Abstract
Antibiotics that interfere reversibly with various aspects of ribosomal function (chloramphenicol, tetracycline, erythromycin, and spectinomycin) are shown to antagonize, at barely inhibitory concentrations, the inhibitory effect of low concentrations of streptomycin (SM) on the growth of Escherichia coli. Paradoxically, these compounds can also replace SM in supporting the growth of conditionally SM-dependent mutants. Chloramphenicol produced about as much phenotypic suppression as SM in SM-sensitive strains, but less than that attainable with high concentrations of SM in resistant strains. The antagonism to SM inhibition and the phenotypic suppression appear to be specific for those growth inhibitors that act on the ribosome. Since inhibitors of the 50S subunit of the ribosome (chloramphenicol, erythromycin) are as active as inhibitors of the 30S subunit, it is suggested that phenotypic suppression by borderline concentrations of ribosome inhibitors does not necessarily depend on an alteration of the recognition region of the ribosome. Alternatively, partial inhibition of the ribosomes might change the environment in a way that would influence the frequency of misreading. Phenotypic suppression by a low concentration of SM as well as by chloramphenicol was found to depend on the presence of a trace of the required growth factor.
MeSH Terms
Bacterial Proteins/biosynthesis
Chloramphenicol/pharmacology
Drug Antagonism
Drug Resistance, Microbial
Erythromycin/pharmacology
Escherichia coli/drug effects
Genetics, Microbial
Molecular Biology
Mutation
Phenotype
Ribosomes/drug effects
Streptomycin/pharmacology
Tetracycline/pharmacology
Chemicals
Bacterial Proteins
Erythromycin
Chloramphenicol
Tetracycline
Streptomycin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kirschmann C
Davis B D
References (31)
31 references, click to expand
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