Antibacterial activity of 2'-esters of erythromycin.
- 1 August 1969
- journal article
- Vol. 18 (2), 159-65
Abstract
The effect of esterification at the 2'-position of desosamine on the antibacterial activity of erythromycin was investigated by determining the bacteriostatic and bactericidal activities of erythromycin and a number of its 2'-esters on S. aureus and relating these activities to the hydrolysis rates of the esters. These studies, together with comparison of the inhibition of protein synthesis in a cell-free system isolated from S. aureus, lead to the conclusion that 2'-esters of erythromycin are inactive until hydrolyzed. Loss of activity appears to result from inability of erythromycin esters to bind to bacterial ribosomes and thus inhibit synthesis of protein.This publication has 5 references indexed in Scilit:
- Mode of action of macrolidesBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1968
- The stoichiometry of erythromycin binding to ribosomal particles of Staphyhloccus aureusBiochemical Pharmacology, 1967
- Interaction of antibiotics with ribosomes: structure-function relationships and a possible common mechanism for the antibacterial action of the macrolides and lincomycin.1967
- EFFECT OF ERYTHROMYCIN ON PROTEIN BIOSYNTHESIS IN BACILLUS SUBTILIS.1963