Croes C, Vanderleyden J, Michiels K
F.A. Janssens Memorial Laboratory for Genetics, Catholic University of Leuven, Heverlee, Belgium.
Mol Gen Genet. 1990 Aug;223(1):152-5. doi: 10.1007/BF00315808.
Cosmid clones encoding the recA gene of Azospirillum brasilense were isolated by intergeneric complementation of an Escherichia coli recA mutant. Site-directed Tn5 mutagenesis and subcloning of one complementing cosmid clone allowed us to localize the A. brasilense recA gene on a 1.2 kb DNA fragment. One Tn5 insertion that inactivates the cloned recA gene was crossed into the chromosome of A. brasilense by marker exchange. The resulting A. brasilense recA mutant showed increased sensitivity to the DNA methylating agent methyl methanesulfonate and to ultraviolet light and had at least one hundredfold reduced recombinational activity compared to the parent strain.
通过大肠杆菌recA突变体的属间互补,分离出了编码巴西固氮螺菌recA基因的黏粒克隆。对一个互补黏粒克隆进行定点Tn5诱变和亚克隆,使我们能够将巴西固氮螺菌recA基因定位在一个1.2 kb的DNA片段上。通过标记交换,将一个使克隆的recA基因失活的Tn5插入片段导入巴西固氮螺菌的染色体中。与亲本菌株相比,所得的巴西固氮螺菌recA突变体对DNA甲基化剂甲磺酸甲酯和紫外线的敏感性增加,重组活性至少降低了100倍。