Biochem PDH Complex

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42 Terms

1
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What is the main fate of pyruvate?

pyruvate dehydrogenase complex (PDH complex)

2
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Where is the PDH complex located?

mitochondrial matrix

3
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What type of reaction is the PDH complex reaction?

catabolic reaction

4
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What are the steps of the synthesis of acetyl CoA from pyruvate?

decarboxylation, oxidation, transfer to CoA

5
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What is the E1 enzyme in the PDH complex?

pyruvate dehydrogenase component

6
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What is the prosthetic group of the E1 enzyme?

TPP

7
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What is the reaction catalyzed by the E1 enzyme?

oxidative decarboxylation of pyruvate

8
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What is the E2 enzyme of the PDH complex?

dihydrolipoyl transacetylase

9
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What is the E3 enzyme of the PDH complex?

dihydrolipoyl dehydrogenase

10
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What is the prosthetic group of the E2 enzyme?

lipoamide

11
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What is the reaction catalyzed by the E2 enzyme?

transfer of acetyl group to CoA

12
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What is the prosthetic group of the E3 enzyme?

FAD

13
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What is the reaction catalyzed by the E3 enzyme?

regeneration of the oxidized form of lipoamide

14
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What does phosphorylation do to the PDH complex?

turns it off

15
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What are acetyl CoA and NADH to the PDH complex?

products and allosteric inhibitors

16
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What does low energy charge do to the PDH complex?

stimulate it

17
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Where does acetyl CoA go after the PDH complex?

the citric acid cycle

18
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What type of reaction is the citric acid cycle?

amphibolic, main cycle is catabolic but intersects with anabolic pathwaysW

19
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Where does the citric acid cycle take place?

the mitochondrial matrix

20
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How many turns of the citric acid cycle are there per glucose?

2AT

21
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What are allosteric inhibitors of the citric acid cycle?

ATP and NADH

22
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Does the TCA cycle change the net concentration of oxaloacetate in the cell?

no because it is recycled

23
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What does a high acetyl-CoA concentration mean?

not enough oxaloacetate, can’t be made into citrate

24
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What is the only enzyme that can catalyze the formation of oxaloacetate?

pyruvate carboxylase

25
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What are the irreversible steps of the citric acid cycle?

1,3,4

26
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What increases in concentration due to PDH complex deficiency?

pyruvate and lactate

27
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When does pyruvate convert to lactate?

low O2 or metabolic deficiency

28
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What enzyme catalyzes the formation of lactate from pyruvate?

lactate dehydrogenase

29
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What is the purpose of the remaining steps of the PDH complex after releasing acetyl CoA?

regenerate oxidized form of lipoyl group

30
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What are catalytic coenzymes?

those that are not consumed in the reaction

31
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What are the catalytic coenzymes in the PDH complex?

TPP, lipoic acid, FAD

32
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What are stoichiometric coenzymes?

those used as substrates

33
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What are the stochiometric coenzymes in the PDH complex?

CoA, NAD+

34
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What do the NADH and FADH2 produced by the citric acid cycle do?

relay electrons extracted from food to the electron transport chain

35
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What is the enzyme of step 4 of the citric acid cycle similar to?

the PDH complex, same cofactors, E3 identical, also affected by complex deficiency

36
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What are the fates of oxaloacetate?

combine with acetyl CoA to form citrate, used to form glucose in gluconeogenesis, forms aspartate which forms other amino acids, purines, and pyrimidines

37
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What enzyme regulates step 1, acetyl CoA + oxaloacetate —→ citrate, of the citric acid cycle?

citrate synthase

38
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What happens to oxaloacetate when energy charge is high?

anabolic pathways decrease amount of oxaloacetate in the cell

39
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What happens to oxaloacetate when energy charge is low?

rate of TCA cycle increases: need more oxaloacetate

40
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Where is pyruvate converted to lactate?

cytoplasm

41
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What are problems caused by PDH complex deficiency?

lactic acidosis, hyperventilation, muscle pain and weakness, abdominal pain, and nausea

42
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Is the citric acid cycle completely stopped when there is PDH complex deficiency?

no