Yamamoto M, Jones J M, Senghas E, Gawron-Burke C, Clewell D B
Appl Environ Microbiol. 1987 May;53(5):1069-72. doi: 10.1128/aem.53.5.1069-1072.1987.
A method has been developed for the introduction of Tn5 into Escherichia coli plasmid chimeras containing Streptococcus faecalis DNA. Tn5 could be introduced via a lambda::Tn5 delivery vehicle. The system proved to be particularly efficient and facilitated insertions at numerous sites on DNA containing the 16-kilobase conjugative transposon Tn916. It was possible to introduce some of the resulting Tn916::Tn5 derivatives back into S. faecalis by using a recently developed protoplast transformation procedure. A presumed zygotic induction resulted in insertion of the Tn916 derivatives at multiple sites in the S. faecalis chromosome.
已开发出一种将Tn5导入含有粪肠球菌DNA的大肠杆菌质粒嵌合体的方法。Tn5可通过λ::Tn5递送载体导入。该系统被证明特别有效,并有助于在含有16千碱基接合转座子Tn916的DNA的多个位点进行插入。通过使用最近开发的原生质体转化程序,有可能将一些所得的Tn916::Tn5衍生物重新导入粪肠球菌。推测的合子诱导导致Tn916衍生物在粪肠球菌染色体的多个位点插入。