A method to invert DNA segments of the Bacillus subtilis 168 genome by recombination between two homologous sequences

被引:25
|
作者
Toda, T
Tanaka, T
Itaya, M
机构
[1] MITSUBISHI KASEI INST LIFE SCI, MACHIDA, TOKYO 194, JAPAN
[2] TOKAI UNIV, SCH MARINE SCI & TECHNOL, SHIMIZU, SHIZUOKA 424, JAPAN
关键词
DNA inversion; recA; neomycin; rare-cutting endonucleases; bacterial genome technology;
D O I
10.1271/bbb.60.773
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We developed a method that allows rapid isolation of mutant Bacillus subtilis 168 carrying an inversion of a specific DNA segment of the genome, Two incomplete neomycin resistance gene cassettes were integrated at both ends of the 1652-kb segment to be inverted, Reciprocal recombination within the 590-bp homologous region of these two cassettes created an intact neomycin resistance gene with concomitant inversion of the 1652-kb segment flanked by the two cassettes, Structure of the mutant genome was verified by analyzing the physical map for rare cutting endonucleases, SfiI, NotI, I-CeuI, and I-SceI, The inversion rate was estimated to be 6.9 +/- 1.4 x 10(-8)/cell/cell division at 37 degrees C, The method should be in principle applicable not only to other regions of the B. subtilis genome but also to other bacterial genomes.
引用
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页码:773 / 778
页数:6
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