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[利用pBR322-red系统对大肠杆菌乳糖操纵子位点进行基因敲除和敲入]

[Gene knockout and knockin on the Escherichia coli lac operon loci using pBR322-red system].

作者信息

Chen Wei, Yu Mei, Li Shan-Hu, Wang Ming-Gang, Zhou Jian-Guang

机构信息

Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100850, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2005 Mar;21(2):192-7.

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.

摘要

pBR322-Red是一种新构建的重组质粒,它包含部分pBR322载体、一系列λ-原噬菌体调控元件和Red重组基因。起初,我们研究了pBR322-Red的最佳工作条件,然后使用该质粒对大肠杆菌W3110染色体中的乳糖操纵子进行如下修饰:首先,我们利用Red介导的重叠单链DNA寡核苷酸重组敲除lacI基因。其次,我们通过Red介导的线性双链DNA同源重组,用报告基因lacZ取代lacA和lacY基因。最后,我们首次检测了这些位点上lacZ的表达。结果表明,pBR322-Red系统适用于通过各种重组策略修饰W3110染色体。

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