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首页> 外文期刊>Applied and Environmental Microbiology >Ammonia Inhibition of Plasmid pRmeGR4a Conjugal Transfer between Rhizobium meliloti Strains.
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Ammonia Inhibition of Plasmid pRmeGR4a Conjugal Transfer between Rhizobium meliloti Strains.

机译:苜蓿根瘤菌菌株之间质粒pRmeGR4a结合转移的氨抑制作用。

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We have examined nutritional factors influencing conjugal transfer of the two nonsymbiotic large plasmids, pRmeGR4a and pRmeGR4b, of Rhizobium meliloti GR4. To monitor transfer, each plasmid was tagged with a different antibiotic resistance marker. Transfer of plasmid pRmeGR4b was dependent upon the presence of plasmid pRmeGR4a on the same donor cell. Transconjugants for pRmeGR4b were obtained at frequencies 5-to 10-fold higher than transconjugants carrying both plasmids, indicating that mobilization of pRmeGR4b by pRmeGR4a probably occurred in trans. Conjugal transfer of the tagged plasmids between R. meliloti strains was tested on minimal medium supplemented with single amino acids, nitrate, or ammonium as the single nitrogen source. A higher number of transconjugants was obtained when glutamate was the only nitrogen source, whereas conjugation was virtually undetectable on ammonium. No relationship was found between donor or recipient growth rate and plasmid transfer rate on a given nitrogen source. Furthermore, in media containing both glutamate and ammonium as nitrogen sources, transfer was reduced almost 100-fold compared with that in media containing glutamate alone. Inhibition was readily detected at 2.5 mM or higher concentrations of either ammonium chloride or ammonium sulfate and appeared to be specific for exogenously supplied ammonium. Inhibition of conjugal transfer between R. meliloti strains by ammonium was only observed for rhizobial plasmids, not for a heterologous plasmid such as RP4. Apparently, ammonium did not affect the plasmid-encoded transfer machinery, as it had no influence on rhizobial plasmid transfer from R. meliloti to Agrobacterium tumefaciens. The effect of ammonium seemed to take place on R. meliloti recipient cells, thereby reducing the efficiency of plasmid conjugation, probably by affecting mating pair formation or stabilization.
机译:我们已经检查了营养因素,影响了两个根瘤菌GR4的两个非共生大质粒pRmeGR4a和pRmeGR4b的结合转移。为了监测转移,每个质粒用不同的抗生素抗性标记物标记。质粒pRmeGR4b的转移取决于在同一供体细胞上质粒pRmeGR4a的存在。获得pRmeGR4b的转导结合体的频率比携带两个质粒的转导结合体高5至10倍,这表明pRmeGR4a可能通过反式转运pRmeGR4b。在添加单一氨基酸,硝酸盐或铵作为单一氮源的基本培养基上测试了苜蓿根瘤菌菌株之间标记质粒的结合转移。当谷氨酸是唯一的氮源时,获得了更多的共轭结合剂,而在铵上却几乎检测不到结合。在给定氮源上,供体或受体的生长速率与质粒转移速率之间没有关系。此外,与仅含有谷氨酸的培养基相比,在含有谷氨酸和铵作为氮源的培养基中,转移几乎减少了100倍。在2.5 mM或更高浓度的氯化铵或硫酸铵中容易检测到抑制作用,并且似乎对外源供应的铵具有特异性。仅在根瘤菌质粒上观察到铵抑制了苜蓿根瘤菌菌株之间的结合转移,而对于异源质粒如RP4则没有观察到。显然,铵不会影响质粒编码的转移机制,因为它对根瘤菌从苜蓿根瘤菌到根癌农杆菌的转移没有影响。铵的作用似乎发生在苜蓿根瘤菌受体细胞上,从而降低了质粒结合的效率,这可能是通过影响交配对的形成或稳定来实现的。

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