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大肠杆菌K-12中nar(硝酸还原酶)基因座的narL和narX基因的鉴定与表达

Identification and expression of genes narL and narX of the nar (nitrate reductase) locus in Escherichia coli K-12.

作者信息

Stewart V, Parales J

机构信息

Department of Microbiology, Cornell University, Ithaca, New York 14853.

出版信息

J Bacteriol. 1988 Apr;170(4):1589-97. doi: 10.1128/jb.170.4.1589-1597.1988.

Abstract

Previous studies have shown that narL+ is required for nitrate induction of nitrate reductase synthesis and for nitrate inhibition of fumarate reductase synthesis in Escherichia coli. We cloned narL on a 5.1-kilobase HindIII fragment. Our clone also contained a previously unidentified gene, which we propose to designate as narX, as well as a portion of narK. Maxicell experiments indicated that narL and narX encode proteins with approximate MrS of 28,000 and 66,000, respectively. narX insertion mutations reduced nitrate reductase structural gene expression by less than twofold. Expression of phi (narL-lacZ) operon fusions was weakly induced by nitrate but was indifferent to aerobiosis and independent of fnr. Expression of phi (narX-lacZ) operon fusions was induced by nitrate and was decreased by narL and fnr mutations. A phi (narK-lacZ) operon fusion was induced by nitrate, and its expression was fully dependent on narL+ and fnr+. Analysis of these operon fusions indicated that narL and narX are transcribed counterclockwise with respect to the E. coli genetic map and that narK is transcribed clockwise.

摘要

先前的研究表明,在大肠杆菌中,narL+是硝酸盐诱导硝酸还原酶合成以及硝酸盐抑制延胡索酸还原酶合成所必需的。我们将narL克隆到一个5.1千碱基的HindIII片段上。我们的克隆还包含一个先前未鉴定的基因,我们提议将其命名为narX,以及一部分narK。大细胞实验表明,narL和narX分别编码分子量约为28,000和66,000的蛋白质。narX插入突变使硝酸还原酶结构基因的表达降低不到两倍。phi(narL-lacZ)操纵子融合体的表达受硝酸盐微弱诱导,但对需氧状态不敏感且不依赖于fnr。phi(narX-lacZ)操纵子融合体的表达受硝酸盐诱导,并因narL和fnr突变而降低。phi(narK-lacZ)操纵子融合体受硝酸盐诱导,其表达完全依赖于narL+和fnr+。对这些操纵子融合体的分析表明,narL和narX相对于大肠杆菌遗传图谱是逆时针转录的,而narK是顺时针转录的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a73/211006/ff5f7be84a3d/jbacter00182-0189-a.jpg

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