Fernández-Tresguerres M E, Martín M, García de Viedma D, Giraldo R, Díaz-Orejas R
Centro de Investigaciones Biológicas, Madrid, Spain.
J Bacteriol. 1995 Aug;177(15):4377-84. doi: 10.1128/jb.177.15.4377-4384.1995.
pPS10 is a replicon isolated from Pseudomonas syringe pv. savastanoi that can be established at 37 degrees C efficiently in Pseudomonas aeruginosa but very inefficiently in Escherichia coli. The establishment of the wild-type pPS10 replicon in E. coli is favored at low temperatures (30 degrees C or below). RepA protein of pPS10 promotes in vitro plasmid replication in extracts from E. coli, and this replication depends on host proteins DnaA, DnaB, DnaG, and SSB. Mutant plasmids able to efficiently replicate in E. coli at 37 degrees C were obtained. Three of four mutants whose mutations were mapped show a conservative Ala-->Val change in the amino-terminal region of the replication protein RepA. Plasmids carrying this mutation maintain the capacity to replicate in P. aeruginosa and have a fourfold increase in copy number in this host. The mutation does not substantially alter the autoregulation mediated by RepA. These results show that the physiological conditions of the host as well as subtle changes in the plasmid replication protein can modulate the host range of the pPS10 replicon.
pPS10是从丁香假单胞菌丁香致病变种中分离出的一个复制子,它能在37℃时在铜绿假单胞菌中高效建立,但在大肠杆菌中效率极低。野生型pPS10复制子在大肠杆菌中于低温(30℃或更低)时易于建立。pPS10的RepA蛋白在大肠杆菌提取物中促进体外质粒复制,且这种复制依赖于宿主蛋白DnaA、DnaB、DnaG和SSB。获得了能够在37℃时在大肠杆菌中高效复制的突变体质粒。其突变已定位的四个突变体中的三个在复制蛋白RepA的氨基末端区域显示出保守的丙氨酸到缬氨酸的变化。携带这种突变的质粒保持了在铜绿假单胞菌中复制的能力,并且在该宿主中的拷贝数增加了四倍。该突变不会显著改变由RepA介导的自动调节。这些结果表明宿主的生理条件以及质粒复制蛋白中的细微变化可以调节pPS10复制子的宿主范围。