McIntire S, Willetts N
J Bacteriol. 1978 Apr;134(1):184-92. doi: 10.1128/jb.134.1.184-192.1978.
Fifteen cointegrates of the plasmid Flac and prophage lambda that had suffered no detectable change in plasmid phenotype were isolated and characterized. The locations of the prophage insertions were determined by genetic analysis of deletion mutants obtained from each cointegrate as survivors of growth at 42 degrees C. In 11 cointegrates, the prophage was inserted between traI and lac, although probably in more than one location; in 3 others, it was on one side or the other of lac; and in 1 it was between lac and pif. Deletions covering all or part of the transfer region, as well as of lac and of pif, were obtained in the course of this analysis. Deletion mutants that had lost all known transfer genes were also oriT, but they retained the capacity to recircularize after transfer. Attempts were made to isolate lambda transducing phages for nearby plasmid genes from the cointegrates, and lambdaptraGD, lambdaptraD, lambdaptraI, and lambdadtraDI phages were obtained.
分离并鉴定了15个质粒Flac和原噬菌体λ的共整合体,这些共整合体的质粒表型未发生可检测到的变化。通过对从每个共整合体获得的缺失突变体进行遗传分析来确定原噬菌体插入的位置,这些缺失突变体是在42℃生长的幸存者。在11个共整合体中,原噬菌体插入在traI和lac之间,尽管可能不止一个位置;在另外3个中,它在lac的一侧或另一侧;在1个中,它在lac和pif之间。在该分析过程中获得了覆盖全部或部分转移区域以及lac和pif的缺失。失去所有已知转移基因的缺失突变体也失去了oriT,但它们在转移后仍保留重新环化的能力。尝试从共整合体中分离用于附近质粒基因的λ转导噬菌体,并获得了λtraGD、λtraD、λtraI和λdtraDI噬菌体。