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大肠杆菌K-12的tol-pal区域的特性:TolQ对tolR表达的翻译控制以及pal下游一个编码周质蛋白的新开放阅读框的鉴定。

Characterization of the tol-pal region of Escherichia coli K-12: translational control of tolR expression by TolQ and identification of a new open reading frame downstream of pal encoding a periplasmic protein.

作者信息

Vianney A, Muller M M, Clavel T, Lazzaroni J C, Portalier R, Webster R E

机构信息

Laboratoire de Microbiologie et Génétique Moléculaire, Centre National de la Recherche Scientifique, Université Claude Bernard Lyon I, France.

出版信息

J Bacteriol. 1996 Jul;178(14):4031-8. doi: 10.1128/jb.178.14.4031-4038.1996.

Abstract

The TolQ, TolR, TolA, TolB, and Pal proteins appear to function in maintaining the integrity of the outer membrane, as well as facilitating the uptake of the group A colicins and the DNA of the infecting filamentous bacteriophages. Sequence data showed that these genes are clustered in a 6-kb segment of DNA with the gene order orf1 tolQ tolR tolA tolB pal orf2 (a newly identified open reading frame encoding a 29-kD9 protein). Like those containing orf1, bacteria containing an insertion mutation in this gene showed no obvious phenotype. Analysis of beta-galactosidase activity from fusion constructs in which the lac operon was fused to various genes in the cluster showed that the genes in this region constitute two separate operons: orf1 tolQRA and tolB pal orf2. In the orf1 tolQRA operon, translation of MR was dependent on translation of the upstream tolQ region. Consistent with this result, no functional ribosome-binding site for TolR synthesis was detected.

摘要

TolQ、TolR、TolA、TolB和Pal蛋白似乎在维持外膜完整性方面发挥作用,同时也促进A群大肠杆菌素的摄取以及感染性丝状噬菌体DNA的摄取。序列数据表明,这些基因聚集在一段6kb的DNA片段中,基因顺序为orf1、tolQ、tolR、tolA、tolB、pal、orf2(一个新鉴定的编码29-kD9蛋白的开放阅读框)。与含有orf1的细菌一样,在该基因中含有插入突变的细菌没有明显的表型。对融合构建体(其中lac操纵子与该簇中的各种基因融合)的β-半乳糖苷酶活性分析表明,该区域的基因构成两个独立的操纵子:orf1、tolQRA和tolB、pal、orf2。在orf1、tolQRA操纵子中,TolR的翻译依赖于上游tolQ区域的翻译。与该结果一致,未检测到TolR合成的功能性核糖体结合位点。

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