Stuy J H
J Bacteriol. 1985 Apr;162(1):1-4. doi: 10.1128/jb.162.1.1-4.1985.
Different Haemophilus cultures were mixed and then spotted onto an agar plate. These mixed colonies were incubated at 37 degrees C and then scored for the presence of recombinants. It was found that conjugative plasmids transferred very efficiently and quickly under these conditions, but only between cells of the same species. Four small plasmids did not transfer at all, nor were they mobilized by the two conjugative plasmids studied. Chromosomal markers transferred very inefficiently. The evidence favored transfer by genetic transformation rather than by conjugation. When mixed cultures were inoculated into broth and then incubated, the transfer of conjugative plasmids was not observed. Transfer of chromosomal markers occurred only when the media used contained Eugonbroth in addition to brain heart infusion, and even then it was very inefficient. The addition of DNase completely eliminated such transfers. This and other evidence indicate that in cell suspensions, chromosomal marker transfer also occurs through transformation. A corrected map of several genetic markers is presented.
将不同的嗜血杆菌培养物混合,然后点种在琼脂平板上。这些混合菌落于37℃培养,然后对重组体的存在情况进行评分。结果发现,在这些条件下,接合质粒能非常高效且快速地转移,但仅在同种细胞之间。四个小质粒根本不转移,也未被所研究的两种接合质粒所动员。染色体标记转移效率极低。证据支持通过基因转化而非接合进行转移。当将混合培养物接种到肉汤中然后培养时,未观察到接合质粒的转移。仅当所用培养基除脑心浸液外还含有优贡肉汤时,染色体标记才会发生转移,即便如此效率也很低。添加DNA酶完全消除了此类转移。这一证据及其他证据表明,在细胞悬液中,染色体标记转移也是通过转化发生的。给出了几个遗传标记的校正图谱。