Pretorius-Güth Inge-M, Pühler Alfred, Simon Reinhard
Lehrstuhl für Genetik, Fakultät für Biologie, Universität Bielefeld, Postfach 8640, D-4800 Bielefeld 1, Federal Republic of Germany.
Appl Environ Microbiol. 1990 Aug;56(8):2354-2359. doi: 10.1128/aem.56.8.2354-2359.1990.
A DNA fragment containing the RP4 mob function, as well as the gentamicin and spectinomycin resistance genes, was inserted by gene replacement onto the megaplasmid 2 (pM2) of Rhizobium meliloti 0540 (Inf EPS), resulting in PG101 (Inf EPS). The self-transfer of pM2 and the mobilization of pM2 by plasmid RP4-4 were investigated during conjugation between PG101 and R. meliloti 2526 (Nod). In filter conjugations, pM2 was readily mobilized by RP4-4. In addition to this, the self-transfer of one megaplasmid (pM) was detected at a frequency of 3 x 10. Bacteria isolated from the nodules of alfalfa and coinoculated with strains PG101 and 2526 showed that pM2 was mobilized at a frequency of approximately 7 x 10. Bacterial cell numbers were too low in the nodules for detection of the self-transfer of pM2 to occur. No pM2 transfer was detected in the inoculum. A comparison of the transfer frequencies for the various conjugation conditions revealed that pM2 transfer occurred as frequently in the nodules as in filter conjugations. These results indicate that the nodule creates conditions for gene transfer that are comparable to optimal laboratory conditions.
一个包含RP4迁移功能以及庆大霉素和壮观霉素抗性基因的DNA片段,通过基因置换插入到苜蓿中华根瘤菌0540(Inf EPS)的大质粒2(pM2)上,得到PG101(Inf EPS)。在PG101与苜蓿中华根瘤菌2526(Nod)的接合过程中,研究了pM2的自我转移以及质粒RP4 - 4对pM2的动员作用。在滤膜接合中,pM2很容易被RP4 - 4动员。除此之外,还检测到一个大质粒(pM)的自我转移频率为3×10 。从苜蓿根瘤中分离并与PG101和2526菌株共同接种的细菌表明,pM2的动员频率约为7×10 。根瘤中的细菌细胞数量过低,无法检测到pM2的自我转移。在接种物中未检测到pM2转移。对各种接合条件下转移频率的比较表明,pM2在根瘤中的转移频率与滤膜接合中的频率相同。这些结果表明,根瘤为基因转移创造了与最佳实验室条件相当的条件。