Exam 3 - Exam Questions From Book Flashcards
2. Identify the metabolite that does NOT serve as a precursor of a dietarily essential amino acid: A. Alpha-ketoglutarate B. 3-phosphoglycerate C. Glutamate D. Aspartate E. Histamine
E. Histamine
Histamine is a catabolite, not a precursor, of histidine.
4. Select the CORRECT answer: The first reaction in the degradation of most of the protein amino acids involves the participation of: A. NAD+ B. Thiamine pyrophosphate (TPP) C. Pyridoxal phosphate D. FAD E. NAD+ and TPP
C. Pyridoxal phosphate
Pyridoxal-dependent transamination is the first reaction in
degradation of all the common amino acids except threonine,
lysine, proline, and hydroxyproline.
5. Identify the amino acid that is the major contributor to the transport of nitrogen destined for excretion as urea: A. Alanine B. Glutamine C. Glycine D. Lysine E. Ornithine
B. Glutamine
- For metabolic disorders of the urea cycle, which statement is NOT CORRECT:
A. Ammonia intoxication is most severe when the metabolic block in the urea cycle occurs prior to the reaction catalyzed by argininosuccinate synthase
B. Clinical symptoms include mental retardation and the avoidance of protein-rich foods
C. Clinical signs can include acidosis
D. Aspartate provides the second nitrogen of argininosuccinate
E. Dietary management focuses on a low-protein diet ingested as frequent small meals
C. Clinical signs can include acidosis
Due to the failure to incorporate NH4+ into urea, clinical
signs of metabolic disorders of the urea cycle include alkalosis,
not acidosis.
- Select one of the following statements that is NOT CORRECT:
A. One metabolic function of glutamine is to sequester nitrogen in a nontoxic form
B. Liver glutamate dehydrogenase is allosterically inhibited by ATP and activated by ADP.
C. Urea is formed both from absorbed ammonia produced by enteric bacteria and from ammonia generated by tissue metabolic activity.
D. The concerted action of glutamate dehydrogenase and glutamate aminotransferase may be termed transdeamination
E. Fumarate generated during biosynthesis of argininosuccinate ultimately forms oxaloacetate in reactions in mitochondria catalyzed successively by fumarase and malate dehydrogenase
E. Fumarate generated during biosynthesis of argininosuccinate ultimately forms oxaloacetate in reactions in mitochondria catalyzed successively by fumarase and malate dehydrogenase
Cytosolic fumarase and cytosolic malate dehydrogenase
convert fumarase to oxaloacetate following a cytosolic reaction of the urea cycle. The mitochondrial fumarase and malate dehydrogenase function in the TCA cycle, not urea biosynthesis.
- Select one of the following statements that is NOT CORRECT:
A. Threonine provides the thioethanol moiety for biosynthesis of coenzyme A
B. Histamine arises by decarboxylation of histidine
C. Ornithine serves as a precursor of both spermine and spermidine
D. Serotonin and melatonin are metabolites of tryptophan
E. Glycine, arginine, and methionine each contribute atoms for biosynthesis of creatinine
A. Threonine provides the thioethanol moiety for biosynthesis of coenzyme A
Serine, not threonine, provides the thioethanol moiety of coenzyme A.
- Select one of the following statements that is NOT CORRECT:
A. Excreted creatinine is a function of muscle mass, and can be used to determine whether a patient has provided a complete 24-hour urine specimen
B. Many drugs and drug catabolites are excreted in urine as glycine conjugates.
C. The major nonprotein metabolic fate of methionine is conversion to S-adenosylmethionine.
D. The concentration of histamine in brain hypothalamus exhibits a circadian rhythm
E. Decarboxylation of glutamine forms the inhibitory neurotransmitter GABA
E. Decarboxylation of glutamine forms the inhibitory neurotransmitter GABA
Decarboxylation of glutamate, not glutamine forms GABA.
15. Which of the following is NOT a hemoprotein? A. Myoglobin B. Cytochrome c C. Catalase D. Cytochrome P450 E. Albumin
E. Albumin
Albumin is not a hemoprotein. In cases of hemolytic anemia, albumin can bind some metheme, but unlike the other proteins listed, albumin is not a hemoprotein.
16. A 30-year old man presented at a clinic with a history of intermittent abdominal pain and episodes of confusion and psychiatric problems. Laboratory tests revealed increases of urinary Gamma-aminolevulinate and porphobilinogen. Mutational analysis revealed a mutation in the gene for uroporphyrinogen I synthase. The probable diagnosis was: A. Acute intermitten porphyria B. X-linked sideroblastic anemia C. Congenital erythropoietic porphyria D. Porphyria cutanea tarda E. Variegate porphyria
A. Acute intermittent porphyria
Acute intermittent porphyria is due to mutations in the gene for uroporphyrin I synthase
- Select one of the following statements that is NOT CORRECT:
A. Bilirubin is a cyclic tetrapyrrole
B. Albumin-bound bilirubin is transported to the liver
C. High levels of bilirubin can cause damage to the brains of newborn infants.
D. Bilirubin contains methyl and vinyl groups
E. Bilirubin does not contain iron
A. Bilirubin is a cyclic tetrapyrrole
Bilirubin is a linear tetrapyrrole.
18. She had noted that her stools had been very pale for some time. Lab tests revealed a very high level of direct bilirubin, and also elevated urinary bilirubin. The plasma level of alanine aminotransferase (ALT) was only slightly elevated, whereas the level of alkaline phosphatase was markedly elevated. Abdominal ultrasonography revealed no evidence of gallstones. Of the following, which is most likely the diagnosis? A. Gilbert Syndrome B. Hemolytic anemia C. Type I Crigler-Najjar syndrome D. Carcinoma of the pancreas E. Infectious hepatitis
D. Carcinoma of the pancreas
The severe jaundice, upper abdominal pain, and weight loss plus the lab results indicating an obstructive type of jaundice are consistent with cancer of the pancreas.
- Which one of the following statements about beta-gamma methylene and beta-gamma imino derivatives of purine and pyrimidine triphosphates is CORRECT?
A. They are potential anticancer drugs
B. They are precursors of B vitamins.
C. They readily undergo hydrolytic removal of the terminal phosphate.
D. They can be used to implicate involvement of nucleotide triphosphates by effects other than phosphoryl transfer.
E. They serve as polynucleotide precursors.
D. They can be used to implicate involvement of nucleotide triphosphates by effects other than phosphoryl transfer.
β,γ-Methylene and β,γ-imino purine and pyrimidine triphosphates do not readily release the terminal phosphate by hydrolysis or by phosphoryl group transfer.
- Which one of the following statements about nucleotide structures is NOT CORRECT?
A. Nucleotides are polyfunctional acids.
B. Caffeine and theobromine differ structurally solely with respect to the number of methyl groups attached to their ring nitrogens.
C. The atoms of the purine ring portion of pyrimidines are numbered in the same direction as those of a pyrimidine
D. NAD+, FMN, “active methionine” and coenzyme A all are derivatives of ribonucleotides
E. 3’,5’-cyclic AMP and GMP (cAMP and cGMP) serve as second messengers in human biochemistry
D. NAD+, FMN, “active methionine” and coenzyme A all are derivatives of ribonucleotides
- Which of the following statements about purine nucleotide metabolism is NOT CORRECT?
A. An early step in purine biosynthesis is the formation of PRPP
B. Inosine monophosphate (IMP) is a precursor of both AMP and GMP
C. Orotic acid is an intermediate in pyrimidine nucleotide biosynthesis
D. Humans catabolize uridine and pseudouridine by analogous reactions
E. Ribonucleotide reductase converts nucleoside diphosphates to the corresponding deoxyribonucleoside diphosphates.
E. Ribonucleotide reductase converts nucleoside diphosphates to the corresponding deoxyribonucleoside diphosphates.
Ribonucleotide reductase converts RIBOnucleoside diphosphates to the corresponding deoxyribonucleoside diphosphates.
- Which of the following statements is NOT CORRECT?
A. Metabolic disorders are only infrequently associated with defects in the catabolism of purines
B. Immune dysfunction are associated both with a defective adenosine deaminase and with a defective purine nucleoside phosphorylase
C. The Lesch-Nyhan syndrome reflects a defect in hypoxanthine-guanine phosphoribosyl transferase
D. Xanthine lithiasis can be due to a severe defect in xanthine oxidase
E. Hyperuricemia can result from conditions such as cancer characterized by enhanced by tissue turnover.
A. Metabolic disorders are only infrequently associated with defects in the catabolism of purines
Metabolic disorders are infrequently associated with
defects in pyrimidine catabolism, which forms water-soluble
- Which of the following components are found in DNA?
A. A phosphate group, adenine, and ribose
B. A phosphate group, guanine, and deoxyribose
C. Cytosine and ribose
D. Thymine and deoxyribose
E. A phosphate group and adenine
B. A phosphate group, guanine, and deoxyribose
- The backbone of a DNA molecule consists of which of the following?
A. Alternating sugars and nitrogenous bases
B. Nitrogenous bases alone
C. Phosphate groups alone
D. Alternating phosphate and sugar groups
E. Five carbon sugars alone
D. Alternating phosphate and sugar groups
7. The interconnecting bonds that connect the nucleotides of RNA and DNA are termed: A. N-glycosidic bonds B. 3’,5’ phosphodiester bonds C. Phosphomonoesters D. -2’ phosphodiester linkages E. peptide nucleic bonds
B. 3’,5’ phosphodiester bonds
8. Which component of the DNA duplex causes the molecule to have a net negative charge at physiological pH? A. Deoxyribose B. Ribose C. Phosphate groups D. Chlorine ion E. Adenine
C. Phosphate groups
11. Name the mechanism through which RNAs are synthesized from DNA A. Replicational duplication B. Translation C. Translesion repair D. Transesterification E. Transcription
E. Transcription
13. Name the enzyme that synthesizes RNA from a double stranded DNA template. A. RNA-dependent RNA polymerase B. DNA-dependent RNA convertase C. RNA-dependent replicase D. DNA-dependent RNA polymerase E. Reverse transcriptase
D. DNA-dependent RNA polymerase
20. What is the name of the unusual repeated stretch of DNA localized at the tips of all eukaryotic chromosomes? A. Kinetochore B. Telomere C. Centriole D. Chromomere E. Micromere
B. Telomere
21. Given that DNA polymerases are unable to synthesize DNA without a primer, what molecule serves as the primer for these enzymes during DNA replication? A. Five carbon sugars B. Deoxyribose alone C. A short RNA molecule D. Proteins with free hydroxyl groups E. Phosphomonoester
C. A short RNA molecule
22. The discontinuous DNA replication that occurs during replication is catalyzed via the production of small DNA segments termed A. Okazaki fragments B. Toshihiro pieces C. Onishi oligonucleotides D. Crick strands E. Watson fragments
A. Okazaki fragments
23. What molecule or force supplies the energy that drives the relief of mechanical strain by DNA gyrase? A. Pyrimidine to purine conversion B. Hydrolysis of GTP C. Hydrolysis of ATP D. Glycolysis E. A proton gradient molecule or force
C. Hydrolysis of ATP
- Eukaryotic RNA polymerases all have a requirement for a large variety of accessory proteins to enable them to bind promoters and form physiologically relevant transcription complexes; these proteins are termed:
A. Basal or general transcription factors
B. Activators
C. Accessory factors
D. Elongation factors
E. Facilitator polypeptides
A. Basal or general transcription factors
31. The DNA segment from which the primary transcript is copied or transcribed is called: A. Coding strand B. Initiator methionine domain C. Translation unit D. Transcriptome E. Initial codon
A. Coding strand