Clermont D, Horaud T
Laboratoire des Staphylocoques et des Streptocoques, Institut Pasteur, Paris, France.
Plasmid. 1994 Jan;31(1):40-8. doi: 10.1006/plas.1994.1005.
The plasmid-free Streptococcus anginosus F22 contained a conjugative element, Tn3705, encoding resistance to erythromycin (Emr) and tetracycline-minocycline (Tcr-Mnr). We mapped a chromosomal region (> 52 kb) of F22, corresponding to the internal part of Tn3705. Molecular analysis of Tn3705 revealed it to be a composite structure: it included in its central part a transposon designated Tn3704 (20.3 kb +/- 0.5 kb), which had a modified structure in comparison with that of Tn916 and on which the Emr Tcr-Mn4 markers were localized. Tn3705 inserted from F22 into the chromosome of various streptococcal transconjugants as well as that of Enterococcus faecalis transconjugants without changing its structure. In contrast, from the chromosome of an E. faecalis::Tn3705 transconjugant only Tn3704 inserted, at various sites, into another E. faecalis chromosome. Sugar fermentations occurred after the insertion of Tn3704 into the chromosome of an asaccharolytic E. faecalis strain. Transposition of only Tn3704 from the chromosome of E. faecalis::Tn3705 onto pIP964, an E. faecalis hemolysin plasmid, yielded two different pIP964 derivatives. The size of the entire element Tn3705 was estimated to be about 70.0 kb by pulsed-field electrophoresis.
无质粒的咽峡炎链球菌F22含有一个接合元件Tn3705,其编码对红霉素(Emr)和四环素-米诺环素(Tcr-Mnr)的抗性。我们绘制了F22的一个染色体区域(>52 kb),该区域对应于Tn3705的内部部分。对Tn3705的分子分析表明它是一个复合结构:其中心部分包含一个名为Tn3704(20.3 kb±0.5 kb)的转座子,与Tn916相比,其结构有所改变,Emr、Tcr-Mn4标记位于该转座子上。Tn3705从F22插入到各种链球菌转接合子以及粪肠球菌转接合子的染色体中,且其结构未发生变化。相比之下,仅Tn3704从粪肠球菌::Tn3705转接合子的染色体插入到另一个粪肠球菌染色体的不同位点。在将Tn3704插入到一个不分解糖的粪肠球菌菌株的染色体后,出现了糖发酵现象。仅将Tn3704从粪肠球菌::Tn3705的染色体转座到粪肠球菌溶血素质粒pIP964上,产生了两种不同的pIP964衍生物。通过脉冲场电泳估计整个元件Tn3705的大小约为70.0 kb。