Pernodet J L, Guerineau M
Mol Gen Genet. 1981;182(1):53-9. doi: 10.1007/BF00422766.
Covalently closed circular DNA was isolated from a strain of Streptomyces coelicolor ATCC 10147 and from a strain of Streptomyces coelicolor subspecies flavus ATCC 19894, using two different methods. The two plasmids were of uniform monomer size: 8.9 kb for pS 10147, the plasmid from S. coelicolor ATCC 10147, and around 125 kb for the plasmid from S. coelicolor ATCC 19894. A restriction enzyme map was constructed for pS 10147, using seven enzymes. Four of the enzymes, (BamHI, Bgl,II, PvuII, and XhoI) cut pS 10147 once while PstI made two cuts. The GC content of this plasmid was calculated to be 72%. The possible utilisation of pS 10147 as a cloning vector in Streptomyces is discussed.
采用两种不同方法,从一株天蓝色链霉菌ATCC 10147和一株黄天蓝色链霉菌亚种ATCC 19894中分离出共价闭合环状DNA。这两种质粒具有统一的单体大小:来自天蓝色链霉菌ATCC 10147的质粒pS 10147为8.9 kb,来自天蓝色链霉菌ATCC 19894的质粒约为125 kb。使用七种酶构建了pS 10147的限制性酶切图谱。其中四种酶(BamHI、BglII、PvuII和XhoI)对pS 10147切割一次,而PstI切割两次。计算得出该质粒的GC含量为72%。文中讨论了pS 10147作为链霉菌克隆载体的可能用途。