Suppr超能文献

副溶血性弧菌的一种新型Na⁺/H⁺逆向转运蛋白NhaD。

A new Na+/H+ antiporter, NhaD, of Vibrio parahaemolyticus.

作者信息

Nozaki K, Kuroda T, Mizushima T, Tsuchiya T

机构信息

Department of Microbiology, Faculty of Pharmaceutical Sciences, Okayama University, Tsushima, Okayama 700, Japan.

出版信息

Biochim Biophys Acta. 1998 Mar 2;1369(2):213-20. doi: 10.1016/s0005-2736(97)00223-x.

Abstract

A gene encoding an Na+/H+ antiporter was cloned from chromosomal DNA of Vibrio parahaemolyticus, a slightly halophilic bacterium, and expressed in Escherichia coli cells. The gene enabled mutant E. coli cells, which were unable to grow in the presence of 10 mM LiCl (or 0.2 M NaCl) because of the lack of major Na+(Li+)/H+ antiporters, to grow under such conditions. We detected Na+/H+ antiport activity due to the gene in membrane vesicles prepared from E. coli cells that harbored the plasmid carrying the gene. Li+ was also a substrate for this antiporter. Activity of this antiporter was pH-dependent with highest activity at pH 8.5 to 9 and no activity at 7.0 to 7.5. Restriction mapping and a Southern blot analysis revealed that the cloned gene was different from the nhaA and the nhaB of V. parahaemolyticus. We designated the gene nhaD. The gene was sequenced, and the amino acid sequence of the NhaD protein was deduced. The NhaD is a unique Na+/H+ antiporter with respect to the primary structure compared with known Na+/H+ antiporters.

摘要

从嗜盐性稍弱的副溶血性弧菌的染色体DNA中克隆出一个编码Na⁺/H⁺逆向转运蛋白的基因,并在大肠杆菌细胞中进行表达。该基因使因缺乏主要的Na⁺(Li⁺)/H⁺逆向转运蛋白而无法在10 mM LiCl(或0.2 M NaCl)存在的情况下生长的突变型大肠杆菌细胞能够在这种条件下生长。我们在从携带该基因的质粒的大肠杆菌细胞制备的膜囊泡中检测到了由于该基因产生的Na⁺/H⁺逆向转运活性。Li⁺也是这种逆向转运蛋白的底物。这种逆向转运蛋白的活性依赖于pH,在pH 8.5至9时活性最高,在7.0至7.5时无活性。限制性图谱分析和Southern印迹分析表明,克隆的基因与副溶血性弧菌的nhaA和nhaB不同。我们将该基因命名为nhaD。对该基因进行了测序,并推导了NhaD蛋白的氨基酸序列。与已知的Na⁺/H⁺逆向转运蛋白相比,NhaD在一级结构方面是一种独特的Na⁺/H⁺逆向转运蛋白。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验