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大肠杆菌K-12中柯氏酸多糖生物合成基因启动子区域的鉴定

Identification of the promoter region for the colanic acid polysaccharide biosynthetic genes in Escherichia coli K-12.

作者信息

Stout V

机构信息

Department of Microbiology and Molecular and Cellular Biology Graduate Program, Arizona State University, Tempe, Arizona 85287-2701, USA.

出版信息

J Bacteriol. 1996 Jul;178(14):4273-80. doi: 10.1128/jb.178.14.4273-4280.1996.

Abstract

The colanic acid polysaccharide capsule biosynthetic genes (cps genes) are primarily clustered at one site located at about 45 min on the Escherichia coli chromosome. The network of proteins involved in regulating the expression of these genes includes the two positive regulators RcsA and RcsB. This work describes the site of action of these two activator proteins and the promoter of the cps genes. It is likely that the cps genes are arranged in a single long operon that is at least 13.5 kb. The promoter region was identified with fusions to lacZ that resulted in regulated expression by the Rcs network of regulatory proteins, and the start site of transcription was identified by primer extension. The operator region was cloned from Kohara phage to multicopy plasmids and identified by titrating RcsA or RcsB. Sequence analysis of the promoter and operator region revealed homology to the JUMPstart element found in the untranslated region of many exopolysaccharide biosynthetic operons. In addition, the deduced amino acid sequence of the amino terminus of the first open reading frame of the cps operon was found to be homologous to proteins encoded by the exopolysaccharide biosynthetic operons of Klebsiella pneumoniae and Erwinia amylovora.

摘要

大肠杆菌酸多糖胶囊生物合成基因(cps基因)主要聚集在大肠杆菌染色体上约45分钟处的一个位点。参与调控这些基因表达的蛋白质网络包括两个正调控因子RcsA和RcsB。这项工作描述了这两种激活蛋白的作用位点以及cps基因的启动子。cps基因可能排列在一个至少13.5 kb的单一长操纵子中。通过与lacZ融合鉴定出启动子区域,该融合导致调节蛋白的Rcs网络进行调控表达,并通过引物延伸鉴定转录起始位点。操纵子区域从Kohara噬菌体克隆到多拷贝质粒中,并通过滴定RcsA或RcsB进行鉴定。启动子和操纵子区域的序列分析显示与许多胞外多糖生物合成操纵子非翻译区中发现的JUMPstart元件具有同源性。此外,发现cps操纵子第一个开放阅读框氨基末端的推导氨基酸序列与肺炎克雷伯菌和梨火疫病菌胞外多糖生物合成操纵子编码的蛋白质具有同源性。

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