Lovett P S, Duvall E J, Keggins K M
J Bacteriol. 1976 Aug;127(2):817-28. doi: 10.1128/jb.127.2.817-828.1976.
Bacillus pumilus ATCC 12140 harbors 10 or more copies per chromosome of each two small plasmids. Variants of this strain were isolated which were sensitive to a killing activity produced by the plasmid-containing parent. Each of 24 such sensitive (S) variants tested lacked detectable levels of supercoiled deoxyribonucleic acid. Transduction of S variants to the Kill+ phenotype was performed using phage PBP1 propagated on a mutant of ATCC 12140, designated strain L10, that remained Kill+ but retained only a single plasmid species (plasmid pPL10; molecular weight, approximately 4.4 X 10(6), approximately 20 copies per chromosome; RHO = 1.698). Resulting Kill+ transductants of S variants contained a single plasmid species having a size and copy number comparable to that of pPL10. Transfer of pPL10 from strain L10 TO B. pumilus strain NRS 576 was accomplished by transduction with selection for the Kill+ phenotype. Strain NRS 576 naturally harbors about two copies per chromosome of a 28-million-dalton plasmid, pPL576. In Kill + transductants of NRS 576, plasmids pPL10 and pPL576 stably coexisted at a ratio of about 11 molecules of pPL10 to 1 molecule of pPL576. Therefore, pPL576 and pPL10 are compatible plasmids. B. subtilis 168 is naturally resistant to pPl10- determined killing activity. Plasmid pPl10 was therefore inserted into B-subtilis 168 by transformation, using an indirect selection procedure and a spoB mutant as recipient. The plasmid is stably maintained at an estimated 10 copies per chromosome in the spore- recipient and in spore+ transformants. pPL10 is sensitive to cleavage by the endonucleases Hind III and EcoR1.
短小芽孢杆菌ATCC 12140每条染色体含有10个或更多拷贝的两种小质粒。分离出该菌株的变体,它们对含质粒的亲本产生的杀伤活性敏感。测试的24个此类敏感(S)变体中的每一个都缺乏可检测水平的超螺旋脱氧核糖核酸。使用在ATCC 12140的突变体(命名为菌株L10)上繁殖的噬菌体PBP1将S变体转导为Kill +表型,该突变体保持Kill +但仅保留一种质粒(质粒pPL10;分子量约为4.4×10⁶,每条染色体约20个拷贝;RHO = 1.698)。S变体产生的Kill +转导子含有一种大小和拷贝数与pPL10相当的单一质粒。通过选择Kill +表型的转导将pPL10从菌株L10转移到短小芽孢杆菌菌株NRS 576。菌株NRS 576每条染色体天然含有约两个拷贝数的2800万道尔顿质粒pPL576。在NRS 576的Kill +转导子中,质粒pPL10和pPL576以约11个pPL10分子比1个pPL576分子的比例稳定共存。因此,pPL576和pPL10是相容质粒。枯草芽孢杆菌168对pPl10确定的杀伤活性天然抗性。因此,使用间接选择程序并以spoB突变体作为受体,通过转化将质粒pPl10插入枯草芽孢杆菌168中。该质粒在孢子受体和孢子+转化体中以每条染色体估计10个拷贝的数量稳定维持。pPL10对核酸内切酶Hind III和EcoR1的切割敏感。