Exam 2 Flashcards

1
Q

What are the inibitors of PDH complex when
Pyruvate -> Acetyl CoA?

A
  • Acetyl-CoA
    • It is product
    • Competative Inhibitor at E2
    • Activates PDH kinases, meaning less active enzyme of PDH complex is available.
  • NADH
    • It is product
    • Activates PDH kinases, meaning less active enzyme of PDH complex is available.
    • Competative Inhibitor at E3
  • ATP
    • High energy charge signals CAC to not be activated as more ATP is not needed, anabolic processses should happen instead
    • Activates PDH kinases, meaning less active enzyme of PDH complex is available.
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2
Q

What are the activators of PDH complex when
Pyruvate -> Acetyl CoA?

A
  • ADP
    • Low energy charge signals for more ATP to be made
    • Inhibits PDH kinases, meaning more active enzyme of PDH complex is available.
  • Insulin
    • Increases PDH phosphatase, meaning more active enzyme of PDH complex is available.
    • Ask Cahill
  • Mg2+ and Ca2+
    • High concetrations of this stablizing ions signal that ATP concetration and thus energy charge is low
    • When this happens, CAC needs to be upregulated
    • Increases PDH phosphatasae, meaning more active enzyme of PDH complex is available.
  • Pyruvate
    • Reactant
    • Inhibits PDH kinases, meaning more active enzyme of PDH complex is available.
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3
Q

Define: “energy charge” of a cell,

Explain: effects on regulation

A

Effects: High energy= High [ATP}

ATP is not only an end product of the ETC and overall catabolism, but it will also phosphrylate enzymes which can lead deactivation

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4
Q

Chemistry and Strucutre of: NAD+

A
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5
Q

Chemistry and Structure: NADP+

A
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6
Q

Chemistry: FAD

A
  • Electron carrier, H(-) transfer, and Redox rxns
  • Similar to NAD+ but allows for H(-) transfer x2
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7
Q

Chemistry and Strucutre: TPP

A
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8
Q

Chemistry and Structure: Lipoamide

A
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9
Q

Chemistry: Biotin

A

Carrier of CO2 equivalents

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10
Q

Chemistry: Coenzyme Q

A

Electron transfer between Complexes I or II and Complex III

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11
Q

When are carbons lost in the CAC?

A
  • Carbons lost @
    • Pyruvate → Ac-SCoa as CO2
      • Not really a part of the CAC
    • Isocitrate → 𝝰-ketoglutarate as CO2
    • 𝝰-ketoglutarate → Succinyl-CoA as CO2
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12
Q

mechanisms in pyruvate dehydrogenase multienzyme complex (pyruvate to AcSCoA + CO2)

A
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13
Q

When does generation of ATP/GTP/NADH/ FADH2 occur in the CAC?

A
  • Pyruvate → acetyl-CoA
    • (1 NADH: not as a direct result of mechanism but from reoxidation of lipoamide via FAD)
  • Isocitrate → 𝝰-ketoglutarate
    • (1 NADH)
  • 𝝰-ketoglutarate → succinyl-CoA
    • (1 NADH: not as a direct result of mechanism but from reoxidation of lipoamide via FAD)
  • succinyl-CoA → succinate
    • (1 GTP: via phosphorylated histidine)
  • Succinate → fumarate
    • (1 FADH2)
  • Malate → OAA
    • (1 NADH)
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14
Q

Explain the amphibolic nature of cycle and feedstocks for CAC intermediates

A
  • Cycle intermediates can be depleted via anabolic pathways
    • citrate to FA synthesis
    • 𝝰-ketoglutarate to glutamate synthesis
    • succinyl-CoA to heme
    • OAA to aspartate
  • Need to replenish intermediates
    • Pyruvate carboxylase: pyruvate +HCO3- + ATP → OAA + ADP + Pi + 2H+ (gluconeogenesis)
    • Malate dehydrogenase: pyruvate + HCO3- + NADPH + H+ → malate + NADP+ + H2O
    • Multiple amino acids (amino group converted to 𝝰-keto acid)
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15
Q

What are the fates of C atoms from entry as AcSCoA to exit as CO2?

A

2 C’s entering as Acetyl-CoA will be incorporated into the new OAA as either C1&2 or C3&4

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16
Q
  • Mechanism:
    • PDH Complex (not really CAC)
      • Pyruvate DH
      • Dihydrolipoyl Transacetylase
      • Dihydrolipoyl DH
A
17
Q

Without using a mechanism, explain the PDH complex

A
18
Q

Mechanism: Citrate Synthase

A
19
Q

Mechanism: Aconitase

A
20
Q

Mechanism: Isocitrate DH

A
21
Q

Mechanism: 𝝰-ketoglutarate DH

A

same as PDH complex

22
Q

Mechanism: Succinyl-CoA Synthase

A
23
Q

Mechanism: Succinate DH

A
24
Q

Mechanism: Fumarase

A
25
Q

Mechanism: Malate DH

A
26
Q

Which reactions of the CAC have large negative delta G’s?

A
27
Q

Explain some Mitochondrion inner membrane features (e.g. selective permeability)

A
28
Q

How do electrons enter pathway? (Complexes I or Complex II)

A
  • Complex I
    • Uses NADH from
      • 2 per glucose from Glycolysis
      • 2 per glucose from Pyruvate → AcSCoA
      • 6 per glucose from CAC
  • NADH binding site in the matrix side
  • Non-covalently bound flavin mononucleotide (FMN) accepts two electrons from NADH
  • Several iron-sulfur centers pass one electron at the time toward the ubiquinone binding site
  • Transfer of two electrons from NADH to ubiquinone is accompanied by a transfer of protons from the matrix (N) to the inter-membrane space (IMS)
  • Experiments suggest that about four protons are transported per one NADH
  • Reduced coenzyme Q picks up two protons
  • Complex II
    • Uses FADH2
      • 2 per glucose from CAC
    • Electrons and protons are passed, one at a time, via iron-sulfur centers to ubiquinone to yield QH2
29
Q

How does each complex contribute to the proton gradient? (# of H+ translocated per 2 e- by each complex)

A

Complex 1: 4 H+

Complex 2: 0 H+

Complex 3: 4 H+

Complex 4: 2 H+

30
Q
A