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I. INTRODUCTION
A rising awareness about health concerns such as diabetes, obesity, and heart diseases has
caused a growing demand for low-calorie products. One contributor of calories in our bodies
comes from added sugar which has little vitamins and minerals. Added sugars, which include
raw sugar, brown sugar, corn syrup, high-fructose corn syrup, malt syrup, maple syrup, and sugar
molecules like dextrose, fructose, lactose, maltose, and sucrose, are the type of sweeteners that
are added to food and beverages during the process. Theses added sugars have many calories but
have little nutritional value. Since there is a need to reduce these added sugars in our diet, the
demand for polyols, also known as sugar alcohols, increased. Polyols, which are often used as
sweetener alternative in low-calorie food, includes sorbitol, mannitol, xylitol, maltitol, lactitol,
erythtritol and isomalt. These polyols have their own sweetness but contains fewer calories.
Erythtritol, a four-carbon sugar alcohol with a chemical formula of C4H10O4, is a lowcalorie substitute for sugar that naturally occurs in fruits such as grapes, pears and watermelons
and in fermented products such as wine, beer, sake, soy sauce, miso bean paste and cheese. It is a
sugar alcohol that has around 60 to 70 percent of the sweetness of sugar but contains less than
0.2 calories per gram. These properties of erythtritol are essential in food and beverage industry.
The application of erythritol is not only limited as an alternative sweetener, it can also
serve as a flavor enhancer, stabilizer, humectant, thickener and formulation aid (Jovanovic et al.,
2014). Erythritol can also be hydrogenated to form hydrocarbons such as butane, butene,
butadiene, and butane-diol (Amada et al., 2012).
oxidation
and
reduction
of
4,6-o-ethylidene-D-glucose,
reduction
of
formaldehyde polymers and hydrogenolysis of sorbitol (Park et al., 2000; Dezeeuw et al., 1973).
Erythtritol can also be produced synthetically by treating an aqueous alkali carbonate solution
with 2-butene-1,4-diol with chlorine and saponifying the chlorohydrin (Dezeeuw et al., 1973).
Production of erythtritol using chemical routes are often expensive and complex. Hence, many
manufacturers produce erythtritol via fermentation.
For industrial production of erythtritol the most common process is through fermentation
using corn as the starting material. Fermentation is usually used because of its simple and low
cost process. In this biological method, various microorganisms are used as yeasts such as
Candida magnolia (Ryu et al., 2000), Yarrowia lipolytica (Tomaszewska et al., 2012), Torula sp
(Kim et al., 2000), Moniliella sp. (Lin et al., 2001), and Trichoderma reesei (Jovanoic et al.,
2014). Other yeasts from the genus of Trichosporonoides and genus of Aureobasidium can also
be used in the fermentation process. After the fermentation, impurities are eliminated. The
erythtritol will then undergo crystallization process to obtain a high purity.
With erythtritols advantages in health and in polyol market and by using the inexpensive
and simple process of fermentation, continuous interest about the production of erythtritol will
keep on increasing.
Erythritol
1,2,3,4 Tetrahydroxybutane; Phycitol; meso-Erythritol
149-32-6
205-737-3
C4H10O4
May cause eye irritation with susceptible person.
May cause skin irritation in susceptible person.
May cause irritation of respiratory tract.
Melting Point
Relative Density
Bulk Density
Specific Gravity
Vapor Pressure
Solubility
Viscosity
Evaporation rate
Risk of Explosion
Class St 1
CAS Number
149-32-6
7732-18-5
% by Weight
99.5
.5
D Uses of Erythritol
Category
Examples
Pharmaceuticals
Beverages
Cosmetics
sweetness.
Used as preservatives in cosmetic and personal care
Food
Other Industries
Handling
Product Packaging
fume hood.
Ground all equipment containing material.
25 kgs plastic woven bags.
Transportation
Disposal
A. Technical specification
Cassava plants can reach up to 4 m in height. Cassava fruits can have a diameter of up to
5 to 10 cm and a length of 15 to 30 cm.
B. Physical and Chemical Properties of Cassava
Physical State
Colour
Odor
Solubility
Flammability limits (%)
Decomposition Point (C)
pH
Powder
White
Neutral
Insoluble in Water
As dust. Min 15g/m3
>150
5-7 (30% suspension)
CAS number
9005-25-8
proportion
>=98%
D. Uses of Cassava
Use
Avoid skin and eye contact and breathing in dust. In common in many
Storage
Linamarase (Enzyme)
An enzyme in the plants which liberates hydrocyanic glycosides in the
same plant. Boiling for 10 minutes destroys the enzyme and renders the
material. Many authors have best suggested the inoculation of fermenting
cassava with a linamarase-producing microorganism to reduce the garri
toxicity.
A. Physical properties
Appearance
Form
Solid
Colour
Off white
Odour
Odourless
B. Composition/information on ingredients
Chemical Characterization
Substances
9001-22-3 glucodidase
EC number
232-589-7
Index number
647-001-00-8
C. Uses of Linamarase
Uses
Handling
Storage
Alpha amylase
The amalyses are enzymes that work by hydrolyzing the straight chain
bonds between the individual glucose molecules that make up the starch
chain.
Physical state
Powder
Appearance
Solid
pH
Fermentation odor
Solubility in water
10g/L (20C)
Vapor density
Not available
Evaporation rate
Not available
Viscosity
Not available
Boiling point
Not available
Not available
Decomposition temperature
Not available
Solubility
liquid
Specific gravity/density
Not available
Molecular formula
Not available
Molecular weight
Not available
CAS #
Chemical Name
EINECS/ELINCS
IUB
9000-90-2
Alpha-Amylase
232-565-6
3.2.1.1
C. Use of Alpha-amylase
Use
Handling
Wash
thoroughly
after
handling.
with
water.
Keep
from
Sodium Hydroxide
Caustic Soda
1310-73-2
NaOH
Sodium hydroxide LD50: Not available. LC50: Not available.
Odorless
Not available
40 g/mole
13.5 [Basic]
1388C (2530.4F)
323C (613.4F)
2.13 (Water = 1)
Not applicable
Not available
Easily soluble in cold water
CAS#
1310-73-2
% by Weight
100
Storage