Hashimoto-Gotoh T, Inselburg J
J Bacteriol. 1979 Aug;139(2):597-607. doi: 10.1128/jb.139.2.597-607.1979.
Replication-defective mutants of plasmid ColE1 were isolated from a chimeric plasmid formed by ligating a temperature-sensitive replication derivative of pSC101, pHSG1, with a ColE1-Tn3-containing plasmid. The replication-defective ColE1 mutants isolated were all spontaneous deletion mutants that had lost the ColE1 replication origin and regions adjacent to it. The extent of a deletion was determined by analyzing restriction endonuclease-generated deoxyribonucleic acid fragments of the ColE1 plasmid component of the chimeras by both agarose and polyacrylamide gel electrophoresis. None of the chimeras containing the replication-defective ColE1 mutants was able to replicate in the presence of chloramphenicol. The expression of ColE1 incompatibility was either markedly reduced or not detectable in the replication mutants isolated.
从通过将pSC101的温度敏感复制衍生物pHSG1与含ColE1 - Tn3的质粒连接形成的嵌合质粒中分离出质粒ColE1的复制缺陷型突变体。所分离出的复制缺陷型ColE1突变体均为自发缺失突变体,它们失去了ColE1复制起点及其相邻区域。通过琼脂糖凝胶电泳和聚丙烯酰胺凝胶电泳分析嵌合体中ColE1质粒成分的限制性内切酶产生的脱氧核糖核酸片段,确定缺失的程度。含有复制缺陷型ColE1突变体的嵌合体在氯霉素存在下均不能复制。在所分离出的复制突变体中,ColE1不相容性的表达要么显著降低,要么检测不到。