Chapter 18. Oxidative Phosphorylation Flashcards

1
Q

the energy inherent in the proton gradient established during the functioning of the respiratory chain; consists of a membrane potential as well as a chemical gradient.

A

Proton-motive force

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2
Q

A cytoplasmic complex that includes cytochrome c released from the mitochondria, which recruits and activates caspase 9, which in turn activates a cascade of caspases that result in programmed cell death (apoptosis).

A

Apoptosome

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3
Q

Molecular assembly of the inner mitochondrial membrane responsible for the respiratory-chain-driven synthesis of ATP. Also called Complex V, mitochondrial ATPase, H+-ATPase, or F0F1-ATPase.

A

ATP synthase (Complex V, F 1F 0 ATPase)

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4
Q

cysteine proteases that participate in the proteolytic cascade that occurs during apoptosis.

A

caspase

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5
Q

a transport protein that carries ADP into the mitochondria and ATP out in a coupled fashion.

A

ATP-ADP translocase (adenine nucleotide translocase, ANT)

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6
Q

the process in which ATP is formed as the result of the transfer of electrons from NADH or FADH2 to O2 via a series of electron carriers.

A

Oxidative phosphorylation

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7
Q

The generation of high-transfer-potential electrons by the citric acid cycle, their flow through the respiratory chain to O2, and the accompanying synthesis of ATP.

A

Cellular respiration

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8
Q

a mobile electron carrier that is a component of the respiratory chain; it shuttles between the oxidized ubiquinone form to the reduced ubiquinol form via a semiquinone intermediate; accepts electrons from NADH-Q reductase as well as succinate-Q reductase.

A

Coenzyme Q (Q, ubiquinone)

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9
Q

A measure of the tendency of chemical to accept electrons and thereby become reduced.

A

Reduction (redux, oxidation-reduction, Eā€™ 0potential

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10
Q

a ubiquitous heme protein that catalyzes the dismutation of hydrogen peroxide into molecular oxygen and water.

A

Catalase

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11
Q

A large component of the respiratory chain that transfers electrons from NADH to ubiquinone and in the process pumps protons across the inner mitochondrial membrane to generate the proton-motive force. Also called NADH dehydrogenase or Complex I.

A

NADH-Q oxidoreductase (Complex I)

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12
Q

an integral membrane protein complex of the inner mitochondrial membrane that transfers electrons from the FADH2 formed in the citric acid cycle to coenzyme Q.

A

Succinate-Q reductase (Complex II)

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13
Q

A coenzyme for oxidation-reduction reactions derived from the vitamin riboflavin. The electron acceptor of FMN, the isoalloxazine ring, is identical with that of FAD, but FMN lacks the adenyl nucleotide component of FAD.

A

flavin mononucleotide (FMN)

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14
Q

the final complex of the respiratory chain, which transfers electrons from cytochrome c to molecular oxygen and concomitantly pumps protons across the inner mitochondrial membrane to generate the proton-motive force.

A

cytochrome c oxidase (complex IV)

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15
Q

an unusual 2Fe-2S center in that one of the iron ions is coordinated by two histidine residues rather than two cysteine residues.

A

Rieske center

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16
Q

a cascade of proteolytic enzymes that result in controlled cell death in response to significant cell damage or specific development programs.

A

Programmed cell death (apoptosis)

17
Q

tight coupling or coordination of the oxidation of reduced cofactors (NADH, FADH2) in the electron transport chain and the phosphorylation of ADP to yield ATP in the mitochondrion; such control ensures that the rate of the citric acid cycle, where reduced cofactors are generated, corresponds to the demand for ATP.

A

Respiratory (acceptor) control

18
Q

A component of the respiratory chain, this oxidoreductase carries electrons from coenzyme Q to cytochrome c and, in the process, pumps protons out of the mitochondrial matrix to generate the proton-motive force. Also called cytochrome reductase or Complex III.

A

Q-cytochrome c oxidoreductase (Complex III)

19
Q

The population of coenzyme Q, reduced and oxidized, that exists in the inner mitochondrial membrane.

A

Q pool

20
Q

The permeablization of the outer mitochondrial membrane, which occurs when mitochondria are damaged. The permeablization initiates the programmed cell death pathway (apoptosis).

A

Mitochondrial outer membrane permeabilization (MOMP)

21
Q

a pathway that transfers electrons from cytoplasmic NADH into the mitochondria; dihydroxyacetone phosphate (DHAP) is reduced by NADH to glycerol 3-phosphate, which enters the mitochondria and is oxidized to yield FADH2and DHAP, which leaves the mitochondria.

A

Glycerol 3-phosphate shuttle

22
Q

Proteins that contain clusters of iron and sulfur that play a role in electron transfer reactions; iron cycles between the Fe2+ and Fe3+ state. Also called nonheme iron proteins.

A

Iron-sulfur (nonheme iron) protein

23
Q

a reversible shuttle, found in the liver and heart, used to transport electrons from cytoplasmic NADH to mitochondrial NAD.

A

Malate-aspartate shuttle

24
Q

a set of reactions in which coenzyme Q cycles between the fully reduced state and the fully oxidized state via one-electron transfer reactions in which one of the electrons is temporarily stored in cytochrome b; provides a means of passing the two electrons of coenzyme Q to the single electron carrier cytochrome c, one electron at a time.

A

Q cycle

25
Q

an enzyme that scavenges superoxide radicals by catalyzing the conversion of two of these radicals into hydrogen peroxide and molecular oxygen. Superoxide dismutase thus protects against damage by reactive oxygen species.

A

Superoxide dismutase

26
Q

A mitochondrial membrane protein that plays a role in thermogenesis by forming a pathway for the flow of protons into the mitochondria, thereby generating heat without synthesizing ATP. Also called thermogenin.

A

Uncoupling protein (UCP)

27
Q

The final complex of the respiratory chain, which transfers electrons from cytochrome c to molecular oxygen and concomitantly pumps protons across the inner mitochondrial membrane to generate the proton-motive force.

A

Cytochrome c (Cyt c)