ATP Production: TCA + Respiratory Chain Flashcards

1
Q

What is the TCA cycle?

A

Final pathway for the oxidation of carbohydrates, lipids, and protein. Synthesizes ATP

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2
Q

What are the 3 important products of the TCA cycle?

A

NADH
FADH2
ATP

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3
Q

What is the irreversible route from glycolysis to the TCA cylce?

A

Formation of Acetyl CoA from Pyruvate

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4
Q

Where is pyruvate converted to Acetyl CoA? Why?

A

The mitochondria because Acetyl CoA cannot cross the mitochondrial membrane

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5
Q

What enzyme complex converts pyruvate to acetyl CoA? What vitamin is required?

A

Pyruvate dehydrogenase complex
Thiamin (Vit B1)

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6
Q

What is the second irreversible step in the TCA cycle? What is the enzyme associated with this step?

A

OAA to Citrate via citrate synthase

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7
Q

What steps of the TCA cycle yields NADH?

A

Isocitrate- alpha KG
Alpha-KG - succinyl CoA
Malate - OAA

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8
Q

What step(s) of the TCA cycle yields ATP?

A

Succinyl CoA - Succinate

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9
Q

What step(s) in the TCA cycle yields FADH2?

A

Succinate - Fumarate

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10
Q

How many total ATP is produced by the TCA cycle alone?

A

9

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11
Q

What enzyme in the TCA cycle can be inhibited by arsenic? what step does this enzyme facilitate?

A

alpha-KG dehydrogenase complex
alpha-KG - succinyl CoA

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12
Q

What is the catabolic function of the TCA cycle?

A

Oxidation of acetyl CoA derived from carbohydrates, lipids, protein metabolism to produce ATP

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13
Q

What are the anabolic functions of the TCA cycle? (3)

A

-Gluconeogenesis
-Fatty acid biosynthesis
-substrates fro amino acid synthesis

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14
Q

Where does fatty acid biosynthesis take place?

A

cytosol

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15
Q

How does acetyl CoA (which is produced in the mitochondria via pyruvate) leave the cell to take part in fatty acid biosynthesis? What is the key enzymes used to ensure this transfer completion?

A

It exits by conversion to citrate by citrate synthase, citrate crosses the membrane, then via citrate lyase converts back to acetyl CoA

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16
Q

Where does the respiratory chain (electron transport) take place?

A

The mitochondrial membrane

17
Q

What is the job of the respiratory chain?

A

Oxidized reduced coenzymes (NADH, FADH2) produced in the TCA cycle and from fatty acid catabolism. Generation of ATP

18
Q

What respiratory chain component is inhibited by cyanide and carbon monoxide, causing total respiratory arrest and subsequent cell death?

A

Component IV

19
Q

How many total ATP is produced after TCA cycle and oxidative phosphorylation?

A

~32

20
Q

NADH cannot penetrate the mitochondrial membrane. How can it take part in the respiratory cycle? List the two ways and how they differ

A
  • Glycerol 3- phosphate shuttle: present in skeletal muscle and brain. converts dihydroxyacetone to glycerol 3- phosphate via NADH & glycerol 3 phosphate dehydrogenase, thus place the electrons on Glycerol 3-P, this then crosses the membrane and is concerted back to dihydroxyacetone, releasing FADH2 which will enter the respiratory cycle
    -Malate Shuttle: OAA is converted to malate via NADH and malate dehydrogenase, malate crosses the membrane, and is converted back to OAA releasing NADH. Problem is OAA cannot cross the mitochondrial membrane so it is transaminated with glutamate to form alpha-KG which will cross readily.
21
Q

What complex is ATP finally synthesized?

A

Complex V

22
Q

What is used as energy in complex V to form ATP?

A

All the H+ that was pumped into the intermembrane space by the other complexes.