Kaiser M, Sawers G
Lehrstuhl für Mikrobiologie der Universität München, Germany.
Mol Microbiol. 1995 Oct;18(2):331-42. doi: 10.1111/j.1365-2958.1995.mmi_18020331.x.
Expression of the Escherichia coli focA-pfl operon is induced by anaerobiosis and transcription is controlled by seven promoters. Anaerobic induction is mediated by the ArcA and Fnr transcription factors. Fnr was purified and its specific interaction with the pfl promoter-regulatory region was characterized. A single binding site could be identified by DNase I footprinting, which was centred at -40.5 bp relative to the start site of promoter 6 (P6) transcription. Activation of P6 transcription in vitro was completely dependent on the Fnr protein. Fnr-dependent transcription could be prevented by mutating the Fnr-binding site, indicating that Fnr must bind to its recognition sequence to be able to activate transcription. An Fnr-independent promoter, which overlaps the P6 promoter, was also identified and characterized in vivo and in vitro. Transcription from this promoter (termed P6A) initiated 10 bp upstream of the P6 start site and assures that low-level synthesis of the FocA protein occurs under aerobic growth conditions.
大肠杆菌focA-pfl操纵子的表达受厌氧诱导,转录由七个启动子控制。厌氧诱导由ArcA和Fnr转录因子介导。纯化了Fnr,并对其与pfl启动子调控区的特异性相互作用进行了表征。通过DNA酶I足迹法可鉴定出一个单一的结合位点,该位点相对于启动子6(P6)转录起始位点位于-40.5 bp处。体外P6转录的激活完全依赖于Fnr蛋白。通过突变Fnr结合位点可阻止Fnr依赖的转录,这表明Fnr必须与其识别序列结合才能激活转录。还在体内和体外鉴定并表征了一个与P6启动子重叠的不依赖Fnr的启动子。该启动子(称为P6A)的转录在P6起始位点上游10 bp处起始,并确保在有氧生长条件下FocA蛋白进行低水平合成。