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Magnesium transport in Salmonella typhimurium: expression of cloned genes for three distinct Mg2+ transport systems.

机译:鼠伤寒沙门氏菌中的镁转运:三个不同的Mg2 +转运系统的克隆基因的表达。

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摘要

In Salmonella typhimurium, the corA, mgtA, and mgtB loci are involved in active transport of Mg2+ (S. P. Hmiel, M. D. Snavely, C. G. Miller, and M. E. Maguire, J. Bacteriol. 168:1444-1450, 1988; S. P. Hmiel, M. D. Snavely, J. B. Florer, M. E. Maguire, and C. G. Miller, J. Bacteriol. 171:4742-4751, 1989). In this study, the gene products coded for by the corA, mgtA, and mgtB genes were identified by using plasmid expression in Escherichia coli maxicells. Complementation was assessed by introducing plasmids into a Mg2+-dependent corA mgtA mgtB strain and determining the ability of the plasmid to restore growth on medium without a Mg2+ supplement. Complementing plasmids containing corA expressed a 42-kilodalton (kDa) protein. This protein was not expressed by plasmids containing insertions or deletions that eliminated complementation. A plasmid containing mgtA expressed 37- and 91-kDa gene products. Data obtained with subclones and insertions in this plasmid indicated that plasmids expressing only the 91-kDa polypeptide complemented; plasmids that did not express this protein did not complement regardless of whether they expressed the 37-kDa protein. Plasmids carrying mgtB expressed a single protein of 102 kDa whose presence or absence correlated with the ability of the plasmid to complement the Mg2+-dependent triple mutant. Fractionation of labeled maxicells demonstrated that the 42-kDa corA, the 91-kDa mgtA, and the 102-kDa mgtB gene products are all tightly associated with the membrane, a location consistent with involvement in a transport process. These data provide further support the for existence of three distinct systems for Mg2+ transport in S. typhimurium.
机译:在鼠伤寒沙门氏菌中,corA,mgtA和mgtB基因座参与Mg2 +的主动转运(SP Hmiel,MD Snavely,CG Miller和ME Maguire,J.Bacteriol.168:1444-1450,1988; SP Hmiel,MD Snavely ,JB Florer,ME Maguire和CG Miller,J.Bacteriol.171:4742-4751,1989)。在这项研究中,通过使用质粒表达在大肠杆菌中鉴定了由corA,mgtA和mgtB基因编码的基因产物。通过将质粒引入依赖于Mg2 +的corA mgtA mgtB菌株中并确定质粒在不含Mg2 +的培养基上恢复生长的能力来评估互补性。含有corA的互补质粒表达了42千达尔顿(kDa)蛋白。含有消除互补作用的插入或缺失的质粒不表达该蛋白。含有mgtA的质粒表达了37 kDa和91 kDa的基因产物。用该质粒的亚克隆和插入获得的数据表明仅表达91-kDa多肽的质粒是互补的。不表达该蛋白的质粒不管它们是否表达37-kDa蛋白都不能互补。携带mgtB的质粒表达102 kDa的单个蛋白质,其存在与否与质粒补充Mg2 +依赖性三重突变体的能力有关。标记的maxicells的分级分离表明42 kDa corA,91 kDa mgtA和102 kDa mgtB基因产物均与膜紧密结合,该位置与参与转运过程一致。这些数据进一步为鼠伤寒沙门氏菌中存在三种不同的Mg2 +传输系统提供了支持。

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