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The Bradyrhizobium japonicum napEDABC genes encoding the periplasmic nitrate reductase are essential for nitrate respiration

机译:编码周质硝酸还原酶的Bradyrhizobium japeDum napedabc基因对于硝酸盐呼吸至关重要

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The napEDABC gene cluster that encodes the periplasmic nitrate reductase from Bradyrhizobium japonicum USDA110 has been isolated and characterized. napA encodes the catalytic subunit, and the napB and napC gene products are predicted to be a soluble dihaem c and a membrane-anchored tetrahaem c-type cytochrome, respectively. napE encodes a transmembrane protein of unknown function, and the napD gene product is a soluble protein which is assumed to play a role in the maturation of NapA. Western blots of the periplasmic fraction from wild-type cells grown anaerobically with nitrate revealed the presence of a protein band with a molecular size of about 90?kDa corresponding to NapA. A B. japonicum mutant carrying an insertion in the napA gene was unable to grow under nitrate-respiring conditions, lacked nitrate reductase activity, and did not show the 90?kDa protein band. Complementation of the mutant with a plasmid bearing the napEDABC genes restored both nitrate-dependent anaerobic growth of the cells and nitrate reductase activity. A membrane-bound and a periplasmic c-type cytochrome, with molecular masses of 25?kDa and 15?kDa, respectively, were not detected in the napA mutant strain incubated anaerobically with nitrate, which identifies those proteins as the NapC and the NapB components of the B. japonicum periplasmic nitrate reductase enzyme. These results suggest that the periplasmic nitrate reductase is the enzyme responsible for anaerobic growth of B. japonicum under nitrate-respiring conditions. The promoter region of the napEDABC genes has been characterized by primer extension. A major transcript initiates 66·5?bp downstream of the centre of a putative FNR-like binding site.
机译:分离和表征编码来自Bradyrhizobium USDA110的周质硝酸还原酶的Napedabc基因簇。 NAPA编码催化亚基,并且预测NaPB和NAPC基因产物分别是可溶性DiHaem C和膜锚固的四血型细胞色素。 Nape编码未知功能的跨膜蛋白,并且NaPD基因产物是可溶性蛋白质,其假设在纳帕的成熟中发挥作用。用硝酸盐生长的野生型细胞的蛋白质斑点揭示了蛋白质带的存在,其分子大小为约90ΩkDa。对应于纳帕。携带插入在纳帕基因中的粳稻突变体不能在硝酸盐呼吸条件下生长,缺乏硝酸还原酶活性,并且没有显示90?KDA蛋白质带。突变体与轴承质粒的互补恢复细胞的硝酸盐依赖性厌氧生长和硝酸还原酶活性。在用硝酸盐孵育的纳帕突变体菌株中,分别未检测到分子量为25μl和15Ω·kDa的膜结合和周质C型细胞色素,其鉴定了那些蛋白质作为NaPC和NaPB组分B.粳稻周质硝酸还原酶酶。这些结果表明,周质硝酸还原酶是硝态呼吸条件下B.粳稻厌氧生长的酶。 NaPEDABC基因的启动子区域的特征在于引物延伸。在推定的FNR样结合位点的中心下游发起66·5?BP的主要转录物。

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