Pyruvate dehydrogenase complex Flashcards
1
Q
Location, function, condition
A
- mitochondrial matrix
- catalyzes irreversible oxidative carboxylation of pyruvate to acetyl CoA
- aerobic
2
Q
Enzymes
A
metabolic: -E1: pyruvate decarboxylase -E2: dihydrolipoyl transacetylase -E3: dihydrolipoyl dehydrogenase regulatory: -PDH kinase( inactivates PDHC) -PDH phosphatase( Activates by phosphorylating E1)
3
Q
First reaction of PDHC
A
pyruvate + thioamine pyrophosphate(TPP) + H+ -> Hydroxyethylthioamine pyrophosphate (HETPP) + CO2
- TPP produced from ATP and vitamin thiamine
- enzyme: PYRUVATE DECARBOXYLASE
4
Q
Second reaction of PDHC
A
Hydroxyethylthioamine pyrophosphate + Lipoamide -> Acetyl-dihydrolipoamide + Thioamine pyrophosphate carboanion
-enzyme: DIHYDROLIPOYL TRANSFERASE
5
Q
Third reaction of PDHC
A
Acetyl-dihydrolipoamide + SH-CoA -> Acetyl CoA + dihydrolipoamide
- acetyl CoA used in TCA or lipid biosynthesis
- enzyme: DIHYDROLIPOYL TRANSFERASE
6
Q
Fourth reaction of PDHC
A
Dihydrolipoamide + FAD -> Lipoamide + FADH2
-enzyme: DIHYDROLIPOYL DEHYDROGENASE
7
Q
Allosteric regulation (of kinase that inactivates PDH)
A
phosphorylated (inactive) / dephosphorylated (active) \+ NADH \+ acetyl CoA \+ pyruvate - NAD+ - SH-CoA - ADP
- Covalent modification
- Arsenic
8
Q
PDHC diseases
A
- Beriberi
- E1/E2 defect
- E3 defect
9
Q
Acetyl CoA
A
- acyl carrier
- derived from pantothenic acid
- production-energy dependent process(G=-32,5kJ/mol)
10
Q
Transport of Acetyl CoA through inner mitochondrial membrane
A
- Carnitine acyltransferase 1
2. Carnitine acyltransferase 2