Oxidative Phosphorylation (Chapter 11.3-11.5 Slides 38-66) Flashcards

1
Q

Each ATP synthase complex has ______ α and ______ β subunits

A

3, 3

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2
Q

The bacterial ATP synthase complex contains a subunit called ______ that associates with the F1 component.

A

ε

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3
Q

The ______ subunit of the yeast ATP synthase complex is homologous to the bacterial ε subunit.

A

δ

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4
Q

What are the three functional components of the ATP synthase complex?

A

rotor, stator, headpiece

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5
Q

The ______ holds the headpiece in place so that it does not turn with the rotor

A

stator

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6
Q

The ______subunits of the headpiece contain the ______ sites for ATP synthesis, and the ______ is responsible for translating proton-motive force into protein conformational changes in the headpiece.

A

β, catalytic, rotor

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7
Q

True or False: The same three functional components are found in all ATP synthase complexes.

A

True

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8
Q

True or False: When one β subunit is in the Lconformation, the other two can be in either L, T or O conformations.

A

False, the other two must be in the T and O conformations.

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9
Q

The yeast mitochondrial ATP synthase complex appears to require ∼______H+ for each ATP synthesized.

A

3

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10
Q

True or False: The number of H+ required for each 120° turn of the γ subunit depends on the number of subunits in the c ring.

A

True

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11
Q

What was the first experiement to demonstrate rotational movement in the ATPase

A

Yoshida and Kinosita

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12
Q

______ drives the γ-subunit rotation in the clockwise direction

A

ATP hydrolysis

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13
Q

ATP ______ results in the conformational sequence O → T → L → O for a given β subunit, which is opposite that of ATP ______.

A

Hydrolysis, synthesis

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14
Q

______ can be used as a nanomotor to drive ATP ______

A

F1, synthesis

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15
Q

The ______ model proposes that protons drive rotation of the c ring in response to the electrochemical proton gradient, through alternate protonation and deprotonation of a charged Asp residue in each c subunit

A

two channel

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16
Q

True or False: In the two-channel model, the electrochemical proton gradient drives rotation of the c ring as protons move from the intermembrane space into the mitochondrial matrix through two half-channels in the a subunit.

A

True

17
Q

True or False: The mitochondria inner membrane allows ions to pass through.

A

False, impervious to ions to allow formation of a proton gradient

18
Q

True or False: Biomolecules required for the electron transport system or oxidative phosphorylation must be transported across the mitochondrial inner membrane

A

True

19
Q

WHat two translocases transport ATP, ADP, and Pi?

A

ATP/ADP translocase

phosphate translocase

20
Q

What two systems transfer electrons to the matrix?

A

malate-aspartate shuttle

glycerol-3-phosphate shuttle

21
Q

True or False: The C state of the mitochondrial ATP/ADP translocase faces toward the ______ and the M state faces toward the ______.

A

Intermembrane space, mitochondrial matrix

22
Q

Atractyloside blocks the ______ state and bongkrekic acid block the ______ state.

A

C, M

23
Q

Phosphate translocase functions as a ______ when is translocates H2PO4− (Pi) and H+P across the membrane

Phosphate translocase functions as a ______ that exchanges H2PO4− for OH−.

A

Symporter, antiporter

24
Q

True or False: In both cases, the movement of H2PO4− into the mitochondrial matrix is electrically neutral.

A

True

25
Q

The flow of _______ H+ into the mitochondrial matrix is required for every ATP synthesized.

A

4 (1 from phosphate translocase, 3 from ATP synthase complex)

26
Q

The malate–aspartate shuttle moves a pair of electrons from ______ NADH to ______ NAD+.

A

cytosolic, mitochondrial

27
Q

What are the four key steps to the malate–aspartate shuttle in liver cells?

A

Reduction of oxaloacetate in the cytosol with NADH + H+ by the enzyme cytosolic malate dehydrogenase to malate and NAD+.

Malate is transported in to the mitochondrial matrix and oxidized by the mitochondrial malate dehydrogenase with NAD+ to form oxaloacetate and NADH + H+.

Transamination of oxaloacetate by mitochondrial aspartate aminotransferase and glutamate to form α-ketoglutarate and aspartate, which is shuttled across the membrane.

Deamination of aspartate in the cytosol by cytosolic aspartate aminotransferase and α-ketoglutarate to form oxaloacetate and glutamate.

28
Q

What are the three steps in the glycerol-3-phosphate shuttle?

A

Reduction of the glycolytic intermediate dihydroxyacetone phosphate in the cytosol, forming glycerol-3-phosphate. The glycerol-3-phosphate then diffuses across the outer mitochondrial membrane through porin channels.

Once in the intermembrane space, the glycerol-3-phosphate is reoxidized to form dihydroxyacetone phosphate. In the process, 2 e− are transferred to an FAD moiety in mitochondrial glycerol-3-phosphate dehydrogenase. (The regenerated dihydroxyacetone phosphate recycles back to the cytoplasm through other porin channels.)

The 2 e− are then passed to Q, which transfers them one at a time to complex III via the Q cycle (see Figures 11.8 and 11.18).

29
Q

True or False: Numerous enzymes in glycolysis and the citrate cycle are regulated by intracellular concentrations of ATP, ADP, AMP, Pi, NAD+, and NADH.

A

True

30
Q

True or False: The chemical uncouplers 2,4-dinitrophenol (DNP) and carbonyl cyanide 4-(trifluoromethoxy) phenylhydrazone (FCCP) activate proton diffusion down the electrochemical proton gradient, which decreases the efficiency of oxidative phosphorylation.

A

True

31
Q

True or False: Decreased expression of uncoupling protein 1 (UCP1) in brown adipose tissue short-circuits the electrochemical proton gradient and diverts redox energy to heat production.

A

False, increased

32
Q

High levels of ______ give brown adipose tissue its dark color

A

Mitochondria

33
Q

True or False: The majority of cytosolic space in white adipose tissue is filled with large fat droplets

A

True

34
Q

Mitochondrial diseases such as LHON are ______ inherited

A

Maternally

35
Q

LHON and MELAS are associated with what complex?

A

I

36
Q

NARP, MILS FBSN are associated with what complex?

A

ATP synthase

37
Q

Sporadic anemia is associated with what complex?

A

IV