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Chromosomal duplications and cointegrates generated by the bacteriophage lamdba Red system in Escherichia coli K-12

机译:大肠杆菌K-12中噬菌体λRed系统产生的染色体重复和共整合

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摘要

BackgroundAn Escherichia coli strain in which RecBCD has been genetically replaced by the bacteriophage λ Red system engages in efficient recombination between its chromosome and linear double-stranded DNA species sharing sequences with the chromosome. Previous studies of this experimental system have focused on a gene replacement-type event, in which a 3.5 kbp dsDNA consisting of the cat gene and flanking lac operon sequences recombines with the E. coli chromosome to generate a chloramphenicol-resistant Lac- recombinant. The dsDNA was delivered into the cell as part of the chromosome of a non-replicating λ vector, from which it was released by the action of a restriction endonuclease in the infected cell. This study characterizes the genetic requirements and outcomes of a variety of additional Red-promoted homologous recombination events producing Lac+ recombinants.
机译:背景技术一种大肠杆菌菌株,其中RecBCD已被噬菌体λRed系统遗传取代,参与其染色体与与该染色体共享序列的线性双链DNA物种之间的有效重组。该实验系统的先前研究集中于基因替换型事件,其中由cat基因和侧翼lac操纵子序列组成的3.5 kbp dsDNA与大肠杆菌染色体重组,以产生耐氯霉素的Lac重组体。 dsDNA作为非复制λ载体染色体的一部分被递送到细胞中,在感染的细胞中通过限制性核酸内切酶的作用将其从dsDNA中释放出来。这项研究的特点是遗传要求和产生Lac +重组体的多种其他Red促进的同源重组事件的结果。

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