Reeves P, Willetts N
J Bacteriol. 1974 Oct;120(1):125-30. doi: 10.1128/jb.120.1.125-130.1974.
The ability of F-like plasmids to promote transfer from the F origin of transfer was determined. Chromosome transfer was measured from plasmid derivatives of RecA(-) Hfr deletion strains which had lost all the F transfer genes but which in some cases retained, and in others had also lost, the origin sequence. ColV2 and ColVBtrp could initiate transfer from the F origin, but R100-1, R1-19, and R538-1 drd could not. These results can be correlated with the plasmid specificity of the traI components of the different plasmid transfer systems, supporting the hypothesis that the origin of transfer is the site of action of the traI product. Most F-like plasmids, including R1-19 and R538-1 drd, could transfer ColE1, consistent with previous findings that the (plasmid-specific) traI product is not necessary for ColE1 transfer by Flac; ColE1 transfer may be initiated by a ColE1-or host-determined product. R100-1 and R136fin(-) could not transfer ColE1 efficiently, apparently because of differences residing in their pilus-forming genes.
测定了F类质粒从F转移起点促进转移的能力。从RecA(-)Hfr缺失菌株的质粒衍生物中检测染色体转移,这些菌株已失去所有F转移基因,但在某些情况下保留了,而在其他情况下也失去了起点序列。ColV2和ColVBtrp可以从F起点起始转移,但R100-1、R1-19和R538-1 drd则不能。这些结果可以与不同质粒转移系统的traI组分的质粒特异性相关联,支持转移起点是traI产物作用位点的假说。大多数F类质粒,包括R1-19和R538-1 drd,可以转移ColE1,这与先前的发现一致,即Flac转移ColE1不需要(质粒特异性的)traI产物;ColE1转移可能由ColE1或宿主决定的产物起始。R100-1和R136fin(-)不能有效地转移ColE1,显然是因为它们的菌毛形成基因存在差异。