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自养黄色杆菌GJ10中编码卤代烷酸脱卤酶的dhlB基因上游区域的序列分析

Sequence analysis of the upstream region of dhlB, the gene encoding haloalkanoic acid dehalogenase of Xanthobacter autotrophicus GJ10.

作者信息

van der Ploeg J, Janssen D B

机构信息

Department of Biochemistry, Groningen Biomolecular Sciences and Biotechnology The Netherlands.

出版信息

Biodegradation. 1995 Sep;6(3):257-63. doi: 10.1007/BF00700465.

Abstract

The DNA sequence upstream of the dhlB gene encoding the haloalkanoic acid dehalogenase of Xanthobacter autotrophicus GJ10 was determined and contained an open reading frame, designated dhlC, which encoded a protein with a significant similarity with the family of Na(+)-dependent symport proteins. The dhlC gene was subcloned under control of a T7 promoter, and found to encode a polypeptide of 45 kDa on SDS-PAGE. Upstream of dhlC, a -24/-12 promoter sequence was found. Further upstream, in the opposite direction of transcription, another open reading frame, designated dhlR, with homology with the family of sigma 54-dependent transcriptional activator proteins was detected. The dhlR gene was cloned and expressed under the control of a T7 promoter and encoded a polypeptide of 51 kDa on SDS-PAGE. The genetic organization of the dhlB region suggested that the expression of dhlC and dhlB was controlled by the product of dhlR and sigma 54 which may explain the observed overexpression of the haloalkanoic acid dehalogenase under starvation conditions.

摘要

测定了自养黄色杆菌GJ10编码卤代烷酸脱卤酶的dhlB基因上游的DNA序列,该序列包含一个开放阅读框,命名为dhlC,它编码一种与Na(+)依赖性同向转运蛋白家族具有显著相似性的蛋白质。dhlC基因在T7启动子的控制下进行亚克隆,在SDS-PAGE上发现它编码一个45 kDa的多肽。在dhlC上游,发现了一个-24/-12启动子序列。进一步在上游,在转录相反方向上,检测到另一个与σ54依赖性转录激活蛋白家族具有同源性的开放阅读框,命名为dhlR。dhlR基因在T7启动子的控制下进行克隆和表达,在SDS-PAGE上编码一个51 kDa的多肽。dhlB区域的基因组织表明,dhlC和dhlB的表达受dhlR和σ54产物的控制,这可能解释了在饥饿条件下观察到的卤代烷酸脱卤酶的过表达现象。

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