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大肠杆菌K-12中uidA和uidR基因的克隆及核酸内切酶限制分析:uidA基因转录方向的确定

Cloning and endonuclease restriction analysis of uidA and uidR genes in Escherichia coli K-12: determination of transcription direction for the uidA gene.

作者信息

Blanco C, Ritzenthaler P, Mata-Gilsinger M

出版信息

J Bacteriol. 1982 Feb;149(2):587-94. doi: 10.1128/jb.149.2.587-594.1982.

Abstract

The two genes of the Escherichia coli K-12 uid region (the structural gene uidA and the regulatory gene uidR) were isolated on a ColE1-uid hybrid plasmid from the bank of Clarke and Carbon. We made a restriction map of this region and correlated it with the genetic map by subcloning the uid restriction fragments into plasmids pBR322, pBR325, and pACYC177. In these plasmids, amplification of the products of the uidA and uidR genes occurred. The enzyme coded for by uidA was identified by polyacrylamide gel electrophoresis of crude extracts from strains containing the uidA plasmid. A 1-megadalton EcoRI-BamHI segment contained the uidAo operator, and the direction of transcription of the uidA gene was determined. The restriction analysis also suggested that the order of the loci in this region is manA, uidA, uidAo, uidR.

摘要

从克拉克和卡尔文文库中,在一个ColE1-uid杂种质粒上分离出了大肠杆菌K-12 uid区域的两个基因(结构基因uidA和调控基因uidR)。我们绘制了该区域的限制性图谱,并通过将uid限制性片段亚克隆到质粒pBR322、pBR325和pACYC177中,将其与遗传图谱进行了关联。在这些质粒中,uidA和uidR基因的产物得到了扩增。通过对含有uidA质粒的菌株粗提物进行聚丙烯酰胺凝胶电泳,鉴定了由uidA编码的酶。一个1兆道尔顿的EcoRI-BamHI片段包含uidAo操纵子,并确定了uidA基因的转录方向。限制性分析还表明,该区域中基因座的顺序是manA、uidA、uidAo、uidR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca1/216546/de919be10fbb/jbacter00261-0189-a.jpg

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