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Antimicrobial peptides (AMPs) frequently work by


A) inhibiting protein synthesis.
B) disrupting the plasma membrane.
C) complementary base pairing with DNA.
D) inhibiting cell-wall synthesis.
E) hydrolyzing peptidoglycan.

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

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Figure 20.2 Figure 20.2    -The antibiotic chloramphenicol binds to the 50S subunit of the ribosome,as shown in Figure 20.2.The effect is to A) prevent mRNA-ribosome binding in eukaryotes. B) prevent peptide bond formation in prokaryotes. C) prevent polypeptide elongation in eukaryotes. D) prevent transcription in prokaryotes. E) prevent ribosome formation in bacteria. -The antibiotic chloramphenicol binds to the 50S subunit of the ribosome,as shown in Figure 20.2.The effect is to


A) prevent mRNA-ribosome binding in eukaryotes.
B) prevent peptide bond formation in prokaryotes.
C) prevent polypeptide elongation in eukaryotes.
D) prevent transcription in prokaryotes.
E) prevent ribosome formation in bacteria.

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

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Which of the following statements about drug resistance is FALSE?


A) It may be carried on a plasmid.
B) It may be transferred from one bacterium to another during conjugation.
C) It may be due to enzymes that degrade some antibiotics.
D) It is found only in gram-negative bacteria.
E) It may be due to decreased uptake of a drug.

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

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PABA serves as the competitive inhibitor in the action of sulfanilamides.

A) True
B) False

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Penicillin does not directly kill bacteria.Why,then,is it considered to be bacteriocidal?

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Figure 20.1 Figure 20.1    -The antibiotic tetracycline binds to the 30S subunit of the ribosome,as shown by the dark black bar on the right portion of the diagram in Figure 20.1.The effect is to A) prevent attachment of DNA. B) prevent peptide bond formation. C) prevent transcription. D) stop the ribosome from moving along the mRNA. E) interfere with the attachment of the tRNA to mRNA-ribosome complex. -The antibiotic tetracycline binds to the 30S subunit of the ribosome,as shown by the dark black bar on the right portion of the diagram in Figure 20.1.The effect is to


A) prevent attachment of DNA.
B) prevent peptide bond formation.
C) prevent transcription.
D) stop the ribosome from moving along the mRNA.
E) interfere with the attachment of the tRNA to mRNA-ribosome complex.

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

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Which of the following antimicrobial agents is recommended for use against fungal infections?


A) amphotericin B
B) bacitracin
C) cephalosporin
D) penicillin
E) polymyxin

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

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Which of the following does NOT affect eukaryotic cells?


A) antiprotozoan drugs
B) antihelminthic drugs
C) antifungal drugs
D) nucleotide analogs
E) semisynthetic penicillins

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

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Penicillin was considered a "miracle drug" for all of the following reasons EXCEPT


A) it was the first antibiotic.
B) it does not affect eukaryotic cells.
C) it inhibits gram-positive cell wall synthesis.
D) it has selective toxicity.
E) it kills bacteria.

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

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From the data in Table 20.1,you can predict that the effect of the drug on a different microbe


A) will be the same.
B) will be weaker.
C) will be stronger.
D) can't be predicted from the information provided.

E) C) and D)
F) B) and C)

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In the presence of penicillin,a cell dies because


A) it lacks a cell wall.
B) it plasmolyzes.
C) it undergoes lysis.
D) it lacks a cell membrane.
E) its contents leak out.

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

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Figure 20.1 Figure 20.1    -In Figure 20.1,why is tetracycline selectively toxic against bacteria? A) Eukaryotic cells will enzymatically destroy the drug. B) Eukaryotic cells will actively pump the drug out of their interiors. C) The drug affects peptidoglycan synthesis,and eukaryotic cells have no peptidoglycan. D) The drug binds to the 30S small ribosomal subunit - eukaryotes have a 40S small subunit. E) Eukaryotes lack a small ribosomal subunit,so the drug cannot negatively affect them. -In Figure 20.1,why is tetracycline selectively toxic against bacteria?


A) Eukaryotic cells will enzymatically destroy the drug.
B) Eukaryotic cells will actively pump the drug out of their interiors.
C) The drug affects peptidoglycan synthesis,and eukaryotic cells have no peptidoglycan.
D) The drug binds to the 30S small ribosomal subunit - eukaryotes have a 40S small subunit.
E) Eukaryotes lack a small ribosomal subunit,so the drug cannot negatively affect them.

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

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Phage therapy has been used in the past as an effective,common antiviral treatment.

A) True
B) False

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An official from an international health agency predicts that if all countries enacted legislation to only sell antibiotics with a prescription,then the rate of antibiotic resistant would "grind to a halt." Do you agree? Explain.

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Mebendazole is used to treat cestode infections.It interferes with microtubule formation;therefore,it would NOT affect


A) bacteria.
B) fungi.
C) helminths.
D) human cells.
E) protozoa.

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

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Figure 20.4 Figure 20.4   The structures of the influenza drug Tamiflu and sialic acid,the substrate for influenza virus's neuramidase,are shown in Figure 20.4.What is the method of action of Tamiflu? A) inhibits cell wall synthesis B) inhibits plasma membrane synthesis C) inhibits synthesis of neuramidase D) competitive inhibition E) prevents synthesis of virus spikes The structures of the influenza drug Tamiflu and sialic acid,the substrate for influenza virus's neuramidase,are shown in Figure 20.4.What is the method of action of Tamiflu?


A) inhibits cell wall synthesis
B) inhibits plasma membrane synthesis
C) inhibits synthesis of neuramidase
D) competitive inhibition
E) prevents synthesis of virus spikes

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

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Most of the available antimicrobial agents are effective against


A) viruses.
B) bacteria.
C) fungi.
D) protozoa.

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

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Due to its target,rifamycins such as rifampin can be effective over a broad spectrum.

A) True
B) False

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Which compound would be the most useful to treat candidiasis?


A) uracil
B) thymine
C) flucytosine
D) guanine
E) penicillin

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

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In what way are semisynthetic penicillins and natural penicillins alike?


A) Both are broad spectrum.
B) Both are resistant to penicillinase.
C) Both are resistant to stomach acids.
D) Both are bactericidal.
E) Both are based on β-lactam.

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

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