Study for the Cengage Microbiology Test with helpful multiple choice questions and detailed explanations. Ace your exam with confidence!

Multiple Choice

Give examples of antibiotics that inhibit protein synthesis and their bacterial ribosomal targets.

Antibiotics that inhibit protein synthesis do so by binding to ribosomal subunits and blocking translation. Tetracyclines bind the 30S ribosomal subunit and prevent aminoacyl-tRNA from entering the A site, stopping the elongation of the protein. This direct mechanism—inhibition of translation via interaction with the 30S subunit—is a classic example of how a drug can stop protein synthesis, making tetracyclines a clear illustration of this concept with a defined ribosomal target. The other listed mechanisms target processes other than protein synthesis: fluoroquinolones interfere with DNA gyrase, and beta-lactams block cell wall synthesis by targeting PBPs. Macrolides and clindamycin also inhibit protein synthesis but do so by binding the 50S subunit and blocking translocation, which is a different ribosomal target from the 30S example.

Antibiotics that inhibit protein synthesis do so by binding to ribosomal subunits and blocking translation. Tetracyclines bind the 30S ribosomal subunit and prevent aminoacyl-tRNA from entering the A site, stopping the elongation of the protein. This direct mechanism—inhibition of translation via interaction with the 30S subunit—is a classic example of how a drug can stop protein synthesis, making tetracyclines a clear illustration of this concept with a defined ribosomal target.

The other listed mechanisms target processes other than protein synthesis: fluoroquinolones interfere with DNA gyrase, and beta-lactams block cell wall synthesis by targeting PBPs. Macrolides and clindamycin also inhibit protein synthesis but do so by binding the 50S subunit and blocking translocation, which is a different ribosomal target from the 30S example.