Exam 4: Metabolism

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What characteristic links the reactions of synthesis of phospholipids and translation of new proteins?

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What is the best definition of exergonic reactions?

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In aerobic conditions pyruvic acid, the product of glycolysis, is transported and metabolized (oxidized) to CO2 and H2O. This takes place in the ______.

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The formation of glucose molecules from non-carbohydrate precursors is called

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Protein anabolism

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Pyruvate kinase deficiency is a genetic condition resulting from a mutation in the gene coding for one of the enzymes of glycolysis, pyruvate kinase. It mostly affects red blood cells, and leads to irregular morphology of red blood cells and hemolytic anemia. Yet, pyruvate kinase is present in all cells where it catalyzes one step of glycolysis. Which of the following best explain why red blood cells are MOST affected in this disorder?

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Lipogenesis is the process of

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What cells are responsible for converting excess of dietary glucose to triglycerides?

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John has been on a low carbohydrate diet for a while and he's started smelling "funny" even if he takes a shower. His urine analysis showed the presence of ketones in his urine. What processes are most likely running in his body?

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What metabolic pathway uses substrate level phosphorylation to make ATP?

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Which of the following is an example of a catabolic reaction?

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What is the net ATP gain after a single round of glycolysis (breakdown of one molecule of glucose)?

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Catabolism of fatty acids begins with

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A nutritional deficiency of niacin will manifest itself with

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Brownian motion is the random movement of molecules suspended in a liquid or a gas. What type of energy makes these molecules move?

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Anabolic reactions are the reactions that

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During a heart attack, blood flow, and therefore oxygen delivery, to the heart muscle is interrupted. How would it change the metabolism of the heart muscle?

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Why is 37o the optimal temperature for enzymatic reactions for most human enzymes?

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What process of ATP production will still proceed normally in people with mitochondrial dysfunction diseases?

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Coenzyme A is derived from

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