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The gntP Gene of Escherichia coli Involved in Gluconate Uptake.:GntP, a high-affinity gluconate permease.

机译:大肠杆菌的gntp基因参与葡萄糖酸盐摄取。:Gntp,一种高亲和力葡萄糖酸盐通透酶。

摘要

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 blotting indicated that the gntP gene was monocistronic and was transcribed as a mRNA with an apparent molecular weight 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 predominantly isolated from the inner-membrane fraction of fractionated host cells. A topology analysis predicted a model 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 was investigated, indicating an apparent Km for gluconate of 25mM.
机译:位于大肠杆菌K-12的fim和uxu基因座之间的gntP基因已被克隆和鉴定。对包含gntP基因的区域进行核苷酸测序,揭示了447个密码子的开放阅读框,该密码子与枯草芽孢杆菌葡萄糖酸通透酶具有显着同源性。 Northern印迹表明,gntP基因是单顺反子,并转录成表观分子量为1.54kb的mRNA。通过引物延伸分析确定转录起点。发现gntP基因处于分解代谢物阻遏下,并且不是由葡萄糖酸盐诱导的。而且,表达似乎受到严格控制。几个观察结果表明,GntP蛋白是一种内膜蛋白。它包含特征性的跨膜区域,主要与分离的宿主细胞的内膜部分分离。拓扑分析预测了一个具有14个跨膜段的模型。通过引入编码gntP基因的质粒可以缓解突变菌株不能在葡萄糖酸盐基本培养基上生长的问题。最后,研究了GntP介导的葡萄糖酸盐摄取的动力学,表明葡萄糖酸盐的表观Km为25mM。

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