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What is the main fate of pyruvate?
pyruvate dehydrogenase complex (PDH complex)
Where is the PDH complex located?
mitochondrial matrix
What type of reaction is the PDH complex reaction?
catabolic reaction
What are the steps of the synthesis of acetyl CoA from pyruvate?
decarboxylation, oxidation, transfer to CoA
What is the E1 enzyme in the PDH complex?
pyruvate dehydrogenase component
What is the prosthetic group of the E1 enzyme?
TPP
What is the reaction catalyzed by the E1 enzyme?
oxidative decarboxylation of pyruvate
What is the E2 enzyme of the PDH complex?
dihydrolipoyl transacetylase
What is the E3 enzyme of the PDH complex?
dihydrolipoyl dehydrogenase
What is the prosthetic group of the E2 enzyme?
lipoamide
What is the reaction catalyzed by the E2 enzyme?
transfer of acetyl group to CoA
What is the prosthetic group of the E3 enzyme?
FAD
What is the reaction catalyzed by the E3 enzyme?
regeneration of the oxidized form of lipoamide
What does phosphorylation do to the PDH complex?
turns it off
What are acetyl CoA and NADH to the PDH complex?
products and allosteric inhibitors
What does low energy charge do to the PDH complex?
stimulate it
Where does acetyl CoA go after the PDH complex?
the citric acid cycle
What type of reaction is the citric acid cycle?
amphibolic, main cycle is catabolic but intersects with anabolic pathwaysW
Where does the citric acid cycle take place?
the mitochondrial matrix
How many turns of the citric acid cycle are there per glucose?
2AT
What are allosteric inhibitors of the citric acid cycle?
ATP and NADH
Does the TCA cycle change the net concentration of oxaloacetate in the cell?
no because it is recycled
What does a high acetyl-CoA concentration mean?
not enough oxaloacetate, can’t be made into citrate
What is the only enzyme that can catalyze the formation of oxaloacetate?
pyruvate carboxylase
What are the irreversible steps of the citric acid cycle?
1,3,4
What increases in concentration due to PDH complex deficiency?
pyruvate and lactate
When does pyruvate convert to lactate?
low O2 or metabolic deficiency
What enzyme catalyzes the formation of lactate from pyruvate?
lactate dehydrogenase
What is the purpose of the remaining steps of the PDH complex after releasing acetyl CoA?
regenerate oxidized form of lipoyl group
What are catalytic coenzymes?
those that are not consumed in the reaction
What are the catalytic coenzymes in the PDH complex?
TPP, lipoic acid, FAD
What are stoichiometric coenzymes?
those used as substrates
What are the stochiometric coenzymes in the PDH complex?
CoA, NAD+
What do the NADH and FADH2 produced by the citric acid cycle do?
relay electrons extracted from food to the electron transport chain
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
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
What enzyme regulates step 1, acetyl CoA + oxaloacetate —→ citrate, of the citric acid cycle?
citrate synthase
What happens to oxaloacetate when energy charge is high?
anabolic pathways decrease amount of oxaloacetate in the cell
What happens to oxaloacetate when energy charge is low?
rate of TCA cycle increases: need more oxaloacetate
Where is pyruvate converted to lactate?
cytoplasm
What are problems caused by PDH complex deficiency?
lactic acidosis, hyperventilation, muscle pain and weakness, abdominal pain, and nausea
Is the citric acid cycle completely stopped when there is PDH complex deficiency?
no