Pyruvate dehydrogenase complex Flashcards

1
Q

Location, function, condition

A
  • mitochondrial matrix
  • catalyzes irreversible oxidative carboxylation of pyruvate to acetyl CoA
  • aerobic
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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)
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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
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4
Q

Second reaction of PDHC

A

Hydroxyethylthioamine pyrophosphate + Lipoamide -> Acetyl-dihydrolipoamide + Thioamine pyrophosphate carboanion
-enzyme: DIHYDROLIPOYL TRANSFERASE

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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
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6
Q

Fourth reaction of PDHC

A

Dihydrolipoamide + FAD -> Lipoamide + FADH2

-enzyme: DIHYDROLIPOYL DEHYDROGENASE

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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
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8
Q

PDHC diseases

A
  • Beriberi
  • E1/E2 defect
  • E3 defect
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9
Q

Acetyl CoA

A
  • acyl carrier
  • derived from pantothenic acid
  • production-energy dependent process(G=-32,5kJ/mol)
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10
Q

Transport of Acetyl CoA through inner mitochondrial membrane

A
  1. Carnitine acyltransferase 1

2. Carnitine acyltransferase 2

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