TCA Cycle Flashcards

1
Q

Where does TCA cycle take place?

A

Mitochondrial matrix

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2
Q

How does pyruvate enter mitochondrion?

A

Pyruvate, hydroxide anti-transporter

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3
Q

How do fatty acids enter mitochondrion?

A

FACoA transporter

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4
Q

What are net products of TCA cycle?

A

6 NADH, 4 CO2, 2 FADH2, 2 ATP

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5
Q

What enzyme converts pyruvate to acetyl CoA?

A

Pyruvate dehydrogenase

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6
Q

What molecules inhibit pyruvate dehydrogenase complex?

A

Acetyl CoA, NADH (feedback inhibition)

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7
Q

How do carbohydrates, fatty acids, and proteins enter the TCA cycle?

A

Carbs - through glycolysis
Fatty acids - exclusively through acetyl CoA
Proteins - directly enter into TCA cycle

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8
Q

What are anaplerotic reactions?

A

Reactions that produce intermediates for TCA cycle

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9
Q

What vitamin is needed to make acetyl CoA? What kind of vitamin is it? What is its deficiency?

A

Pantatheine - B vitamin - no known deficiency

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10
Q

Where is pyruvate converted to acetyl-CoA?

A

Mitochondrial matrix (pyruvate transporter moves it from cytoplasm into matrix)

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11
Q

How is ATP generated in mitochondria exported to cytoplasm?

A

Specific ATP-ADP exchanger that ensures ADP is brought into mitochondrial matrix and ATP is exported out

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12
Q

What’s the pyruvate dehydrogenase complex do?

A

Oxidizes pyruvate to acetyl-CoA resulting in loss of CO2 and large negative free energy, making it irreversible

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13
Q

What cofactors are involved in pyruvate dehydrogenase complex?

A

NAD, TPP, Lipoic acid, FAD

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14
Q

Which cofactor is involved in pyruvate decarboxylase part of PDC? What kind of vitamin is it?

A

TPP (thiamine pyrophosphate)

B1 vitamin

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15
Q

What would a deficiency in TPP cause?

A

Beriberi, GI symptoms, neurological findings

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16
Q

What three enzymes make up PDC?

A

pyruvate decarboxylase, dihydrolipyl transacetylase, dihydrolipyl dehydrogenase

17
Q

Which enzyme and its cofactor are involved in acetyl group transfer to CoASH and transfer of electrons to riboflavin?

A

Dihydrolipoyl acetyl transferase and Lipoic Acid

18
Q

Which cofactor accepts electrons from lipoic acid?

19
Q

What kind of vitamin is NAD? What would a deficiency in niacin or nicotinamide (NAD) cause?

A

Vitamin B3 - Pellagra skin disease, diarrhea, dementia, ultimately death (in dogs - black tongue)

20
Q

What kind of vitamin is riboflavin? What does a deficiency in riboflavin cause?

A

B2 vitamin - Fissures in corners of mouth, inflammation of tongue, skin disease, sever irritation of eye

21
Q

What’s the order of cofactors used during PDC rxns?

A

TPP, lipoic acid, FAD, NAD

22
Q

What enzyme in TCA catalyzes the reaction of oxaloacetate with acetyl-CoA?

A

Citrate synthase

23
Q

What enzyme in TCA catalyzes the reaction of isocitrate to alpha-ketoglutarate?
What molecules are given off?

A

isocitrate dehydrogenase; NADH and CO2

24
Q

What enzyme is involved in substrate-level phosphorylation in TCA? It turns ______ into _________ and a ______.

A

Succinyl-CoA synthetase; it turns succinyl CoA into succinate and a GTP

25
How is TCA cycle regulated by phosphorylation?
Phosphorylated PDH complex is inactive. Dephosphorylated PDH complex is active. If there is low energy in the cell, Ca2+ will activate phosphatase and PDH activity will increase. If there is high energy in the cell, ATP-like signals decrease PDH complex activity.
26
Which enzyme generates FADH? Where does the FADH go?
Succinate dehydrogenase | Goes directly to CoQ
27
How much ATP does a single NADH and FADH2 molecule generate?
NADH - 2.5 | FADH2 - 1.5
28
How many ATP does one acetyl-CoA generate?
About 12.5 through oxidative phosphorylation including the NADH from PDC
29
What does pyruvate carboylase do? What cofactor is needed for this reaction?
Carboxylation of pyruvate to yield oxaloacetate; requires biotin
30
What pathology is associated with biotin deficiency?
Dermatitis, GI symptoms
31
What low energy signals regulate TCA enzymes?
AMP-like signals AMP, ADP, NAD, Ca2+, cAMP, CoASH
32
What high energy signals regulate TCA enzymes?
ATP-like signals ATP, NADH, citrate, acetyl CoA, malonyl-CoA