Khasanov F K, Zhvingila D Iu, Zaĭhudlin A A, Prozorov A A, Bashkirov V I
Genetika. 1992 Jul;28(7):38-45.
With a view to determine a minimal sequence length of homology necessary for RecE-dependent homologous recombination in Bacillus subtilis cells, we developed a system, based on interaction between plasmid replicon and bacterial chromosome. Recombination frequencies were measured between ts plasmid pE194 derivatives carrying chromosomal beta-glucuronidase gene (bglS) fragments of various length, and a bacterial chromosome. The homologous recombination events resulted in bglS gene disruption. Approx. 70 bp of homology were found to be necessary for detectable homologous recombination. Homologous recombination was not detected when homology was equal 25 bp. These data indicate that homology requirement for recombination in B. subtilis differs from that in Escherichia coli.
为了确定枯草芽孢杆菌细胞中RecE依赖性同源重组所需的最小同源序列长度,我们基于质粒复制子与细菌染色体之间的相互作用开发了一个系统。我们测定了携带不同长度染色体β-葡萄糖醛酸酶基因(bglS)片段的温度敏感型质粒pE194衍生物与细菌染色体之间的重组频率。同源重组事件导致bglS基因破坏。发现约70 bp的同源性对于可检测到的同源重组是必要的。当同源性为25 bp时未检测到同源重组。这些数据表明枯草芽孢杆菌中重组的同源性要求与大肠杆菌中的不同。