Abstract
The aminoglycosides, a group of structurally related antibiotics, bind to rRNA in the small subunit of the prokaryotic ribosome. Most aminoglycosides are inactive or weakly active against eukaryotic ribosomes. A major difference in the binding site for these antibiotics between prokaryotic and eukaryotic ribosomes is the identity of the nucleotide at position 1408 (Escherichia coli numbering), which is an adenosine in prokaryotic ribosomes and a guanosine in eukaryotic ribosomes. Expression in E.coli of plasmid-encoded 16S rRNA containing an A1408 to G substitution confers resistance to a subclass of the aminoglycoside antibiotics that contain a 6' amino group on ring I. Chemical footprinting experiments indicate that resistance arises from the lower affinity of the drug for the eukaryotic rRNA sequence. The 1408G ribosomes are resistant to the same subclass of aminoglycosides as previously observed both for eukaryotic ribosomes and bacterial ribosomes containing a methylation at the N1 position of A1408. The results indicate that the identity of the nucleotide at position 1408 is a major determinant of specificity of aminoglycoside action, and agree with prior structural studies of aminoglycoside-rRNA complexes.
MeSH Terms
Adenosine/genetics,metabolism
Amino Acid Substitution
Aminoglycosides
Ampicillin/pharmacology
Anti-Bacterial Agents/chemistry,metabolism,pharmacology
Base Sequence
Binding Sites
Drug Resistance, Microbial/genetics
Escherichia coli/drug effects,genetics,growth & development
Eukaryotic Cells/drug effects,metabolism
Guanosine/genetics,metabolism
Methylation
Microbial Sensitivity Tests
RNA, Ribosomal, 16S/genetics,metabolism
Ribosomes/chemistry,drug effects,genetics,metabolism
Species Specificity
Spectinomycin/pharmacology
Substrate Specificity
Sulfuric Acid Esters
Chemicals
Aminoglycosides
Anti-Bacterial Agents
RNA, Ribosomal, 16S
Sulfuric Acid Esters
Guanosine
Ampicillin
Spectinomycin
dimethyl sulfate
Adenosine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Recht M I
Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305-5126, USA.
Douthwaite S
Puglisi J D
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