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Expression of cre gene in Escherichia coli and bioassay its expression product / 生物工程学报
Chinese Journal of Biotechnology ; (12): 497-500, 2002.
Article in Zh | WPRIM | ID: wpr-256177
Responsible library: WPRO
ABSTRACT
The Cre recombinase from bacteriophage P1 can recognize specific DNA sequences, cleave DNA at specific target sites, and then ligate it to the cleaved DNA of a second site. In this study, cre gene was cloned into the pGEM-T Easy vector via PCR procedure. Then the cre gene was inserted into an expression vector pET-29a and expressed in E. coli BL21 (DE3). A 38 kD soluble protein was expressed and named CRE. CRE was purified by DEAE-52 chromatography. Bioassay of the partially purified product showed that CRE can cleave the plasmid pGLGFP which contains two loxP site with the same direction.
Subject(s)
Full text: 1 Index: WPRIM Main subject: Plasmids / Viral Proteins / Recombinant Proteins / Gene Expression Regulation, Enzymologic / Chromatography, DEAE-Cellulose / Integrases / Green Fluorescent Proteins / Escherichia coli / Genetics / Luminescent Proteins Language: Zh Journal: Chinese Journal of Biotechnology Year: 2002 Type: Article
Full text: 1 Index: WPRIM Main subject: Plasmids / Viral Proteins / Recombinant Proteins / Gene Expression Regulation, Enzymologic / Chromatography, DEAE-Cellulose / Integrases / Green Fluorescent Proteins / Escherichia coli / Genetics / Luminescent Proteins Language: Zh Journal: Chinese Journal of Biotechnology Year: 2002 Type: Article