Choe M, Reznikoff W S
Department of Biochemistry, University of Wisconsin, Madison 53706.
J Bacteriol. 1993 Feb;175(4):1165-72. doi: 10.1128/jb.175.4.1165-1172.1993.
A newly identified anaerobically expressed locus, aeg-46.5, which is located at min 46.5 on Escherichia coli linkage map, was cloned and analyzed. The phenotype of this gene was studied by using a lacZ operon fusion. aeg-46.5 is induced anaerobically in the presence of nitrate in wild-type and narL cells. It is repressed by the narL gene product, as it showed derepressed anaerobic expression in narL mutant cells. We postulate that aeg-46.5 is subject to multiple regulatory systems, activation as a result of anaerobiosis, narL-independent nitrate-dependent activation, and narL-mediated repression. The regulatory region of aeg-46.5 was identified. A 304-bp DNA sequence which includes the regulatory elements was obtained, and the 5' end of aeg-46.5 mRNA was identified. It was verified that the anaerobic regulation of aeg-46.5 expression is controlled on the transcriptional level. Computer analysis predicted possible control sites for the NarL and FNR proteins. The proposed NarL site was found in a perfect-symmetry element. The aeg-46.5 regulatory elements are adjacent to, but divergent from, those of the eco gene.
一个新鉴定出的厌氧表达基因座aeg - 46.5被克隆并分析,该基因座位于大肠杆菌连锁图谱的46.5分钟处。通过使用lacZ操纵子融合来研究该基因的表型。在野生型和narL细胞中,aeg - 46.5在硝酸盐存在下厌氧诱导表达。它受到narL基因产物的抑制,因为在narL突变细胞中它表现出去阻遏的厌氧表达。我们推测aeg - 46.5受到多种调控系统的作用,因无氧状态而激活、不依赖narL的硝酸盐依赖性激活以及narL介导的抑制。确定了aeg - 46.5的调控区域。获得了一个包含调控元件的304 bp DNA序列,并确定了aeg - 46.5 mRNA的5'末端。证实了aeg - 46.5表达的厌氧调控是在转录水平上进行的。计算机分析预测了NarL和FNR蛋白可能的控制位点。在一个完美对称元件中发现了推测的NarL位点。aeg - 46.5的调控元件与eco基因的调控元件相邻,但方向相反。