TCA Flashcards

1
Q

Are neverending amounts of NAD+ available in a cell?

A

No (limited)

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2
Q

What does glycolysis do to NAD?

A

reduces it

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3
Q

How is NAD regenerated?

A

through pyruvate metabolism

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4
Q

Where are enzymes for TCA?

A

matrix of mitochondrion

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5
Q

What catalyses the oxidative decarboxylation of pyruvate to acetyl-CoA?

A

pyruvate dehydrogenase complex (PDC)

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6
Q

How many enzymes does the pyruvate dehydrogenase complex (PDC) consist of?

A

3 enzymes involved in the actual reaction mechanism
E1, E2 and E3
2 enzymes involved in the control of PDC
(a kinase and a phosphatase in a single polypeptide)
5 coenzymes
thiamine, lipoic acid, coenzyme A, FAD, NAD+

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7
Q

Is oxidative decarboxylation of pyruvate to acetyl-CoA reversible?

A

No

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8
Q

How many reactions occur in total in TCA?

A

8

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9
Q

How many oxidation reactions occur?

A

4

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10
Q

How manny GTP molecules are formed?

A

1

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11
Q

Which enzyme of TCA is not located in the matrix of the mitrochondrion?

A

Succinate dehydrogenase (integrated in the inner mitochondrial membrane)

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12
Q

What does each turn of the TCA cycle involve in terms of carbon atoms?

A

the uptake of two carbon atoms in the form of acetyl-CoA and the release of two carbon atoms as CO2

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13
Q

How many pairs of electrons are transferred from NAD+ to form NADH + H+ per turn of cycle?

A

3

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14
Q

How many pairs of electrons are used to reduce FAD+ to FADH2 per turn of cycle?

A

1

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15
Q

Does high ADP and NAD+ mean high or low energy?

A

low

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16
Q

High succinyl-CoA and acetyl-CoA means what?

A

plenty of precursor molecules for biosynthetic reactions