951102
spaces AU 9523988 : A1 : 19951116 Board of Regents, University of Texas System, USA EM
JP 7216095 : A2 : 19950815
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Biodegradable multiblock polymers for use as drug delivering matrix US 5548035 : A : 19960820 Sam Yang Co., Ltd., S. Korea EM
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CA 2190121 : AA : 19950921
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Polymeric gene delivery system EP 804249 : A2 : 19971105 Brown University Research Foundation, USA DD
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Method for making a bioerodible material for the sustained release of a EP 693923 : A1 : 19960131
medicament and the material made from the method JP 8512288 : T2 : 19961224 Cambridge Scientific, Inc., USA DD EM
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
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High molecular weight polyesterpolycarbonates and the use thereof for the JP 9504565 : T2 : 19970506
preparation of bioerosible matrixes for controlled release of drugs US 5698661 : A : 19971216 Mediolanum Farmaceutica S.p.A., Italy EM
Bone cements containing biodegradable polymers, bioceramics, thrombin,
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WO 9522318 : A1 : 19950824
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Drugs, vaccines and hormones in polylactide coated microspheres JP 9509161 : T2 : 19970916 Can. DD microcapsule
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Biodegradable polymer fibers for surgical sutures SU 1835296 : A1 : 19930823 Volokon EM
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Process for preparing a controlled-release pharmaceutical composition of CH 681425 : A : 19930331
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WO 9503356 : A1 : 19950202
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Nanoparticles and microparticles of non-linear hydrophilic-hydrophobic JP 9504308 : T2 : 19970428
multiblock copolymers US 6007845 : A : 19991228 Massachusetts Institute of Technology, USA DD microcapsule
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CA 2156718 : AA : 19950629
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Immunological response potentiation with biodegradable microparticles CN 1120809 : A : 19960417 Forschung, Switz. DD
WO 9513799 : A1 : 19950526
CA 2176716 : AA : 19950526
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EP 729353 : A1 : 19960904
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Preparation of biocompatible and biodegradable polymer conjugates with FR 2707653 : A1 : 19950120
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Biodegradable polycaprolactone-polyether block copolymers and their CN 1087098 : A : 19940525 Chinese Academy of Sciences, Institute of Chemistry, Peop.
manufacture CN 1035678 : B : 19970820 Rep. China EM
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Improved process and device for treating and healing a bone void US 5736160 : A : 19980407 THM Biomedical, Inc., USA TE
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9506077 : A2 : 19950302
WO 9506077 : A3 : 19950504
CA 2168012 : AA : 19950302
AU 9476557 : A1 : 19950321
AU 697995 : B2 : 19981022
ZA 9406536 : A : 19960226
EP 719295 : A1 : 19960703
BR 9407370 : A : 19960716
CN 1129947 : A : 19960828
HU 74568 : A2 : 19970128
JP 9501967 : T2 : 19970225
EP 1028137 : A2 : 20000816
NO 9600721 : A : 19960426
FI 9600892 : A : 19960418
AU 9881920 : A1 : 19981210 Sandoz Ltd., Switz.
Polymeric matrices and their uses in pharmaceutical compositions US 6083521 : A : 20000704 Sandoz-Erfindugen Verwaltungsgellshcaft m.b.H. DD EM
WO 9509659 : A1 : 19950413
US 5575815 : A : 19961119
AU 9479671 : A1 : 19950501
AU 703003 : B2 : 19990311
EP 723462 : A1 : 19960731
Local polymeric gel cellular therapy JP 9506011 : T2 : 19970617 USA EM
US 5410016 : A : 19950425
US 5380536 : A : 19950110
US 5468505 : A : 19951121
US 5626863 : A : 19970506
US 5567435 : A : 19961022
Photopolymerizable biodegradable hydrogels as tissue contacting materials US 5986043 : A : 19991116
and controlled-release carriers US 6060582 : A : 20000509 University of Texas, USA EM
WO 9509613 : A1 : 19950413
Controlled-release microspheres AU 9458959 : A1 : 19950501 USA DD microcapsule
WO 9507072 : A2 : 19950316
WO 9507072 : A3 : 19950406
DE 4330958 : A1 : 19950316
DE 4416818 : A1 : 19951116
AU 9476551 : A1 : 19950327
EP 717617 : A1 : 19960626
JP 9502191 : T2 : 19970304
Active principle-containing gas-filled microparticles for ultrasonically NO 9600973 : A : 19960308
controlled release of active principles US 6068857 : A : 20000530 Germany DD
JP 6298917 : A2 : 19941025
JP 2644971 : B2 : 19970825
KR 9615447 : B1 : 19961114
Biodegradable polymers for medical goods and their manufacture US 5476909 : A : 19951219 Sam Yang Co., Ltd., S. Korea EM
US 5349047 : A : 19940920
US 5256762 : A : 19931026
CA 2099999 : AA : 19940115
Polyesters having predetermined monomeric sequence and good physical EP 579173 : A2 : 19940119
properties EP 579173 : A3 : 19940316 United States Surgical Corp., USA EM
6.9 Patents in medical and pharmaceutical applications.xls - page 463
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
DE 4330958 : A1 : 19950316
CA 2171303 : AA : 19950316
WO 9507072 : A2 : 19950316
WO 9507072 : A3 : 19950406
AU 9476551 : A1 : 19950327
EP 717617 : A1 : 19960626
HU 74509 : A2 : 19970128
JP 9502191 : T2 : 19970304
NO 9600973 : A : 19960308
US 6068857 : A : 20000530
Microparticle compositions for release of active agents by ultrasound AU 9877299 : A1 : 19980910 Schering A.-G., Germany DD microcapsule
WO 9502415 : A1 : 19950126
US 5562909 : A : 19961008
CA 2166208 : AA : 19950126
AU 9473261 : A1 : 19950213
AU 691824 : B2 : 19980528
EP 710117 : A1 : 19960508
BR 9407051 : A : 19960813
CN 1128954 : A : 19960814
JP 9500629 : T2 : 19970121
Phosphazene polyelectrolytes as immunoadjuvants WO 9502628 : A1 : 19950126 Virus Research Institute, USA DD
EP 635276 : A1 : 19950125
FR 2707878 : A1 : 19950127
FR 2707878 : B1 : 19970214
AU 9467579 : A1 : 19950202
US 5496872 : A : 19960305
CA 2128463 : AA : 19950122
Adhesive compositions for surgical use comprising sulfur-containing BR 9402861 : A : 19950404
polymers JP 7163650 : A2 : 19950627 Imedex S.A., Fr. EM
WO 9503357 : A1 : 19950202
US 5543158 : A : 19960806
US 5565215 : A : 19961015
EP 710261 : A1 : 19960508
Biodegradable particles for diagnosis and therapy JP 9504042 : T2 : 19970422 Massachusetts Institute of Technology, USA DD microcapsule
WO 9501810 : A1 : 19950119
AU 9470789 : A1 : 19950206
AU 692779 : B2 : 19980618
EP 707498 : A1 : 19960424
JP 9500298 : T2 : 19970114
AU 9885153 : A1 : 19981224
Implantable prosthesis containing polymer matrix seeded with fibroblasts AU 722956 : B2 : 20000817 Smith Nephew PLC, UK TE
US 5384333 : A : 19950124
CA 2138474 : AA : 19960620
EP 717999 : A1 : 19960626
AU 677115 : B2 : 19970410
Biodegradable injectable drug delivery polymer AU 9481544 : A1 : 19960711 University of Miami, USA DD
Polymerization of hydroxyalkanoic acids in presence of acetaldehyde JP 6279577 : A2 : 19941004 Mitsui Toatsu Chemicals, Japan EM
WO 9428935 : A1 : 19941222
US 5447725 : A : 19950905
CA 2164933 : AA : 19941222
CA 2164933 : C : 19990112
EP 702567 : A1 : 19960327
CN 1126948 : A : 19960717
Methods and compositions for aiding periodontal tissue regeneration JP 8511528 : T2 : 19961203 Procter and Gamble Co., USA DD EM
6.9 Patents in medical and pharmaceutical applications.xls - page 464
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 633020 : A1 : 19950111
EP 633020 : B1 : 19990915
CA 2127317 : AA : 19950106
NO 9402515 : A : 19950106
AU 9466145 : A1 : 19950112
AU 674077 : B2 : 19961205
FI 9403205 : A : 19950106
CN 1106653 : A : 19950816
JP 8003055 : A2 : 19960109
US 5534269 : A : 19960709
Sustained-release microcapsules containing polypeptides AT 184480 : E : 19991015 Takeda Chemical Industries, Ltd., Japan DD microcapsule
slow-release pharmaceuticals of water-soluble peptide hormones JP 6321803 : A2 : 19941122 Kirin Brewery, Japan DD
Preparation of lactide polymers using aluminum acetylacetonate catalyst PL 159692 : B1 : 19921231 Polska Akademia Nauk Zaklad Polimerow, Pol. EM
Massachusetts Institute of Technology, USA
Porous biodegradable polymeric materials for cell transplantation WO 9425079 : A1 : 19941110 Children's Medical Center Corp. TE
US 5329044 : A : 19940712
US 5473035 : A : 19951205
Glucaric acid monoamides and their use to prepare poly(glucaramides) US 5478374 : A : 19951226 USA EM
WO 9423698 : A1 : 19941027
US 5456917 : A : 19951010
EP 693923 : A1 : 19960131
Sustained-release implant comprising bioerodible polymers JP 8512288 : T2 : 19961224 Cambridge Scientific, Inc., USA DD
WO 9423699 : A1 : 19941027
CA 2160877 : AA : 19941027
AU 9466373 : A1 : 19941108
Slow-release delivery of antisense oligodeoxyribonucleotides from EP 695170 : A1 : 19960207
biodegradable microparticles JP 8511418 : T2 : 19961203 Medisorb Technologies International L.P., USA DD microcapsule
WO 9422424 : A1 : 19941013
Biodegradable, water-permeable membrane for fluid-imbibing pumps AU 9465266 : A1 : 19941024 Alza Corp., USA DD
Sustained-release pharmaceuticals containing peptides JP 6234656 : A2 : 19940823 Takeda Chemical Industries Ltd, Japan DD microcapsule
Preparation of polypeptide-polymer ion conjugates for treatment of wounds JP 6080694 : A2 : 19940322 Ra Hoya Kyansaa Risaachi Fuaun, USA DD EM
Preparation of polyesters with rare earth alkoxides as initiators JP 6157729 : A2 : 19940607 Japan Synthetic Rubber Co Ltd, Japan EM
US 5336505 : A : 19940809
US 5030457 : A : 19910709
Bioerodible polymers useful for the controlled release of therapeutic agents LV 10871 : B : 19960620 Pharmaceutical Delivery Systems, USA DD EM
WO 9415587 : A2 : 19940721
WO 9415587 : A3 : 19940901
CA 2150574 : AA : 19940721
AU 9459921 : A1 : 19940815
AU 680650 : B2 : 19970807
EP 678018 : A1 : 19951025
JP 8505395 : T2 : 19960611
HU 73188 : A2 : 19960628
PL 174772 : B1 : 19980930
ZA 9400077 : A : 19940811
CN 1115252 : A : 19960124
US 5672659 : A : 19970930
Ionic molecular conjugates of biodegradable polyester and bioactive FI 9503314 : A : 19950705
polypeptides US 5863985 : A : 19990126 Kinerton Ltd., Ire. DD EM
6.9 Patents in medical and pharmaceutical applications.xls - page 465
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
US 5328695 : A : 19940712
US 4906474 : A : 19900306
US 4757128 : A : 19880712
US 4888176 : A : 19891219
US 5356630 : A : 19941018
US 5545409 : A : 19960813
Muscle morphogenic protein and use thereof US 5629009 : A : 19970513 Massachusetts Institute of Technology, USA TE
GB 2273874 : A1 : 19940706
WO 9415588 : A1 : 19940721
AU 9457017 : A1 : 19940815
EP 676956 : A1 : 19951018
EP 676956 : B1 : 19980304
FI 9503056 : A : 19950620
Preparation of pharmaceuticals in a polymer matrix US 5620697 : A : 19970415 Finland DD
WO 9415640 : A1 : 19940721
CA 2153661 : AA : 19940721
Methods and compositions for the direct concentrated delivery of passive EP 680337 : A1 : 19951108
immunity JP 8508240 : T2 : 19960903 USA DD
FR 2699076 : A1 : 19940617
CA 2111136 : AA : 19940612
AU 9352336 : A1 : 19940623
AU 664504 : B2 : 19951116
DE 4342842 : A1 : 19940721
GB 2274586 : A1 : 19940803
Pharmaceutical dosage form for delivery to periodontal pocket GB 2274586 : B2 : 19960911 Colgate-Palmolive Co., USA DD
WO 9414416 : A1 : 19940707
CA 2153063 : AA : 19940707
AU 9458016 : A1 : 19940719
AU 673885 : B2 : 19961128
EP 676952 : A1 : 19951018
EP 676952 : B1 : 20000712
JP 8505138 : T2 : 19960604
AT 194489 : E : 20000715
ZA 9309470 : A : 19940810
Bioerodible controlled delivery system CN 1094610 : A : 19941109 Instie Vision Inc., USA DD
WO 9414417 : A1 : 19940707
CA 2153064 : AA : 19940707
AU 9458017 : A1 : 19940719
AU 674382 : B2 : 19961219
EP 676953 : A1 : 19951018
EP 676953 : B1 : 19990506
JP 8505139 : T2 : 19960604
AT 179597 : E : 19990515
ZA 9309469 : A : 19940810
Plasticized bioerodible controlled delivery system CN 1094643 : A : 19941109 Insite Vision Inc., USA DD
6.9 Patents in medical and pharmaceutical applications.xls - page 466
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 601799 : A1 : 19940615
AU 9352113 : A1 : 19940616
AU 669939 : B2 : 19960627
LT 3265 : B : 19950525
CA 2110730 : AA : 19940608
NO 9304423 : A : 19940608
FI 9305471 : A : 19940608
WO 9413317 : A1 : 19940623
CN 1096221 : A : 19941214
JP 7097334 : A2 : 19950411
ZA 9309163 : A : 19950607
US 5480868 : A : 19960102
RU 2128055 : C1 : 19990327
US 5668111 : A : 19970916
LV 10927 : B : 19960420
Sustained-release emulsion of LH-RH antagonists US 5972891 : A : 19991026 Takeda Chemical Industries, Ltd., Japan DD
WO 9415636 : A1 : 19940721
CA 2152949 : AA : 19940721
AU 9458053 : A1 : 19940815
AU 667003 : B2 : 19960229
EP 678035 : A1 : 19951025
JP 8505152 : T2 : 19960604
Vaccine preparations in stable particulate forms US 5902565 : A : 19990511 CSL Ltd., Australia DD
WO 9409760 : A1 : 19940511
US 5399665 : A : 19950321
CA 2127463 : AA : 19940511
EP 619732 : A1 : 19941019 Massachusetts Institute of Technology, USA
Biodegradable polymers for cell transplantation JP 7506622 : T2 : 19950720 Children's Hospital EM TE
EP 579503 : A2 : 19940119
EP 579503 : A3 : 19940615
Radiation-curable, urethane-acrylate prepolymers and crosslinked polymers EP 579503 : B1 : 19971105
for wound closure devices US 5674921 : A : 19971007 Ethicon Inc., USA EM
Flexible, elastic and biodegradable film made of polymers based on lactic
acid for medical dressings US 5296229 : A : 19940322 Solvay et Cie., Belg. EM
Sogo Yatsuko Kk, Japan
Aqueous solution of reduced gliadin JP 6107696 : A2 : 19940419 Yamauchi Kyoshi DD EM
WO 9409898 : A1 : 19940511
CA 2126685 : AA : 19931018
EP 625069 : A1 : 19941123
EP 625069 : B1 : 19981230
JP 7502686 : T2 : 19950323
HU 70418 : A2 : 19951030
AT 175132 : E : 19990115
ES 2127835 : T3 : 19990501
CN 1090172 : A : 19940803
US 5648096 : A : 19970715
Method of manufacturing microcapsules FI 9403067 : A : 19940623 Schwarz Pharma AG, Germany DD
Biodegradable polymer implant materials for prevention of post-surgical WO 9408635 : A1 : 19940428
adhesions AU 9453411 : A1 : 19940509 Materials Technology Consultants Ltd., UK EM
WO 9320126 : A1 : 19931014
EP 633905 : A1 : 19950118 Sandoz-Erfindungen Verwaltungsgeselschaft M.B.H., Austria
JP 7505420 : T2 : 19950615 Sandoz-Patent-GmbH
Preparation of biodegradable polycarbonates, and their use as drug carriers US 5849859 : A : 19981215 Sandoz Ltd. EM
6.9 Patents in medical and pharmaceutical applications.xls - page 467
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 595030 : A2 : 19940504
JP 6211648 : A2 : 19940802
Sustained-release multi-core microsphere preparation and method for JP 2911732 : B2 : 19990623
producing the same US 5603961 : A : 19970218 Tanabe Seiyaku Co., Ltd., Japan DD
WO 9320134 : A1 : 19931014
AU 9339417 : A1 : 19931108
ZA 9302273 : A : 19931126
Acid and base additives for bioerodible polymers to regulate degradation for EP 633907 : A1 : 19950118
sustained-release drug-delivery formulations US 5571525 : A : 19961105 Alza Corp., USA DD EM
WO 9320127 : A1 : 19931014
Poly(orthoesters) and poly(orthocarbonates) for sustained-release drug ZA 9302269 : A : 19931018
delivery having improved stability and bioerosion behavior AU 9339411 : A1 : 19931108 Alza Corp., USA DD EM
CA 2099941 : AA : 19940117
JP 6032732 : A2 : 19940208
JP 2651320 : B2 : 19970910
US 5556642 : A : 19960917
EP 586838 : A1 : 19940316
EP 586838 : B1 : 19971105
AT 159854 : E : 19971115
Method for producing sustained-release microsphere preparation ES 2110544 : T3 : 19980216 Tanabe Seiyaku Co., Ltd., Japan DD
WO 9405265 : A1 : 19940317
EP 659073 : A1 : 19950628
AU 683022 : B2 : 19971030
JP 3007687 : B2 : 20000207
Biodegradable polymer matrixes for sustained delivery of local anesthetics JP 8503695 : T2 : 19960423 Children's Medical Center Corp., USA EM
EP 586238 : A2 : 19940309
EP 586238 : A3 : 19940629
EP 586238 : B1 : 19990107
JP 6192068 : A2 : 19940712
CA 2105374 : AA : 19940303
AT 175345 : E : 19990115
ES 2125953 : T3 : 19990316
US 5575987 : A : 19961119
Sustained-release microcapsules manufactured from aliphatic polyesters US 5716640 : A : 19980210 Takeda Chemical Industries, Ltd., Japan DD microcapsule
6.9 Patents in medical and pharmaceutical applications.xls - page 468
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9318070 : A1 : 19930916
ZA 9301594 : A : 19930927
AU 9336423 : A1 : 19931005
AU 670069 : B2 : 19960704
ZA 9301599 : A : 19931228
CN 1084524 : A : 19940330
CN 1038940 : B : 19980701
EP 629214 : A1 : 19941221
EP 629214 : B1 : 19961023
LT 3199 : B : 19950327
LT 3216 : B : 19950425
JP 7505177 : T2 : 19950608
HU 69070 : A2 : 19950828
LV 10294 : B : 19951220
IL 104962 : A1 : 19960131
AT 144540 : E : 19961115
ES 2093413 : T3 : 19961216
CZ 281738 : B6 : 19970115
BR 9306043 : A : 19971118
PL 174125 : B1 : 19980630
RU 2114865 : C1 : 19980710
FI 9404078 : A : 19940905
NO 9403273 : A : 19940905
Noncrosslinked nonpolypeptide polymers for biodegradable medical goods US 5574097 : A : 19961112 Nycomed Imaging AS, Norway EM
Novel biodegradable polyesters DE 4224401 : A1 : 19940127 Pharmatech GmbH, Germany EM
EP 573024 : A1 : 19931208
EP 573024 : B1 : 19980826
Preparation of biodegradable polyesters DE 4218510 : A1 : 19931209 Pharmatech GmbH, Germany EM
WO 9400484 : A1 : 19940106
AU 9345431 : A1 : 19940124
Scar inhibitory factor and use thereof US 5827735 : A : 19981027 USA TE
Institut fuer Polymerenchemie, Germany
Manufacture of biodegradable aliphatic polyesters by ring-opening Berlin-Chemie AG
polymerization in presence of zinc salts DD 301573 : A7 : 19930325 Institut fuer Wirkstofforschung EM
Biodegradable drug delivery system for the prevention and treatment of
osteomyelitis US 5281419 : A : 19940125 Thomas Jefferson University, USA DD
EP 580428 : A1 : 19940126
EP 580428 : B1 : 19971001
AU 9341987 : A1 : 19940127
JP 6293636 : A2 : 19941021
AT 158718 : E : 19971015
CA 2101183 : AA : 19940125
HU 67277 : A2 : 19950328
CN 1088092 : A : 19940622
Pharmaceutical microparticle preparation and production thereof US 5723269 : A : 19980303 Takeda Chemical Industries, Ltd., Japan DD microcapsule
Manufacture of microcapsules with biodegradable polymer containing
cisplatin JP 5294839 : A2 : 19931109 Bio Material Univers Kk, Japan DD microcapsule
WO 9324154 : A1 : 19931209
US 5518730 : A : 19960521
AU 9344058 : A1 : 19931230
AU 665844 : B2 : 19960118
JP 7507548 : T2 : 19950824
Biodegradable controlled release melt-spun delivery system EP 746342 : A1 : 19961211 Fuisz Technologies, Ltd., USA DD
6.9 Patents in medical and pharmaceutical applications.xls - page 469
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9325191 : A2 : 19931223
WO 9325191 : A3 : 19940217
FR 2692147 : A1 : 19931217
FR 2692147 : B1 : 19950224
EP 646001 : A1 : 19950405
EP 646001 : B1 : 19970917
Bioresorbable poly(hydroxyacid) microspheres free from surface active JP 8505836 : T2 : 19960625
agents US 5662938 : A : 19970902 Centre National de la Recherche Scientifique, Fr. DD microcapsule
WO 9325221 : A1 : 19931223
AU 9346308 : A1 : 19940104
AU 680422 : B2 : 19970731
EP 644771 : A1 : 19950329
JP 7507806 : T2 : 19950831
AU 9742755 : A1 : 19980115
Pharmaceutical microspheres containing erythropoietin AU 698016 : B2 : 19981022 Alkermes Controlled Therapeutics, Inc., USA DD microcapsule
WO 9324097 : A1 : 19931209
FR 2691901 : A1 : 19931210
FR 2691901 : B1 : 19950519
AU 9343309 : A1 : 19931230
ZA 9303946 : A : 19931230
EP 649300 : A1 : 19950426
Use of mixtures of polymers derived from lactic acids in the preparation of EP 649300 : B1 : 19970305
bioresorbable membranes for guided tissue regeneration, particularly in JP 8500981 : T2 : 19960206
periodontology AT 149342 : E : 19970315 Centre National de la Recherche Scientifique (CNRS), Fr. TE
DE 4219724 : A1 : 19931216
WO 9325241 : A1 : 19931223
EP 644776 : A1 : 19950329
EP 644776 : B1 : 19981202
JP 7507778 : T2 : 19950831
AT 173937 : E : 19981215
ES 2127277 : T3 : 19990416
Use of microcapsules as contrast agents for color Doppler sonography NO 9404806 : A : 19941212 Schering A.-G., Germany EM imaging
EP 537000 : A2 : 19930414
EP 537000 : A3 : 19930804
US 5254345 : A : 19931019
CA 2079988 : AA : 19930412
JP 5214093 : A2 : 19930824
JP 7030177 : B4 : 19950405
JP 7165908 : A2 : 19950627
Poly(orthocarbonate acetal) bioerodible polymers JP 7094548 : B4 : 19951011 Merck and Co., Inc., USA EM
WO 9320138 : A2 : 19931014
WO 9320138 : A3 : 19940217
AU 9339709 : A1 : 19931108
Polymer matrix system containing a partially soluble compound ZA 9302268 : A : 19931111 Alza Corp., USA DD EM
EP 567391 : A1 : 19931027
CA 2093836 : AA : 19931025
ZA 9302661 : A : 19931126
NO 9301431 : A : 19931021
AU 9336990 : A1 : 19931028
A biodegradable .beta.-transforming growth factors delivery system for bone JP 6025009 : A2 : 19940201
regeneration HU 64863 : A2 : 19940328 Bristol-Myers Squibb Co., USA EM composite
WO 9317704 : A1 : 19930916
Biodegradable bursting release system EP 641219 : A1 : 19950308 Cambridge Scientific, Inc., USA DD
6.9 Patents in medical and pharmaceutical applications.xls - page 470
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9317669 : A1 : 19930916
AU 9337353 : A1 : 19931005
AU 673160 : B2 : 19961031
EP 627911 : A1 : 19941214
JP 7507056 : T2 : 19950803
JP 3011768 : B2 : 20000221
Photopolymerizable biodegradable hydrogels as tissue contacting material BR 9306038 : A : 19980113
and controlled-release carriers CA 2117588 : C : 19980825 University of Texas System, USA DD EM
EP 556818 : A1 : 19930825
Polyester-type polyfunctional macromonomer, gel and drug release JP 6016799 : A2 : 19940125
controlling material responsive to changes in temperature US 5417983 : A : 19950523 Sagami Chemical Research Center, Japan DD EM
Manufacture of sustained-release microparticles containing water-soluble
polypeptide hormones JP 5194253 : A2 : 19930803 Kirin Brewery, Japan DD
JP 5039347 : A2 : 19930219
Biodegradable polymers in sustained-release pharmaceuticals JP 2704330 : B2 : 19980126 Taki Kagaku K. K., Japan EM
WO 9315694 : A1 : 19930819
AU 9336192 : A1 : 19930903
AU 667877 : B2 : 19960418
EP 625891 : A1 : 19941130
EP 625891 : B1 : 19970108
Multi-phase bioerodible polymer implant/carrier. JP 7503869 : T2 : 19950427 University of Texas System, USA EM TE
EP 560014 : A1 : 19930915
AU 9331174 : A1 : 19930916
JP 6007423 : A2 : 19940118
Biodegradable film dressing containing thermoplastic polymers CA 2091552 : AA : 19930913 Atrix Laboratories, Inc., USA EM
US 5179189 : A : 19930112
US 5171812 : A : 19921215
CA 2073561 : AA : 19910720
ZA 9100381 : A : 19920226
WO 9305096 : A1 : 19930318
AU 9226444 : A1 : 19930405
AU 667325 : B2 : 19960321
EP 605536 : A1 : 19940713
JP 7503030 : T2 : 19950330
US 5270419 : A : 19931214
US 5240963 : A : 19930831
US 5317079 : A : 19940531
Fatty acid-terminated polyanhydrides as controlled-release pharmaceutical FI 9401087 : A : 19940428
matrixes NO 9400837 : A : 19940502 Nova Pharmaceutical Corp., USA DD
US 5219980 : A : 19930615
Biodegradable polyesters for medical uses WO 9321253 : A1 : 19931028 SRI International, USA EM
WO 9311805 : A1 : 19930624
AU 9333467 : A1 : 19930719
AU 669148 : B2 : 19960530
EP 625056 : A1 : 19941123
EP 625056 : B1 : 19991020
JP 7502431 : T2 : 19950316
HU 68706 : A2 : 19950728
RO 111200 : B1 : 19960730
US 5622707 : A : 19970422
RU 2128057 : C1 : 19990327
AT 185699 : E : 19991115
ES 2141145 : T3 : 20000316
FI 9402895 : A : 19940818
Composite membranes for the guided regeneration of tissues NO 9402329 : A : 19940817 M.U.R.S.T., Italy TE
6.9 Patents in medical and pharmaceutical applications.xls - page 471
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9315767 : A1 : 19930819
Implant therapy for bone growth stimulation AU 9336072 : A1 : 19930903 Merck and Co., Inc., USA DD
US 5227412 : A : 19930713
JP 2587664 : B2 : 19970305
Biodegradable and resorbable surgical material and process for preparation EP 349656 : B1 : 19940316 Biomaterials Universe, Inc., Japan
of the same JP 8196616 : A2 : 19960806 Takiron Co., Ltd. EM
US 5206341 : A : 19930427
WO 9310169 : A1 : 19930527
AU 9331282 : A1 : 19930615
Polymers from hydroxy acids and polycarboxylic acids EP 705292 : A1 : 19960410 Southern Research Institute, USA EM
EP 544948 : A1 : 19930609
Intraocular and intraorbital implants for the controlled release of EP 544948 : B1 : 19950927
pharmacological agents ES 2077813 : T3 : 19951201 University of Miami, USA DD
Biodegradable lactic acid polymer-based thermoplastic compositions JP 4335060 : A2 : 19921124 Mitsui Toatsu Chemicals, Inc., Japan EM
DE 4223284 : A1 : 19930128
DE 4223284 : C2 : 19970731
CH 683149 : A : 19940131
WO 9301802 : A1 : 19930204
HU 64234 : A2 : 19931228
BR 9205375 : A : 19940308
CH 683592 : A : 19940415
PL 169387 : B1 : 19960731
RU 2103994 : C1 : 19980210
US 5445832 : A : 19950829
BE 1005696 : A3 : 19931221
BE 1005697 : A5 : 19931221
CA 2074320 : AA : 19930123
CA 2074320 : C : 19990406
CA 2074322 : AA : 19930123
DK 9200938 : A : 19930123
DK 9200939 : A : 19930123
SE 9202212 : A : 19930123
SE 512609 : C2 : 20000410
SE 9202213 : A : 19930123
SE 512670 : C2 : 20000417
NO 9202885 : A : 19930125
NO 9202886 : A : 19930125
GB 2257909 : A1 : 19930127
GB 2257909 : B2 : 19960110
GB 2257973 : A1 : 19930127
GB 2257973 : B2 : 19960228
AU 9220436 : A1 : 19930128
AU 651711 : B2 : 19940728
AU 9220437 : A1 : 19930128
AU 652844 : B2 : 19940908
FR 2679450 : A1 : 19930129
FR 2679450 : B1 : 19950609
FR 2680109 : A1 : 19930212
FR 2680109 : B1 : 19940902
NL 9201309 : A : 19930216
NL 9201310 : A : 19930216
CN 1070344 : A : 19930331
Formulatin of peptide drugs as sustained-release microspheres CN 1054543 : B : 20000719 Debio Recherche Pharmaceutique S. A., Switz. DD
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Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9307861 : A1 : 19930429
US 5288502 : A : 19940222
Multiphase pharmaceutical microspheres AU 9227845 : A1 : 19930521 University of Texas System, USA DD microcapsule
EP 539751 : A1 : 19930505
EP 539751 : B1 : 19980218
AU 9226054 : A1 : 19930429
AU 666676 : B2 : 19960222
AT 163261 : E : 19980315
ES 2114901 : T3 : 19980616
CA 2079831 : AA : 19930429
Biodegradable polymer compositions for implants JP 5305135 : A2 : 19931119 Atrix Laboratories, Inc., USA DD
EP 537559 : A1 : 19930421
EP 537559 : B1 : 19980121
AU 9226055 : A1 : 19930422
AT 162398 : E : 19980215
ES 2113906 : T3 : 19980516
CA 2079830 : AA : 19930416
JP 5286850 : A2 : 19931102
US 5702716 : A : 19971230
Polymeric compositions useful as controlled-release implants US 5945115 : A : 19990831 Atrix Laboratories, Inc., USA DD
US 5176907 : A : 19930105
Biocompatible and biodegradable poly (phosphoester-urethane) WO 9303739 : A1 : 19930304 Johns Hopkins University, USA
EP 535937 : A1 : 19930407
EP 535937 : B1 : 19970611
CA 2079509 : AA : 19930402
JP 5194200 : A2 : 19930803
AT 154241 : E : 19970615
US 5651990 : A : 19970729
Prolonged-release microparticles containing biodegradable polymers US 5622657 : A : 19970422 Takeda Chemical Industries, Ltd., Japan DD microcapsule
JP 4359014 : A2 : 19921211
Manufacture of biodegradable lactide polymers JP 3065384 : B2 : 20000717 Asahi Glass Co., Ltd., Japan EM
WO 9300936 : A1 : 19930121
SE 9101867 : A : 19930111
SE 469109 : B : 19930517
SE 469109 : C : 19930909
CA 2113091 : AA : 19930121
AU 9223314 : A1 : 19930211
A barrier for tissue separation EP 596940 : A1 : 19940518 Medinvent, Swed. EM
DE 4226465 : A1 : 19930211
JP 5042202 : A2 : 19930223
Jaw bone-reproducing bioabsorbable and biodegradable polymer material JP 3071004 : B2 : 20000731 Gunze Ltd., Japan EM
EP 521455 : A2 : 19930107
EP 521455 : A3 : 19930421
Aerosol composition containing a film-forming hydroxycarboxylic acid CA 2072812 : AA : 19930103 Takeda Chemical Industries, Ltd., Japan
polymer JP 5294824 : A2 : 19931109 Osaka Aerosol Industries Corp. DD
Pulsed release of high molecular weight therapeutic agents, such as WO 9300383 : A1 : 19930107
peptides, from bioerodible polymer compositions AU 9222615 : A1 : 19930125 Pharmaceutical Delivery Systems, Inc., USA DD
WO 9219241 : A1 : 19921112
CA 2102507 : AA : 19921108
AU 9220160 : A1 : 19921221
AU 657973 : B2 : 19950330
JP 6507416 : T2 : 19940825
HU 69390 : A2 : 19950928
EP 720478 : A1 : 19960710
A controlled-release delivery system for smoking cessation containing US 5486362 : A : 19960123
lobeline NO 9303971 : A : 19940107 Dynagen, Inc., USA DD
6.9 Patents in medical and pharmaceutical applications.xls - page 473
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9222336 : A1 : 19921223
AU 9219757 : A1 : 19930112
AU 657768 : B2 : 19950323
EP 588890 : A1 : 19940330
EP 588890 : B1 : 19970604
JP 6508536 : T2 : 19940929
AT 153861 : E : 19970615
ES 2102507 : T3 : 19970801
NO 9304506 : A : 19940209
Method of producing a microstructure in a bioresorbable element US 5486546 : A : 19960123 GUIDOR AB, Swed. TE
FR 2668707 : A1 : 19920507
FR 2668707 : B1 : 19950524
CH 681425 : A : 19930331
BE 1004923 : A5 : 19930223
GB 2249725 : A1 : 19920520
GB 2249725 : B2 : 19940810
CA 2055115 : AA : 19920515
NL 9101877 : A : 19920601
DE 4136930 : A1 : 19920820
AT 9102235 : A : 19930715
AT 397198 : B : 19940225
SE 9103348 : A : 19920515
SE 506448 : C2 : 19971215
JP 4288021 : A2 : 19921013
controlled-release pharmaceutical composition containing peptide ES 2049617 : A1 : 19940416
derivatives ES 2049617 : B1 : 19970316 Debio Recherche Pharmaceutique, Switz. DD
WO 9219226 : A1 : 19921112
CA 2102507 : AA : 19921108
AU 9221548 : A1 : 19921221
A controlled, sustained-release delivery system for treating drug HU 69390 : A2 : 19950928
dependency US 5486362 : A : 19960123 Dynagen, Inc., USA DD microcapsule
WO 9213567 : A1 : 19920820
AU 9216432 : A1 : 19920907
AU 669479 : B2 : 19960613
EP 568651 : A1 : 19931110
Biodegradable polymer blends for drug delivery JP 6508863 : T2 : 19941006 Nova Pharmaceutical Corp., USA DD
WO 9216191 : A1 : 19921001
Swelling agent and biodegradable polymer substances in long-acting EP 576675 : A1 : 19940105
pharmaceutical granule preparations US 5654009 : A : 19970805 Fujisawa Pharmaceutical Co., Ltd., Japan DD microcapsule
WO 9209312 : A1 : 19920611
Porous implant materials containing denatured albumins or biodegradable CA 2074362 : AA : 19920523
polyesters EP 512122 : A1 : 19921111 Toray Industries, Inc., Japan TE
US 5153002 : A : 19921006
CA 2040761 : AA : 19920905
Biocompatible gradient controlled-release implant CA 2055339 : AA : 19921019 University of Montreal, Can. DD
WO 9215282 : A2 : 19920917
CA 2105079 : AA : 19920829
AU 9215752 : A1 : 19921006
AU 652625 : B2 : 19940901
JP 6505661 : T2 : 19940630
EP 724429 : A1 : 19960807
EP 724429 : B1 : 19990707
AT 181825 : E : 19990715
Polymeric microparticles for drug targeting ES 2137947 : T3 : 20000101 Indiana University Foundation, USA DD microcapsule
6.9 Patents in medical and pharmaceutical applications.xls - page 474
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9215340 : A1 : 19920917
CA 2103541 : AA : 19920905
EP 574474 : A1 : 19931222
EP 574474 : B1 : 19980729
JP 6504702 : T2 : 19940602
AT 168889 : E : 19980815
AU 667048 : B2 : 19960307
AU 9222823 : A1 : 19940331
NO 9303139 : A : 19931103
Bioresorbable implant material comprising plasticized polymers US 5525646 : A : 19960611 Guidor AB, Swed. EM
GB 2246295 : A1 : 19920129
GB 2246295 : B2 : 19940511
FI 9103410 : A : 19920124
EP 473268 : A2 : 19920304
EP 473268 : A3 : 19920916
ZA 9105555 : A : 19920429
CA 2047540 : AA : 19920124
AU 9181238 : A1 : 19920130
AU 655187 : B2 : 19941208
HU 60632 : A2 : 19921028
JP 5032559 : A2 : 19930209
Polypeptide-polymer conjugate continuous-release pharmaceutical US 5320840 : A : 19940614
compositions US 5773581 : A : 19980630 Imperial Chemical Industries PLC, UK DD
WO 9211843 : A1 : 19920723
ZA 9200088 : A : 19921028
Bioerodible devices and compositions for diffusional release of drugs US 5543156 : A : 19960806 Alza Corp., USA DD
Multiphasic sustained-release microcapsules US 5126147 : A : 19920630 BioSearch, Inc., USA DD microcapsule
EP 486959 : A1 : 19920527
EP 486959 : B1 : 19960828
AT 141788 : E : 19960915
ES 2094781 : T3 : 19970201
JP 4283510 : A2 : 19921008
Pharmaceutical composition of microparticles with controlled release and US 5536508 : A : 19960716
process of preparing it US 5700486 : A : 19971223 Vectorpharma International S.p.A., Italy DD microcapsule
EP 491983 : A1 : 19920701
Biodegradable and resorbable molded article for surgical use EP 491983 : B1 : 19960320 Takiron Co. Ltd., Japan EM
Polyanhydride bioerodible controlled-release implants for administration of Massachusetts Institute of Technology, USA
stabilized growth hormone US 5122367 : A : 19920616 Nova Pharmaceutical Corp. DD
WO 9207555 : A1 : 19920514
AU 9189355 : A1 : 19920526
ZA 9108526 : A : 19920826
US 5620700 : A : 19970415
Drug delivery system for periodontal pocket US 5783205 : A : 19980721 Alza Corp., USA DD
EP 473223 : A1 : 19920304
EP 473223 : B1 : 19950510
IL 99180 : A1 : 19980104
AT 122230 : E : 19950515
ES 2072530 : T3 : 19950716
AU 9182678 : A1 : 19920227
AU 645594 : B2 : 19940120
JP 4230621 : A2 : 19920819
JP 2588328 : B2 : 19970305
CA 2049668 : AA : 19920223
Bioerodible pharmaceutical implants US 5837228 : A : 19981117 Merck and Co., Inc., USA DD
6.9 Patents in medical and pharmaceutical applications.xls - page 475
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 452111 : A2 : 19911016
EP 452111 : A3 : 19920805
EP 452111 : B1 : 19980715
CA 2040141 : AA : 19911014
AT 168391 : E : 19980815
JP 4218528 : A2 : 19920810
Biodegradable high-molecular weight polyesters for the preparation of HU 59943 : A2 : 19920728
microcapsules US 5585460 : A : 19961217 Takeda Chemical Industries, Ltd., Japan DD microcapsule
Sustained-release pharmaceutical microcapsules JP 4036233 : A2 : 19920206 Biomaterials Universe, Inc., Japan DD microcapsule
WO 9202211 : A1 : 19920220
CA 2088982 : AA : 19920210
AU 9186103 : A1 : 19920302
AU 660290 : B2 : 19950622
EP 542915 : A1 : 19930526
HU 69680 : A2 : 19950928
Sustained-release implant containing core covered by a polymer sheath JP 11508224 : T2 : 19990721 Endocon, Inc., USA DD
Sustained-release pharmaceuticals containing biodegradable carriers JP 3181414 : A2 : 19910807 Osteotech, Inc., USA DD
Sustained-release pharmaceuticals containing biodegradable and
absorbable polymers JP 3287544 : A2 : 19911218 Biomaterials Universe, Inc., Japan DD
WO 9115193 : A1 : 19911017
FR 2660556 : A1 : 19911011
FR 2660556 : B1 : 19940916
EP 523183 : A1 : 19930120
EP 523183 : B1 : 19940202
JP 5507063 : T2 : 19931014
AT 101031 : E : 19940215
Pharmaceutical microspheres containing biocompatible and biodegradable ES 2062786 : T3 : 19941216
surfactants and polymers US 6120805 : A : 20000919 Rhone-Poulenc Rorer S. A., Fr. DD microcapsule
Preparation of bioresorbable polymers free of monomers and solvents for
injection molding, extrusion, and melt-spinning DE 4014974 : A1 : 19911114 Boehringer Ingelheim K.-G., Germany EM
WO 9112882 : A1 : 19910905
FR 2658432 : A1 : 19910823
CA 2053913 : AA : 19910823
EP 469110 : A1 : 19920205
EP 469110 : B1 : 19940727
JP 4505420 : T2 : 19920924
Biocompatible microspheres for the controlled release of water-soluble US 5478564 : A : 19951226
substances and process for preparing them US 5609886 : A : 19970311 Medgenix Group S. A., Belg. DD microcapsule
Preparation of ortho and thio-ortho ester polymer for sustained-release
drugs US 5013821 : A : 19910507 Pharmaceutical Delivery Systems, Inc., USA DD microcapsule
WO 9109079 : A1 : 19910627
EP 464163 : A1 : 19920108
Use of supercritical fluids to obtain porous sponges of biodegradable EP 464163 : B1 : 19950405
polymers for pharmaceutical implants or drug delivery systems JP 4505775 : T2 : 19921008 Farmitalia Carlo Erba S.r.l., Italy EM
Enteric-coated pharmaceuticals and their preparation JP 3083917 : A2 : 19910409 Biomaterial Universe K. K., Japan DD EM
Chemotherapeutic treatment of bacterial infections with an antibiotic WO 9113595 : A1 : 19910919
encapsulated within a biodegradable polymeric matrix AU 9175589 : A1 : 19911010 United States Dept. of the Army, USA DD microcapsule
DE 4002736 : A1 : 19910801
EP 439846 : A1 : 19910807
EP 439846 : B1 : 19940202
EP 439846 : B2 : 19981028
ES 2062289 : T3 : 19941216
US 5229469 : A : 19930720
CA 2035279 : AA : 19910801
Preparation of biodegradable polymers for the controlled release of JP 4364161 : A2 : 19921216
substances US 5317065 : A : 19940531 Hoechst A.-G., Fed. Rep. Ger. EM
6.9 Patents in medical and pharmaceutical applications.xls - page 476
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
Controlled-release dosage forms with tubular structures WO 9111176 : A1 : 19910808 AKZO N. V., Neth. DD
CA 2024130 : AA : 19910301
Bioerodible polymers useful for the controlled-release pharmaceuticals US 5030457 : A : 19910709 Pharmaceutical Delivery Systems, Inc., USA DD
Poly(amide anhydride) and poly(imide anhydrides) for biological application US 5010167 : A : 19910423 Massachusetts Institute of Technology, USA EM
WO 9105001 : A1 : 19910418
US 5028667 : A : 19910702
CA 2066029 : AA : 19910330
AU 9066244 : A1 : 19910428
EP 493529 : A1 : 19920708
EP 493529 : B1 : 19950705
BR 9007686 : A : 19920818
JP 5500982 : T2 : 19930225
JP 2858947 : B2 : 19990217
DD 298247 : A5 : 19920213
ZA 9007797 : A : 19920527
CN 1051367 : A : 19910515
US 5095098 : A : 19920310
US 5028667 : B1 : 19930209
Yttrium and rare earth compound catalysts for lactone polymerization for NO 9201190 : A : 19920326
preparation of biogradable polyesters FI 9201351 : A : 19920327 du Pont de Nemours, E. I., and Co., USA EM
WO 9101126 : A1 : 19910207
CA 2063729 : AA : 19910125
AU 9060718 : A1 : 19910222
AU 653498 : B2 : 19941006
EP 484387 : A1 : 19920513
EP 484387 : B1 : 19940119
JP 5504941 : T2 : 19930729
AT 100308 : E : 19940215
ES 2062540 : T3 : 19941216
Biodegradable system for regenerating the periodontium NO 9200302 : A : 19920124 Atrix Laboratories, Inc., USA EM
EP 398472 : A2 : 19901122
EP 398472 : A3 : 19910918
EP 398472 : B1 : 19941130
JP 3007718 : A2 : 19910114
JP 2855463 : B2 : 19990210
ES 2072976 : T3 : 19950801
CA 2012469 : AA : 19900917
CA 2012469 : C : 19980512
Azo group-containing biodegradable polyurethanes in the large intestine US 5225514 : A : 19930706 Ono Pharmaceutical Co., Ltd., Japan DD
US 4999417 : A : 19910312
CA 2029062 : AA : 19920501
Biodegradable polymer compositions EP 483429 : A1 : 19920506 Nova Pharmaceutical Corp., USA EM
EP 414416 : A2 : 19910227
EP 414416 : A3 : 19910703
EP 414416 : B1 : 19970604
US 4997904 : A : 19910305
CA 2022939 : AA : 19910226
AT 154050 : E : 19970615
ES 2104586 : T3 : 19971016
Biodegradable aromatic polyanhydrides with good solubility and uses in JP 3091530 : A2 : 19910417
medical application JP 4170429 : A2 : 19920618 Nova Pharmaceutical Corp., USA EM
6.9 Patents in medical and pharmaceutical applications.xls - page 477
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 419156 : A2 : 19910327
EP 419156 : A3 : 19911016
US 5047464 : A : 19910910
CA 2025480 : AA : 19910321
JP 3128934 : A2 : 19910531
Preparation and uses of bioerodible thermoset polyester elastomers US 5217712 : A : 19930608 Merck and Co., Inc., USA EM
WO 9103510 : A1 : 19910321
US 5030457 : A : 19910709
AU 9064024 : A1 : 19910408
EP 489843 : A1 : 19920617
Biodegradable orthoester polymers useful for the controlled release of JP 5502465 : T2 : 19930428
therapeutic agents LV 10871 : B : 19960620 Pharmaceutical Delivery Systems, Inc., USA EM
EP 420541 : A2 : 19910403
EP 420541 : A3 : 19920422
CA 2025626 : AA : 19910328
AU 9063643 : A1 : 19910411
AU 633361 : B2 : 19930128
Biodegradable resorbable ureteral stent JP 3205059 : A2 : 19910906 Bristol-Myers Squibb Co., USA EM
Encapsulated osteoprogenitor cells for promoting hard tissue healing WO 9101720 : A1 : 19910221 USA TE
WO 9015586 : A2 : 19901227
WO 9015586 : A3 : 19910321
CA 2056384 : AA : 19901206
CA 2056384 : C : 19980623
EP 476045 : A1 : 19920325
EP 476045 : B1 : 19960828
JP 5503286 : T2 : 19930603
AT 141804 : E : 19960915
Bioerodible polymer composite implants for drug delivery in bone ES 2093647 : T3 : 19970101 Massachusetts Institute of Technology, USA DD
WO 9012605 : A1 : 19901101
CA 2031529 : AA : 19901028
EP 422208 : A1 : 19910417 SRI International, USA
Biodegradable composites for internal medical use JP 3505541 : T2 : 19911205 University of Utah DD EM
WO 9013780 : A1 : 19901115
US 5019400 : A : 19910528
CA 2030550 : AA : 19901102
AU 9055309 : A1 : 19901129
AU 621751 : B2 : 19920319
EP 424516 : A1 : 19910502
EP 424516 : B1 : 19921209
JP 3504389 : T2 : 19910926
JP 7039338 : B4 : 19950501
AT 83310 : E : 19921215
Very low temperature casting of controlled release microspheres ES 2037563 : T3 : 19930616 Enzytech, Inc., USA DD microcapsule EM
WO 9009783 : A1 : 19900907
US 5545409 : A : 19960813
Pharmaceutical implants comprising water-soluble bioactive proteins US 5629009 : A : 19970513 Massachusetts Institute of Technology, USA EM TE
WO 9009166 : A1 : 19900823
US 4990336 : A : 19910205
AU 9051091 : A1 : 19900905
EP 457834 : A1 : 19911127
EP 457834 : B1 : 19940608
Multiphasic sustained-release injectable containing microencapsulated AT 106716 : E : 19940615
biomacromolecular agents ES 2057537 : T3 : 19941016 Biosearch, Inc., USA DD microcapsule
6.9 Patents in medical and pharmaceutical applications.xls - page 478
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 9012603 : A1 : 19901101
US 5041138 : A : 19910820
CA 2051663 : AA : 19901018
CA 2051663 : C : 19960806
AU 9055568 : A1 : 19901116
AU 635025 : B2 : 19930311
EP 469070 : A1 : 19920205
EP 469070 : B1 : 19960911
JP 4505717 : T2 : 19921008
JP 6006155 : B4 : 19940126
AT 142511 : E : 19960915
ES 2095252 : T3 : 19970216
CA 2031532 : AA : 19901026
WO 9012604 : A1 : 19901101
AU 9055691 : A1 : 19901116
AU 636346 : B2 : 19930429
EP 422209 : A1 : 19910417
JP 4501080 : T2 : 19920227
AT 119787 : E : 19950415
Implantation of polymers with attached chondroycte for regeneration of bone ES 2072434 : T3 : 19950716
and cartilage JP 10263070 : A2 : 19981006 USA TE
WO 9007308 : A1 : 19900712
EP 449941 : A1 : 19911009
EP 449941 : B1 : 19940302
JP 3505684 : T2 : 19911212
JP 6083713 : B4 : 19941026
AT 101994 : E : 19940315
ES 2049971 : T3 : 19940501
NO 9102439 : A : 19910621
NO 177035 : B : 19950403
NO 177035 : C : 19950726
DK 171525 : B1 : 19961223
WO 9403121 : A1 : 19940217
EP 773750 : A1 : 19970521
Surgical barrier manufacture from polymers for gingival tissues US 5700479 : A : 19971223 Procordia Oratech AB, Swed. EM
US 4957998 : A : 19900918
Biodegradable polymers containing acetal, carboxy-acetal, ortho ester and WO 9202210 : A1 : 19920220
carboxyortho ester linkages CA 2022817 : AA : 19920208 Pharmaceutical Delivery Systems, Inc., USA EM
WO 9004982 : A1 : 19900517
FI 85223 : B : 19911213
FI 85223 : C : 19920325
AU 8945032 : A1 : 19900528
AU 636311 : B2 : 19930429
EP 442911 : A1 : 19910828
EP 442911 : B1 : 19960417
JP 4502715 : T2 : 19920521
JP 2931004 : B2 : 19990809
AT 136796 : E : 19960515
Biodegradable surgical implants CA 2010274 : AA : 19910816 Biocon Oy, Finland EM
US 4888176 : A : 19891219
US 4906474 : A : 19900306
US 4757128 : A : 19880712
US 5328695 : A : 19940712
Controlled drug delivery using high molecular weight polyanhydrides US 5286763 : A : 19940215 Massachusetts Institute of Technology, USA DD
6.9 Patents in medical and pharmaceutical applications.xls - page 479
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 374532 : A2 : 19900627
EP 374532 : A3 : 19910807
EP 374532 : B1 : 19940921
ES 2059683 : T3 : 19941116
IL 92699 : A1 : 19940826
CA 2006106 : AA : 19900622
DK 8906559 : A : 19900623
AU 8947078 : A1 : 19900628
AU 635913 : B2 : 19930408
JP 2212418 : A2 : 19900823
JP 2901673 : B2 : 19990607
Sustained-release pharmaceutical microparticles for delivery to periodontal ZA 8909863 : A : 19901031
pocket US 5500228 : A : 19960319 American Cyanamid Co., USA DD microcapsule
EP 374531 : A2 : 19900627
EP 374531 : A3 : 19910731
EP 374531 : B1 : 19940504
AT 105177 : E : 19940515
ES 2051968 : T3 : 19940701
IL 92700 : A1 : 19940530
CA 2006105 : AA : 19900622
DK 8906558 : A : 19900623
NO 8905167 : A : 19900625
NO 178605 : B : 19960122
NO 178605 : C : 19960502
AU 8947077 : A1 : 19900628
AU 635912 : B2 : 19930408
JP 2184620 : A2 : 19900719
JP 2901674 : B2 : 19990607
Pharmaceutical composition containing antibotics for sustained delivery to ZA 8909857 : A : 19901031
periodontal pockets US 5366733 : A : 19941122 American Cyanamid Co., USA DD microcapsule
US 4950735 : A : 19900821
Biodegradable polyamides US 5068220 : A : 19911126 Sharpoint, L. P., USA EM
US 4938763 : A : 19900703
US 4938763 : B1 : 19950704
BR 8907686 : A : 19910730
JP 4503163 : T2 : 19920611
JP 2992046 : B2 : 19991220
AU 644581 : B2 : 19931216
EP 773034 : A1 : 19970514
IL 91850 : A1 : 19950330
IL 107393 : A1 : 19950629
ZA 8907511 : A : 19910626
NO 9101277 : A : 19910531
US 5278202 : A : 19940111
US 5340849 : A : 19940823
AU 9350677 : A1 : 19940217
AU 666050 : B2 : 19960125
US 5725491 : A : 19980310
US 5733950 : A : 19980331
Biodegradable in-situ forming implants and methods of producing the same US 5990194 : A : 19991123 USA EM
Lactide block copolymers and porphyrin complex catalysts for their JP 2084431 : A2 : 19900326
preparation JP 2525043 : B2 : 19960814 Tokuyama Soda Co., Ltd., Japan EM
Biodegradable, biocompatible, and sustained-release peptide preparations JP 2078629 : A2 : 19900319
containing block copolymers JP 6004540 : B4 : 19940119 Taki Chemical Co., Ltd., Japan DD EM
Manufacture of microspheres sensitive to temperature changes for JP 2045417 : A2 : 19900215
pharmaceutical formulations JP 2727326 : B2 : 19980311 Lion Corp., Japan DD
6.9 Patents in medical and pharmaceutical applications.xls - page 480
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
US 4919929 : A : 19900424
AU 605159 : B2 : 19910110
AU 8776086 : A1 : 19890127
US 4956349 : A : 19900911
US 5242691 : A : 19930907
CA 2072658 : AA : 19910507
WO 9106321 : A1 : 19910516
AU 9066149 : A1 : 19910531
AU 644820 : B2 : 19931223
JP 5501801 : T2 : 19930408
JP 2912451 : B2 : 19990628
EP 593440 : A1 : 19940427
EP 593440 : B1 : 19960821
AT 141513 : E : 19960915
NO 9201748 : A : 19920701
US 5352462 : A : 19941004
CA 2163737 : AA : 19941208
WO 9427623 : A1 : 19941208
AU 9345979 : A1 : 19941220
AU 690521 : B2 : 19980430
BR 9307851 : A : 19960319
EP 707485 : A1 : 19960424
Milk antibody production with shaped polymer microparticles for controlled- NO 9504717 : A : 19960126
release of antigens FI 9505692 : A : 19960124 Stolle Research and Development Corp., USA DD microcapsule
EP 349505 : A2 : 19900103
EP 349505 : A3 : 19900808
EP 349505 : B1 : 19980916
JP 3500139 : T2 : 19910117
JP 2842649 : B2 : 19990106
AU 636570 : B2 : 19930506
EP 754467 : A1 : 19970122
AT 171076 : E : 19981015
ES 2121741 : T3 : 19981216
Polymer sheets for tissue separation in wound heeling ZA 8904694 : A : 19900228 Astra Meditec AB, Swed. EM
US 4904524 : A : 19900227
CA 1325560 : A1 : 19931228
AU 8941777 : A1 : 19900426
AU 612100 : B2 : 19910627
EP 365160 : A2 : 19900425
EP 365160 : A3 : 19911106
EP 365160 : B1 : 19941214
ES 2065392 : T3 : 19950216
DK 8905145 : A : 19900419
JP 2157217 : A2 : 19900618
Manufacture and uses of wet wipes JP 2557987 : B2 : 19961127 Scott Paper Co., USA
6.9 Patents in medical and pharmaceutical applications.xls - page 481
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 8905664 : A1 : 19890629
US 4891263 : A : 19900102
US 5120802 : A : 19920609
US 4916193 : A : 19900410
US 4920203 : A : 19900424
US 4916207 : A : 19900410
EP 390860 : A1 : 19901010
EP 390860 : B1 : 19950412
JP 3502651 : T2 : 19910620
US 5145945 : A : 19920908
US 5066772 : A : 19911119
US 5185408 : A : 19930209
US 5152781 : A : 19921006
US 5256764 : A : 19931026
US 5274074 : A : 19931228
US 5531998 : A : 19960702
Medical devices fabricated from homopolymers and copolymers having US 5412068 : A : 19950502
recurring carbonate units US 5486593 : A : 19960123 Allied-Signal, Inc., USA EM
WO 8905830 : A1 : 19890629
Biodegradable polyurethanes, products based thereon, and polyester polyol NL 8703115 : A : 19890717
prepolymers EP 417095 : A1 : 19910320 Stichting Biomat, Neth. EM
JP 1216917 : A2 : 19890830
Slow-release implants containing pharmaceuticals JP 2702729 : B2 : 19980126 Eisai Co., Ltd., Japan DD
EP 322319 : A2 : 19890628
EP 322319 : A3 : 19890802
EP 322319 : B1 : 19920812
CA 1330421 : A1 : 19940628
JP 2000702 : A2 : 19900105
JP 8022814 : B4 : 19960306
AT 79252 : E : 19920815
ES 2051882 : T3 : 19940701
JP 11189527 : A2 : 19990713
JP 10067650 : A2 : 19980310
Ophthalmic drug implants containing biodegradable polymers JP 2975332 : B2 : 19991110 USA DD
EP 311065 : A1 : 19890412
EP 311065 : B1 : 19940202
DE 3734223 : A1 : 19890420
AT 101035 : E : 19940215
ES 2061589 : T3 : 19941216
DK 8805615 : A : 19890410
FI 8804604 : A : 19890410
NO 8804474 : A : 19890410
NO 176304 : B : 19941205
NO 176304 : C : 19950322
AU 8823522 : A1 : 19890413
AU 609194 : B2 : 19910426
JP 2000117 : A2 : 19900105
JP 2763303 : B2 : 19980611
ZA 8807535 : A : 19900627
IL 87973 : A1 : 19920818
CA 1333770 : A1 : 19950103 Boehringer Ingelheim K.-G., Fed. Rep. Ger.
Implantable biodegradable drug delivery system containing polylactide KR 9706082 : B1 : 19970423 Boehringer Ingelheim International G.m.b.H. DD
6.9 Patents in medical and pharmaceutical applications.xls - page 482
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
DE 3835099 : A1 : 19890427
CH 672887 : A : 19900115
GB 2211091 : A1 : 19890628
GB 2211091 : B2 : 19910213
NL 8802490 : A : 19890501
ES 2009347 : A6 : 19890916
DK 8805714 : A : 19890415
FR 2622105 : A1 : 19890428
FR 2622105 : B1 : 19930514
CA 1332808 : A1 : 19941101
JP 1157920 : A2 : 19890621
Controlled- or sustained-release dosage form containing biodegradable BE 1001687 : A5 : 19900206
polyesters US 5187150 : A : 19930216 Debiopharm S. A., Switz. DD
JP 1096139 : A2 : 19890414 Japan Atomic Energy Research Institute, Japan
Biodegradable copolymers for slow release of drugs JP 5046328 : B4 : 19930713 Taki Chemical Co., Ltd. EM
EP 332530 : A1 : 19890913
FR 2628432 : A1 : 19890915
FR 2628432 : B1 : 19901221
Preparation of citric acid-diamine copolymers as carriers for US 5026821 : A : 19910625
pharmaceuticals JP 2022327 : A2 : 19900125 SANOFI, Fr. EM
JP 1156912 : A2 : 19890620
Manufacture of slow-release pharmaceutical microgranules JP 2837675 : B2 : 19981216 Chugai Pharmaceutical Co., Ltd., Japan DD
JP 1015059 : A2 : 19890119
Manufacture of antithrombotic materials absorbable by the body JP 2508105 : B2 : 19960619 Mitsubishi Kasei Corp., Japan EM
DE 3822459 : A1 : 19890330
DE 3822459 : C2 : 19940707
GB 2209937 : A1 : 19890601
GB 2209937 : B2 : 19910703
AT 8802234 : A : 19930615
AT 397035 : B : 19940125
ZA 8806827 : A : 19890530
CA 1326438 : A1 : 19940125
FR 2620621 : A1 : 19890324
FR 2620621 : B1 : 19930219
DK 8805189 : A : 19890322
AU 8822326 : A1 : 19890323
AU 611944 : B2 : 19910627
ES 2009346 : A6 : 19890916
FI 8804297 : A : 19890322
FI 96919 : B : 19960614
FI 96919 : C : 19960925
NO 8804154 : A : 19890322
NO 178604 : B : 19960122
NO 178604 : C : 19960502
IL 87790 : A1 : 19920525
SE 8803321 : A : 19890322
SE 503406 : C2 : 19960610
NL 8802323 : A : 19890417
BE 1001685 : A5 : 19900206
CH 675968 : A : 19901130
US 5192741 : A : 19930309
JP 1121222 : A2 : 19890512
Sustained/controlled-release pharmaceuticals containing biodegradable JP 7013023 : B4 : 19950215
polymeric carriers and water-insoluble peptides US 5776885 : A : 19980707 Biopharm Developments Ltd. (BPD), UK DD
6.9 Patents in medical and pharmaceutical applications.xls - page 483
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 302582 : A1 : 19890208
EP 302582 : B1 : 19940727
EP 302582 : B2 : 19971217
CA 1302260 : A1 : 19920602
AU 8810992 : A1 : 19890209
AU 611662 : B2 : 19910620
JP 1042420 : A2 : 19890214
BR 8801242 : A : 19890221
ES 2056915 : T3 : 19941016
IL 86221 : A1 : 19920818
Sustained-release microencapsulated peptide hormones IN 173577 : A : 19940604 Southern Research Institute, USA DD microcapsule
WO 8900855 : A1 : 19890209
US 4857311 : A : 19890815
CA 1335858 : A1 : 19950606
AU 8822580 : A1 : 19890301
EP 368912 : A1 : 19900523
EP 368912 : B1 : 19940316
JP 2504158 : T2 : 19901129
Polyanhydrides with improved hydrolytic degradation properties, as matrices JP 7057797 : B4 : 19950621
for sustained-release drugs AT 102833 : E : 19940415 Massachusetts Institute of Technology, USA DD EM
EP 301856 : A2 : 19890201
EP 301856 : A3 : 19900725
EP 301856 : B1 : 19950524
US 4894231 : A : 19900116
JP 2500521 : T2 : 19900222
Sustained-release drug delivery systems coated with a barrier substance CA 1332356 : A1 : 19941011
such as silicone oil ES 2074050 : T3 : 19950901 Biomeasure, Inc., USA DD
JP 1108226 : A2 : 19890425
Block copolymers of lactides and films and fibers manufactured from them JP 8002955 : B4 : 19960117 Mitsui Toatsu Chemicals, Inc., Japan EM
EP 295055 : A2 : 19881214
EP 295055 : A3 : 19900502
IL 82834 : A1 : 19901105
US 4826945 : A : 19890502
Bioabsorbable polyester-polyether multiblock polymers or polyester- JP 1195862 : A2 : 19890807
polyether-polyurethane block polymers for surgical articles CA 1329854 : A1 : 19940524 Yissum Research Development Company, Israel EM
EP 314245 : A1 : 19890503
EP 314245 : B1 : 19940608
NL 8702563 : A : 19890516
AT 106913 : E : 19940615
Lactide polymers, their preparation and compositions with biologically active JP 1146924 : A2 : 19890608
substances US 5053485 : A : 19911001 C.C.A. Biochem B. V., Neth. EM
EP 263490 : A2 : 19880413
EP 263490 : A3 : 19900516
EP 263490 : B1 : 19950104
JP 63091325 : A2 : 19880422
JP 7025689 : B4 : 19950322
AU 8779404 : A1 : 19880414
AU 608250 : B2 : 19910328
CA 1315200 : A1 : 19930330
Sustained-release microspheres containing a biodegradable polymer and a ES 2068810 : T3 : 19950501
compound of sugar origin for subcutaneous administration US 4853226 : A : 19890801 Chugai Pharmaceutical Co., Ltd., Japan DD microcapsule
6.9 Patents in medical and pharmaceutical applications.xls - page 484
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
DE 3700128 : A1 : 19880714
JP 63174937 : A2 : 19880719
JP 8025909 : B4 : 19960313
EP 274127 : A2 : 19880713
EP 274127 : A3 : 19900627
EP 274127 : B1 : 19931201
AT 97930 : E : 19931215
Preparation of amino acid acyloxyalkylamide polymers as biodegradable US 4906473 : A : 19900306
matrices for controlled-release drug preparations US 5041291 : A : 19910820 Hoechst A.-G., Fed. Rep. Ger. EM
WO 8806873 : A1 : 19880922
US 4843112 : A : 19890627
AU 8815754 : A1 : 19881010
Bioerodable bone cements containing crosslinked polyester matrix with CA 1324082 : A1 : 19931109
calcium phosphate ceramic and bioresorbable calcium salts US 5085861 : A : 19920204 Beth Israel Hospital Assoc., USA EM composite
Biologically degradable fiber meshes for repairing chest walls in surgical JP 63122459 : A2 : 19880526
operations JP 7041063 : B4 : 19950510 Gunze Ltd., Japan EM
WO 8802262 : A1 : 19880407
Implantable biodegradable polymeric drug delivery system with adjuvant US 4863735 : A : 19890905
activity CA 1323566 : A1 : 19931026 Massachusetts Institute of Technology, USA DD EM
EP 266119 : A2 : 19880504
EP 266119 : A3 : 19890726
EP 266119 : B1 : 19940720
IL 84167 : A1 : 19910415
CA 1331738 : A1 : 19940830
AU 8779929 : A1 : 19880428
AU 607439 : B2 : 19910307
ES 2056068 : T3 : 19941001
ZA 8707946 : A : 19880629
DK 8705577 : A : 19880425
JP 63190833 : A2 : 19880808
JP 2741728 : B2 : 19980422
CN 1036326 : A : 19891018
CN 1040946 : B : 19981202
IN 170283 : A : 19920307
US 5811128 : A : 19980922
US 6024983 : A : 20000215
CN 1111157 : A : 19951108
US 5814344 : A : 19980929
US 5820883 : A : 19981013
US 5853763 : A : 19981229
Oral delivery of bioactive agents to and through the Peyer's patch by use of US 5942252 : A : 19990824 Southern Research Institute, USA
microencapsulation CN 1205204 : A : 19990120 University of Alabama DD microcapsule
EP 245840 : A2 : 19871119
EP 245840 : A3 : 19890322
EP 245840 : B1 : 19931201
DE 3616320 : A1 : 19871119
DE 3707369 : A1 : 19880915
AT 97929 : E : 19931215
AT 8702581 : A : 19931115
Biodegradable polymers for retarding preparations with controlled release AT 397804 : B : 19940725 Hoechst A.-G., Fed. Rep. Ger. DD EM
6.9 Patents in medical and pharmaceutical applications.xls - page 485
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
WO 8800837 : A2 : 19880211
WO 8800837 : A3 : 19880310
IN 165717 : A : 19891223
AU 8777887 : A1 : 19880224
AU 608531 : B2 : 19910411
EP 259904 : A1 : 19880316
EP 259904 : B1 : 19910612
JP 1500435 : T2 : 19890216
AT 64305 : E : 19910615
US 5087616 : A : 19920211
CA 1323303 : A1 : 19931019
Conjugates containing tumor-specific agents, cytotoxic agents and FI 8801579 : A : 19880406
biodegradable polymeric carriers for selective delivery of cytotoxic drugs to NO 8801473 : A : 19880406
tumor cells and methods of destroying tumor cells using the conjugates DK 8801847 : A : 19880606 Battelle Memorial Institute, Switz. DD EM
WO 8803417 : A1 : 19880519
FI 8604457 : A : 19880504
FI 80605 : B : 19900330
FI 80605 : C : 19900710
ES 2005049 : A6 : 19890216
CA 1297795 : A1 : 19920324
AU 8782357 : A1 : 19880601
AU 606903 : B2 : 19910221
EP 289562 : A1 : 19881109
EP 289562 : B1 : 19930203
JP 1501289 : T2 : 19890511
Bioceramic composites covered with reinforcing fibers for use in bone AT 85225 : E : 19930215
surgery, and their manufacture SU 1769715 : A3 : 19921015 Materials Consultants Oy, Finland EM composite
EP 281482 : A1 : 19880907
AU 8811435 : A1 : 19880908
Polymer blends having a biodegradability rate different from that of the AU 606383 : B2 : 19910207
blend components JP 1013034 : A2 : 19890117 Research Triangle Institute, USA EM
EP 246341 : A1 : 19871125
EP 246341 : B1 : 19900411
Noninflammatory, nontoxic, biodegradable polyanhydride implants, which JP 63031667 : A2 : 19880210
have predictable degradation rates. JP 7096025 : B4 : 19951018 Massachusetts Institute of Technology, USA EM
EP 257369 : A1 : 19880302
EP 257369 : B1 : 19920415
US 4758435 : A : 19880719
AT 74751 : E : 19920515
ES 2031096 : T3 : 19921201
CA 1297020 : A1 : 19920310
AU 8776724 : A1 : 19880218
AU 599406 : B2 : 19900719
Improved estradiol implant composition and method for preparation ZA 8705897 : A : 19880525 American Cyanamid Co., USA DD
6.9 Patents in medical and pharmaceutical applications.xls - page 486
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 245820 : A2 : 19871119
EP 245820 : A3 : 19910130
EP 245820 : B1 : 19951227
US 4741872 : A : 19880503
AU 8772668 : A1 : 19871119
AU 600723 : B2 : 19900823
AT 132035 : E : 19960115
ES 2080715 : T3 : 19960216
DK 8702446 : A : 19871117
JP 63028445 : A2 : 19880206
JP 2634813 : B2 : 19970730
CA 1309657 : A1 : 19921103
Biodegradable microspheres as a carrier for macromolecules US 5160745 : A : 19921103 University of Kentucky Research Foundation, USA DD
SE 452469 : B : 19871130
SE 452469 : C : 19880310
WO 8707898 : A1 : 19871230
EP 272300 : A1 : 19880629
EP 272300 : B1 : 19941102
JP 63503551 : T2 : 19881222
Process for the manufacture of crosslinked carboxy group-containing JP 7116242 : B4 : 19951213
polysaccharides US 4963666 : A : 19901016 Pharmacia AB, Swed. EM
DE 3616320 : A1 : 19871119
EP 245840 : A2 : 19871119
EP 245840 : A3 : 19890322
EP 245840 : B1 : 19931201
AT 97929 : E : 19931215
US 4835248 : A : 19890530
DK 8702468 : A : 19871116
NO 8702015 : A : 19871116
NO 169133 : B : 19920203
NO 169133 : C : 19920513
JP 62297325 : A2 : 19871224
JP 8032781 : B4 : 19960329
Biologically degradable polymers for controlled release of active materials CA 1297627 : A1 : 19920317 Hoechst A.-G. , Fed. Rep. Ger. EM
BE 905487 : A1 : 19870325
CH 671402 : A : 19890831
DE 3632251 : A1 : 19870430
FR 2590262 : A1 : 19870522
FR 2590262 : B1 : 19920612
GB 2185979 : A1 : 19870805
GB 2185979 : B2 : 19891206
US 4792598 : A : 19881220
Preparation of bis(carboxyphenoxy)(poly)(alkyleneoxy) monomers, their JP 62091527 : A2 : 19870427
polyanhydrides, and their use in sustained release pharmaceuticals US 5091565 : A : 19920225 Sandoz S. A., Switz. DD
EP 226061 : A2 : 19870624
EP 226061 : A3 : 19880720
EP 226061 : B1 : 19940216
High molecular weight bioresorbable polymers and implantation devices, JP 62144663 : A2 : 19870627
especially for promotion of nerve growth JP 5052749 : B4 : 19930806 Allied Corp., USA EM TE
6.9 Patents in medical and pharmaceutical applications.xls - page 487
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 202065 : A2 : 19861120
EP 202065 : A3 : 19871021
EP 202065 : B1 : 19930407
JP 62054760 : A2 : 19870310
JP 2551756 : B2 : 19961106
US 4728721 : A : 19880301
CA 1262005 : A1 : 19890926
AT 87946 : E : 19930415
HU 43488 : A2 : 19871130
HU 196703 : B : 19890130
Preparation of a biodegradable high molecular polymer and its use as a US 4849228 : A : 19890718 Takeda Chemical Industries, Ltd. , Japan
pharmaceutical excipient JP 8169818 : A2 : 19960702 Wako Pure Chemical Industries, Ltd. DD microcapsule
EP 192068 : A1 : 19860827
EP 192068 : B1 : 19900523
US 4634720 : A : 19870106
US 4636526 : A : 19870113
AU 8652661 : A1 : 19860828
AU 589393 : B2 : 19891012
CA 1290881 : A1 : 19911015
JP 61193666 : A2 : 19860828
Hard tissue prosthetics US 4698375 : A : 19871006 Dow Chemical Co., USA EM composite
EP 171907 : A1 : 19860219
EP 171907 : B1 : 19890111
EP 171907 : B2 : 19940810
JP 61028521 : A2 : 19860208
JP 6078425 : B4 : 19941005
JP 11001443 : A2 : 19990106
CA 1236641 : A1 : 19880510
CA 1256638 : A1 : 19890627
EP 172636 : A1 : 19860226
EP 172636 : B1 : 19890111
EP 172636 : B2 : 19921111
US 4677191 : A : 19870630
US 4683288 : A : 19870728
AT 39935 : E : 19890115
AT 39936 : E : 19890115
JP 61111326 : A2 : 19860529
JP 6010252 : B4 : 19940209
JP 6049185 : A2 : 19940222 Wako Pure Chemical Industries, Ltd. , Japan
Copolymer of lactic acid and glycolic acid JP 7033433 : B4 : 19950412 Takeda Chemical Industries, Ltd. EM
NL 8401912 : A : 19860102
EP 168862 : A2 : 19860122
EP 168862 : A3 : 19860827
EP 168862 : B1 : 19920318
JP 61041321 : A2 : 19860227
Biodegradable polymeric substrate loaded with active substance for AT 73649 : E : 19920415 Nederlandse Centrale Organisatie voor Toegepast-
controlled release of the active substance through a membrane US 4965128 : A : 19901023 Natuurwetenschappelijk Onderzoek, Neth. DD
6.9 Patents in medical and pharmaceutical applications.xls - page 488
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 166596 : A2 : 19860102
EP 166596 : A3 : 19870527
EP 166596 : B1 : 19910313
AU 8543150 : A1 : 19860102
AU 587977 : B2 : 19890907
ZA 8504188 : A : 19860226
IL 75407 : A1 : 19881130
FI 8502374 : A : 19851227
FI 81591 : B : 19900731
FI 81591 : C : 19901112
US 4745160 : A : 19880517
HU 38261 : A2 : 19860528
HU 193994 : B : 19871228
HU 196301 : B : 19881128
AT 61613 : E : 19910315
NO 8502547 : A : 19851227
NO 167752 : B : 19910826
NO 167752 : C : 19911204
DK 8502878 : A : 19851227
JP 61015846 : A2 : 19860123
JP 7051517 : B4 : 19950605
CA 1247271 : A1 : 19881220
ES 544580 : A1 : 19860901
ES 551370 : A1 : 19870416
ES 551371 : A1 : 19870501
ES 551372 : A1 : 19870501
US 4877606 : A : 19891031
NO 9001686 : A : 19851227
NO 175135 : B : 19940530
NO 175135 : C : 19940907
JP 7069929 : A2 : 19950314
JP 7106987 : B4 : 19951115
JP 7069930 : A2 : 19950314
Biodegradable amphipathic copolymers JP 7106988 : B4 : 19951115 Imperial Chemical Industries PLC, UK DD
6.9 Patents in medical and pharmaceutical applications.xls - page 489
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
DE 3422160 : A1 : 19841220
DE 3422160 : C2 : 19940908
US 4496446 : A : 19850129
GB 2141435 : A1 : 19841219
GB 2141435 : B2 : 19870121
CA 1247041 : A1 : 19881220
DK 8402961 : A : 19841217
DK 160409 : B : 19910311
DK 160409 : C : 19910819
SE 8403239 : A : 19841217
SE 461794 : B : 19900326
SE 461794 : C : 19900719
FI 8402435 : A : 19841217
FI 80213 : B : 19900131
FI 80213 : C : 19900510
AU 8429433 : A1 : 19841220
AU 569891 : B2 : 19880225
JP 60012068 : A2 : 19850122
JP 6024590 : B4 : 19940406
ZA 8404569 : A : 19860226
NO 159238 : B : 19880905
NO 159238 : C : 19881214
BE 899939 : A1 : 19841218
NL 8401926 : A : 19850116
NL 191081 : B : 19940816
NL 191081 : C : 19950116
Modifying a surgical structural element from bioresorbable polymers IL 72205 : A1 : 19880731 American Cyanamid Co. , USA EM
JP 59066425 : A2 : 19840414
Microcapsules production using biodegradable polymers JP 3072097 : B4 : 19911115 Mitsui Toatsu Chemicals, Inc., Japan DD microcapsule
WO 8400303 : A1 : 19840202
NL 8202894 : A : 19840216
AU 8317701 : A1 : 19840208
AU 568813 : B2 : 19880114
BR 8307449 : A : 19840717
EP 113739 : A1 : 19840725
EP 113739 : B1 : 19870506
JP 59501301 : T2 : 19840726
JP 63022829 : B4 : 19880513
DK 8401333 : A : 19840229
DK 159997 : B : 19910114
DK 159997 : C : 19910603
US 4915893 : A : 19900410
FI 8401051 : A : 19840315
FI 75609 : B : 19880331
FI 75609 : C : 19880711
NO 8401009 : A : 19840315
NO 158783 : B : 19880725
NO 158783 : C : 19881102
Polyester-containing filament material US 5110852 : A : 19920505 Rijksuniversiteit Groningen, Neth. EM
6.9 Patents in medical and pharmaceutical applications.xls - page 490
Title PATENT :KIND: DATE Patent assignee Drug delivery Eng. Materials Tissue Eng.
EP 92918 : A2 : 19831102
EP 92918 : A3 : 19850116
EP 92918 : B1 : 19881019
AT 37983 : E : 19881115
AU 8313280 : A1 : 19831027
AU 566010 : B2 : 19871008
ZA 8302601 : A : 19840229
US 4526938 : A : 19850702
IL 68426 : A1 : 19860831
HU 30969 : O : 19840428
HU 198093 : B : 19890728
CA 1246265 : A1 : 19881206
FI 8301368 : A : 19831023
FI 80284 : B : 19900131
FI 80284 : C : 19900510
NO 8301413 : A : 19831024
NO 162368 : B : 19890911
ES 521713 : A1 : 19841201
DK 8301785 : A : 19831023
DK 165458 : B : 19921130
DK 165458 : C : 19930413
JP 58191714 : A2 : 19831109
JP 5017245 : B4 : 19930308
NO 8401544 : A : 19831024
NO 164302 : B : 19900611
NO 164302 : C : 19900919
ES 535112 : A1 : 19851201
US 4942035 : A : 19900717
JP 4210928 : A2 : 19920803
Continuous release formulations JP 7088312 : B4 : 19950927 Imperial Chemical Industries PLC, UK DD
EP 52510 : A2 : 19820526
EP 52510 : A3 : 19820908
EP 52510 : B1 : 19860827
EP 52510 : B2 : 19941019
AU 8177560 : A1 : 19820527
AU 556754 : B2 : 19861120
JP 57118512 : A2 : 19820723
JP 4040329 : B4 : 19920702
ZA 8107973 : A : 19830727
CA 1176565 : A1 : 19841023
IL 64298 : A1 : 19850731
Microencapsulation of water soluble polypeptides AT 21624 : E : 19860915 Syntex (U.S.A.), Inc., USA DD microcapsule
Appendix 7. List of R&D Institutions on EDPs
Research Institute Department Associate Address additional www ref.
Case Western Reserve Institute of Pathology Anderson, J.M. 2085 Adelbert Road, http://www.cwru.edu/med/pathol book 11
University Cleveland, Ohio 44106, USA ogy/
Children's Hospital Boston Dept. of Surgery Chaignaud, B.E.; Enders 1161; Longwood Av., book 12
Vacanti, J.P. Boston, MA 02115, USA
Children's Medical Center Atala, A. PCT Int. Appl. WO 9922781 CA
Corporation A2 12 may 1999 130:343055
Clemson University Shalaby, S.W. Clemson, South Carolina bone repair and poly(a- http://www.clemson.edu/ book 11
29634, USA esters)
Fiber and polymer science, Dept. of Textiles and Apparel Chu, C.-C. Ithaca, NY, USA suture materials www.cornell.edu/ book 04/11
Cornell University www.human.cornell.edu/TXA/fa
culty/chu/whois_frame.html
Ethicon, Inc. Jamiolkowski, D.D. Somerville, New Jersey , bone repair and poly(a- book 11
USA esters)
F. Edward Hebert School of Mayer, M.H. Bethesda, Maryland, USA bone fixation devices book 11
Medicine
Georgia Institute of Institute for Bioengineering Nerem, R.M. Atlanta, GA 30332-0363, tissue engineering/ vascular http://www.ibb.gatech.edu/ book 12
Technology and Bioscience USA http://www.bme.gatech.edu/fac
ulty/nerem.htm
Han Yang University Dept. of Chemistry Han, Y.-K. 17 Haegdang dong, PGLA scaffolds for tissue http://www.hanyang.ac.kr/englis
Seongdong-ku, Seoul 133- engineering h/
791, Korea
Lab. For tissue engineering, Dept. of Surgery Atala, A. 300 Longwood Avenue, tissue engineering/ liver http://www.bidmc.harvard.edu/s book 12
Harvard Medical School Boston, MA 02115, USA urgery/
School of Pharmacy, Dept. of Medicinal Chemistry Domb, A.J. Jerusalem 91120, Israel polyesters/ polyanhydrides/ JBMR 45
Hebrew University drug release
Institute of Physical and Polymer Chemistry Laboratory Doi, Y. Hirosawa, Wako-shi, Saitama polyhydroxyalkanoates
Chemical Research 351-01, Japan
Johns Hopkins Oncolgy Depts. Of Radiobiology lab.; Yuan, X.; Williams, Baltimore, MD, USA device for release CA
Center Divisionof Radiation Oncology J.A. 131:233451
Johns Hopkins University Dept. of Chemical Engineering Lo, H. Baltimore, MD, USA poly(phosphoesters) book 11
491
Johns Hopkins University Dept. of Biomedical Kadiyala, S> Baltimore, MD, USA poly(phosphoesters) book 11
Engineering
Orthopeadic Biomechanis Dept. of Orthopedics Aro, H.T. Baltimore, MD, USA book 11
Lab., Johns Hopkins
University
Johns Hopkins University, Dept. of Biomedical Leong, K.W. Baltimore, MD, USA drug dlivery book 12
School of Medicine Engineering
Kansai University Fac. Of Engineering Ouchi, T. Osaka, 564-8680, Japan PLA and poly(depsi-
peptides)
Korea Advanced Institute of Dept. of Biological Sciences Park, Tae Gwan Taejon 305-701, Korea PLGA; drug delivery http://bama.kaist.ac.kr/main.htm
Science and Technology
Kwangju Institute of Science Bae, You Han 1 Oryong-dong, Puk-gu, PEO based hydrogels http://www.kjist.ac.kr/hindex.ht
and Technology Kwangju 500-712, Korea ml
Long Island University Wu, X.S. Brooklyn, USA
Ludwig-Maximilians Dept. of Otorhinolaryngology Kastenbauer, E.; Munich, Germany hyaluronic acid benzyl www.med-muenchen.de JBMR 42
University of Munich Naumann, A.; ester; tissue engineering
Aigner, J.
Malcolm and Dorothy Coutts Coutts, R.D. San Diego Articular cartilage repair book 11
Institute for joint Rec
Massachusetts Institute of Dept. of chemical engineering Langer, R. 77 Massachusetts Avenue, poly(anhydrides) book 11/12
Technology Cambridge, USA
Mayo Clinic and foundation Anethesia Research Masters, D.M. Rochester, USA polyanhydrides
Medical college of Dept. of Orthopaedic surgery Laurencin, C. USA poly(anhydrides) book 11
Pennsylvania and
Hahnemann University
National Tsing Hua Dept. of Chemical Engineering Wang, C.H. 101, Section 2 Kuang Fu poly(oxazoline-lactide) http://www.nthu.edu.tw/english/i
University Road, Hsinchu, R.China ndex.html
Oregon Health Sciences Northwest Wound Healing Hollinger, J.O. Portland, USA bone repair and poly(a- www.ohsu.edu book 11/
University Center esters) JBMR 41
492
college of engineering, Dept. of Applied Chemistry Tsunooka, M. 1-1 Gakuen-cho, Sakai, book 01
Osaka Prefecture University Osaka 599-8531, Japan
Oxford Bioresearch The Magdalen Centre Cederholm- Oxfort Science Park, Oxford
Laboratory Williams S.A. OX4 4GA, UK
Purdue University School of Pharmacy Park, K. Robert E. Heine Pharmacie hydrogels book 03
Building, West Lafayette,
IN 47907, USA
Institute of Biosciences and Cox Laboratory for Biomedical Mikos, G. P.O.Box 1892, Houston, poly(propylene fumarate): http://www.rice.edu/ JBMR 46
Bioengineering and De, Rice Engineering Texas 77251-1892, USA polyesters; retinal pigment
University epithelial regeneration;
guided tissue regeneration
Rudgers University Dept. of Chemical and Moghe, P.V. Piscataway, New Jersey porous polyesters/ tissue http://www.rudgers.edu JBMR 43
Biochemical Engineering 08854, USA engineering/ drug delivery
systems
Russian Academy of N.N. Semenov's Institute of Zaikov, G.E./ 4 Kosygin str., Moscow book 02/14
Sciences Chemical Physics or N.M. Gumargalieva, K.Z. 117334, Russia
Emanuel's Inst. Of
Biochemical Physics
493
School of Medicine, Department of Medicine Accavitti-Loper; THT 466, Birmingham, AL http://info.dom.uab.edu/index.ht
University of Alabama M.A. 35294, USA m
University of California Medical Center Kampner, S.L. San Francisco, USA Joint replacement www.ucsf.edu book 06
University of California at Dept. of Orthopedics Chu, C.R. Lajolla, California, USA Articular cartilage repair www.ucsd.edu book 11
San Diego
University of Connecticut Institute of Materials Science Edelman, P.G. Storrs, CT 06269-3136, USA www.ims.uconn.edu book 08
University of Connecticut Institute of Materials Science Huang, S.J. Storrs, CT 06269-3136, USA www.ims.uconn.edu/polymer/fa book 08
culty/huang.htm
Polymer Materials Research vakgroep organische chemie Lemmoughi, Y.; Krijgslaan 281 S4bis, Gent, polyphosphazenes http://www.rug.ac.be/index_e.ht book 10
Group;University of Gent Schacht, E. Belgium ml
University of Hamburg Inst. Of Inorganic and Applied Epple, M. Martin Luther King Platz 6, D- Porous polyglycolide/ http://www.chemie.uni- JBMR 43
Chemistry 20146 Hamburg, Germany wound healing/ bone hamburg.de/ac/
regeneration
University of Kentucky College of Pharmacy Thanoo, B.C. Lexington, KY 40536-0082, polyester http://www.uky.edu/Pharmacy/
USA
Bascom Palmer Eye Dept. of Ophtalmology Parel, J.-M.; Miami, Florida 33136, USA Poly(a-hydroxyacids)/ spinal JBMR 42
Institue, University of Miami Gautier, S.M. cord
School of Medicine
University of Michigan Depts. Of Biologic and Ma, P.X.; Zhang, Ann Harbor, MI 48109, USA nanoscale fibrous http://www.bme.umich.edu/ CA
Materials Sciences R. extracellular matrix 131:134571
University of Michigan Depts. of biologic and Mooney, D.J.; Ann Arbor, Michigan 48109- tissue engineering http://www.engin.umich.edu/dep book
Materials Sci. and Chemical Wong, W.H. 2136, USA t/cheme/ 12/JBMR 42
Engineering
University of Montpellier 1 Faculty of Pharmacy Vert, M. 15 avenue Charles Flahault, http://www.univ- book 08
34060 Montpellier, France montp1.fr/CentresDeRecherche
/Pharma/crba.htm
University of Montreal Fac. Of Pharmacy Hildgen, P.P. Montreal, H3C-3J7, Canada polyester http://www.pharm.umontreal.ca/
Division of Mechanical Mechanical, materials, Rudd, D.C. UK PCT Int. Appl. WO 9911297 http://www.nottingham.ac.uk/sc CA
Engineering, A54University manufacturing engineering A2 11 Mar. 1999 hool4m 130:227736
of Nottingham+A77 and management
Laboratoire de Physio- Faculte de Pharmacie Couvreur, P. URA CNRS 1218, Paris, poly(alkylcyanoacrylates) http://www.u-
Chimie, Pharmacotechnie, France psud.fr/Chatenay/Pharmacie.ns
Bio; University of Paris XI f
University of Puerto Rico Dept. of Chemistry Carrasquillo, K.G.; San Juan hormone delivery; PLGA CA
Griebenow, K. films 130:187092
494
Dept. of Ophtalmology, Health Science Center Garcia, C.A. 6411 Fannin, Houston, PLA-PGA in orthopedics/ http://www.med.uth.tmc.edu/ book 05/
University of Texas Texas 77030, USA tissue regeneration/ retinal JBMR 46
pigment epithelium
transplantation
University of Texas Dept. of Plastic and Miller, M.J. 1515 Holcombe Blvd. Box poly(propylene fumarate)
Reconstructive Surgery 62, Houston, Texas 77030,
USA
University of Twente Dept. of Chemical Engineering Feijen, J. P.O.Box 217, 7500 AE http://pbm.ct.utwente.nl/
and Institute of Biomedical Enschede, The Netherlands
Engineering
Center for Controlled School of medicine Andriano, K.P.; Salt Lake City, Utah, USA Orthopedic http://www.med.utah.edu/som/ book 05
Chemical Delivery, Daniels, A.U.
University of Utah
University of Utah Dept. of Pharmaceutics and Kim, Sung Wan Salt Lake City, Utah 84112, polyesters; drug delivery http://www.pharmaceutics.utah.
Pharmaceutical Chemistry USA edu/kim/personnel/swkim.html
Fac. Of Pharmacy, Dept. of Pharmaceutics Crommelin, D.J.A.; P.O. Box 80.082, 3508 TB http://www.pharm.uu.nl/
University of Utrecht Hennink,W.E. Utrecht, The Netherlands
Walter Reed Army Medical Mayer, M.H. Washington D.C. , USA bone fixation devices book 11
Center
Wilford Hall Medical Center Dept. of Orthopaedic Surgery Yaszemski, M.J. Texas 78236, USA poly(propylene fumarate)
Tampere University of Dept. of Materials Engineering Prof. Pertti P.O.Box 527, FIN-33101 poly(D,L)lacticacid http://www.tut.fi/units/ms/biom/
Technology Törmälä Tampere, Finland
Wuhan University of Institute of Materials Science Fu, J.; Li, S. Wuhan 430070, Peop. Rep. CA
Technology and Engineering China 131:229636
Note:
The book 11/12 in the ref. Colume correspond to those in the table of Appendix 4.7
495