Dosch D C, Helmer G L, Sutton S H, Salvacion F F, Epstein W
Department of Microbiology, University of Chicago, Illinois 60637.
J Bacteriol. 1991 Jan;173(2):687-96. doi: 10.1128/jb.173.2.687-696.1991.
The analysis of mutants of Escherichia coli that require elevated concentrations of K+ for growth has revealed two new genes, trkG, near minute 30 within the cryptic rac prophage, and trkH, near minute 87, the products of which affect constitutive K+ transport. The analysis of these and other trk mutations suggests that high rates of transport, previously considered to represent the activity of a single system, named TrkA, appear to be the sum of two systems, here named TrkG and TrkH. Each of these two is absolutely dependent on the product of the trkA gene, a cytoplasmic protein associated with the inner membrane (D. Bossemeyer, A. Borchard, D. C. Dosch, G. C. Helmer, W. Epstein, I. R. Booth, and E. P. Bakker, J. Biol. Chem. 264:16403-16410, 1989). The TrkH system is also dependent on the products of the trkH and trkE genes, while the TrkG system is also dependent on the product of the trkG gene and partially dependent on the product of the trkE gene. It is suggested that the trkH and trkG products are membrane proteins that form the transmembrane path for the K+ movement of the respective systems. Two mutations altering the trkA product reduce the affinity for K+ of both TrkG and TrkH, indicating that changes in peripheral protein can alter the conformation of the sites at which K+ is bound prior to transport. The TrkD system has a relatively modest rate of transport, is dependent solely on the product of the trkD gene, and is the sole saturable system for Cs+ uptake in this species (D. Bossemeyer, A. Schlösser, and E. P. Bakker, J. Bacteriol. 171:2219-2221, 1989).
对生长需要高浓度钾离子的大肠杆菌突变体进行分析,发现了两个新基因,trkG,位于隐蔽性rac原噬菌体的约30分钟处附近,以及trkH,位于约87分钟处附近,它们的产物影响组成型钾离子转运。对这些以及其他trk突变的分析表明,先前被认为代表单个名为TrkA系统活性的高转运速率,似乎是两个系统的总和,这里命名为TrkG和TrkH。这两个系统中的每一个都绝对依赖于trkA基因的产物,trkA基因产物是一种与内膜相关的胞质蛋白(D. Bossemeyer、A. Borchard、D. C. Dosch、G. C. Helmer、W. Epstein、I. R. Booth和E. P. Bakker,《生物化学杂志》264:16403 - 16410,1989年)。TrkH系统还依赖于trkH和trkE基因的产物,而TrkG系统还依赖于trkG基因的产物,并部分依赖于trkE基因的产物。有人提出,trkH和trkG产物是膜蛋白,它们形成各自系统钾离子移动的跨膜通道。两个改变trkA产物的突变降低了TrkG和TrkH对钾离子的亲和力,表明外周蛋白的变化可以改变钾离子在转运前结合位点的构象。TrkD系统的转运速率相对适中,仅依赖于trkD基因的产物,并且是该物种中铯离子摄取的唯一可饱和系统(D. Bossemeyer、A. Schlösser和E. P. Bakker,《细菌学杂志》171:2219 - 2221,1989年)。