Franke A E, Clewell D B
J Bacteriol. 1981 Jan;145(1):494-502. doi: 10.1128/jb.145.1.494-502.1981.
Streptococcus faecalis strain DS16 harbors the conjugative hemolysin-bacteriocin plasmid pAD1 (35 megadaltons) and the nonconjugative R-plasmid pAD2 determining resistance to streptomycin, kanamycin, and erythromycin; a tetracycline resistance (Tetr) determinant is located on the chromosome. When strain DS16 was mated (on membrane filters) with the plasmid-free strain JH2-2, Tetr transconjugants could be obtained at a frequency of about 10(-6) per recipient. Analyses of transconjugants showed that some contained the Tetr determinant linked to pAD1. Subsequent studies showed that the Tetr determinant was located on a 10-megaldalton transposon, designated Tn916, which could insert into two hemolysin plasmids: pAM gamma 1 and pOB1. In addition, derivatives of DS16 devoid of pAD1 were capable of transferring Tetr to recipient strains. Transconjugants (plasmid-free) from such matings could subsequently act as donors in the transfer of Tetr. Both transposition and transfer were found to be rec independent.
粪肠球菌DS16菌株携带接合性溶血素-细菌素质粒pAD1(35兆道尔顿)和决定对链霉素、卡那霉素及红霉素耐药性的非接合性R质粒pAD2;四环素抗性(Tetr)决定簇位于染色体上。当DS16菌株(在滤膜上)与无质粒菌株JH2-2进行接合时,每受体可获得频率约为10(-6)的Tetr转接合子。对转接合子的分析表明,有些含有与pAD1相连的Tetr决定簇。随后的研究表明,Tetr决定簇位于一个10兆道尔顿的转座子上,命名为Tn916,它可插入两种溶血素质粒:pAMγ1和pOB1。此外,不含pAD1的DS衍生产物能够将Tetr转移至受体菌株。此类接合产生的转接合子(无质粒)随后可作为Tetr转移的供体。转座和转移均发现与rec无关。