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Dr. Farhana Atia
Assistant Professor
Department of Biochemistry
Nilphamari Medical College, Nilphamari
Email: farhana.atia@gmail.com
FUNDAMENTALS OF MOLECULAR BIOLOGY
AND GENETICS
NUCLEIC ACID
ī‚¨ DNA
ī‚¨ RNA
ī‚¨ NA are polymer of nucleotide covalently linked
with one another.
ī‚¨ Nucleotide: Building blocks of NA consisting
ī‚¤ Nitrogenous base
ī‚¤ Pentose sugar
ī‚¤ Phosphate group
ī‚¤ Nucleoside: Derivatives of purine & pyrimidine
that have a sugar linked to a ring nitrogen.
(base+ sugar).
NITROGENOUS BASE
Nitrogenous base
īŽPurine: adenine, guanine
īŽPyrimidine: cytosine, uracil, thymine
īŽUnusual base
ī‚¨ Heterogenous ring
ī‚¨ Numbered as
ī‚¤ 1-6 in pyrimidine
ī‚¤ 1-9 in purine
SUGAR
ī‚¨ Sugar
ī‚¤Deoxyribose
ī‚¤Ribose
ī‚¨ Ring
ī‚¨ C are numbered as
1′- 5′ (prime)
ī‚¨ Structure
PURINE
ī‚¨ 9 MEMBERED RING
ī‚¨ Arranged in anti-clockwise
ī‚¨ Adenine : 6 amino purine
ī‚¨ Guanine : 2 amino 6 oxopurine
ī‚¨ Unusual base (during metabolism of
purine)
ī‚¤Hypoxanthine : 6 oxopurine
ī‚¤Xanthine : 2, 6 dioxopurine
ī‚¤Uric acid : 3 oxopurine
Adenine Guanine
ī‚¨ Pharmacologically
Methylated purine of plants have
pharmacological properties
ī‚¤ Methylated xanthine derivative of caffeine of
coffee (1, 3, 7 trimethyl xanthine)
ī‚¤ Theophylline of tea ( 1, 3 dimethyl xanthine)
ī‚¤ Theobromine of coca ( 3, 7 dimethyl xanthine)
PYRIMIDINE
ī‚¨ 6 membered ring
ī‚¨ Arranged in clockwise direction
ī‚¨ Cytosine : 2 oxo 4 amino pyrimidine
ī‚¨ Uracil : 2, 4 dioxo pyrimidine
ī‚¨ Thymine : 2, 4 dioxo 5 methyl pyrimidine (only
base that have methyl group)
ī‚¨ Methylation : 5 methyl cytosine
ī‚¨ Hydroxy methylation : 5 hydroxy methyl
cytosine
ī‚¨ Glycosylation & acetylation : 4 acetyl cytosine
ī‚¨ Uracil : 2, 4 dioxo pyrimidine
ī‚¨ Thymine : 2, 4 dioxo 5 methyl pyrimidine
ī‚¨ Cytosine : 2 oxo 4 amino pyrimidine
Base Nucleoside Nucleotide
Adenine Adenosine
AMP
ADP
ATP
Guanine Guanosine
GMP
GDP
GTP
Cytosine Cytidine CMP
Uracil Uridine UMP
Thymine Thymidine TMP
Position of attachment
ī‚¨ Nucleoside consists of purine/ pyrimidine & a
cyclized sugar.
ī‚¨ Most of a D-ribose or 2′ deoxyribose linked
via a covalent β N glycosidic bond to N9 of
purine & N1 of pyrimidine.
ī‚¨ Numbering of a sugar atom employ a prime,
distinguished sugar from those of heterocyclic
base.
Nucleoside
NUCLEOTIDE
ī‚¨ Mono, di or tri phosphate ester of nucleoside.
ī‚¨ First PO₄ group is attached by an ester
linkage to the 5′ hydroxyl group of pentose.
ī‚¨ DNA- 5′ deoxyribonucleotide
ī‚¨ RNA- 5′ ribonucleotide
ī‚¨ 2nd & 3rd PO₄ groups are attached by high
energy phosphate bond.
ī‚¨ PO₄ groups are responsible for negative
charge of Ntide & Nside.
FUNCTIONS OF N’TIDE
ī‚¨ Essential for all living cells. DNA & RNA can
not be synthesized without nucleotide.
ī‚¨ N’tide has group transfer potential or
participate in energy transfer (ie. Energy
currency of cell).
ī‚¨ Serve as a carrier of activated intermediates in
the synthesis of some carbohydrate, lipid &
protein, Eg. UDP-glucose, UDP-galactose.
ī‚¨ Act as a physiological mediator. Eg. C-AMP, c-
GMP, ADP in platelet agregation.
ī‚¨ As a 2nd messenger participate in diverse
regulatory functions of cells.
ī‚¤ Inhibit or activate key enzymes- c-AMP
dependent protein kinase
ī‚¤ ADP level regulates the rate of mitochondrial
phosphorylation.
ī‚¨ Structural component of coenzymes- NAD,
NADP, FAD, FMN.
ī‚¨ Allosteric modifier of some enzymes- ATP,
CTP
ī‚¨ Act as a carrier of active molecule in anabolic
process (CHO, prot, lipid)
ī‚¨ Synthetic N’tide analog are used as
chemotherapy- Allopurinol treat hyperuricemia &
gout.
ī‚¨ Non hydrolyzable analog of N’tide provide
research tool.
ī‚¨ Hazardous effect: N’tide absorb UVL. UVL is a
potent mutagen.
Nucleic acids are polynucleotide

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Molecular biology and genetics

  • 1. Dr. Farhana Atia Assistant Professor Department of Biochemistry Nilphamari Medical College, Nilphamari Email: farhana.atia@gmail.com FUNDAMENTALS OF MOLECULAR BIOLOGY AND GENETICS
  • 2. NUCLEIC ACID ī‚¨ DNA ī‚¨ RNA ī‚¨ NA are polymer of nucleotide covalently linked with one another. ī‚¨ Nucleotide: Building blocks of NA consisting ī‚¤ Nitrogenous base ī‚¤ Pentose sugar ī‚¤ Phosphate group ī‚¤ Nucleoside: Derivatives of purine & pyrimidine that have a sugar linked to a ring nitrogen. (base+ sugar).
  • 3. NITROGENOUS BASE Nitrogenous base īŽPurine: adenine, guanine īŽPyrimidine: cytosine, uracil, thymine īŽUnusual base ī‚¨ Heterogenous ring ī‚¨ Numbered as ī‚¤ 1-6 in pyrimidine ī‚¤ 1-9 in purine
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  • 5. SUGAR ī‚¨ Sugar ī‚¤Deoxyribose ī‚¤Ribose ī‚¨ Ring ī‚¨ C are numbered as 1′- 5′ (prime) ī‚¨ Structure
  • 6. PURINE ī‚¨ 9 MEMBERED RING ī‚¨ Arranged in anti-clockwise ī‚¨ Adenine : 6 amino purine ī‚¨ Guanine : 2 amino 6 oxopurine ī‚¨ Unusual base (during metabolism of purine) ī‚¤Hypoxanthine : 6 oxopurine ī‚¤Xanthine : 2, 6 dioxopurine ī‚¤Uric acid : 3 oxopurine
  • 8. ī‚¨ Pharmacologically Methylated purine of plants have pharmacological properties ī‚¤ Methylated xanthine derivative of caffeine of coffee (1, 3, 7 trimethyl xanthine) ī‚¤ Theophylline of tea ( 1, 3 dimethyl xanthine) ī‚¤ Theobromine of coca ( 3, 7 dimethyl xanthine)
  • 9. PYRIMIDINE ī‚¨ 6 membered ring ī‚¨ Arranged in clockwise direction ī‚¨ Cytosine : 2 oxo 4 amino pyrimidine ī‚¨ Uracil : 2, 4 dioxo pyrimidine ī‚¨ Thymine : 2, 4 dioxo 5 methyl pyrimidine (only base that have methyl group) ī‚¨ Methylation : 5 methyl cytosine ī‚¨ Hydroxy methylation : 5 hydroxy methyl cytosine ī‚¨ Glycosylation & acetylation : 4 acetyl cytosine
  • 10. ī‚¨ Uracil : 2, 4 dioxo pyrimidine ī‚¨ Thymine : 2, 4 dioxo 5 methyl pyrimidine ī‚¨ Cytosine : 2 oxo 4 amino pyrimidine
  • 11. Base Nucleoside Nucleotide Adenine Adenosine AMP ADP ATP Guanine Guanosine GMP GDP GTP Cytosine Cytidine CMP Uracil Uridine UMP Thymine Thymidine TMP
  • 12. Position of attachment ī‚¨ Nucleoside consists of purine/ pyrimidine & a cyclized sugar. ī‚¨ Most of a D-ribose or 2′ deoxyribose linked via a covalent β N glycosidic bond to N9 of purine & N1 of pyrimidine. ī‚¨ Numbering of a sugar atom employ a prime, distinguished sugar from those of heterocyclic base.
  • 14. NUCLEOTIDE ī‚¨ Mono, di or tri phosphate ester of nucleoside. ī‚¨ First PO₄ group is attached by an ester linkage to the 5′ hydroxyl group of pentose. ī‚¨ DNA- 5′ deoxyribonucleotide ī‚¨ RNA- 5′ ribonucleotide ī‚¨ 2nd & 3rd PO₄ groups are attached by high energy phosphate bond. ī‚¨ PO₄ groups are responsible for negative charge of Ntide & Nside.
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  • 16. FUNCTIONS OF N’TIDE ī‚¨ Essential for all living cells. DNA & RNA can not be synthesized without nucleotide. ī‚¨ N’tide has group transfer potential or participate in energy transfer (ie. Energy currency of cell). ī‚¨ Serve as a carrier of activated intermediates in the synthesis of some carbohydrate, lipid & protein, Eg. UDP-glucose, UDP-galactose. ī‚¨ Act as a physiological mediator. Eg. C-AMP, c- GMP, ADP in platelet agregation.
  • 17. ī‚¨ As a 2nd messenger participate in diverse regulatory functions of cells. ī‚¤ Inhibit or activate key enzymes- c-AMP dependent protein kinase ī‚¤ ADP level regulates the rate of mitochondrial phosphorylation. ī‚¨ Structural component of coenzymes- NAD, NADP, FAD, FMN. ī‚¨ Allosteric modifier of some enzymes- ATP, CTP
  • 18. ī‚¨ Act as a carrier of active molecule in anabolic process (CHO, prot, lipid) ī‚¨ Synthetic N’tide analog are used as chemotherapy- Allopurinol treat hyperuricemia & gout. ī‚¨ Non hydrolyzable analog of N’tide provide research tool. ī‚¨ Hazardous effect: N’tide absorb UVL. UVL is a potent mutagen.
  • 19. Nucleic acids are polynucleotide