Hamada S E, Luckey J P, Farrand S K
J Bacteriol. 1979 Jul;139(1):280-6. doi: 10.1128/jb.139.1.280-286.1979.
Although several techniques are available for transferring the Ti plasmids from one strain of agrobacterium tumefaciens to another, there are no reproducible methods for analysis of chromosomal markers in this phytopathogen. The R plasmid, R68.45, is known to show chromosomal mobilizing ability in several bacterial genera including the closely related Rhizobia. R68.45 was transferred into the prototrophic A. tumefaciens strain 15955. Ten kanamycin-resistant transconjugant clones were tested for chromosomal mobilizing ability by mating with strain SA10, rifampin- and streptomycin-resistant histidine auxotroph of strain 15955. Of the 10 donor clones, 2 showed high chromosomal mobilizing ability. Between 1,000 and 2,000 His+ colony-forming units per ml were obtained, a value 10 to 20 times greater than can be accounted for by spontaneous reversion. Sequential recloning and matings resulted in the isolation of relatively stable donor cultures. Chromosome gene transfer is dependent upon the presence in the donor of R68.45. Donors lacking an R plasmid or harboring the closely related plasmid RP4 failed to yield His+ transconjugants. With strain SA11, a methionine auxotroph of strain SA10, coinheritance of histidine and methionine independence could be demonstrated. Approximately half of the transconjugants also inherited R68.45. These results indicate that A. tumefaciens 15955 is capable of undergoing host chromosomal genetic exchange.
虽然有几种技术可用于将Ti质粒从一种根癌土壤杆菌菌株转移到另一种,但在这种植物病原体中,尚无用于分析染色体标记的可重复方法。已知R质粒R68.45在包括密切相关的根瘤菌在内的几个细菌属中表现出染色体动员能力。将R68.45转移到原养型根癌土壤杆菌菌株15955中。通过与菌株SA10(15955菌株的耐利福平、耐链霉素的组氨酸营养缺陷型)交配,对10个卡那霉素抗性转接合子克隆进行染色体动员能力测试。在10个供体克隆中,有2个表现出高染色体动员能力。每毫升获得1000至2000个His⁺菌落形成单位,该值比自发回复突变所能解释的值大10至20倍。连续的再克隆和交配导致分离出相对稳定的供体培养物。染色体基因转移取决于供体中R68.45的存在。缺乏R质粒或携带密切相关质粒RP4的供体未能产生His⁺转接合子。对于菌株SA11(SA10的甲硫氨酸营养缺陷型),可以证明组氨酸和甲硫氨酸独立性的共同遗传。大约一半的转接合子也继承了R68.45。这些结果表明,根癌土壤杆菌15955能够进行宿主染色体基因交换。