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Plasmid pBRINT: a vector for chromosomal insertion of cloned DNA.

作者信息

Balbás P, Alvarado X, Bolívar F, Valle F

机构信息

Instituto de Biotecnología, Universidad Nacional Autónoma de Mexico, Cuernavaca, Morelos.

出版信息

Gene. 1993 Dec 22;136(1-2):211-3. doi: 10.1016/0378-1119(93)90466-g.

DOI:10.1016/0378-1119(93)90466-g
PMID:8294004
Abstract

Plasmid pBRINT is a pBR322 derivative [Bolivar et al., Gene 2 (1977) 95-113; Balbás et al., Gene 50 (1986) 3-40] that allows the insertion and replacement of DNA sequences into the Escherichia coli chromosome by homologous recombination. This method uses the inability of E. coli strain ATCC47002 (JC7623) to replicate covalently closed circular (ccc) pBR322-derived plasmids, and the convenience of XGal+IPTG screening for recombinants. The vector also contains suitable selection markers (Ap and Cm), as well as a multiple cloning site (MCS) derived from the pUC vectors [Yanisch-Perron et al., Gene 33 (1985) 103-119] to facilitate cloning. A simple PCR scheme was developed to scan for DNA insertions into the bacterial chromosome. Once introduced into the chromosome, the inserted DNA sequences can be transferred to other strains by bacteriophage P1-mediated transduction.

摘要

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引用本文的文献

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Chromosomal editing in Escherichia coli. Vectors for DNA integration and excision.大肠杆菌中的染色体编辑。DNA整合与切除载体。
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