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大肠杆菌rep基因:rep蛋白启动子及N端的鉴定

Escherichia coli rep gene: identification of the promoter and N terminus of the rep protein.

作者信息

Bialkowska-Hobrzanska H, Gilchrist C A, Denhardt D T

出版信息

J Bacteriol. 1985 Dec;164(3):1004-10. doi: 10.1128/jb.164.3.1004-1010.1985.

Abstract

The functional Escherichia coli rep gene, which encodes the Mr 67,000 Rep helicase, has been localized within a 2.55-kilobase sequence. Its regulatory region has been characterized by the use of rep-lacZ fusions. The direction of transcription of the rep gene is clockwise on the E. coli chromosome, as are the nearby ilvC and rho genes. The sequence of the rep control region was determined, and putative regulatory sequences were identified; no evidence for autoregulation of expression was obtained. Transcription of the gene was not enhanced during the SOS response. The location of the promoter and the beginning of the protein were confirmed by S1 nuclease mapping of the 5' end of rep mRNA and determination of the NH2-terminal sequence of the rep protein.

摘要

编码分子量为67,000的Rep解旋酶的功能性大肠杆菌rep基因已定位在一段2.55千碱基的序列内。其调控区域已通过使用rep-lacZ融合体进行了表征。rep基因在大肠杆菌染色体上的转录方向是顺时针的,附近的ilvC和rho基因也是如此。确定了rep控制区域的序列,并鉴定了推定的调控序列;未获得表达自动调控的证据。在SOS反应期间,该基因的转录未增强。通过对rep mRNA 5'端进行S1核酸酶图谱分析以及确定rep蛋白的NH2末端序列,证实了启动子的位置和蛋白质的起始位置。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ab1/219290/6d91b39e8fa6/jbacter00217-0040-a.jpg

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