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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 em Zh | WPRIM | ID: wpr-256177
Biblioteca responsável: 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.
Assuntos
Texto completo: 1 Índice: WPRIM Assunto principal: Plasmídeos / Proteínas Virais / Proteínas Recombinantes / Regulação Enzimológica da Expressão Gênica / Cromatografia DEAE-Celulose / Integrases / Proteínas de Fluorescência Verde / Escherichia coli / Genética / Proteínas Luminescentes Idioma: Zh Revista: Chinese Journal of Biotechnology Ano de publicação: 2002 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Plasmídeos / Proteínas Virais / Proteínas Recombinantes / Regulação Enzimológica da Expressão Gênica / Cromatografia DEAE-Celulose / Integrases / Proteínas de Fluorescência Verde / Escherichia coli / Genética / Proteínas Luminescentes Idioma: Zh Revista: Chinese Journal of Biotechnology Ano de publicação: 2002 Tipo de documento: Article