反硝化副球菌IFO 12442一氧化氮还原酶位点的克隆及核苷酸序列分析

Kiyohito Murai, Katsuhide Miyake, Jun Andoh, Shinji Iijima
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引用次数: 2

摘要

从反硝化副球菌IFO 12442中克隆出含有亚硝酸盐还原酶上游基因(nirS)的5.2 kb DNA片段,并测定其序列。在该片段中,观察到四个开放阅读框(orf)。其中位于nirS基因上游3kb处的两个orf通过同源性分析编码一氧化氮还原酶(norC, norB)。norC和norB编码该酶的细胞色素c和b亚基,蛋白质产物的预测分子量分别为17 kDa(150个氨基酸残基)和52.5 kDa(462个氨基酸残基)。另外两个开放阅读框分别为ORF1 (73 kDa, 681个氨基酸残基)和ORF2 (32.5 kDa, 304个氨基酸残基),分别位于nir和nor基因之间。ORF1的氨基酸序列与已知的stutzeri假单胞菌N2O还原酶基因簇的转录调控蛋白NosR的氨基酸序列具有很高的相似性(35%的同源性)。由于ORF1蛋白具有一个保守的半胱氨酸簇和5个类似于NosR蛋白的疏水跨膜重复序列,ORF1可能作为反硝化的膜结合传感器。Northern blot分析表明ORF1-2和norCB可能是作为独立的操作子转录的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning and nucleotide sequence of the nitric oxide reductase locus in Paracoccus denitrificans IFO 12442

A 5.2-kb DNA fragment containing the upstream region of the nitrite reductase gene (nirS) was cloned from Paracoccus denitrificans IFO 12442 and its DNA sequence was determined. In this fragment, four open reading frames (ORFs) were observed. Among these, two ORFs, located 3 kb upstream of the nirS gene were found to encode nitric oxide reductase (norC, norB) by homology analysis. The norC and norB encoded cytochrome c and b subunits of the enzyme, and the predicted molecular weights of the protein products were 17 kDa (150 amino acid residues) and 52.5 kDa (462 amino acid residues), respectively. The other two open reading frames, designated ORF1 (73 kDa, 681 amino acid residues) and ORF2 (32.5 kDa, 304 amino acid residues), were found between the nir and nor genes. The deduced amino acid sequence of ORF1 showed high similarity (35% identity) to that of NosR which is known to be a transcriptional regulatory protein for the N2O reductase gene cluster of Pseudomonas stutzeri. Since the ORF1 protein has a well conserved cysteine cluster and 5 hydrophobic transmembrane repeats similar to those of the NosR protein, ORF1 probably functions as a membrane bound sensor for denitrification. Northern blot analysis indicated that the ORF1–2 and norCB regions are probably transcribed as independent operons.

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