Causey S C, Brown L R
J Bacteriol. 1978 Sep;135(3):1070-9. doi: 10.1128/jb.135.3.1070-1079.1978.
We used the sequence-specific endonucleases EcoRI, SmaI, BamHI, HsuI, and HaeIII as identification tools in following the conjugal transfer of the well-studied R plasmids Sa, R388, RP4, and R6K. Transfers were both intergeneric and intrageneric. Plasmid fingerprints were generated from both single- and combination-enzyme digests. The Sa transconjugants yielded plasmids showing consistent fingerprints for each of the respective endonucleases used, whereas the three other R-plasmid transconjugants showed fingerprint changes.
我们使用序列特异性核酸内切酶EcoRI、SmaI、BamHI、HsuI和HaeIII作为鉴定工具,追踪已充分研究的R质粒Sa、R388、RP4和R6K的接合转移。转移包括属间和属内转移。通过单酶切和双酶切产生质粒指纹图谱。Sa转接合子产生的质粒对于所使用的每种相应核酸内切酶都显示出一致的指纹图谱,而其他三种R质粒转接合子则显示出指纹图谱变化。