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Gene knockout and knockin on the Escherichia coli lac operon loci using pBR322-red system / 生物工程学报
Chinese Journal of Biotechnology ; (12): 192-197, 2005.
Article en Zh | WPRIM | ID: wpr-249926
Biblioteca responsable: WPRO
ABSTRACT
pBR322-Red is a newly constructed recombineering plasmid, which contains a part of the pBR322 vector, a series of regulatory elements of lambda-prophage and Red recombination genes. In the beginning, we studied the best working conditions of pBR322-Red, and then modified lac operon in E. coli W3110 chromosome using the plasmid as follow: Firstly, we knockout the lacI gene using Red-mediated recombineering with overlapping single stranded DNA oligonucleotides. Secondly, we substituded the lacA and lacY genes with lacZ, a report gene, by Red-mediated linearized double strands DNA homologous recombination. Finally, we detected the expression of lacZ on these loci for the first time. The results suggested that pBR322-Red system is suitable for modifying W3110 chromosome with various recombination strategies.
Asunto(s)
Texto completo: 1 Índice: WPRIM Asunto principal: Plásmidos / Recombinación Genética / Cromosomas Bacterianos / Bacteriófago lambda / Escherichia coli / Técnicas de Sustitución del Gen / Técnicas de Inactivación de Genes / Genética / Operón Lac / Métodos Límite: Humans Idioma: Zh Revista: Chinese Journal of Biotechnology Año: 2005 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Plásmidos / Recombinación Genética / Cromosomas Bacterianos / Bacteriófago lambda / Escherichia coli / Técnicas de Sustitución del Gen / Técnicas de Inactivación de Genes / Genética / Operón Lac / Métodos Límite: Humans Idioma: Zh Revista: Chinese Journal of Biotechnology Año: 2005 Tipo del documento: Article