Landini P, Hajec L I, Volkert M R
Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester 01655.
J Bacteriol. 1994 Nov;176(21):6583-9. doi: 10.1128/jb.176.21.6583-6589.1994.
Expression of the Escherichia coli aidB gene is induced in vivo by alkylation damage in an ada-dependent pathway and by anaerobiosis or by acetate at pH 6.5 in an ada-independent fashion. In this report, we present data on aidB gene structure, function, and regulation. The aidB gene encodes a protein of ca. 60 kDa that is homologous to several mammalian acyl coenzyme A dehydrogenases. Accordingly, crude extracts from an aidB-overexpressing strain showed isovaleryl coenzyme A dehydrogenase activity. aidB overexpression also reduced N-methyl-N'-nitro-N-nitrosoguanidine-induced mutagenesis. Both ada- and acetate/pH-dependent induction of aidB are regulated at the transcriptional level, and the same transcriptional start point is used for both kinds of induction. Ada protein plays a direct role in aidB regulation: methylated Ada is able to bind to the aidB promoter region and to activate transcription from aidB in an in vitro transcription-translation system using crude E. coli extracts.
大肠杆菌aidB基因的表达在体内可通过ada依赖途径由烷基化损伤诱导,也可通过厌氧状态或在pH 6.5时由乙酸盐以ada非依赖方式诱导。在本报告中,我们展示了关于aidB基因结构、功能和调控的数据。aidB基因编码一种约60 kDa的蛋白质,该蛋白质与几种哺乳动物酰基辅酶A脱氢酶同源。因此,来自aidB过表达菌株的粗提物显示出异戊酰辅酶A脱氢酶活性。aidB过表达还降低了N-甲基-N'-硝基-N-亚硝基胍诱导的诱变作用。aidB的ada依赖型和乙酸盐/pH依赖型诱导均在转录水平受到调控,且两种诱导方式使用相同的转录起始点。Ada蛋白在aidB调控中起直接作用:甲基化的Ada能够结合到aidB启动子区域,并在使用大肠杆菌粗提物的体外转录-翻译系统中激活aidB的转录。