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[大肠杆菌中功能活性缩短的lon基因的克隆、表达及结构]

[Cloning, expression and structure of the functionally active shortened lon gene in Escherichia coli].

作者信息

Amerik A Iu, Chistiakov L G, Ostroumova N I, Gurevich A I, Antonov V K

出版信息

Bioorg Khim. 1988 Mar;14(3):408-11.

PMID:3289547
Abstract

Lon gene of E. coli has been cloned into the plasmid pBR327. Full nucleotide sequence of the gene has been established. It was shown that the cloned gene does not possess the terminal codon and is somewhat shortened. Nevertheless it retains full phenotypic activity and expresses the C-end modified La proteinase which retains ATP-dependent proteolytic activity.

摘要

大肠杆菌的Lon基因已被克隆到质粒pBR327中。该基因的完整核苷酸序列已确定。结果表明,克隆的基因没有终止密码子,且有所缩短。然而,它仍保留了完整的表型活性,并表达C端修饰的La蛋白酶,该蛋白酶保留了ATP依赖性蛋白水解活性。

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