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鉴定大肠杆菌K-12中控制新型外膜孔蛋白产生的三个基因。

Identification of three genes controlling production of new outer membrane pore proteins in Escherichia coli K-12.

作者信息

Pugsley A P, Schnaitman C A

出版信息

J Bacteriol. 1978 Sep;135(3):1118-29. doi: 10.1128/jb.135.3.1118-1129.1978.

Abstract

Escherichia coli K-12 strains carrying mutations in the ompB gene or double mutations in the tolF and par genes lack the major outer membrane proteins 1a and 1b. These strains are deficient in the transport of small hydrophylic compounds and are multiply colicin resistant. When revertants of these strains were sought, a number of extragenic pseudorevertants were obtained which produced new outer membrane proteins. These new proteins could be divided into three classes by differences in electrophoretic mobility on polyacrylamide gels, by differing specificities for transport of small molecules, and by the identification of three different genetic loci for genes controlling their production. These genetic loci are designated as nmpA (at approximately 82.5 min on the E. coli K-12 genetic map), nmpB (8.6 min), and nmpC (12 min). The new proteins produced in strains carrying nmpA, nmpB, or nmpC mutations did not cross-react with antiserum against a mixture of proteins 1a and 1b, or with antiserum against phage-directed protein 2. Production of the new membrane proteins restored sensitivity to some of the colicins.

摘要

携带ompB基因突变或tolF和par基因双突变的大肠杆菌K - 12菌株缺乏主要外膜蛋白1a和1b。这些菌株在亲水性小分子化合物的转运方面存在缺陷,并且对多种大肠杆菌素具有抗性。在寻找这些菌株的回复突变体时,获得了一些基因外假回复突变体,它们产生了新的外膜蛋白。通过聚丙烯酰胺凝胶电泳迁移率的差异、小分子转运特异性的不同以及鉴定控制其产生的三个不同基因位点,可以将这些新蛋白分为三类。这些基因位点分别被命名为nmpA(在大肠杆菌K - 12基因图谱上约82.5分钟处)、nmpB(8.6分钟)和nmpC(12分钟)。携带nmpA、nmpB或nmpC突变的菌株中产生的新蛋白,与针对蛋白1a和1b混合物的抗血清或针对噬菌体导向蛋白2的抗血清均无交叉反应。新膜蛋白的产生恢复了对某些大肠杆菌素的敏感性。

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