来自Bacillus circulans WZ-12的二氯甲烷脱卤酶基因dcmR的克隆和表达

通过PCR方法从Bacillus circulans WZ-12中分离到二氯甲烷脱卤酶基因dcmR,构建具T7强启动子的pET28b(+)-dcmR质粒,电击转化Escherichia.coli BL21(DE3),构建了二氯甲烷生物降解基因工程菌BL21pET28b(+)-dcmR].重组菌经IPTG诱导后,表达蛋白占总蛋白的32%.表达蛋白的酶活最高可达25.78 U/mL,酶的比活(以蛋白计)为88.86 U/mg.重组菌周质中酶活2.92 U/mL,胞内酶活22.86 U/mL.重组菌产生的酶的活力和比活较原降解菌株高1~2倍.对工程菌的生长特性和降解特性的研究表明,工程菌在LB培养基中的生长特性与原始菌株没有差别,生长至对数期A600 nm值都可达2.4左右.重组菌株dcmR-1在25 h的降解率达90%以上,降解效率比原降解菌株有明显提高.该基因工程菌的构建对二氯甲烷生物降解机制研究以及复合污染环境的生物修复和工程应用具有实际意义.

Gene Cloning and Overexpression of Dichloromethane Dehalogenase from Bacillus circulans WZ-12

The dcmR gene encoding dichloromethane dehalogenase was amplified by PCR from Bacillus circulans WZ-12 and cloned to expression vector pET28b(+),yielding recombinant plasmid pET28b(+)-dcmR.Then plasmid pET28b(+)-dcmR was introduced into Escherichia.coli BL21(DE3).Expression was induced by IPTG,and the enzyme activity reached 25.78(U/mL),the specific enzyme activity reached 88.86(U/mg) protein.The periplasmic and cytoplasmic enzyme activity reached 2.92(U/mL) and 22.86(U/mL) respectively.All results analysis...