Professional Documents
Culture Documents
METABOLISM
Naresh panigrahi
Gitam university
Nucleic Acid
Definition
• The nitrogenous bases found in DNA are adenine, guanine, cytosine and
thymine.
• Adenine and guanine are purine bases while cytosine and thymine are
pyrimidnes.
• They are linked by a phosphate group on the 5th position of sugar residue
becomes linked to 3' hydroxyl group of the preceeding sugar molecule.
• The double stranded model of the DNA was worked out by Watson and
Crick in 1953.
• The double helix model consists of two strands wound around a central
axis with the bases stacked inside.
• The order of the strand is in opposite directions, i.e., from 5' to 3' direction
in one and 3'to 5' direction in the other.
• The bases stacked in the center of the helix as they interact with each
other through weak hydrogen bonds.
• Hydrogen bonds are weaker than covalent bonds, they are continually
forming and disassociating.
• In the double stranded nucleic acids, the adenine form hydrogen bonds
only with thymine (or uracil) molecule. While cytidine will only form
hydrogen bonds with guanine.
• The per cent of the G-T and the A-T is variable from species to species.
•The base pairs form a flat plain in the helix, the adenine
forming two hydrogen bonds with thymine, and the
cytidine forming three bonds with guanine.
•Using the concept of base pairing, all the enzymes and
substrates necessary, the two DNA strands when copied
separately, wherever there is adenine in the original
strand, the duplicated strand will have thymidine, and
guanine would be matched to cytosine.
•After replication, each original strand (parent strand), is
paired with a new (daughter) strand. This type of
replication is known as semi-conservative mode of
duplication.
•The double stranded DNA can be denatured by alkaline
conditions or heat.
Nucleoside, Nucleotide & Nucleic acid
phosphate
sugar base
phosphate phosphate
sugar base
sugar base sugar base
phosphate
nucleoside nucleotides
sugar base
nucleic acids
Dr Siham Gritly 8
DNA, RNA and the nucleobases
Dr Siham Gritly 11
Functions of Nucleic Acids
• The main functions is store and transfer genetic information.
• The deoxyribonucleic acid is the storage for place for genetic information in the cell.
• The genetic information is transmitted from DNA to the protein synthesizers in the cell.
• RNA also directs the production of new protein by transmitting genetic information to the protein building
structures.
• The function of the nitrogenous base sequences in the DNA backbone determines the proteins being
synthesized.
• The function of the double helix of the DNA is that no disorders occur in the genetic information if it is lost
or damaged.
• r-RNA are mostly present in the ribosomes, and responsible for stability of m-RNA.
• Deoxyribonucleotide; monomeric building
block of DNA; a phosphate group and a
nitrogenous base both bonded to deoxyribose
• Ribonucleotide; monomeric building block of
RNA; a phosphate group and a nitrogenous
base both bonded to ribose sugar
• Duplex; two complementary strands of DNA
• Mutant; genetically altered species or cell
Dr Siham Gritly 14
• Nucleoside; nitrogenous base bonded to ribose
or deoxyribose
• Nucleotide; monomeric building block of
RNA and DNA; a phosphate group and a
nitrogenous base both bonded to ribose or
deoxyribose
• Nucleic Acids are Polynucleotides
• Phosphodiester; two different alcohols
forming ester linkages with one phosphate ion
Dr Siham Gritly 15
• Replication; DNA synthesis
• Template; a section of DNA which is being
replicated or transcribed; mRNA which is
being translated
• Transcription; synthesis of RNA from DNA
• Translation; synthesis of proteins from an
RNA template
16
Nucleotides
Nucleoside phosphates
• Nucleotides are monomers of nucleic acids
Dr Siham Gritly 17
Nucleotide Structures of purine and pyrimidine
Heterocyclic ring compounds
Nitrogenous Bases
Dr Siham Gritly 19
The derivatives of purine ; adenine and guanine (found in both
DNA & RNA) 1-Adenine 6-aminopurine, 2-Guanine 2-amino-
6-oxypurine
Dr Siham Gritly 20
the derivatives of pyrimidine are thymine, cytosine and uracil.
Cytosine- 2-oxy-4-aminopyrimidine, Uracil-n2,4-
dioxypyrimidineThymine-2,4-dioxy-, 5-methyl
Dr Siham Gritly 21
• The common abbreviations used for these five
bases are, A, G, T, C and U.
Dr Siham Gritly 22
Nucleotides mainly;
Pentose sugar+ β-N-glycosidic bond+
phosphoryl group
Dr Siham Gritly 23
Nucleotides mainly;
1-pentose sugar. 2-phosphate groups. 3-a
nitrogeous base
• 1-5–carbon sugar component
• Ribose
• Deoxyribose
Dr Siham Gritly 24
5–carbon sugar component; Ribose and Deoxyribose
Furanose structures
Dr Siham Gritly 25
• 2-Phosphate group Attached to the sugar's
5' carbon with a phosphodiester bond
• 3-Nitrogen Base component attached to the
sugar's 1'carbon.
Dr Siham Gritly 26
Nucleosides
• Nucleoside consist of purine and pyrimidine
bases and a sugar β-D-ribose or β-D-2-
deoxyribose linked through a covalent β-N-
glycosidic bond
• Therefore Nucleosides are Formed by Joining
a Nitrogenous Base to a Sugar
• Base is linked via a β-N-glycosidic bond
Dr Siham Gritly 27
β-N-glycosidic bond linked nitrogen-9 of the purine
base or nitrogen-1 of the pyrinidine base with
carbon1 of pentose sugar
Dr Siham Gritly 28
• The nucleosides of A, G, C,T, U are named
• Adenine ---Adenosine
• Guanine ----Guanisine
• Cytosine ----Cytidine
• Thymine ----Thymidine
• Uracil -----Uridine
• Purine nucleosides end “osine”
• Pyrinidine ends in “idine”
• Ribose sugar produced; ribonucleoside
• 2-deoxyribose sugar produced;
deoxyribonucleosides
Dr Siham Gritly 29
Common nucleosides
30
The genetic code