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插入序列IS5的5A蛋白的合成与过量产生。

Synthesis and overproduction of the 5A protein of insertion sequence IS5.

作者信息

Chernak J M, Schlaffer E J, Smith H O

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

J Bacteriol. 1988 Nov;170(11):5368-70. doi: 10.1128/jb.170.11.5368-5370.1988.

Abstract

We have demonstrated both the synthesis and overproduction of the 5A protein encoded by the longest open reading frame of the bacterial insertion sequence IS5. Expression was obtained in vitro and in Escherichia coli maxicells from plasmids containing IS5 in either orientation, as well as in vitro from a restriction fragment containing exclusively IS5 DNA. When IS5 was cloned in the appropriate orientation downstream of a strong tac promoter, production of the 5A protein was increased to 10 to 20% of the total protein synthesized in vitro.

摘要

我们已经证明了细菌插入序列IS5最长开放阅读框编码的5A蛋白的合成与过量产生。在体外以及在大肠杆菌最大细胞中,从含有两种方向的IS5的质粒中都获得了表达,并且在体外从仅包含IS5 DNA的限制片段中也获得了表达。当IS5以适当的方向克隆在强tac启动子下游时,5A蛋白的产量增加到体外合成的总蛋白的10%至20%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbde/211615/47c13dae73d9/jbacter00189-0377-a.jpg

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