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[大肠杆菌硫氧还蛋白基因的克隆与表达]

[Cloning and expression of the Escherichia coli thioredoxin gene].

作者信息

Barenboĭm M G, Shingarova L N, Korobko V G

出版信息

Bioorg Khim. 1995 Jul;21(7):524-7.

PMID:7488267
Abstract

The gene encoding thioredoxin (trxA) was isolated from chromosomal DNA of E. coli HB101 strain using the polymerase chain reaction. The cloned structural gene with a synthetic Shine-Dalgarno sequence was placed under the control of either inducible tac-promoter or a tandem of two strong constitutive promoters A2 and A3 from early region of bacteriophage T7. Both constructions were shown to provide high levels of biosynthesis of recombinant thioredoxin.

摘要

利用聚合酶链反应从大肠杆菌HB101菌株的染色体DNA中分离出编码硫氧还蛋白(trxA)的基因。带有合成的Shine-Dalgarno序列的克隆结构基因置于可诱导的tac启动子或来自噬菌体T7早期区域的两个强组成型启动子A2和A3串联的控制之下。结果表明,这两种构建体都能实现重组硫氧还蛋白的高水平生物合成。

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