WELCOME
Muhammad Abdul Jalil
Department of Pharmacy,
University of Chittagong
NUCLEOTIDE
Nucleotides are organic molecules consisting of a
nucleoside( contain one nitrogenous base & a
pentose sugar) and one or more phosphate group.
Nucleotides are the monomer of DNA
(Deoxyribonucleic acid) and RNA (Ribonucleic acid)
both of which are essential bio-molecules within all
life-forms on Earth.
• Pentose sugar : Deoxyribose sugar
and Ribose sugar.
• Phosphate : Two nucleotide link-
up by phosphate group and create
polynucleotide.Ex-DNA,RNA.
• Nitrogenous base: One or two ring bases that contains Nitrogen
in the ring.Two types-
1. Purine base - larger double ring structure. Ex:
Adenine(A),Guanine(G).
2. Pyrimidine base – single ring structure. Ex:
Cytosine(C),Thymine(T),Uracil(U).
Types of nucleotides:
1. Purine(Adenine & Guanine) nucleotide.
2. Pyrimidin(Thymine,Cytosine & Uracil)
nucleotide.
Pathways for the biosynthesis of nucleotides: Nucleotide
biosynthesis in the cell can be grouped into two broad classes –
1. De-novo synthesis (synthesis from scratch): It is a biochemical
pathway in which nucleotides are synthesized new from simple
precursor molecules.Such as sugar or amino acids.
2. Salvage pathway ( recycle pathway): This pathway is used to
recover bases and nucleosides formed during the degradation of
RNA and DNA.
PURINE SYNTHESIS
De-novo pathway:
ATP GTP
Adenylsuccinate
synthetase
IMP
dehydrogenase
Adenylsuccinate lyase
GMP
synthetase
PURINE SYNTHESIS
Salvage pathway :
purine or pyrimidine
bases or nucleosides Nucleotides
ANTICANCER DRUGS
Structural analogues purine synthesis inhibitors:
This structural analogues act as competitive
inhibitor of the naturally occurring nucleotides
that are used to synthesized DNA.when wrong
Bases are in corporated the DNA becomes
functionally inactive. There by cell division is
Arrested,so they are useful as anticancer drug.
Example :
Mercaptopurine
Azaserine
Inhibits the conversion of
IMP to GMP & AMP
Glutamine antagonist
PYRIMIDINE
BIOSYNTHESIS
De-novo synthesis :
II(CPSII)
3.Aspartate
transcarbamoylase
3’Dihydroorotase
4.Dihydroorotate
dehydrogenase
5.OPRT
6.OMP decarboxylase
6’CTP synthase
7.Ribonucleotide reductase
10.Thymidylate
Synthase,N5,N10 Methyl
THF.
**CAD tri-functional enzyme
**3 rate limiting enzyme
**CPSII most regulated enzyme
PYRIMIDINE SYNTHESIS
THANK YOU

Nucleotide Metabolism

  • 1.
  • 2.
    Muhammad Abdul Jalil Departmentof Pharmacy, University of Chittagong
  • 3.
    NUCLEOTIDE Nucleotides are organicmolecules consisting of a nucleoside( contain one nitrogenous base & a pentose sugar) and one or more phosphate group. Nucleotides are the monomer of DNA (Deoxyribonucleic acid) and RNA (Ribonucleic acid) both of which are essential bio-molecules within all life-forms on Earth.
  • 4.
    • Pentose sugar: Deoxyribose sugar and Ribose sugar. • Phosphate : Two nucleotide link- up by phosphate group and create polynucleotide.Ex-DNA,RNA. • Nitrogenous base: One or two ring bases that contains Nitrogen in the ring.Two types- 1. Purine base - larger double ring structure. Ex: Adenine(A),Guanine(G). 2. Pyrimidine base – single ring structure. Ex: Cytosine(C),Thymine(T),Uracil(U).
  • 5.
    Types of nucleotides: 1.Purine(Adenine & Guanine) nucleotide. 2. Pyrimidin(Thymine,Cytosine & Uracil) nucleotide.
  • 6.
    Pathways for thebiosynthesis of nucleotides: Nucleotide biosynthesis in the cell can be grouped into two broad classes – 1. De-novo synthesis (synthesis from scratch): It is a biochemical pathway in which nucleotides are synthesized new from simple precursor molecules.Such as sugar or amino acids. 2. Salvage pathway ( recycle pathway): This pathway is used to recover bases and nucleosides formed during the degradation of RNA and DNA.
  • 8.
    PURINE SYNTHESIS De-novo pathway: ATPGTP Adenylsuccinate synthetase IMP dehydrogenase Adenylsuccinate lyase GMP synthetase
  • 9.
    PURINE SYNTHESIS Salvage pathway: purine or pyrimidine bases or nucleosides Nucleotides
  • 10.
    ANTICANCER DRUGS Structural analoguespurine synthesis inhibitors: This structural analogues act as competitive inhibitor of the naturally occurring nucleotides that are used to synthesized DNA.when wrong Bases are in corporated the DNA becomes functionally inactive. There by cell division is Arrested,so they are useful as anticancer drug. Example : Mercaptopurine Azaserine Inhibits the conversion of IMP to GMP & AMP Glutamine antagonist
  • 11.
    PYRIMIDINE BIOSYNTHESIS De-novo synthesis : II(CPSII) 3.Aspartate transcarbamoylase 3’Dihydroorotase 4.Dihydroorotate dehydrogenase 5.OPRT 6.OMPdecarboxylase 6’CTP synthase 7.Ribonucleotide reductase 10.Thymidylate Synthase,N5,N10 Methyl THF. **CAD tri-functional enzyme **3 rate limiting enzyme **CPSII most regulated enzyme
  • 12.
  • 13.