Abstract
5-Azacytidine was found to be bactericidal to Escherichia coli carrying plasmids specifying EcoRII restriction-modification systems, but not to the same strains lacking these plasmids. Of other base analogs tested, only 5(beta-D-ribofuranosyl)isocytidine had similar, although weaker, effects. Plasmids that had lost the EcoRII restriction-modification system did not confer sensitivity to 5-azacytidine. Mutants defective in the restriction function remained sensitive to the toxic effects of the drug; however, a mutant defective in the modification function lost most of the sensitivity to 5-azacytidine. For the bactericidal effect to be seen, the cells had to be growing; cells in the stationary phase of growth were not killed by the drug. The drug inhibited the methylase enzyme, and an inhibitor of the enzyme could be detected in vitro in extracts of cells that had been treated with 5-azacytidine. This nalidixic acid inhibited its formation. Coumermycin but not nalidixic acid antagonized the bactericidal effect of the drug; however, coumermycin was more effective in preventing the inhibition of the methylase by 5-azacytidine than was nalidixic acid.
MeSH Terms
Azacitidine/pharmacology
Cell Survival/drug effects
Coliphages/drug effects,genetics
DNA Restriction Enzymes/genetics
Deoxyribonucleases, Type II Site-Specific
Escherichia coli/drug effects,enzymology,genetics
Plasmids
Species Specificity
Chemicals
DNA Restriction Enzymes
CCWGG-specific type II deoxyribonucleases
Deoxyribonucleases, Type II Site-Specific
Azacitidine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Friedman S
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