Bremer E, Gerlach P, Middendorf A
Department of Biology, University of Konstanz, Federal Republic of Germany.
J Bacteriol. 1988 Jan;170(1):108-16. doi: 10.1128/jb.170.1.108-116.1988.
The Escherichia coli tsx gene encodes an outer membrane protein that is involved in nucleoside uptake and serves as the receptor protein for colicin K and several bacteriophages. Regulation of its expression was studied by using tsx-lacZ protein and operon fusion strains carrying mutations in deoR, cytR, and crp. The cytR-encoded repressor had a stronger influence on tsx transcription than the DeoR repressor did, and the level of tsx expression in a deoR cytR double mutant was approximately the sum of those found in the single deoR and cytR strains. This double negative control of Tsx synthesis was superceded by a positive control mechanism mediated by the cyclic AMP-catabolite activator protein (cAMP-CAP) complex. Our results suggest that tsx expression is controlled at two separate and differently regulated promoters: the weaker promoter (P1) is repressible by DeoR, while the stronger promoter (P2) is subject to negative and positive control by the CytR repressor and the cAMP-CAP complex, respectively. A mutant was isolated that showed unaltered tsx regulation by DeoR and the cAMP-CAP complex but strongly reduced repression by CytR. This tsx operator mutant was used to obtain a suppressor mutation located on a plasmid carrying the cloned cytR gene that restored CytR control of tsx expression. The direction of tsx transcription was determined and found to be counterclockwise on the E. coli chromosome.
大肠杆菌tsx基因编码一种外膜蛋白,该蛋白参与核苷摄取,并作为大肠杆菌素K和几种噬菌体的受体蛋白。通过使用tsx - lacZ蛋白以及携带deoR、cytR和crp突变的操纵子融合菌株,研究了其表达调控。与DeoR阻遏物相比,由cytR编码的阻遏物对tsx转录的影响更强,并且在deoR cytR双突变体中tsx的表达水平大约是在单个deoR和cytR菌株中所发现水平的总和。Tsx合成的这种双重负调控被由环腺苷酸 - 分解代谢物激活蛋白(cAMP - CAP)复合物介导的正调控机制所取代。我们的结果表明,tsx的表达受两个单独且调控方式不同的启动子控制:较弱的启动子(P1)可被DeoR阻遏,而较强的启动子(P2)分别受CytR阻遏物的负调控和cAMP - CAP复合物的正调控。分离出了一个突变体,该突变体显示DeoR和cAMP - CAP复合物对tsx的调控未改变,但CytR的阻遏作用大幅降低。这个tsx操纵基因突变体被用于获得位于携带克隆cytR基因的质粒上的一个抑制突变,该抑制突变恢复了CytR对tsx表达的控制。确定了tsx转录的方向,发现在大肠杆菌染色体上是逆时针方向。