Buchet A, Eichler K, Mandrand-Berthelot M A
Laboratoire de Génétique Moléculaire des Microorganismes et des Interactions Cellulaires, CNRS UMR 5577, Institut National des Sciences Appliquées, F-69621 Villeurbanne Cedex, France.
J Bacteriol. 1998 May;180(10):2599-608. doi: 10.1128/JB.180.10.2599-2608.1998.
The divergent structural operons caiTABCDE and fixABCX of Escherichia coli are required for anaerobic carnitine metabolism. Transcriptional monocopy lacZ fusion studies showed that both operons are coexpressed during anaerobic growth in the presence of carnitine, respond to common environmental stimuli (like glucose and nitrate), and are modulated positively by the same general regulators, CRP and FNR, and negatively by H-NS. Overproduction of the CaiF specific regulatory protein mediating the carnitine signal restored induction in an fnr mutant, corresponding to its role as the primary target for anaerobiosis. Transcript analysis identified two divergent transcription start points initiating 289 bp apart. DNase I footprinting revealed three sites with various affinities for the binding of the cAMP-CRP complex inside this regulatory region. Site-directed mutagenesis experiments indicated that previously reported perfect CRP motif 1, centered at -41.5 of the cai transcriptional start site, plays a direct role in the sole cai activation. In contrast, mutation in CRP site 2, positioned at -69.5 of the fix promoter, caused only a threefold reduction in fix expression. Thus, the role of the third CRP site, located at -126.5 of fix, might be to reinforce the action of site 2. A critical 50-bp cis-acting sequence overlapping the fix mRNA start site was found, by deletion analysis, to be necessary for cai transcription. This region is thought to be involved in transduction of the signal mediated by the CaiF regulator.
大肠杆菌的不同结构操纵子caiTABCDE和fixABCX是厌氧肉碱代谢所必需的。转录单拷贝lacZ融合研究表明,在肉碱存在的情况下,这两个操纵子在厌氧生长过程中共同表达,对常见的环境刺激(如葡萄糖和硝酸盐)有反应,并受到相同的一般调节因子CRP和FNR的正向调节以及H-NS的负向调节。介导肉碱信号的CaiF特异性调节蛋白的过量表达恢复了fnr突变体中的诱导作用,这与其作为厌氧的主要靶点的作用相对应。转录分析确定了两个相距289 bp起始的不同转录起始点。DNase I足迹分析揭示了在该调节区域内对cAMP-CRP复合物结合具有不同亲和力的三个位点。定点诱变实验表明,先前报道的以cai转录起始位点-41.5为中心的完美CRP基序1在cai的唯一激活中起直接作用。相反,位于fix启动子-69.5处的CRP位点2的突变仅导致fix表达降低三倍。因此,位于fix -126.5处的第三个CRP位点的作用可能是加强位点2的作用。通过缺失分析发现,一个与fix mRNA起始位点重叠的关键50 bp顺式作用序列对于cai转录是必需的。该区域被认为参与了由CaiF调节因子介导的信号转导。