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产气克雷伯菌谷氨酸脱氢酶(gdhA)基因:在大肠杆菌中的克隆、高水平表达及杂交酶形成

The Klebsiella aerogenes glutamate dehydrogenase (gdhA) gene: cloning, high-level expression and hybrid enzyme formation in Escherichia coli.

作者信息

Mountain A, McPherson M J, Baron A J, Wootton J C

出版信息

Mol Gen Genet. 1985;199(1):141-5. doi: 10.1007/BF00327523.

Abstract

The NADP-dependent glutamate dehydrogenase gene of Klebsiella aerogenes was cloned in E. coli in the expression plasmid pRK9. The cloned gene shows a high level of expression in E. coli in the hybrid plasmid pKG3 and such expression is independent of the vector promoter, as shown by experiments in which the promoter was deleted. Active hybrid GDH hexamers were shown in cell-free extracts of an E. coli strain carrying cloned gdhA genes of both E. coli and K. aerogenes. The nucleotide sequence of the N-terminal coding region of the K. aerogenes gdhA gene was determined and found to be strongly homologous with that of E. coli.

摘要

产气克雷伯菌的依赖NADP的谷氨酸脱氢酶基因被克隆到大肠杆菌的表达质粒pRK9中。克隆基因在杂交质粒pKG3中能在大肠杆菌中高水平表达,并且如缺失启动子的实验所示,这种表达不依赖于载体启动子。在携带大肠杆菌和产气克雷伯菌克隆gdhA基因的大肠杆菌菌株的无细胞提取物中显示出有活性的杂交GDH六聚体。测定了产气克雷伯菌gdhA基因N端编码区的核苷酸序列,发现其与大肠杆菌的该序列高度同源。

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