Verger J M, Grayon M, Chaslus-Dancla E, Meurisse M, Lafont J P
Laboratoire de Pathologie Infectieuse et d'Immunologie, Centre de Recherche de Tours, Institut National de la Recherche Agronomique, Nouzilly, France.
Plasmid. 1993 Mar;29(2):142-6. doi: 10.1006/plas.1993.1016.
Escherichia coli strain K12 BM14, carrying plasmid R751 (51.4 kb; Tpr, Tra+, IncP), was used as donor in matings with reference strains of the six Brucella nomenspecies, not known so far to harbor naturally occurring plasmids. R751 was easily transferred to and between Brucella spp., at frequencies ranging between 10(-1) and 10(-4). All Brucella transconjugants stably maintained plasmid R751 both in vitro and in vivo in our experimental conditions. No genetic modification of the plasmid during and after the conjugal transfer process could be deduced from the comparative restriction analysis (BamHI, HindIII, and EcoRI) in each Brucella transconjugant and in the E. coli donor.
携带质粒R751(51.4 kb;Tpr,Tra+,IncP)的大肠杆菌K12 BM14菌株,被用作与布鲁氏菌属六个种的参考菌株进行接合试验的供体,目前尚不清楚这些菌株是否天然携带质粒。R751很容易转移到布鲁氏菌属细菌中,也能在它们之间转移,转移频率在10^(-1)到10^(-4)之间。在我们的实验条件下,所有布鲁氏菌属的接合子在体外和体内都能稳定维持质粒R751。通过对每个布鲁氏菌属接合子和大肠杆菌供体进行比较限制性分析(BamHI、HindIII和EcoRI),未推断出在接合转移过程中及之后质粒发生基因修饰。