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大肠杆菌的硝酸还原酶:第二种硝酸还原酶的序列及其与narGHJI操纵子所编码的硝酸还原酶的比较。

Nitrate reductases of Escherichia coli: sequence of the second nitrate reductase and comparison with that encoded by the narGHJI operon.

作者信息

Blasco F, Iobbi C, Ratouchniak J, Bonnefoy V, Chippaux M

机构信息

Laboratoire de Chimie Bactérienne, CNRS, Marseille, France.

出版信息

Mol Gen Genet. 1990 Jun;222(1):104-11. doi: 10.1007/BF00283030.

Abstract

The structural genes for NRZ, the second nitrate reductase of Escherichia coli, have been sequenced. They are organized in a transcription unit, narZYWV, encoding four subunits, NarZ, NarY, NarW and NarV. The transcription unit is homologous (73% identity) to the narGHJI operon which encodes the genes for NRA, the better characterized nitrate reductase of this organism. The level of homology between the corresponding polypeptides ranges from 69% for the NarW/NarJ pair to 86% for the NarV/NarI pair. The NarZ polypeptide contains the five conserved regions present in all other known molybdoproteins of E. coli and their relative order is the same. The NarY polypeptide, which contains the same four cysteine clusters in the same order as NarH, is probably an electron transfer unit of the complex. Upstream of narZ, an open reading frame, ORFA, is present which could encode a product which has homology (73% identity) with the COOH-terminal end of NarK. The ORFA-narZ intergenic region, however, is about 80 nucleotides long and does not contain the cis-acting elements, NarL and Fnr boxes, nor the terC4 terminator sequence present in the 500 nucleotide narK-narG intergenic region. This might explain why the narZYWV and the narGHJI operons are regulated differently. Our results tend to support the hypothesis that a DNA fragment larger than that encompassing the narGHJI genes has been duplicated.

摘要

已对大肠杆菌第二种硝酸还原酶NRZ的结构基因进行了测序。它们被组织在一个转录单元narZYWV中,该单元编码四个亚基,即NarZ、NarY、NarW和NarV。该转录单元与narGHJI操纵子同源(同一性为73%),narGHJI操纵子编码该生物体中特征更明确的硝酸还原酶NRA的基因。相应多肽之间的同源性水平范围从NarW/NarJ对的69%到NarV/NarI对的86%。NarZ多肽包含大肠杆菌所有其他已知钼蛋白中存在的五个保守区域,并且它们的相对顺序相同。NarY多肽与NarH一样按相同顺序包含相同的四个半胱氨酸簇,可能是该复合物的电子传递单元。在narZ上游存在一个开放阅读框ORFA,它可能编码一种与NarK的COOH末端具有同源性(同一性为73%)的产物。然而,ORFA-narZ基因间区域约80个核苷酸长,不包含顺式作用元件NarL和Fnr框,也不包含500个核苷酸的narK-narG基因间区域中存在的terC4终止序列。这可能解释了为什么narZYWV和narGHJI操纵子受到不同的调控。我们的结果倾向于支持这样一种假设,即一个大于包含narGHJI基因的DNA片段发生了重复。

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