Chapter 19: Problem 11
Aminolevulinic acid synthase A. requires NAD for activity. B. is allosterically activated by heme. C. synthesis is inhibited by steroids. D. is synthesized in mitochondria. E. synthesis can be induced by a variety of drugs.
Chapter 19: Problem 11
Aminolevulinic acid synthase A. requires NAD for activity. B. is allosterically activated by heme. C. synthesis is inhibited by steroids. D. is synthesized in mitochondria. E. synthesis can be induced by a variety of drugs.
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Get started for freeThe production of ammonia in the reaction catalyzed by glutamate dehydrogenase A. requires the participation of NADH or NADPH. B. proceeds through a Schiff base intermediate. C. may be reversed to consume ammonia if it is present in excess. D. is favored by high levels of ATP or GTP. E. would be inhibited when gluconeogenesis is active.
Conjugated bilirubin is A. transported in blood bound to serum albumin. B. deficient in Crigler-Najjar syndrome, a deficiency of a UDPglucuronosyltransferase. C. reduced in serum in biliary tract obstruction. D. the form of bilirubin most elevated in hepatic (liver) disease. E. less soluble in aqueous solution than the unconjugated form.
Aminotransferases A. usually require \(\alpha\) -ketoglutarate or glutamine as one of the reacting pair. B. catalyze reactions that result in a net use or production of amino acids. C. catalyze irreversible reactions. D. require pyridoxal phosphate as an essential cofactor for the reaction. E. are not able to catalyze transamination reactions with essential amino acids.
Valine and isoleucine give rise to propionyl CoA, a precursor of succinyl CoA. A disease related to a defect in this conversion is methylmalonic aciduria. Some patients respond to megadoses of vitamin \(\mathrm{B}_{12}\). Which of the following statements about the conversion of propionyl CoA to succinyl CoA is/are correct? A. The first step in the conversion is a biotin-dependent carboxylation. B. Some methylmalonic aciduria patients respond to \(\mathrm{B}_{12}\) because the defect in the mutase converting malonyl CoA to succinyl CoA is poor binding of the cofactor. C. The same pathway of propionyl CoA to succinyl CoA is part of the metabolism of odd-chain fatty acids. D. All of the above. E. None of the above.
Heme oxygenase A. can oxidize the methene bridge between any two pyrrole rings of heme. B. requires molecular oxygen. C. produces bilirubin. D. produces carbon dioxide. E. can use either heme or protoporphyrin IX as substrate.
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