Nakamura T, Katoh Y, Shimizu Y, Matsuba Y, Unemoto T
Laboratory of Membrane Biochemistry, Faculty of Pharmaceutical Sciences, Chiba University, Japan.
Biochim Biophys Acta. 1996 Dec 18;1277(3):201-8. doi: 10.1016/s0005-2728(96)00097-7.
Novel genes that functionally complement the growth of K+ uptake-deficient mutant strain of Escherichia coli TK420 have been cloned from the marine bacterium Vibrio alginolyticus. The nucleotide sequence revealed three open reading frames. The second gene was homologous to proC gene and allowed the growth of proC-defective mutant strain of E. coli chi 342 in the absence of proline. The first and third genes, but not proC, were required for the growth of TK420 in a synthetic medium containing 10 mM K+ and 100 mM Na+. Since K+ uptake activity of TK420 was restored by the introduction of these genes, these two genes were considered to be directly related to K+ transport. Homologous genes were found in E. coli, but their functions have not been reported.
已从海洋细菌溶藻弧菌中克隆出了在功能上能补充大肠杆菌TK420钾离子摄取缺陷突变株生长的新基因。核苷酸序列显示有三个开放阅读框。第二个基因与脯氨酸合成酶基因proC同源,能使大肠杆菌chi 342的proC缺陷突变株在无脯氨酸的情况下生长。在含有10 mM钾离子和100 mM钠离子的合成培养基中,TK420的生长需要第一个和第三个基因,但不需要proC基因。由于导入这些基因后恢复了TK420的钾离子摄取活性,因此认为这两个基因与钾离子转运直接相关。在大肠杆菌中发现了同源基因,但其功能尚未见报道。