Milliken C E, Clowes R C
J Bacteriol. 1973 Feb;113(2):1026-33. doi: 10.1128/jb.113.2.1026-1033.1973.
Plasmid DNA from Escherichia coli strains harboring drug resistance either of the infectious or noninfectious kind has been separated by CsCl centrifugation of crude cell lysates in the presence of ethidium bromide and examined by electron microscopy. Plasmid deoxyribonucleic acid (DNA) from an S(+) strain (which has the property of noninfectious streptomycin-sulfonamide resistance) consists of a monomolecular covalently closed circular species of 2.7 mum in contour length (5.6 x 10(6) atomic mass units; amu). DNA from a strain carrying a transfer factor, termed Delta, but no determinant for drug resistance, is a monomolecular covalently closed circular species of 29.3 mum in contour length (61 x 10(6) amu). DNA from either Delta(+)A(+) or Delta(+)S(+) strains, (which are respectively ampicillin or streptomycin-sulfonamide resistant, and can transfer this drug resistance), shows a bimodal distribution of molecules of contour lengths 2.7 mum and 29.3 mum, whereas DNA from a (Delta-T)(+) strain (showing infectious tetracycline resistance) contains only one species of molecule measuring 32.3 mum (67 x 10(6) amu). We conclude that ampicillin resistance is carried by a DNA molecule (the A determinant) of 2.7 mum, and streptomycin-sulfonamide resistance is carried by an independent molecule (the S determinant) of similar size. These molecules are not able to effect their own transfer, but can be transmitted to other cells due to the simultaneous presence of the transfer factor, Delta, which also constitutes an independent molecule, of size 29.3 mum. In general, there appears to be little recombination or integration of the A or S molecules into that of Delta, although a small proportion (5-10%) of recombinant molecules cannot be excluded. In contrast, the third drug-resistance determinant, that for tetracycline resistance (denoted as T), is integrated in the Delta molecule to form the composite structure Delta-T of size 32.3 mum, which determines infectious tetracycline resistance. The Delta(+)A(+) and Delta(+)S(+) strains are defined as harboring plasmid aggregates, and the (Delta-T)(+) strain is defined as carrying a plasmid cointegrate; the properties of all three strains are characteristic of strains harboring R factors. These results are compatible with the previously published genetic data. The number of Delta molecules per cell appears to be equal to the chromosomal number irrespective of growth phase, and this plasmid can thus be defined as stringently regulated in DNA replication. In contrast, S and A exist as multiple copies, probably in at least a 10-fold excess of chromosomal copy number. S and A can thus be defined as relaxed in the regulation of their DNA replication.
通过在溴化乙锭存在的情况下对粗细胞裂解物进行氯化铯离心,已分离出携带传染性或非传染性耐药性的大肠杆菌菌株的质粒DNA,并通过电子显微镜进行了检查。来自S(+)菌株(具有非传染性链霉素 - 磺胺抗性特性)的质粒脱氧核糖核酸(DNA)由一个轮廓长度为2.7μm(5.6×10⁶原子质量单位;amu)的单分子共价闭合环状分子组成。来自携带称为Delta的转移因子但无耐药性决定簇的菌株的DNA是一个轮廓长度为29.3μm(61×10⁶amu)的单分子共价闭合环状分子。来自Delta(+)A(+)或Delta(+)S(+)菌株(分别对氨苄青霉素或链霉素 - 磺胺具有抗性,并可转移这种耐药性)的DNA显示出轮廓长度为2.7μm和29.3μm的分子的双峰分布,而来自(Delta - T)(+)菌株(显示传染性四环素抗性)的DNA仅包含一种尺寸为32.3μm(67×10⁶amu)的分子。我们得出结论,氨苄青霉素抗性由一个2.7μm的DNA分子(A决定簇)携带,链霉素 - 磺胺抗性由一个大小相似的独立分子(S决定簇)携带。这些分子自身无法实现转移,但由于转移因子Delta(其也是一个大小为29.3μm的独立分子)的同时存在,可被传递到其他细胞。一般来说,A或S分子与Delta分子之间似乎很少发生重组或整合,尽管不能排除一小部分(5 - 10%)的重组分子。相比之下,第三个耐药性决定簇,即四环素抗性决定簇(表示为T),整合在Delta分子中形成大小为32.3μm的复合结构Delta - T,它决定传染性四环素抗性。Delta(+)A(+)和Delta(+)S(+)菌株被定义为携带质粒聚集体,(Delta - T)(+)菌株被定义为携带质粒共整合体;所有这三种菌株的特性都是携带R因子的菌株的特征。这些结果与先前发表的遗传数据一致。每个细胞中Delta分子的数量似乎与染色体数量相等,而与生长阶段无关,因此这种质粒在DNA复制中可被定义为严格调控。相比之下,S和A以多拷贝形式存在,可能至少比染色体拷贝数多10倍。因此,S和A在其DNA复制调控中可被定义为松弛调控。