Tian Yongqiang, Jiang Weihong, Zhao Guoping, Qin Zhongjun
Key Laboratory of Synthetic Biology, Shanghai Institute of Plant Physiology and Ecology, The Chinese Academy of Sciences, 300 Fenglin Road, Shanghai, 200032, China.
Biotechnol Lett. 2009 Aug;31(8):1253-8. doi: 10.1007/s10529-009-0005-6. Epub 2009 Apr 29.
The high efficiency of homologous recombination in yeast and bacteria makes it useful for recombinational cloning of large genomic segments in vivo. The low efficiency of homologous recombination in Streptomyces has hindered the development of this cloning method. Unlike the inefficient mobilization of chromosomal markers, conjugative plasmid transfer is very efficient in Streptomyces. Here we report that the conjugation-coupled recombination procedure can be used to transfer a 10 kb chromosomal telomeric segment of Streptomyces lividans into a linear plasmid. The plasmid predominated in the population of cells after transfer into recipients. These results may promote the development of the recombinational cloning of large chromosomal segments in Streptomyces in vivo.
酵母和细菌中同源重组的高效率使其在体内对大基因组片段的重组克隆很有用。链霉菌中同源重组的低效率阻碍了这种克隆方法的发展。与染色体标记的低效转移不同,接合性质粒转移在链霉菌中非常高效。在此,我们报道接合偶联重组程序可用于将天蓝色链霉菌的一个10 kb染色体端粒片段转移到线性质粒中。转移到受体细胞后,该质粒在细胞群体中占主导地位。这些结果可能会促进链霉菌体内大染色体片段重组克隆的发展。