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来自坚强芽孢杆菌OF4的一种假定新型Mg2+转运蛋白MgtE的克隆与特性分析

Cloning and characterization of MgtE, a putative new class of Mg2+ transporter from Bacillus firmus OF4.

作者信息

Smith R L, Thompson L J, Maguire M E

机构信息

Department of Pharmacology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4965.

出版信息

J Bacteriol. 1995 Mar;177(5):1233-8. doi: 10.1128/jb.177.5.1233-1238.1995.

Abstract

The MM281 strain of Salmonella typhimurium which possesses mutations in each its three known Mg2+ transport systems and requires 100 mM Mg2+ for growth was used to screen a genomic library from the gram-positive alkaliphilic bacterium Bacillus firmus OF4 for clones that could restore the ability to grow without Mg2+ supplementation. Of the clones obtained, five also conferred sensitivity to Co2+, similar to the phenotype of mutants with mutations in the S. typhimurium corA Mg2+ transport locus. All five contained identical inserts by restriction analysis. Using 63Ni2+ as a surrogate for the unavailable 28Mg2+, the plasmid insert was shown to restore cation uptake with properties similar but not identical to those of the S. typhimurium CorA Mg2+ transporter. Sequence analysis of one clone identified a single open reading frame with multiple possible initiation sites. Deletion and mutation analysis identified a minimum open reading frame of 939 bp encoding a polypeptide with a predicted molecular mass of 34 kDa. Disruption of the open reading frame eliminated cation influx activity and restored resistance to Co2+. This putative transporter, designated MgtE, has no sequence similarity to any known protein including CorA and appears to represent a new class of Mg2+ transport system.

摘要

鼠伤寒沙门氏菌MM281菌株在其三个已知的Mg2+转运系统中均有突变,生长需要100 mM Mg2+,该菌株被用于筛选来自革兰氏阳性嗜碱芽孢杆菌OF4的基因组文库,以寻找能够恢复在不添加Mg2+情况下生长能力的克隆。在获得的克隆中,有五个也对Co2+敏感,类似于鼠伤寒沙门氏菌corA Mg2+转运位点发生突变的突变体的表型。通过限制性分析,所有五个克隆都含有相同的插入片段。用63Ni2+替代无法获得的28Mg2+,结果表明质粒插入片段可恢复阳离子摄取,其特性与鼠伤寒沙门氏菌CorA Mg2+转运体相似但不完全相同。对一个克隆的序列分析确定了一个具有多个可能起始位点的单一开放阅读框。缺失和突变分析确定了一个939 bp的最小开放阅读框,其编码一个预测分子量为34 kDa的多肽。开放阅读框的破坏消除了阳离子流入活性并恢复了对Co2+的抗性。这个假定的转运体被命名为MgtE,它与包括CorA在内的任何已知蛋白质都没有序列相似性,似乎代表了一类新的Mg2+转运系统。

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