Aerobic Respiration Flashcards

1
Q

Where does the CAC/KC take place & what is the main function of this pathway?

A

Mitochondria

Functions to oxidize acetyl coA to CO2 & H2O

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2
Q

What are the pyruvate dehydrogenase complex enzymes needed to catalyze acetyl-CoA from pyruvate, & what are their functions ?

A
  1. PDH: oxidizes pyruvate, yields CO2
  2. Dihydrolipoly transacetylase: oxidizes 2 C molecules bonded to thiamine pyrophosphate & transfers them to lipoic acid; also catalyzes CoA-SH to acteyl-CoA
  3. D. dehydrogenase: FAD reoxidizes lipoic acid (for future use) & reduced to FADH2
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3
Q

What other pathways are capable of forming acetyl-CoA?

A
  • Fatty acid oxidation (beta-oxidation)
  • Amino acid catabolism
  • Ketone bodies
  • Alcohol
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4
Q

Where in the mitochondria does the CAC specifically take place ?

A

Mitochondrial matrix

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5
Q

What rxns take place in the CAC?

A
  1. Acetyl-CoA & oxaloacetate undergo condensation to form citryl-CoA—-> hydrolysis of citryl yields citrate & CoA-SH
  2. Citrate is isomerized to isocitrate
  3. Isocitrate oxidized to oxalosuccinate (via isocitrate dehydrogenase: rate limiting step of CAC)—>oxalosuccinate decarboxylated to a-ketoglutarate & CO2
  4. a-ketoglutarate & CoA-SH form succinyl CoA & CO2
  5. Hydrolysis of thioester bond on succinyl CoA yields succinate & CoA-SH (coupled yo phosphorylation of GDP to GTP)
  6. Succinate oxidized to fumarate & FAD reduced to FADH2 in the inner mitochondrial membrane
  7. Fumarase catalyzes hydrolysis of fumarate & forms malate (L-malate)
  8. Malate dehydrogenase catalyzes oxidation of malate to oxaloacetate
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6
Q

What are the 3 essential checkpoints that regulate the CAC from within ?

A
  1. Citric synthase: ATP & NADH function as allosteric inhibitors
  2. Isocitrate dehydrogenase: Inhibited by ATP & NADH
  3. a-ketoglutarate dehydrogenase complex: reaction products of succinyl CoA, ATP, & NADH serve as inhibitory factors
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7
Q

What are the final 2 steps of aerobic respiration ?

A

ETC & generation of ATP via ADP phosphorylation

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8
Q

The transfer of electrons from NADH to coenzyme Q is catalyzed where ?

A

Complex I

1. NADH—>FMN—->NAD+ & FMNH2—>CoQ (ubiquinone)—–>CoQH2

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9
Q

What is the main difference between Complex I & II ?

A

CI receives e- from NADH while C2 receives e- from succinate

  • No H+ pumping occurs in C2
  • C2: succinate—>FAD & FADH2—> CoQ—-> fumarate & CoQH2
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10
Q

What is the main function of complex III ?

A

To facilitate transfer of e- from CoQH2 to cytochrome c

*Q cycle : 2 e- transferred from ubiquinol (intermembrane space) to ubiquinone (near mitochondrial matrix)

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11
Q

Complex IV facilitates the transfer of e- from cytochrome c to what final e- acceptor ?

A

O2

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12
Q

What happens when H+ increases in the intermembrane space ?

A

pH drops & voltage difference between intermembrane space & matrix increases (create electrochemical gradient)

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13
Q

NADH formed via glycolysis cannot directly cross into the mitochondrial matrix. What shuttle mechanisms aid in transferring the e- transporters through the membrane?

A
  • Glycerol-3-phosphate shuttle

- Malate-aspartate shuttle

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14
Q

What is the F0 portion of ATP synthase & what is its function ?

A

F0 is the part of ATP synthase that spans the membrane, & it functions as an ion channel (chemiosmotic coupling occurs simultaneously to all chemical energy of gradient to be harnessed for ADP->ATP)
*F1 portion: phosphorylates ADP to ATP

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15
Q

Chemiosmotic coupling describes a direct relationship between what ?

A

proton gradient & ATP synthesis

*Conformational coupling says its indirect

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