Final: Chapter 11 Oxidative Phosphorylation Flashcards

1
Q

What is the chemiosmotic theory?

A

Theory proposed by Peter Mitchell that describes energy conversion in essentially all organisms

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2
Q

Where in the cell is does the chemiosmotic theory take place?

A

The mitochondria

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3
Q

How is the proton gradient in the chemiosmotic theory established across the mitochondrial inner membrane?

A

With chemiosmosis (the movement of protons down a concentration gradient). The gradients moves from high concentrations of protons to low concentrations.

ALSO ATP is produced :)

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4
Q

What initiates a proton gradient?

A

Outward pumping of H+ from the mitochondrial matrix by three large protein complexes

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5
Q

What does inward flow of H+ through the membrane bound ATP synthase protein accomplish?

A

ATP synthesis

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6
Q

What is the electron transport chain ?

A

The combined redox reactions that occur in a set of protein complexes embedded in the inner mitochondrial membranes. NADH is oxidized to form NAD+ and O2 (the final electron acceptor) is reduced to H2O

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7
Q

The proton circuit behaves like an electrical circuit. What molecules act as the resistor, capacitor, and battery?

A

ATP synthase is the resistor, the proton gradient is the capacitor, and the battery is the electron transport system

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8
Q

How does proton uncoupling stop ATP synthesis?

A

Proton uncoupling is when a fraction of the proton gradient generated by the electron transport chain is not used to drive ATP synthesis. It causes a proton “leakage” and produces heat

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9
Q

What are the main structural features of the mitochondria?

A

Outer mitochondrial membrane, intermembrane space, inner mitochondrial membrane, cristae (folds within the inner mitochondrial membrane), and the mitochondrial matrix

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10
Q

Referring to protein components of the electron transport chain: What protein is in Complex I?

A

NADH-ubiquinone oxidoreductase

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11
Q

Referring to protein components of the electron transport chain: What protein is in Complex II?

A

Succinate dehydrogenase

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12
Q

Referring to protein components of the electron transport chain: What protein is in Complex III?

A

Ubiquinone-cytochrome c oxidoreductase

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13
Q

Referring to protein components of the electron transport chain: What protein is in Complex IV?

A

Cytochrome oxidase

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14
Q

Referring to protein components of the electron transport chain: What protein is in Complex V?

A

ATP synthase complex

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15
Q

Which complexes in the electron transport system contain transmembrane regions that are embedded in the inner mitochondrial membrane as well as functional domains that face toward the mitochondrial matrix?

A

Complexes I - IV

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16
Q

In which complex does NADH oxidation occur?

A

Complex I which can pump four hydrogen ions across the membrane from the matrix into the intermembrane space, thereby establishing a proton gradient

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17
Q

Where does the ETC take place?

A

On the matrix side of the inner mitochondrial membrane

18
Q

What are the main inhibitors of the ETC?

A

Rotenone, hydrogen cyanide, carbon monoxide, and antimycin A

19
Q

What are redox loops?

A

A type of arrangement where protons and electrons are separated on opposite sides of the membrane.

20
Q

Which complex is a redox loop?

A

Complex III (Q cycle)

21
Q

Proton pumps for the ETC are dependent on what?

A

The conformational changes of Complexes I and IV

22
Q

What happens in Complex I and what important protein is involved?

A
  • This complex includes flavin mononucleotide (FMN) and NADH-ubiquinone oxidoreductase
  • NADH is oxidized while Coenzyme Q is reduced
  • FMN accepts 2 electrons from NADH
23
Q

How is semiquinone and reduced flavin mononucleotide formed from flavin mononucleotides?

A

Flavin mononucleotides are reduced one electron at a time

24
Q

What does Coenzyme Q do?

A

Acts as mobile electron carrier and transports electrons from Complex I to Complex III

25
Q

Coenzyme Q’s activity serves as an entry point for what other molecules/pathways?

A

Citrate cycle, fatty acid oxidation, and glycerol-3-phosphate dehydrogenase

26
Q

What happens when Coenzyme Q is reduced?

A

Ubiquinol (QH2) forms and 4H+ are translocated from the matrix side of the membrane to the intermembrane space

27
Q

What happens in Complex II and what important protein is involved?

A
  • With succinate dehydrogenase, this complex catalyzes the oxidation-reduction reaction of succinate to fumarate.
  • Coupled redox reaction using FAD and reduction of coenzyme Q to QH2
28
Q

What happens in Complex III and what important protein is involved?

A
  • With Ubiquinone-cytochrome C oxidoreductase, cytochrome C is reduced while translocating 4H+
  • This complex is a docking site for QH2 and cytochrome c
29
Q

What does the Q cycle convert?

A

Converts a 2 electron transport process into two 1 electron transfers

30
Q

Where do electrons come from in the Q cycle?

A

Coenzyme Q

31
Q

Where does Q cycle occur and what happens during it?

A

Occurs in Complex III. Cytochrome c is reduced and transports 1 electron from Complex III to Complex IV

32
Q

What are cytochrome proteins?

A

Membrane associated, heme-containing proteins involved in electron transport-redox reactions

33
Q

What happens in Complex IV and what important protein involved?

A

Cytochrome c oxidase accepts electrons one at a time. While cytochrome c is oxidized, oxygen is reduced to water. ALSO, 2H+ are translocated across the membrane

34
Q

What two large structural components comprise the ATP synthase complex?

A

F1 (encodes catalytic activity) and F0 (acts as a proton channel crossing the inner mitochondrial membrane)

35
Q

Where do protein flow through in ATP synthase and what happens?

A

They flow through the F0 component which induces the F1 subunit to undergo a conformation change (loose to tight and then open). ATP is released only in the open position

36
Q

What two shuttles are used to shuttle biomolecules required for the ETC and oxidative phosphorylation?

A

Malate-aspartate shuttle (liver) and glycerol-3-phosphate (muscle) which transport electrons from cystolic NADH to the mitochondria

37
Q

How is the import of ADP and P into the mitochondrial matrix accomplished?

A

By using two translocase proteins located in the inner mitrochondrial matrix: ATP/ADP translocase (exports one ATP for every ADP imported) and phosphate translocase (translocates one P and one H+ into the matrix)

38
Q

What is ATP-ADP translocase?

A

An antiporter membrane transport protein

39
Q

What is phosphate translocase?

A

Protein similar to a channel that can act as a symporter (two molecules moved in the same direction) or antiporter (two molecules moved in opposite directions). It is also electrically neutral

40
Q

What is the malate-aspartate shuttle and what’s important about it?

A

It is the primary shuttle in liver cells whose reactions are all reversible. It maintains the supply of NAD+

41
Q

What is the glycerol-3-phosphate shuttle and what’s important about it?

A

Shuttle that consists of two isozymes of glycerol-3-phosphate dehydrogenase. It delivers electrons from NADH to the mitochondrial matrix using FAD. Electrons from NADH got into the ETC through coenzyme Q