L 42 Purine Nucleotide Biosyn Flashcards
Basic characteristics of bases
purines: 9 memebered bicyclic aromatic rings
- osine
- only one IMP not named by base: hypoxanthine, inosine, inosine monophosphate
- made of SIX components: aspartate, glycine, Amide of two glutamines, THF, CO2. ribose 5 phosphate (from HMP shunt) (all from AA)
- liver is the major site of synthesis, in CYTOSOL (most tissues limited in making purines)
pyrimidines : six membered planar aromatic rings
-idine
Nucleoside: base and sugar
Nucleotide: phophorylated nucleoside
-more negative: usually associated with Mg2+ as counter ion
PRPP Synthetase
RL step in puring and py synthesis(found in nearly ALL tissues)
- transfers pyrophosphate to group from ATP to R5P creating PRPP (activated sugar)
- allosterically inhibited by both pur and pu
Glutamine PRPP amido transferase
- FIRST COMMITED STEP TO PURING SYNTHESIS
- sequentially adds carbons and nitrogens directly to ribose moiety
- replaces pyrophosphate w/ amide nitrogen of glutaminee releasing glutamate and resulting in a 5PR Amine
- requires glutamine and H2O
- allosterically inhibited by AMP GMP IMP
- allosterically activated by PRPP
IMP Inosine Monophosphate Production
- six ATP required
- 2 N10F-THF required
- required for purines and thymidine
- deficiency in FOLIC ACID results in insufficient nucleotides for normal DNA replication and results in anemia - hypoxanthine in IMP is first recognizeable purine
- 7 of 9 stems to IMP are catalyzed by multifuntional enzymes
-after IMP formed the path splits to either AMP or GMP
Starting with IMP going to AMP and GMP, there are two levels of regulation
- the first committed step in each branch is allosterically regulated via feedback inhibition by its product (GMP and AMP)
- GTP supplies entegy for AMP syn and ATP supplies energy for GMP synthesis
NMP to NDP and NTP
specific nucleoside monophosphate kinases (adenylate kinase, guanylate kinase)
nucleoside DIphosphate kinases: broad specificty and will inter convert most nucleotides to thier triphosphate derivative.
ADP-ATP by ATP synthase in mitochondria (OxPhos)
ATP is present at highest concentration
Salvage Pathway: Recycling Nucleic acid breakdown products
extrahepatic tissues!!
APRT
- Adenine to AMP
- require PRPP
and HGPRT(most)
- hypxanthine to IMP
- guanine to GMP
- require PRPP
90% of daily purines come from salvage
salvage requires far less entergy (12 atp compared to 1 ATP)
regualtion:
- decrease in salvage makes more available to stimlate denovo syn
- decrease in salvage decreases nucleotides available to INHIBIT de novo syn.
Degradation of purines six steps
- DNA/RNA or high E compound (ATP/GTP) dephosphorylated to release AMP GMP
- AMP and GMP converted back to IMP
- AMP GMP IMP lost phophate group first (forming nucleosides) and thier sugar moeity (free bases)
- HGPRT is able to recycle from hypoxanthine or guanine and APRT is able to recyle Adenine
- if not recycled, converted to xanthine
- XO (Xanthide Oxidase) breaks down in two more steps to Uric Acid (STOP-what is the sig?).
NO ENERY PRODUCTION
-plamsa ammonia levels increase die to AMP degradation
slide 28?
balance of purine nucleotides
balance of uric acid produced and denovo purines synthesized change in direct relationship
increase in denovo prod, comparable increase in uric acid prod.