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大肠杆菌K-12脂多糖核心生物合成基因rfaQ、rfaP和rfaG的鉴定及序列分析

Identification and sequences of the lipopolysaccharide core biosynthetic genes rfaQ, rfaP, and rfaG of Escherichia coli K-12.

作者信息

Parker C T, Pradel E, Schnaitman C A

机构信息

Department of Microbiology, Arizona State University, Tempe 85287.

出版信息

J Bacteriol. 1992 Feb;174(3):930-4. doi: 10.1128/jb.174.3.930-934.1992.

Abstract

The rfa locus of Escherichia coli K-12 includes a block of about 10 closely spaced genes transcribed in the same direction which are involved in synthesis and modification of the hexose region of the lipopolysaccharide core. We have sequenced the first three genes in this block. The function of the first of these genes is unknown, but we have designated it rfaQ on the basis of its location and similarity to other rfa genes. Complementation of Salmonella typhimurium rfa mutants with E. coli rfa restriction fragments indicated that the second and third genes in the block were rfaG and rfaP. The deduced sizes of the RfaQ, RfaG, and RfaP proteins are 36,298, 42,284, and 30,872 Da, respectively, and the proteins are basic and lack extensive hydrophobic domains. RfaQ shares regions of homology with proteins RfaC and RfaF, which are involved in synthesis of the heptose region of the core. Proteins RfaB, RfaG, and RfaK share a region of homology, which suggests that they belong to a second family of Rfa proteins which are thought to be hexose transferases.

摘要

大肠杆菌K-12的rfa基因座包含一组约10个紧密排列且同向转录的基因,这些基因参与脂多糖核心己糖区域的合成与修饰。我们已对该基因簇中的前三个基因进行了测序。其中第一个基因的功能尚不清楚,但基于其位置以及与其他rfa基因的相似性,我们将其命名为rfaQ。用大肠杆菌rfa限制片段对鼠伤寒沙门氏菌rfa突变体进行互补试验表明,该基因簇中的第二个和第三个基因分别是rfaG和rfaP。推导的RfaQ、RfaG和RfaP蛋白的大小分别为36,298、42,284和30,872道尔顿,这些蛋白呈碱性且缺乏广泛的疏水结构域。RfaQ与参与核心庚糖区域合成的RfaC和RfaF蛋白具有同源区域。RfaB、RfaG和RfaK蛋白共享一个同源区域,这表明它们属于Rfa蛋白的第二个家族,被认为是己糖转移酶。

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