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PMID: 6177680 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Bactericidal effect of 5-azacytidine on Escherichia coli carrying EcoRII restriction-modification enzymes.

Journal of bacteriology ·Vol. 151 ·No. 1 ·1982-07-00 ·Pages 262-8

Friedman S

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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21 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1982-07-00
Pages
262-8
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC220236
Subset
IM
Grants
NIGMS NIH HHS · GM2778702 · United States
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