Bio 10 - Energy Metabolism Flashcards

1
Q

Which type of pyruvate is used to feed into the TCA cycle?

A

The pyruvate that has been converted to Acetyl-CoA.

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2
Q

What are the co-factors need to make pyruvate to Acetyl-CoA?

A

[TLC For Nobody] Thiamine pyrophosphate (TPP; the active form of thiamine). Lipoic acid. Coenzyme A (vitamin B5). FAD (vitamin B2). NAD+ (vitamin B3).

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3
Q

Which poison can inhibit Lipoic acid?

A

Arsenic; causes garlic breath, vomiting, rice-water stools.

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4
Q

What are the causes of PDH deficiency?

A

X-linked congenital defect. Acquired defect (arsenic exposure). Deficient in one of the B vitamins (especially B1; thiamine).

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5
Q

What does Citrate synthase do?

A

It converts Acetyl-CoA into citrate in the TCA (Krebs) cycle.

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6
Q

What is the rate-limiting enzyme in TCA cycle? What does it do?

A

It is Isocitrate dehydrogenase. It converts Isocitrate into alpha-ketoglutarate.

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7
Q

What does alpha-ketoglutarate dehydrogenase do?

A

Converts alpha-ketoglutarate into succinyl-CoA. It requires all the same co-factors as pyruvate dehydrogenase (TPP, Lipoic Acid, Coenzyme A, FAD, NAD+).

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8
Q

Where does TCA take place?

A

In the inner mitochondrial membrane.

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9
Q

What is Complex I in the mitochondria?

A

It is NADH reductase. It converts NADH to NAD+, while pumping a H+ ion into the intermembrane space. It also generates an electron that goes into Complex II.

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10
Q

Which substances inhibit Complex I?

A

Amytal. Rotenone. MPP.

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11
Q

Which substances inhibit Complex III?

A

Antimycin A.

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12
Q

Which substances inhibit Complex IV?

A

Cianide. Sodium Azide. Carbon monoxide. Hydrogen Sulfide.

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13
Q

Which substances inhibit ATPase?

A

Oligomycin A.

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14
Q

What is an uncoupling agent?

A

Uncouples the electron transport chain from the ATPase: it increases the permeability of the inner mitochondrial membrane to hydrogen ions, generating more heat in the body.

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15
Q

What are three uncoupling agents?

A

Thermogenin. Aspirin. 2,4-DNP.

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16
Q

Why are alanine and glutamine found in such high concentrations in the blood?

A

They are the two major carriers of nitrogen from tissue.

17
Q

What is generally involved in transamination? What enzyme catalyses this reaction?

A

Transfer of the amino group of an amino acid to alpha-ketoglutarate to form glutamate. The remaining deaminated amino acid is a ketoacid (such as pyruvate) that is used in energy metabolism. Aminotransferase catalyzes the reaction.

18
Q

How are aminotransferases named?

A

By donor of the amino group (alanine aminotransferase converts alanine to pyruvate and forms glutamate).

19
Q

In addition to substrates, what is required by all aminotransferases?

A

Pyridoxal phosphate (a derivative of vitamin B6).

20
Q

What are the two most important amintransferase enzymes? What reactions do they catalyze?

A

Alanine aminotransferase (ALT): converts alanine + alpha-ketoglutarate into glutamate + pyruvate. Aspartate Aminotransferase (AST): converts Glutamate + Oxaloacetate into alpha-ketoglutarate + Aspartate.

21
Q

What are the two main transporters of nitrogen in the blood?

A

Alanine. Glutamine.

22
Q

What are the major regulatory enzymes of the citric acid (TCA) cycle?

A

Citrate synthase. Isocitrate dehydrogenase. Alpha-ketoglutarate dehydrogenase.

23
Q

What are the four things that can be done to pyruvate?

A

Converted to Oxaloacetate (using pyruvate carboxylase), Acetyl-CoA (using pyruvate dehydrogenase), Lactate (Lactate dehydrogenase), or Alanine (using ALT).