Burman L G
J Bacteriol. 1977 Jul;131(1):76-81. doi: 10.1128/jb.131.1.76-81.1977.
The conjugational transfer efficiency of 41 wild-type R-plasmids was studied in Escherichia coli K-12. Type I R-plasmids were transferred at comparatively high and rather uniform frequencies, whereas type F R-plasmids showed less uniform and, on average, somewhat lower transfer frequencies. R-plasmids not mediating sensitivity to F-, I-, or N-specific phages showed moderate transfer frequencies, and type N R-plasmids showed very low transfer frequencies. Various lines of evidence suggest that a well-expressed, but functionally inefficient, conjugation apparatus is the cause of the poor transfer of type N R-plasmids in liquid medium. Nalidixic acid efficiently inhibited transfer of type I and particularly type F R-plasmids, whereas the transfer of type N plasmids was resistant to the drug. Type F and type I plasmids appear to depend on at least one host function for their transfer, namely, the nalidixic acid-sensitive reaction in vegetative chromosome replication, whereas type N plasmids are independent of this function.
在大肠杆菌K-12中研究了41种野生型R质粒的接合转移效率。I型R质粒以相对较高且较为均匀的频率进行转移,而F型R质粒的转移频率不太均匀,且平均而言略低。不介导对F-、I-或N特异性噬菌体敏感性的R质粒表现出中等转移频率,而N型R质粒的转移频率非常低。各种证据表明,表达良好但功能低效的接合装置是N型R质粒在液体培养基中转移不佳的原因。萘啶酸能有效抑制I型尤其是F型R质粒的转移,而N型质粒的转移对该药物具有抗性。F型和I型质粒的转移似乎至少依赖一种宿主功能,即营养染色体复制中对萘啶酸敏感的反应,而N型质粒则不依赖此功能。