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Under which circumstances are amino acids not metabolized via oxidative degradation?


A) Starvation
B) Plants growing in nutrient-rich soils
C) Normal protein turnover
D) A diet rich in proteins
E) Uncontrolled diabetes

F) All of the above
G) A) and E)

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In the urea cycle,ornithine transcarbamoylase catalyzes:


A) cleavage of urea to ammonia.
B) formation of citrulline from ornithine and another reactant.
C) formation of ornithine from citrulline and another reactant.
D) formation of urea from arginine.
E) transamination of arginine.

F) A) and D)
G) None of the above

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The coenzyme involved in a transaminase reaction is:


A) biotin phosphate.
B) lipoic acid.
C) nicotinamide adenine dinucleotide phosphate (NADP+) .
D) pyridoxal phosphate (PLP) .
E) thiamine pyrophosphate (TPP) .

F) A) and B)
G) A) and C)

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Suppose you are responsible for formulating the diet for a 4-year-old boy with phenylketonuria.How do you decide what kind and amount of protein to include in the diet?

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A growing child needs a certain amount o...

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Which substance is not involved in the production of urea from NH4+ via the urea cycle?


A) Aspartate
B) ATP
C) Carbamoyl phosphate
D) Malate
E) Ornithine

F) B) and C)
G) A) and E)

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Transamination reactions are catalyzed by a family of enzymes,all of which require __________ as a coenzyme.In the first step of a transamination,the coenzyme in the aldehyde form condenses with the _________ group of an amino acid to form a(n)_________.

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pyridoxal phosphate ...

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Name four amino acids that can be converted directly (in one step)into pyruvate or a citric acid cycle intermediate,and name the intermediate formed from each.

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(1)aspartate;oxaloacetate; (2)...

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In the digestion of protein that occurs in the small intestine,which enzyme is critical in the activation of zymogens?


A) Enteropeptidase
B) Hexokinase
C) Papain
D) Pepsin
E) Secretin

F) A) and B)
G) B) and D)

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A

Describe (a)the fundamental nutritional problem faced by individuals with genetic defects in enzymes involved in urea formation and (b)two approaches to treatment of these diseases.

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(a)A defect in urea synthesis can result...

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In the treatment of diabetes,insulin is given intravenously.Why can't this hormone,a small protein,be taken orally?

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First,the biological activity of insulin...

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Degradation of amino acids yields compounds that are common intermediates in the major metabolic pathways.Explain the distinction between glucogenic and ketogenic amino acids in terms of their metabolic fates.

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The glucogenic amino acids are those that are catabolized to intermediates that can serve as substrates for gluconeogenesis: pyruvate and any of the four- or five-carbon intermediates of the citric acid cycle.Ketogenic amino acids are catabolized to yield acetyl-CoA or acetoacetyl-CoA,the precursors for ketone body formation.

Which of the following statements is false in reference to the mammalian synthesis of urea?


A) Krebs was a major contributor to the elucidation of the pathway involved.
B) The amino acid arginine is the immediate precursor to urea.
C) The carbon atom of urea is derived from mitochondrial HCO3-.
D) The precursor to one of the nitrogens of urea is aspartate.
E) The process of urea production is an energy-yielding series of reactions.

F) B) and E)
G) None of the above

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The conversion of glutamate to an α\alpha -ketoacid and NH4+:


A) does not require any cofactors.
B) is a reductive deamination.
C) is accompanied by ATP hydrolysis catalyzed by the same enzyme.
D) is catalyzed by glutamate dehydrogenase.
E) requires ATP.

F) A) and D)
G) B) and E)

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The human genetic disease phenylketonuria (PKU) can result from:


A) deficiency of protein in the diet.
B) inability to catabolize ketone bodies.
C) inability to convert phenylalanine to tyrosine.
D) inability to synthesize phenylalanine.
E) production of enzymes containing no phenylalanine.

F) A) and B)
G) None of the above

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In the human genetic disease maple syrup urine disease,the metabolic defect involves:


A) a deficiency of the vitamin niacin.
B) oxidative decarboxylation.
C) synthesis of branched chain amino acids.
D) transamination of an amino acid.
E) uptake of branched chain amino acids into liver.

F) A) and B)
G) C) and D)

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Give the name and draw the structure of the α\alpha -keto acid resulting when the following amino acids undergo transamination with α\alpha -ketoglutarate: (a)glutamate; (b)aspartate; (b)alanine.

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(a)blured image-ketogl...

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Which of these is not a protease that acts in the small intestine?


A) Chymotrypsin
B) Elastase
C) Enteropeptidase
D) Secretin
E) Trypsin

F) A) and D)
G) A) and E)

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Describe the three different forms of nitrogen by which different organisms dispose of excess nitrogen obtained in the diet.Give examples of organisms that produce these different forms.

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(1)Ammonotelic: release into the surroun...

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Diagram the degradative pathway from proline to an intermediate of either glycolysis or the citric acid cycle.Show structures of intermediates and indicate where cofactors are involved.

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The shortest pathway is from p...

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Which of these directly donates a nitrogen atom for the formation of urea during the urea cycle?


A) Adenine
B) Aspartate
C) Creatine
D) Glutamate
E) Ornithine

F) B) and D)
G) A) and C)

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B

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