Von Tersch M A, Carlton B C
J Bacteriol. 1984 Dec;160(3):854-9. doi: 10.1128/jb.160.3.854-859.1984.
A host-vector system was developed for molecular cloning in Bacillus megaterium and used to clone the structural and immunity genes for megacins A-216 and A-19213. Recombinant clones that expressed immunity only or both immunity to and production of each megacin were obtained. Restriction mapping of native megacinogenic plasmids and recombinant clones was used to construct physical and genetic maps of megacinogenic plasmids pBM309 and pBM113. Limited sequence homology between pBM309 and pBM113 was detected by Southern blot hybridization and was mapped to, at most, a 6.4-kilobase-pair region of pBM309 and a 6.1-kilobase-pair region of pBM113.
构建了一种用于巨大芽孢杆菌分子克隆的宿主-载体系统,并用于克隆巨霉素A-216和A-19213的结构基因和免疫基因。获得了仅表达免疫性或同时表达对每种巨霉素的免疫性和产生能力的重组克隆。利用天然产巨霉素质粒和重组克隆的限制性酶切图谱构建了产巨霉素质粒pBM309和pBM113的物理图谱和遗传图谱。通过Southern印迹杂交检测到pBM309和pBM113之间有限的序列同源性,该同源性最多定位于pBM309的一个6.4千碱基对区域和pBM113的一个6.1千碱基对区域。