首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >New tester strains of Salmonella typhimurium lacking O6-methylguanine DNA methyltransferases and highly sensitive to mutagenic alkylating agents.
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New tester strains of Salmonella typhimurium lacking O6-methylguanine DNA methyltransferases and highly sensitive to mutagenic alkylating agents.

机译:新的测试株鼠伤寒沙门氏菌缺乏O6-甲基鸟嘌呤DNA甲基转移酶,并且对诱变的烷基化剂高度敏感。

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摘要

Salmonella typhimurium YG7104 and YG7108 are derivatives of the Ames tester strain TA1535, and have chromosomal deletions of the ogtST gene or both the ogtST and adaST genes, respectively. The ogtST and adaST genes encode O6-methylguanine DNA methyltransferases that are involved in the repair of DNA damage caused by alkylating agents. The sensitivities of these strains to 15 mutagens with different structures were tested and compared with those of the parent strain TA1535. Deletion of ogtST or ogtST plus adaST substantially increased the sensitivity of strain TA1535 to the mutagenicity of alkylating agents, such as N-ethyl-N'-nitro-N-nitrosoguanidine, ethyl methanesulfonate or dimethylnitrosamine (DMN). Preincubation of the chemical with S9 mix and bacteria for 20 min at 37 degrees C before pouring them together on agar plates was not necessary to detect the mutagenicity of DMN when strain YG7104 or YG7108 was used as a tester strain. Introduction of plasmid pKM101 did not enhance but rather decreased the sensitivity of YG7104 and YG7108 to alkylating agents. Since the new strains are highly sensitive only to alkylating agents, they will be useful to detect the mutagenicity with high efficiency and to study the mechanism of mutagenesis induced by environmental alkylating agents.
机译:鼠伤寒沙门氏菌YG7104和YG7108是Ames测试仪菌株TA1535的衍生物,分别具有ogtST基因或ogtST和adaST基因的染色体缺失。 ogtST和adaST基因编码O6-甲基鸟嘌呤DNA甲基转移酶,这些酶参与修复烷化剂引起的DNA损伤。测试了这些菌株对15种具有不同结构的诱变剂的敏感性,并与亲本菌株TA1535进行了比较。删除ogtST或ogtST加上adaST大大提高了菌株TA1535对烷基化试剂(例如N-乙基-N'-硝基-N-亚硝基胍,甲烷磺酸乙酯或二甲基亚硝胺(DMN))致突变性的敏感性。将菌株YG7104或YG7108用作测试菌株时,在将S9混合物和细菌在琼脂平板上倒入一起之前在37摄氏度下预孵育20分钟对于检测DMN的致突变性不是必需的。质粒pKM101的引入没有增强而是降低了YG7104和YG7108对烷基化剂的敏感性。由于新菌株仅对烷基化剂高度敏感,因此它们可用于高效检测诱变性和研究环境烷基化剂诱导的诱变机理。

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