Exam 16: The Citric Acid Cycle
Exam 1: The Foundations of Biochemistry109 Questions
Exam 2: Water87 Questions
Exam 3: Amino Acids, Peptides, and Proteins112 Questions
Exam 4: The Three-Dimensional Structure of Proteins100 Questions
Exam 5: Protein Function101 Questions
Exam 6: Enzymes106 Questions
Exam 7: Carbohydrates and Glycobiology109 Questions
Exam 8: Nucleotides and Nucleic Acids98 Questions
Exam 9: DNA-Based Information Technologies102 Questions
Exam 10: Lipids102 Questions
Exam 11: Biological Membranes and Transport105 Questions
Exam 12: Biosignaling98 Questions
Exam 13: Bioenergetics and Biochemical Reaction Types105 Questions
Exam 14: Glycolysis, Gluconeogenesis, and the Pentose Phosphate Pathway112 Questions
Exam 15: Principles of Metabolic Regulation101 Questions
Exam 16: The Citric Acid Cycle105 Questions
Exam 17: Fatty Acid Catabolism97 Questions
Exam 18: Amino Acid Oxidation and the Production of Urea98 Questions
Exam 19: Oxidative Phosphorylation and Photophosphorylation96 Questions
Exam 20: Carbohydrate Biosynthesis in Plants and Bacteria94 Questions
Exam 21: Lipid Biosynthesis100 Questions
Exam 22: Biosynthesis of Amino Acids, Nucleotides, and Related Molecules98 Questions
Exam 23: Hormonal Regulation and Integration of Mammalian Metabolism100 Questions
Exam 24: Genes and Chromosomes99 Questions
Exam 25: DNA Metabolism101 Questions
Exam 26: RNA Metabolism101 Questions
Exam 27: Protein Metabolism99 Questions
Exam 28: Regulation of Gene Expression99 Questions
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Which statement is FALSE regarding regulation of the pyruvate dehydrogenase complex?
(Multiple Choice)
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Which high-energy bond is associated with the succinyl-CoA synthetase reaction?
(Multiple Choice)
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The glyoxylate cycle in germinating seeds is a pathway that has some similarity to the citric acid cycle. It uses the carbon-based products from the catabolism of fatty acids as the precursors for gluconeogenesis. How can the glyoxylate cycle accomplish this?
(Multiple Choice)
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Which vitamin is NOT a precursor for a cofactor in the pyruvate dehydrogenase complex?
(Multiple Choice)
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Acetyl-CoA labeled with 14C in both of its acetate carbon atoms is incubated with unlabeled oxaloacetate and a crude tissue preparation capable of carrying out the reactions of the citric acid cycle. After one turn of the cycle, oxaloacetate would have 14C in:
(Multiple Choice)
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CO2 is produced in two reactions in the citric acid cycle. For each of these reactions, name and show the structures of reactant and product, name the enzyme, and show how any cofactors participate.
(Essay)
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Oxaloacetate uniformly labeled with 14C (i.e., with equal amounts of 14C in each of its carbon atoms) is condensed with unlabeled acetyl-CoA. After a single pass through the citric acid cycle back to oxaloacetate, what fraction of the original radioactivity will be found in the oxaloacetate?
(Multiple Choice)
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Which enzymatic activity would be decreased by thiamine deficiency?
(Multiple Choice)
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Which statement is NOT true of the reaction catalyzed by the pyruvate dehydrogenase complex?
(Multiple Choice)
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Which reaction of the citric acid cycle requires a water molecule?
(Multiple Choice)
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Which step is NOT catalyzed by the pyruvate dehydrogenase complex?
(Multiple Choice)
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Describe the enzymes, cofactors, intermediates, and products the pyruvate dehydrogenase complex.
(Essay)
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Arsenic inhibits the pyruvate dehydrogenase complex by inactivating the dihydrolipoamide component of dihydrolipoyl transacetylase. Which enzyme is also MOST likely to be inhibited by arsenic?
(Multiple Choice)
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The oxidative step of the citric acid cycle that is NOT linked to the reduction of NAD+ is the reaction catalyzed by:
(Multiple Choice)
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Two of the steps in the oxidative decarboxylation of pyruvate to acetyl-CoA do not involve the three carbons of pyruvate, yet are essential to the operation of the pyruvate dehydrogenase complex. Explain.
(Essay)
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Why is flux through the citric acid low in the resting state?
(Multiple Choice)
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Suppose you found an overly high level of pyruvate in a patient's blood and urine. One possible cause is a genetic defect in the enzyme pyruvate dehydrogenase, but another plausible cause is a specific vitamin deficiency. Explain what vitamin might be deficient in the diet, and why that would account for high levels of pyruvate to be excreted in the urine. How would you determine which explanation is correct?
(Essay)
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There are few, if any, humans with defects in the enzymes of the citric acid cycle. Explain this observation in terms of the role of the citric acid cycle.
(Essay)
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Glucose labeled with 14C in C-3 and C-4 is completely converted to acetyl-CoA via glycolysis and the pyruvate dehydrogenase complex. What percentage of the acetyl-CoA molecules formed will be labeled with 14C, and in which position of the acetyl moiety will the 14C label be found?
(Multiple Choice)
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