Rostås K, Dobritsa S V, Dobritsa A P, Koncz C, Alföldi L
Mol Gen Genet. 1980;180(2):323-9. doi: 10.1007/BF00425844.
Ability to produce megacin A, a bacteriocin of B. megaterium, was transferred from the strain B. megaterium 216 into auxotrophic derivatives of the strain B. megaterium KM via protoplast fusion and polyethylene-glycol-induced protoplast transformation by plasmid DNA, respectively. A 30.9 megadalton plasmid was detected in cells with MegA phenotype, and the loss of this phenotype was accompanied in each case with the elimination of that plasmid. The megacinogenic plasmid pBM309 has a single site for both BamHI and XhoI. It is cleaved by the endonucleases SalI, BglII, PstI, PvuII, and EcoRI into 3, 3, 4, 4, and 9 fragments, respectively. The physical map of this plasmid is presented.
巨大芽孢杆菌的细菌素——巨霉素A的产生能力,分别通过原生质体融合以及聚乙二醇诱导的质粒DNA原生质体转化,从巨大芽孢杆菌216菌株转移至巨大芽孢杆菌KM菌株的营养缺陷型衍生物中。在具有MegA表型的细胞中检测到一个30.9兆道尔顿的质粒,并且在每种情况下该表型的丧失都伴随着该质粒的消除。产巨霉素质粒pBM309对BamHI和XhoI均有一个单一酶切位点。它分别被内切酶SalI、BglII、PstI、PvuII和EcoRI切割成3、3、4、4和9个片段。给出了该质粒的物理图谱。