Morohoshi F, Munakata N
J Bacteriol. 1985 Mar;161(3):825-30. doi: 10.1128/jb.161.3.825-830.1985.
Three mutant strains exhibiting hyper-sensitivity to N-methyl-N'-nitro-N-nitrosoguanidine, but not to methyl methanesulfonate, were selected by a replica method from mutagenized spores of Bacillus subtilis. All three were totally deficient in the adaptive response to N-methyl-N'-nitro-N-nitrosoguanidine with regard to both lethality and mutagenesis. The activity to destroy O6-methylguanine residues in the methylated DNA was not elevated in the mutant cells by the pretreatment with sublethal concentrations of N-methyl-N'-nitro-N-nitrosoguanidine. This deficiency corresponded to the persistence of O6-methylguanine residues in the DNA of both control and pretreated mutant cells challenged with the drug. The lethal and mutagenic sensitivity of the mutant strains were observed only for methyl- or ethyl-nitroso compounds that are thought to be active as inducers and are also active in O-alkylation. Except for the insensitivity to methyl methanesulfonate, the phenotypes of these mutants look very similar to those of ada mutants isolated previously in Escherichia coli.
通过影印法从枯草芽孢杆菌诱变孢子中筛选出三株对N-甲基-N'-硝基-N-亚硝基胍表现出超敏感性但对甲磺酸甲酯不敏感的突变菌株。这三株菌株在对N-甲基-N'-硝基-N-亚硝基胍的致死性和诱变作用方面的适应性反应均完全缺失。用亚致死浓度的N-甲基-N'-硝基-N-亚硝基胍预处理后,突变细胞中破坏甲基化DNA中O6-甲基鸟嘌呤残基的活性并未升高。这种缺陷与用该药物攻击的对照和预处理突变细胞的DNA中O6-甲基鸟嘌呤残基的持续存在相对应。仅对被认为作为诱导剂有活性且在O-烷基化中也有活性的甲基或乙基亚硝基化合物观察到突变菌株的致死性和诱变敏感性。除了对甲磺酸甲酯不敏感外,这些突变体的表型与先前在大肠杆菌中分离出的ada突变体非常相似。