Härtig Elisabeth, Geng Hao, Hartmann Anja, Hubacek Angela, Münch Richard, Ye Rick W, Jahn Dieter, Nakano Michiko M
Institute of Microbiology, University of Braunschweig, Braunschweig, Germany.
J Bacteriol. 2004 Oct;186(19):6477-84. doi: 10.1128/JB.186.19.6477-6484.2004.
Transcription of the yclJK operon, which encodes a potential two-component regulatory system, is activated in response to oxygen limitation in Bacillus subtilis. Northern blot analysis and assays of yclJ-lacZ reporter gene fusion activity revealed that the anaerobic induction is dependent on another two-component signal transduction system encoded by resDE. ResDE was previously shown to be required for the induction of anaerobic energy metabolism. Electrophoretic mobility shift assays and DNase I footprinting experiments showed that the response regulator ResD binds specifically to the yclJK regulatory region upstream of the transcriptional start site. In vitro transcription experiments demonstrated that ResD is sufficient to activate yclJ transcription. The phosphorylation of ResD by its sensor kinase, ResE, highly stimulates its activity as a transcriptional activator. Multiple nucleotide substitutions in the ResD binding regions of the yclJ promoter abolished ResD binding in vitro and prevented the anaerobic induction of yclJK in vivo. A weight matrix for the ResD binding site was defined by a bioinformatic approach. The results obtained suggest the existence of a new branch of the complex regulatory system employed for the adaptation of B. subtilis to anaerobic growth conditions.
编码一种潜在双组分调节系统的yclJK操纵子的转录,在枯草芽孢杆菌中会因氧限制而被激活。Northern印迹分析和yclJ-lacZ报告基因融合活性测定表明,厌氧诱导依赖于resDE编码的另一种双组分信号转导系统。先前已证明ResDE是诱导厌氧能量代谢所必需的。电泳迁移率变动分析和DNase I足迹实验表明,应答调节因子ResD特异性结合转录起始位点上游的yclJK调节区域。体外转录实验表明,ResD足以激活yclJ转录。ResD被其传感激酶ResE磷酸化后,作为转录激活因子的活性会大大增强。yclJ启动子的ResD结合区域中的多个核苷酸替换在体外消除了ResD结合,并在体内阻止了yclJK的厌氧诱导。通过生物信息学方法定义了ResD结合位点的权重矩阵。所得结果表明,存在一种用于枯草芽孢杆菌适应厌氧生长条件的复杂调节系统的新分支。