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An inducible expression system of histidine-tagged proteins in Streptomyces lividans for one-step purification by Ni2+ affinity chromatography.

作者信息

Enguita F J, de la Fuente J L, Martín J F, Liras P

机构信息

Department of Ecology, Genetics and Microbiology, Faculty of Biology, University of León, Spain.

出版信息

FEMS Microbiol Lett. 1996 Apr 1;137(2-3):135-40. doi: 10.1111/j.1574-6968.1996.tb08095.x.

Abstract

An expression and purification cassette containing the aminoglycoside phosphotransferase gene (aph) as selective marker has been constructed in the Escherichia coli vector pULHis2. DNA fragments inserted in the cassette can be easily subcloned in pIJ699 to give vectors for overexpression of genes in Streptomyces and purification of proteins by a one-step procedure. The expression system uses the thiostrepton-inducible promoter tipA for expression and a six histidine coding nucleotide sequence that is fused in frame to the foreign gene inserted in the polylinker. The pULHis2-derived expression vector has been used satisfactorily to express and to purify the P7 and P8 proteins of Nocardia lactamdurans which carry out the methoxylation of cephalosporin C to 7-methoxycephalosporin C.

摘要

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