Iordanescu S, Surdeanu M
Mol Gen Genet. 1983;191(2):201-6. doi: 10.1007/BF00334814.
Temperature-sensitive replication (Tsr) mutants have been isolated from the Staphylococcus aureus plasmid pC194. For three of the four mutant plasmids tested (pSAO801, pSAO802, and pSAO804) the segregation kinetics suggested a complete block of plasmid replication at 43 degrees C. The replication defects of three mutant plasmids: pSAO802, pSAO803, and pSAO804 could be complemented by recombinant plasmids carrying a segment from either the wild type or the other mutant, pSAO801. There was no complementation when the segment carried by the recombinant plasmid was derived from one of the three complementable mutants. These data were taken as evidence for the involvement of a diffusible, plasmid-encoded product, RepH, in pC194 replication. The complementation of the fourth Tsr mutant, pSAO801, could not be tested due to an abnormal susceptibility of this mutant to the incompatibility expressed by recombinants carrying segments derived from pC194 or its mutants. A single mutation was found to be responsible for both pSAO801 instability and its altered incompatibility properties but the nature of the defect has not yet been elucidated.
温度敏感复制(Tsr)突变体已从金黄色葡萄球菌质粒pC194中分离出来。对于所测试的四个突变体质粒中的三个(pSAO801、pSAO802和pSAO804),分离动力学表明在43℃时质粒复制完全受阻。三个突变体质粒pSAO802、pSAO803和pSAO804的复制缺陷可由携带野生型或另一个突变体pSAO801片段的重组质粒互补。当重组质粒携带的片段来源于三个可互补突变体之一时,则不存在互补作用。这些数据被视为一种可扩散的、由质粒编码的产物RepH参与pC194复制的证据。由于该突变体对携带来源于pC194或其突变体片段的重组体所表现出的不相容性异常敏感,因此无法测试第四个Tsr突变体pSAO801的互补作用。发现单个突变是pSAO801不稳定性及其不相容性改变的原因,但缺陷的本质尚未阐明。