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苜蓿中华根瘤菌中参与细胞色素c生物合成的cycHJKL基因对于离体“呼吸性”硝酸盐还原以及共生期间的固氮作用是必需的。

The cycHJKL genes of Rhizobium meliloti involved in cytochrome c biogenesis are required for "respiratory" nitrate reduction ex planta and for nitrogen fixation during symbiosis.

作者信息

Kereszt A, Slaska-Kiss K, Putnoky P, Banfalvi Z, Kondorosi A

机构信息

Institute of Genetics, Hungarian Academy of Sciences, Szeged.

出版信息

Mol Gen Genet. 1995 Apr 10;247(1):39-47. doi: 10.1007/BF00425819.

Abstract

We report the genetic and biochemical analysis of Rhizobium meliloti mutants defective in symbiotic nitrogen fixation (Fix-) and "respiratory" nitrate reduction (Rnr-). The mutations were mapped close to the ade-1 and cys-46 chromosomal markers and the mutated locus proved to be identical to the previously described fix-14 locus. By directed Tn5 mutagenesis, a 4.5 kb segment of the chromosome was delimited in which all mutations resulted in Rnr- and Fix- phenotypes. Nucleotide sequence analysis of this region revealed the presence of four open reading frames coding for integral membrane and membrane-anchored proteins. Biochemical analysis of the mutants showed that the four proteins were necessary for the biogenesis of all cellular c-type cytochromes. In agreement with the nomenclature proposed for rhizobial genes involved in the formation of c-type cytochromes, the four genes were designated cycH, cycJ, cycK, and cycL, respectively. The predicted protein product of cycH exhibited a high degree of similarity to the Bradyrhizobium japonicum counterpart, while CycK and CycL shared more than 50% amino acid sequence identity with the Rhodobacter capsulatus Cc11 and Cc12 proteins, respectively. cycJ encodes a novel membrane anchored protein of 150 amino acids. We suggest that this gene cluster codes for (parts of) a multisubunit cytochrome c haem lyase. Moreover, our results indicate that in R. meliloti c-type cytochromes are required for respiratory nitrate reduction ex planta, as well as for symbiotic nitrogen fixation in root nodules.

摘要

我们报告了苜蓿根瘤菌在共生固氮(Fix-)和“呼吸性”硝酸盐还原(Rnr-)方面存在缺陷的突变体的遗传和生化分析。这些突变被定位在靠近ade-1和cys-46染色体标记的位置,并且突变位点被证明与先前描述的fix-14位点相同。通过定向Tn5诱变,确定了染色体上一个4.5 kb的片段,其中所有突变都导致了Rnr-和Fix-表型。对该区域的核苷酸序列分析揭示了存在四个编码整合膜蛋白和膜锚定蛋白的开放阅读框。对突变体的生化分析表明,这四种蛋白质是所有细胞c型细胞色素生物合成所必需的。与为参与c型细胞色素形成的根瘤菌基因所提议的命名法一致,这四个基因分别被命名为cycH、cycJ、cycK和cycL。cycH预测的蛋白质产物与日本慢生根瘤菌的对应物具有高度相似性,而CycK和CycL分别与荚膜红细菌的Cc11和Cc12蛋白共享超过50%的氨基酸序列同一性。cycJ编码一种由150个氨基酸组成的新型膜锚定蛋白。我们认为这个基因簇编码多亚基细胞色素c血红素裂解酶的(部分)成分。此外,我们的结果表明,在苜蓿根瘤菌中,c型细胞色素是离体呼吸性硝酸盐还原以及根瘤中共生固氮所必需的。

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