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梨火疫病菌rcsA基因的分子克隆、表达及核苷酸序列,该基因编码荚膜表达的正调控因子:相关荚膜激活蛋白家族的证据

Molecular cloning, expression and nucleotide sequence of the rcsA gene of Erwinia amylovora, encoding a positive regulator of capsule expression: evidence for a family of related capsule activator proteins.

作者信息

Coleman M, Pearce R, Hitchin E, Busfield F, Mansfield J W, Roberts I S

机构信息

Department of Microbiology, University of Leicester, UK.

出版信息

J Gen Microbiol. 1990 Sep;136(9):1799-806. doi: 10.1099/00221287-136-9-1799.

Abstract

A gene encoding a positive activator of the expression of extracellular polysaccharide (EPS) synthesis in the phytopathogen Erwinia amylovora has been isolated from a genomic library in Escherichia coli. The presence of the cloned gene in E. coli stimulated transcription of the genes encoding colanic acid biosynthesis and could complement rcsA mutations. Introduction of the gene on a multicopy plasmid into Er. amylovora caused a threefold increase in EPS expression. The nucleotide sequence of the gene (designated rcsA) was determined. This revealed a single open reading frame encoding an RcsA protein of 23-7 kDa. This was confirmed by minicell analysis in E. coli. The predicted amino acid sequence of this RcsA protein showed a high degree of homology to the RcsA protein of Klebsiella aerogenes, demonstrating the existence of a family of related RcsA activator proteins capable of stimulating EPS expression. The protein had no significant homology to known DNA-binding activator proteins, indicating, for the first time, that the RcsA family of activator proteins may stimulate expression of EPS synthesis indirectly by acting on other regulatory proteins.

摘要

已从大肠杆菌基因组文库中分离出一个编码植物病原菌梨火疫欧文氏菌胞外多糖(EPS)合成表达正激活因子的基因。该克隆基因在大肠杆菌中的存在刺激了编码柯氏酸生物合成基因的转录,并可弥补rcsA突变。将该基因导入多拷贝质粒并转入梨火疫欧文氏菌后,EPS表达增加了三倍。测定了该基因(命名为rcsA)的核苷酸序列。结果显示有一个单一的开放阅读框,编码一个23.7 kDa的RcsA蛋白。这一点在大肠杆菌的微小细胞分析中得到了证实。该RcsA蛋白的预测氨基酸序列与产气克雷伯菌的RcsA蛋白高度同源,证明存在一个能够刺激EPS表达的相关RcsA激活蛋白家族。该蛋白与已知的DNA结合激活蛋白没有显著同源性,这首次表明RcsA激活蛋白家族可能通过作用于其他调节蛋白间接刺激EPS合成的表达。

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