Tiganova I G, Rusina O Iu, Andreeva I V, Skavronskaia A G
Gamaleya's Research Institute for Epidemiology and Microbiology, Russian Academy of Medical Sciences, Moscow, Russia.
Mol Gen Mikrobiol Virusol. 2003(2):16-20.
The study focused on plasmid pKM101, which is a necessary component of the short-term test of Eim's system (Salmonella-microsome test), to detect the potential carcinogens through their mutagen activity. We found a previously unknown feature of the plasmid to enhance the expression of certain plasmid and chromosome genes. The purpose of the present study was to examine and specify the role of operon mucAB responsible for the mutation properties of the plasmid in activating the expression of bacterial genes. An ultraviolet-induction examination of bacterial genes, with the mutants of plasmid pKM101 affecting operon mucAB being used, showed that the function of genes mucAB did activate, but, on the contrary, suppressed the induction of genes elt (i.e. of genes controlling the formation of LT-toxin of Escherichia coli) and of sfiA (SOS-regulated gen E. col controlling the cell division.
该研究聚焦于质粒pKM101,它是艾姆斯系统(沙门氏菌-微粒体试验)短期检测的必要组成部分,用于通过潜在致癌物的诱变活性来检测它们。我们发现了该质粒一个此前未知的特性,即增强某些质粒和染色体基因的表达。本研究的目的是研究并明确负责质粒突变特性的操纵子mucAB在激活细菌基因表达中的作用。使用影响操纵子mucAB的质粒pKM101突变体对细菌基因进行紫外线诱导检测,结果表明,mucAB基因的功能确实起到了激活作用,但相反地,却抑制了elt基因(即控制大肠杆菌LT毒素形成的基因)和sfiA基因(调控大肠杆菌细胞分裂的SOS调节基因E)的诱导。