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Tellurite reductase activity of nitrate reductase is responsible for the basal resistance of Escherichia coli to tellurite

机译:硝酸盐还原酶的碲酸盐还原酶活性负责大肠杆菌对碲酸盐的基础抗性

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Tellurite and selenate reductase activities were identified in extracts of Escherichia coli. These activities were detected on non-denaturing polyacrylamide gels using an in situ methyl viologen activity-staining technique. The activity bands produced from membrane-protein extracts had the same RF values as those of nitrate reductases (NRs) A and Z. Tellurite and selenate reductase activities were absent from membranes obtained from mutants deleted in NRs A and Z. Further evidence of the tellurite and selenate reductase activities of NR was demonstrated using rocket immunoelectrophoresis analysis, where the tellurite and selenate reductase activities corresponded to the precipitation arc of NR. Additionally, hypersensitivity to potassium tellurite was observed under aerobic growth conditions in nar mutants. The tac promoter expression of NR A resulted in elevated tellurite resistance. The data obtained also imply that a minimal threshold level of NR A is required to increase resistance. Under anaerobic growth conditions additional tellurite reductase activity was identified in the soluble fraction on non-denaturing gels. Nitrate reductase mutants were not hypersensitive under anaerobic conditions, possibly due to the presence of this additional reductase activity.
机译:在大肠杆菌提取物中鉴定了碲和硒还原酶活性。使用原位甲基Viologen活性染色技术在非变性聚丙烯酰胺凝胶上检测这些活性。由膜 - 蛋白质提取物产生的活动带具有与硝酸还原酶(NRS)A和Z.碲酸盐和硒化物还原酶活性的射频和硒酸盐酶活性与在NRS A和Z中删除的突变体中获得的膜中不存在。进一步证据使用火箭免疫电泳分析证明了NR的硒还原酶活性,其中碲酸盐和硒化物还原酶活性对应于NR的沉淀弧。另外,在NAR突变体中的有氧生长条件下观察到对碲酸钾的过敏率。 NR A的TAC启动子表达导致碲沸石耐受升高。所获得的数据也意味着需要增加NR A的最小阈值水平来增加电阻。在厌氧生长条件下,在非变性凝胶上的可溶性级分中鉴定出额外的碲化酯还原酶活性。硝酸还原酶突变体在厌氧条件下不过敏,可能是由于这种另外的还原酶活性的存在。

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