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大肠杆菌deoR和cytR基因产物的鉴定。

Identification of the Escherichia coli deoR and cytR gene products.

作者信息

Singer J T, Barbier C S, Short S A

出版信息

J Bacteriol. 1985 Sep;163(3):1095-100. doi: 10.1128/jb.163.3.1095-1100.1985.

Abstract

The protein products encoded by the Escherichia coli deoR and cytR structural genes have been identified based on results obtained from E. coli maxicells harboring (i) recombinant plasmids carrying wild-type deoR and cytR genes, (ii) deletion derivatives of the deoR+ and cytR+ plasmids, (iii) plasmids containing site-specific mutations in the deoR and cytR structural genes, and (iv) plasmids which have transposon Tn1000 inserted into the deoR and cytR structural genes. Analysis of the protein profiles obtained from all the maxicell experiments demonstrated that the deoR gene encodes a protein with a subunit molecular weight of 30,500 and that the product of the cytR gene is a protein with a subunit molecular weight of 37,000.

摘要

基于从含有以下物质的大肠杆菌大细胞中获得的结果,已鉴定出大肠杆菌deoR和cytR结构基因编码的蛋白质产物:(i)携带野生型deoR和cytR基因的重组质粒;(ii)deoR⁺和cytR⁺质粒的缺失衍生物;(iii)在deoR和cytR结构基因中含有位点特异性突变的质粒;以及(iv)转座子Tn1000插入到deoR和cytR结构基因中的质粒。对所有大细胞实验获得的蛋白质谱分析表明,deoR基因编码一种亚基分子量为30,500的蛋白质,cytR基因的产物是一种亚基分子量为37,000的蛋白质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34b1/219243/804f33c23b1c/jbacter00220-0292-a.jpg

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