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Integration of narrow-host-range vectors from Escherichia coli into the genomes of amino acid-producing corynebacteria after intergeneric conjugation.

机译:基因间缀合后,将大肠杆菌的狭窄宿主范围载体整合到氨基酸生产棒状杆菌的基因组中。

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摘要

Conjugative transfer of mobilizable derivatives of the Escherichia coli narrow-host-range plasmids pBR322, pBR325, pACYC177, and pACYC184 from E. coli to species of the gram-positive genera Corynebacterium and Brevibacterium resulted in the integration of the plasmids into the genomes of the recipient bacteria. Transconjugants appeared at low frequencies and reproducibly with a delay of 2 to 3 days compared with matings with replicative vectors. Southern analysis of corynebacterial transconjugants and nucleotide sequences from insertion sites revealed that integration occurs at different locations and that different parts of the vector are involved in the process. Integration is not dependent on indigenous insertion sequence elements but results from recombination between very short homologous DNA segments (8 to 12 bp) present in the vector and in the host DNA. In the majority of the cases (90%), integration led to cointegrate formation, and in some cases, deletions or rearrangements occurred during the recombination event. Insertions were found to be quite stable even in the absence of selective pressure.
机译:大肠杆菌的窄宿主范围质粒pBR322,pBR325,pACYC177和pACYC184的可动员衍生物从大肠杆菌向革兰氏阳性菌棒状杆菌和短杆菌属物种的共轭转移,导致该质粒整合到大肠杆菌的基因组中受体细菌。与复制载体的交配相比,转导结合体的出现频率较低,可再现地延迟了2至3天。插入位点的棒状杆菌转导结合物和核苷酸序列的Southern分析表明,整合发生在不同的位置,并且载体的不同部分参与了该过程。整合不依赖于本地插入序列元件,而是源自载体和宿主DNA中存在的非常短的同源DNA片段(8至12 bp)之间的重组。在大多数情况下(90%),整合导致共整合形成,在某些情况下,重组事件发生缺失或重排。发现即使在没有选择压力的情况下插入也相当稳定。

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