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大肠杆菌mfd启动子的特性分析。

Characterisation of the Escherichia coli mfd promoter.

作者信息

Stanley Louise K, Savery Nigel J

机构信息

Department of Biochemistry, University of Bristol, School of Medical Sciences, University Walk, BS8 1TD, Bristol, UK.

出版信息

Arch Microbiol. 2003 May;179(5):381-5. doi: 10.1007/s00203-003-0540-9. Epub 2003 Mar 26.

Abstract

The bacterial mfd gene encodes a transcription-repair coupling factor that mediates the preferential repair of DNA damage in the template strand of active transcriptional units. In this report, the transcription start site for the Escherichia coli mfd gene was determined in vivo and in vitro, and the DNA determinants for mfd transcription by deletion and site-directed mutagenesis were defined. A canonical sigma(70)-dependent promoter, mfd P1, was responsible for the majority of mfd transcription, and a core region consisting of residues -42 to +5 was sufficient for full activity in rich and minimal media.

摘要

细菌的mfd基因编码一种转录修复偶联因子,该因子介导活性转录单元模板链中DNA损伤的优先修复。在本报告中,在体内和体外确定了大肠杆菌mfd基因的转录起始位点,并通过缺失和定点诱变确定了mfd转录的DNA决定因素。一个典型的依赖σ70的启动子mfd P1负责大部分的mfd转录,由-42至+5位残基组成的核心区域在丰富培养基和基本培养基中具有充分活性。

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