Klemm P, Tong S, Nielsen H, Conway T
Department of Microbiology, Technical University of Denmark, Lyngby, Denmark.
J Bacteriol. 1996 Jan;178(1):61-7. doi: 10.1128/jb.178.1.61-67.1996.
The gntP gene, located between the fim and uxu loci in Escherichia coli K-12, has been cloned and characterized. Nucleotide sequencing of a region encompassing the gntP gene revealed an open reading frame of 447 codons with significant homology to the Bacillus subtilis gluconate permease. Northern (RNA) blotting indicated that the gntP gene was monocistronic and was transcribed as an mRNA with an apparent molecular size of 1.54 kb. The transcriptional start point was determined by primer extension analysis. The gntP gene was found to be under catabolite repression and was not induced by gluconate. Also, expression seemed to be stringently controlled. Several observations indicated that the GntP protein is an inner membrane protein; it contains characteristic membrane-spanning regions and was isolated predominantly from the inner-membrane fraction of fractionated host cells. A topology analysis predicted a protein with 14 membrane-spanning segments. The inability of a mutant strain to grow on gluconate minimal medium could be relieved by introduction of a plasmid encoding the gntP gene. Finally, the kinetics of GntP-mediated gluconate uptake were investigated, indicating an apparent Km for gluconate of 25 microM.
位于大肠杆菌K-12菌毛(fim)和木糖异构酶(uxu)基因座之间的gntP基因已被克隆并进行了特性分析。对包含gntP基因的区域进行核苷酸测序,发现一个由447个密码子组成的开放阅读框,与枯草芽孢杆菌葡萄糖酸盐通透酶具有显著同源性。Northern(RNA)印迹分析表明,gntP基因是单顺反子,转录成一条表观分子大小为1.54 kb的mRNA。通过引物延伸分析确定了转录起始点。发现gntP基因受到分解代谢物阻遏,且不受葡萄糖酸盐诱导。此外,其表达似乎受到严格调控。多项观察结果表明,GntP蛋白是一种内膜蛋白;它含有特征性的跨膜区域,主要从分级分离的宿主细胞内膜组分中分离得到。拓扑结构分析预测该蛋白有14个跨膜区段。通过导入编码gntP基因的质粒,可以挽救突变菌株在葡萄糖酸盐基本培养基上生长的缺陷。最后,研究了GntP介导的葡萄糖酸盐摄取动力学,结果表明葡萄糖酸盐的表观Km值为25 μM。