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TRANSCRIPT
Chapter 18 Oxidative Phosphorylation
Matching Questions Use the following to answer questions 1-10:
Choose the correct answer from the list below. Not all of the answers will be used.
a) mitochondria
b) chemiosmotic theory
c) coenzyme Q
d) FMN
e) iron-sulfur clusters
f) respiration
g) transporters
h) porins
i) succinate dehydrogenase
j) cytochrome c oxidase
k) ATP-ADP translocase
l) malate-aspartate shuttle
1. ____________ This is where oxidative phosphorylation occurs in eukaryotes.
Ans: a
Section: Introduction
2. ____________ An ATP-generating process in which an inorganic substance such as oxygen
serves as the ultimate electron acceptor.
Ans: f
Section: Introduction
3. ____________ The permeability of the outer mitochondrial membrane is primarily due to the
presence of these substances.
Ans: h
Section: 18.1
4. ____________ This electron carrier is a derivative of quinone and has an isoprenoid tail.
Ans: c
Section: 18.3
5. ____________ This enzyme catalyzes the reduction of O2.
Ans: j
Section: 18.3
Chapter 18 Oxidative Phosphorylation
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6. ____________ This prosthetic group is present in complexes I, II, and III of electron
transport.
Ans: e
Section: 18.3
7. ____________ This citric acid cycle enzyme is also part of an electron-transport complex.
Ans: i
Section: 18.3
8. ____________ This is the name given to the hypothesis proposed by Peter Mitchell to explain
how ATP synthesis is coupled to electron transport.
Ans: b
Section: 18.4
9. ____________ Atractyloside inhibits this mitochondrial protein.
Ans: k
Section: 18.6
10. ____________ This is a process by which cytoplasmic NADH can be re-oxidized by O2 using
the electron-transport system.
Ans: l
Section: 18.5
Fill in the Blank Questions
11. A strong oxidizing agent has a strong tendency to ____________ (accept, donate) electron(s).
Ans: accept Section: 18.2
12. In the initial step of Complex I, two high-potential electrons are transferred from NADH to the
___________ prosthetic group of this complex.
Ans: FMN Section: 18.3
13. Cytochrome ________ is the only water-soluble cytochrome of the electron-transport chain.
Ans: c Section: 18.3
14. Cytochrome c oxidase contains two heme A groups and three ______________ ions.
Ans: copper Section: 18.3
15. ________________ carries electrons from Complex III to Complex IV.
Ans: Cytochrome c Section: 18.3
16. The transfer of a single electron to O2 forms the reactive _______________ ion.
Ans: superoxide Section: 18.3
Chapter 18 Oxidative Phosphorylation
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17. _______________ is a molecular assembly in the inner mitochondrial membrane that carries out
the synthesis of ATP.
Ans: F1Fo ATPase, or ATP synthase Section: 18.3
18. In the glycerol phosphate shuttle, cytoplasmic glycerol phosphate dehydrogenase uses
cytoplasmic NADH to reduce _________________ to glycerol-3-phosphate.
Ans: dihydroxyacetone phosphate Section: 18.5
19. Acceptor control of oxidative phosphorylation means that the rate of respiration depends upon
the level of __________.
Ans: ADP Section: 18.6
20. _________________ is a poison because it blocks the flow of electrons from cytochrome c to
oxygen.
Ans: Carbon monoxide (CO), or Cyanide (CN-)or Azide (N3 ) Section: 18.6
Multiple Choice Questions
21. What type of gradient is critical to ATP formation by oxidative phosphorylation?
A) sodium ion D) potassium ion
B) chloride ion E) None of the above.
C) proton
Ans: C Section: Introduction
22. When glucose is totally oxidized to CO2 and H2O, how many ATP molecules are made by
oxidative phosphorylation relative to the maximum yield?
A) 12 out of 30
B) 26 out of 30
C) 26 out of 32
D) 12 out of 38
E) None of the above.
Ans: B Section: 18.6
23. What is the chemical effect of oligomycin on aerobic metabolism?
A) The flow of electrons from NADH to CoQ is blocked.
B) The flow of electrons from Cyt a-a3 to oxygen is blocked.
C) Oligomycin blocks the proton transfer through Fo of ATP synthase and therefore blocks
the phosphorylation of ADP to form ATP.
D) The transport of ATP out of and ADP into the mitochondria is blocked.
E) Oxidative phosphorylation is uncoupled from electron transport and all the energy is lost
as heat.
Ans: C Section: 18.6
Chapter 18 Oxidative Phosphorylation
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24. Choose the correct path taken by a pair of electrons as it travels down the electron-transport
chain.
A) NADH complex I CoQ Complex III Cyt c complex IV O2
B) FADH2 complex I CoQ Complex III Cyt c complex IV O2
C) NADH complex I complex II Complex III Cyt c complex IV O2
D) FADH2 complex II CoQ Complex III Cyt c complex IV O2
E) a and d
Ans: E Section: 18.3
25. Which of the following does not participate in, nor is a component of, the electron-transport
chain?
A) coenzyme A
B) non-heme, iron-sulfur proteins
C) coenzyme Q
D) cytochrome c1
E) NADH
Ans: A Section: 18.3
26. In prokaryotes the site of ATP-synthesizing machinery is
A) the mitochondrial matrix. D) the nucleolus.
B) the outer cell wall. E) none of the above.
C) the cytoplasmic membrane.
Ans: C Section: 18.1
27. Electron flow down the electron-transport chain leads to the
A) transport of protons across the inner mitochondrial membrane from inside the matrix to
the intermembrane space.
B) transport of protons across the inner mitochondrial membrane from the intermembrane
space into the matrix.
C) coupled synthesis of GTP.
D) a dangerous imbalance of K+ ions across the mitochondiral membrane.
E) none of the above.
Ans: A Section: 18.3
28. Coenzyme Q is also called
A) NADH. D) all of the above.
B) oxidoreductase. E) none of the above.
C) ubiquinone.
Ans: C Section: 18.3
29. Which of the following does not pump protons?
A) Complex I D) Complex IV
B) Complex II E) All of the above.
C) Complex III
Ans: B Section: 18.3
30. In proteins these amino acid residues usually complex to the iron-sulfur clusters.
A) Gly B) Arg C) Cys D) All of the above. E) None of the above.
Ans: C Section: 18.3
Chapter 18 Oxidative Phosphorylation
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31. What is a cytochrome?
A) a protein that transfers electrons, and that also contains a heme prosthetic group
B) a chloroplast protein that transfers electrons, and that also contains an iron sulfur
prosthetic group
C) a protein that pumps ATP, and that also contains iron
D) All of the above.
E) None of the above.
Ans: A Section: 18.3
32. In the Rieske center, the iron-sulfur center is coordinated to the amino acid(s) _______.
A) His B) Cys C) His and Cys D) Cys and Met E) none of these
Ans: A Section: 18.3
33. What is the reaction of ATP synthase?
A) AMP3
+ 2 HPO42
+ H+
ATP4
+ H2O
B) ADP3
+ HPO42
+ H+ ATP
4 + H2O
C) ADP3
+ HPO42
+ 2H+
ATP4
+ H2O
D) AMP3
+ 2 HPO42
+ 2H+ ATP
4 + H2O
E) None of the above
Ans: B Section: 18.4
34. What is the net ATP obtained from one cytoplasmic NADH when it is reoxidized by the
electron-transport chain using the glycerol 3-phosphate shuttle?
A) 2.5. B) 1.5. C) 2.0. D) 1.0. E) None of the above.
Ans: B Section: 18.5
35. In the malate-aspartate shuttle, electrons from NADH are transferred to ________, forming
malate.
A) oxaloacetate D) glutamate
B) aspartate E) none of the above
C) acetate
Ans: A Section: 18.5
Short-Answer Questions
36. Provide a brief description of oxidative phosphorylation.
Ans: It is the process in which ATP is formed, due to the transfer of electrons from NADH or
FADH2 to O2 by a series of electron carriers in the inner membrane of the mitochondria.
Section: Introduction
37. Draw the structure of a mitochondrion and indicate the sites of oxidative phosphorylation and
the citric acid cycle.
Ans: The drawing should include the overall shape with the outer membrane and the inner
membrane, the inner-membrane space, matrix, and cristae labeled. Most of the TCA cycle
takes place in the matrix, while oxidative phosphorylation occurs in the inner
mitochondrial membrane. It should closely resemble text Figure 18.2.
Section: 18.1
Chapter 18 Oxidative Phosphorylation
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38. What is the current belief for the presence of mitochondria in eukaryotic cells? What is the
proof?
Ans: It is believed that the organelles are the result of an endosymbiotic event. The structure of
mitochondria is consistent with this theory. Furthermore, DNA sequence analysis
suggests that an ancestor of an existing bacterium is the source for extant mitochondria.
Section: 18.2
39. Describe the path by which electrons from FADH2 enter the electron transport chain.
Ans: Succinate dehydrogenase, which forms FADH2, is part of the succinate-Q reductase
complex. The FADH2 does not leave this complex, but transfers electrons to the iron
sulfur centers of the complex, and then to Q.
Section: 18.3
40. Explain why less ATP is made from the reoxidation of FADH2 as compared to NADH.
Ans: Complex II is not a proton pump. When electrons flow from FADH2 to oxygen, as
catalyzed by complex II, complex III, and complex IV, fewer protons are pumped out of
the matrix as compared to NADH. Thus, fewer ATP molecules are ultimately made.
Section: 18.3
41. Give the balanced equation for the net reaction catalyzed by Q-cytochrome c oxido-reducatase.
Ans: QH2 + 2Cyt cox + 2H+
matrix Q + 2Cyt cred + 4H+
cytosol
Section: 18.3
42. What is a major defense strategy against oxidative damage caused by reactive oxygen species
(ROS)?
Ans: Superoxide dismutase converts superoxide radicals to peroxide and oxygen (requires
protons), and catalase converts hydrogen peroxide to water and oxygen.
Section: 18.3
43. Discuss the evolution of the cytochrome c protein.
Ans: Cytochrome c has been studied in many organisms with mitochondrial respiratory
systems, and shows little divergence. Cytochrome c from the many different organisms
can react with the cytochrome c oxidase, demonstrating little structural difference at their
interfaces. The amino acid sequences of the various cytochrome c proteins are similar
and, over a billion years of evolution, 25% of the amino acids remained unchanged.
Section: 18.3
44. What is the actual function of the protons in the synthesis of ATP by FoF1 ATP synthase?
Ans: The proton gradient is necessary for ATP synthesis because the binding of a proton to the
enzyme causes a conformational change that releases the bound ATP. The role of the proton
gradient is not to form ATP but to release it from the synthase.
Section: 18.4
45. What was the proof that the ATP synthase was rotating?
Ans: Using cloned 3 3 subunits, with the subunits tagged with a histidine that attached it to
a nickel coated slide, and using another fluorescent tag linked to the subunit, the
rotation could be observed using a fluorescent microscope.
Section: 18.4. and Figure 18.30
Chapter 18 Oxidative Phosphorylation
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46. How does the glycerol 3-phosphate shuttle function?
Ans: Electrons from NADH are transferred to DHAP, to form glycerol-3-P, a reaction that
occurs in the cytosol. Glycerol-3-P diffuses through the outer membrane and then
transfers the electrons to FAD of glycerol-3-phosphate dehydrogenase located in the
inner membrane. The FADH2 then transfers the electrons to Q.
Section: 18.5
47. In the malate-aspartate shuttle, how is oxaloacetate regenerated since there is no transporter for
oxaloacetate across the inner membrane?
Ans: Inside the mitochondria, the malate is converted to OAA by malate dehydrogenase. The
OAA is converted to aspartate, which can be transported out of the mitochondria. The
aspartate can then be converted to oxaloacetate. The aspartate-oxaloacetate reactions
require glutamate and -ketoglutarate.
Section: 18.5
48. How is oxidative phosphorylation regulated?
Ans: The electrons do not flow unless ADP is available to be simultaneously phosphorylated to
ATP. Thus, the synthesis of ATP does not occur unless ADP levels are high. This is
referred to as acceptor control.
Section: 18.6
49. What are uncouplers? Provide an example of when this might be useful.
Ans: Uncouplers destroy the proton gradient across the inner membrane by carrying protons
back into the matrix. This disrupts the coupling of electron transport to oxidative
phosphorylation, and the energy is released as heat instead of being used to drive
phosphorylation of ADP. Non-shivering thermogenesis, to generate heat for newborns, is
one example provided (due to the uncoupler UCP-1).
Section: 18.6
50. Explain why carbon monoxide is toxic.
Ans: Carbon monoxide bond to the ferrous ion of cytochrome a3 of cytochrome c oxidase.
This blocks the electron flow to oxygen and the proton-motive force can no longer be
generated. Without the proton gradient, the phosphorylation of ADP cannot occur. Thus
energy production ceases.
Section: 18.6