Chemistry of Nucleic Acids..slide
Chemistry of Nucleic Acids..slide
Chemistry of Nucleic Acids..slide
NUCLEIC ACIDS
dr. Winarsi
DNA and RNA are nucleic acids (deoxyribonucleic acids
and ribonucleic acids).
Nucleic acid is a polymer of nucleotides.
A nucleotide consisits of:
1. a heterocyclic nucleobase (purine or pyrimidine),
2. a pentose sugar (ribose or deoxyribose),
3. A phosphate or polyphosphate group
(monophosphate, diphosphate, or triphosphate).
Nucleotides are phosphate esters of C5 sugars (ribose or
deoxyribose) linked to a nitrogenous base.
The purine bases, adenin and guanin are 2 purines found in all
nucleic acids.
The pyrimidine bases
Nucleosides:
- in DNA : deoxyadenosine, deoxyguanosine, deoxycytidine,
deoxythymidine.
- in RNA : adenosine, guanosine, cytidine, uridine.
Nucleotides:
- in DNA: deoxyadenilate (dAMP), deoxyguanylate (dGMP),
deoxycytidylate (dCMP), thymidylate (dTMP).
- in RNA: adenylate (AMP), guanylate (GMP), cytidylate (CMP),
uridilate (UMP).
Primary polymeric structure of nucleic acids.
Linkage of nucleotides.
Nucleotides are linked together by phosphodiester bonds between
the 3’ hydroxyl on the sugar of one nucleotide through a
phosphate molecule to the 5’ hydroxyl on the sugar of another
nucleotide.
The sugar-phosphate linkages form a symmetrical “backbone”,
with the 5’ end of one sugar always linked through a phosphate
molecule to the 3’ end of the adjacent sugar.
It is standard to use the one-letter abbreviation for the bases when
writing the order of nucleic acid polymer. By convention, DNA
sequences are written in the 5’ to 3’ direction.
DNA secondary structure.