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Nickel and cobalt resistance properties of Sinorhizobium meliloti isolated from Medicago lupulina growing in gold mine tailing

机译:从金尾矿中生长的紫花苜蓿分离的中华根瘤菌的耐镍和钴性能

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摘要

Sinorhizobium meliloti CCNWSX0020, isolated from root nodules of Medicago lupulina growing in gold mine tailings in the northwest of China, displayed multiple heavy metal resistance and growth promotion of M. lupulina. In our previous work, the expression level of dmeR and dmeF genes were induced by Cu2+ through comparative transcriptome approach. Based on protein analysis, the dmeF encoded for a protein which showed a 37% similarity to the cation transporter DmeF of Cupriavidus metallidurans, whereas dmeR encoded transcriptional regulator which was highly homologous with DmeR belonging to RcnR/CsoR family metal-responsive transcriptional regulator. In addition to copper, quantitative real-time PCR analysis showed that dmeR and dmeF were also induced by nickel and cobalt. To investigate the functions of dmeR and dmeF in S. meliloti CCNWSX0020, the dmeR and dmeF deletion mutants were constructed. The dmeF mutant was more sensitive to Co2 + and Ni2 + than the wild type strain. Pot experiments were carried out to determine whether the growth of M. lupulina was affected when the dmeF gene was knocked out in the presence of nickel or cobalt. Results indicated that the nodule number of the host plant inoculated with the dmeF deletion mutant was significantly less than the S. meliloti CCNWSX0020 wild-type in the presence of Co2 + or Ni2 +. However, when standardized by nodule fresh weight, the nitrogenase activities of nodules infected by the dmeF deletion mutant was similar to nitrogenase activity of the wild type nodule.
机译:从生长在中国西北部金矿尾矿中的紫花苜蓿的根瘤中分离出的中华根瘤菌CCNWSX0020表现出多重重金属抗性并促进了紫花苜蓿的生长。在我们以前的工作中,通过比较转录组方法,Cu 2 + 诱导了dmeR和dmeF基因的表达水平。基于蛋白质分析,dmeF编码的蛋白质与铜尿酸铜阳离子阳离子转运蛋白DmeF具有37%的相似性,而dmeR编码的转录调节子与RcnR / CsoR家族金属反应性转录调节子的DmeR高度同源。除铜外,实时荧光定量PCR分析表明dmeR和dmeF也被镍和钴诱导。为了研究dmeR和dmeF在苜蓿链球菌CCNWSX0020中的功能,构建了dmeR和dmeF缺失突变体。 dmeF突变体比野生型菌株对Co 2 + 和Ni 2 + 更敏感。进行盆栽实验以确定 M的生长。当在镍或钴存在下敲除 dmeF 基因时,会影响lupulina 。结果表明,接种了 dme F缺失突变体的寄主植物的根瘤数明显少于 S。在Co 2 + 或Ni 2 + 存在的情况下,meliloti CCNWSX0020野生型。然而,当按结节鲜重标准化时,被 dme F缺失突变体感染的结节的固氮酶活性类似于野生型结节的固氮酶活性。

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