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参与表皮菌素免疫的表皮葡萄球菌基因epiF、-E和-G的分析

Analysis of the Staphylococcus epidermidis genes epiF, -E, and -G involved in epidermin immunity.

作者信息

Peschel A, Götz F

机构信息

Mikrobielle Genetik, Universität Tübingen, Federal Republic of Germany.

出版信息

J Bacteriol. 1996 Jan;178(2):531-6. doi: 10.1128/jb.178.2.531-536.1996.

Abstract

The lantibiotic epidermin is produced by Staphylococcus epidermidis Tü3298. The known genes involved in epidermin biosynthesis and regulation are organized as operons (epiABCD and epiQP) that are encoded on the 54-kb plasmid pTü32. Here we describe the characterization of a DNA region that mediates immunity and increased epidermin production, located upstream of the structural gene epiA. The sequence of a 2.6-kb DNA fragment revealed three open reading frames, epiF, -E, and -G, which may form an operon. In the cloning host Staphylococcus carnosus, the three genes mediated an increased tolerance to epidermin, and the highest level of immunity (sevenfold) was achieved with S. carnosus carrying epiFEG and epiQ. The promoter of the first gene, epiF, responded to the activator protein EpiQ and contained a palindromic sequence similar to the EpiQ binding site of the epiA promoter, which is also activated by EpiQ. Inactivation of epiF, -E, or -G resulted in the complete loss of the immunity phenotype. An epidermin-sensitive S. epidermidis Tü3298 mutant was complemented by a DNA fragment containing all three genes. When the epiFEG genes were cloned together with plasmid pTepi14, containing the biosynthetic genes epiABCDQP, the level of epidermin production was approximately fivefold higher. The proteins EpiF, -E, and -G are similar in deduced sequence and proposed structure to the components of various ABC transporter systems. EpiF is a hydrophilic protein with conserved ATP-binding sites, while EpiE and -G have six alternating hydrophobic regions and very likely constitute the integral membrane domains. When EpiF was overproduced in S. carnosus, it was at least partially associated with the cytoplasmic membrane. A potential mechanism for how EpiFEG mediates immunity is discussed.

摘要

羊毛硫抗生素表皮菌素由表皮葡萄球菌Tü3298产生。已知参与表皮菌素生物合成和调控的基因被组织成操纵子(epiABCD和epiQP),它们编码在54 kb的质粒pTü32上。在此,我们描述了位于结构基因epiA上游的一个介导免疫和表皮菌素产量增加的DNA区域的特征。一个2.6 kb DNA片段的序列揭示了三个开放阅读框epiF、-E和-G,它们可能形成一个操纵子。在克隆宿主肉葡萄球菌中,这三个基因介导了对表皮菌素耐受性的增加,携带epiFEG和epiQ的肉葡萄球菌实现了最高水平的免疫(七倍)。第一个基因epiF的启动子对激活蛋白EpiQ有反应,并且包含一个与epiA启动子的EpiQ结合位点相似的回文序列,epiA启动子也被EpiQ激活。epiF、-E或-G的失活导致免疫表型完全丧失。一个对表皮菌素敏感的表皮葡萄球菌Tü3298突变体被一个包含所有三个基因的DNA片段互补。当epiFEG基因与包含生物合成基因epiABCDQP的质粒pTepi14一起克隆时,表皮菌素的产量水平大约高五倍。蛋白质EpiF、-E和-G在推导序列和推测结构上与各种ABC转运系统的组分相似。EpiF是一种具有保守ATP结合位点的亲水蛋白,而EpiE和-G有六个交替的疏水区域,很可能构成整合膜结构域。当EpiF在肉葡萄球菌中过量表达时,它至少部分与细胞质膜相关联。文中讨论了EpiFEG介导免疫的潜在机制。

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