Morimoto Takuya, Ara Katsutoshi, Ozaki Katsuya, Ogasawara Naotake
Graduate School of Information Science, Nara Institute of Science and Technology, Nara 630-0101, Japan.
Genes Genet Syst. 2009 Aug;84(4):315-8. doi: 10.1266/ggs.84.315.
A genetic tool to introduce marker-free deletions is essential for multiple manipulations of genomes. We report a simple and efficient method to create marker-free deletion mutants of Bacillus subtilis through transformation with recombinant PCR products, using the Escherichia coli mazF gene encoding an endoribonuclease that cleaves free mRNAs as a counter-selection tool. Our method will be applicable to any bacterium in which introduction of the mazF cassette into the genome by double crossover homologous recombination is possible.
一种用于引入无标记缺失的基因工具对于基因组的多种操作至关重要。我们报告了一种简单有效的方法,通过用重组PCR产物转化来创建枯草芽孢杆菌的无标记缺失突变体,使用编码内切核糖核酸酶的大肠杆菌mazF基因,该酶可切割游离mRNA作为反选择工具。我们的方法将适用于任何能够通过双交换同源重组将mazF盒引入基因组的细菌。