A) serine
B) glycine
C) cysteine
D) lysine
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Multiple Choice
A) precursor in the synthesis of aspartate
B) an intermediate in the urea cycle
C) formation of ornithine from serine
D) condenses with aspartate to form argininosuccinate
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Multiple Choice
A) urine turning dark on standing due to air oxidation
B) deficiency or defect in phenylalanine hydroxylase
C) treated by putting patient on a diet high in phenylalanine
D) treated patients suffering severe mental retardation
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Multiple Choice
A) the enzyme nitrogenase
B) GTP
C) H₂Ofree conditions
D) a strong oxidizer such as ferredoxin
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Multiple Choice
A) glutamate dehydrogenase and glutamine synthetase
B) nitrogenase and glutamate dehydrogenase
C) glutamine synthetase and nitrogenase
D) α-ketoglutarate dehydrogenase and glutamate synthetase
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Multiple Choice
A) The coenzyme needed is thiamine pyrophosphate (TPP) .
B) It is characterized by the transfer of an α-carboxyl group from an amino acid to the α-keto position of an α-keto acid.
C) The amino donor becomes an α-keto acid.
D) Humans are capable of synthesizing the α-keto acid analog of essential amino acids and using transamination to form the amino acids,but are not able to construct carbon skeletons of the non-essential amino acids.
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Multiple Choice
A) They lack the enzyme aminotransferase.
B) They lack the enzymes to reduce N₂ and NO₃- to NH₄⁺.
C) They lack carbamoyl-phosphate synthetase I.
D) They lack glutamate dehydrogenase.
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Multiple Choice
A) asparagine
B) aspartame
C) oxaloacetate
D) α-ketoglutarate
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Multiple Choice
A) breaks the N₂ triple bond
B) provides electrons
C) phosphorylates the enzyme
D) transfers electrons from ferredoxin
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Multiple Choice
A) They have an extra amino group.
B) They have an additional methylene group.
C) They have an additional carboxyl group.
D) They have an aldehyde group.
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Multiple Choice
A) proline
B) valine
C) alanine
D) glutamate
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Multiple Choice
A) the amide N of Asn
B) the N of Asp
C) the R-group N of Lys
D) the N of glucosamine
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Multiple Choice
A) reducing NO₃- to N₂
B) using NO₃- as an electron acceptor in their energy-producing pathways
C) oxidizing NH₄⁺ to NO₃-
D) reducing the combined-nitrogen levels
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Multiple Choice
A) nitrogen
B) carbon
C) nitrite
D) carbon dioxide
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Multiple Choice
A) excess folic acid
B) homocystinuria at very low levels
C) lower risk of heart attack and stroke
D) folic acid-dependent conversion of homocysteine to methionine
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Multiple Choice
A) threonine
B) homocysteine
C) tyrosine
D) alanine
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Multiple Choice
A) It catalyzes the adenylation of glutamine synthetase.
B) It exists in 2 forms,PIIA and PIID.PIIA causes the deadenylation of glutamine synthetase,and its activity increases with an increase in glutamine.
C) AT:PIIA needs ATP to complete the reaction.
D) It is an enzyme that causes the adenylation/deadenylation of a specific tyrosine residue.
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Multiple Choice
A) methionine
B) isoleucine
C) glutamate
D) cysteine
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Multiple Choice
A) those that are precursors for glucose synthesis
B) those degraded to yield acetyl-CoA or acetoacetate
C) those that cannot be converted to fatty acids or ketone bodies
D) those degraded to yield succinyl-CoA,pyruvate,a-ketoglutarate,fumarate,and oxaloacetate
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Multiple Choice
A) They lack the enzymes for photosynthesis.
B) They lack the enzymes for the glyoxylate cycle.
C) They lack the enzymes for the glutamine synthesis pathway .
D) They lack the enzymes for the Phe,Val,Leu,Ile,and His biosynthetic pathways.
Correct Answer
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