Class 2: OX Phos I Flashcards

1
Q

Mitochondria membrane systems:

A

Outer membrane: permeable d.t porin VDAC

Inner membrane: impermeable, folded in cristae.

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2
Q

2 compartments of the mito. :

A

Intermembrane space

Matrix: TCA and FA oxidation

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3
Q

WHere does ox phos occur?

A

Inner membrane of mito.

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4
Q

Semi-autonomous organelles.
HAVE THEIR OWN DNA, MAKE PROTEINS AND RNAs.
All mito. Derived from rickettsia prowazekii by endosymbiotic event.
Human DNA has 16,569 bp and encodes 13 respiratory chain proteins, rRNAs, tRNAs.

A

Mitochondrial genome.

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5
Q

TCA cycle generates :

A

Electron carriers. NADH and FADH2

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6
Q

Electrons reduce->

A

O2 to water

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7
Q

Which 3 complexes pump H+ into the intermembrane space?

A

1,3, and 4

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8
Q

How do H+s return to the matrix from intermembrane space?

A

ATP synthase - powers synthesis of ATP

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9
Q

NADH Q oxidoreductase

A

Complex 1

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10
Q

Succinct Q reductase

A

Complex 2

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11
Q

Q cytochrome c oxidoreductase

A

Complex 3

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12
Q

Cytochrome c oxidase

A

Complex 4

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13
Q

Electron flow is ________

A

Exergonic

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14
Q

Succincte Q reductase generates FADH2 and has what enzyme from TCA in it?

A

Succinate dehydrogenase

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15
Q

Which complex doesnt pump electrons across membrane to intermembrane space?

A

Succinate Q reductase

Or

Complex 2

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16
Q

Complex 1,3,4 collectively are called

A

Respirasome

17
Q

Transfers e- from NADH Q oxidoreductase and then succinate Q reductase to Q cytochrome c oxidoreductase

A

Coenzyme Q

Or

Ubiquinone

18
Q

Shuttles e- from Q cytochrome c oxidoreductase(3) to cytochrome c oxidase (4)

Final component of ETC

Catalyzes the reduction of O2

A

Cytochrome c

19
Q

Prosthetic groups for complex 1:

A

FMN

Fe-S

20
Q

Complex 2 prosthetic groups:

A

FAD

Fe-S

21
Q

Complex 3 prosthetic groups:

A

Heme b and c

Fe-S

22
Q

Complex 4 prosthetic groups:

A

heme a

Cu

23
Q

Play a role in reduction reactions.

Oxidation-reduction reactions but the H+’s never leave the protein.

A

Fe-S clusters

24
Q

Rare inherited RECESSIVE disease.
Caused by mutation in the protein FRATAXIN.
Issue: synthesis of Fe-S clusters.
Affects CNS, PNS, heart, and skeletal system –excitable cells.
Common mutation is trinucleotide expansion in fraxtaxin gene.

A

Friedreich’s ataxia

25
Q

First point of entry of electrons from NADH.

Pumps 4 protons into intermembrane space.

A

Complex 1

26
Q

FADH2 enters ETC and doesnt leave through:

Leave ATP synthesized from oxidation of FADH2

A

Complex 2

27
Q

Electrons from QH2 are passed on to cytochrome c by:

2 protons pumped into intermembrane space

A

Complex 3

28
Q

Solves problem of cyt c only carrying 1 e- from CoQ

A

Q cycle

29
Q

Catalyzes transfer of e-‘s from reduced cyt c to molecular O2, the final acceptor

Makes these reactions aerobic, makes ppl breath.

4 e-s funneled to O2 to reduce it to water

A

Complex 4

30
Q

4 protons are pumped and 4 protons are used to form 2 molecules of water :

A

Peroxide bridge

31
Q

Complete reduction of O2 forms water.
Partial reduction forms dangerous species.
Can form superoxide anion or hydrogen peroxide.

Hydroxyl radical formed from both

A

Free radicals

32
Q

Dz asso. W/ free radicals:

A

Parkinson’s Dz

Ischemia; reperfusion injury

33
Q

Enzymes for antioxidants:

A
  1. Superoxide dismutase (SOD) uses selenium. To turn superoxide anion to H2O2
  2. Catalase converted H2O2 to 2 molecules of water.
34
Q

This protein has been conserved throughout nearly all of evo.

A

Cytochrome c