Many antibiotics are effective as drugs to fight off bacterial infections because they inhibit protein synthesis in bacterial cells. Using the information provided in the following table that highlights several antibiotics and their mode of action, discuss which phase of translation is inhibited: initiation, elongation, or termination. What other components of the translational machinery could be targeted to inhibit bacterial protein synthesis? Antibiotic Action 1. Streptomycin Binds to 30S ribosomal subunit 2. Chloramphenicol Inhibits peptidyl transferase of 70S ribosome 3. Tetracycline Inhibits binding of charged tRNA to the A site of the ribosome 4. Erythromycin Binds to free 50S particle and prevents formation of 70S ribosome 5. Kasugamycin Inhibits binding of tRNAfMet 6. Thiostrepton Prevents translocation by inhibiting EF-G

Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN:9781305251052
Author:Michael Cummings
Publisher:Michael Cummings
Chapter9: Gene Expression And Gene Regulation
Section9.6: Translation Requires The Interaction Of Several Components
Problem 2EG: Antibiotics and Protein Synthesis Antibiotics are molecules produced by microorganisms as defense...
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Many antibiotics are effective as drugs to fight off bacterial infections
because they inhibit protein synthesis in bacterial cells.
Using the information provided in the following table that highlights
several antibiotics and their mode of action, discuss which
phase of translation is inhibited: initiation, elongation, or termination.
What other components of the translational machinery
could be targeted to inhibit bacterial protein synthesis?
Antibiotic Action
1. Streptomycin Binds to 30S ribosomal subunit
2. Chloramphenicol Inhibits peptidyl transferase of
70S ribosome
3. Tetracycline Inhibits binding of charged tRNA to
the A site of the ribosome
4. Erythromycin Binds to free 50S particle and prevents
formation of 70S ribosome
5. Kasugamycin Inhibits binding of tRNAfMet
6. Thiostrepton Prevents translocation by
inhibiting EF-G

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