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5-氮杂胞苷对携带EcoRII限制修饰酶的大肠杆菌的杀菌作用。

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

作者信息

Friedman S

出版信息

J Bacteriol. 1982 Jul;151(1):262-8. doi: 10.1128/jb.151.1.262-268.1982.

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.

摘要

发现5-氮杂胞苷对携带指定EcoRII限制修饰系统质粒的大肠杆菌具有杀菌作用,但对缺乏这些质粒的相同菌株则无此作用。在测试的其他碱基类似物中,只有5-(β-D-呋喃核糖基)异胞苷具有类似但较弱的效果。失去EcoRII限制修饰系统的质粒不会使细菌对5-氮杂胞苷敏感。限制功能有缺陷的突变体对该药物的毒性作用仍敏感;然而,修饰功能有缺陷的突变体对5-氮杂胞苷的敏感性大部分丧失。为了观察到杀菌效果,细胞必须处于生长状态;处于生长稳定期的细胞不会被该药物杀死。该药物抑制甲基化酶,并且在用5-氮杂胞苷处理的细胞提取物中可在体外检测到该酶的抑制剂。萘啶酸抑制其形成。香豆霉素而非萘啶酸可拮抗该药物的杀菌作用;然而,香豆霉素在防止5-氮杂胞苷对甲基化酶的抑制方面比萘啶酸更有效。

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