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大肠杆菌recA蛋白过度产生而未刺激其蛋白水解活性。

Overproduction of the Escherichia coli recA protein without stimulation of its proteolytic activity.

作者信息

Uhlin B E, Clark A J

出版信息

J Bacteriol. 1981 Oct;148(1):386-90. doi: 10.1128/jb.148.1.386-390.1981.

Abstract

Plasmid pBEU14, which carries the Escherichia coli recA+ gene and which can be amplified by manipulation of growth temperature, was constructed. When pBEU14 deoxyribonucleic acid was amplified, a high rate of synthesis and accumulation of recA protein resulted. Amplification of the recA gene and protein did not cause induction of prophage lambda, indicating that the proteolytic activity of the recA protein was not stimulated.

摘要

构建了携带大肠杆菌recA⁺基因且可通过调节生长温度进行扩增的质粒pBEU14。当pBEU14脱氧核糖核酸被扩增时,recA蛋白会以高合成率和积累量产生。recA基因和蛋白的扩增并未导致原噬菌体λ的诱导,这表明recA蛋白的蛋白水解活性未被刺激。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22fc/216207/56470f83ddcd/jbacter00263-0396-a.jpg

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