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大肠杆菌中用于硝酸盐依赖性基因调控的第二种硝酸盐传感器narQ的鉴定与表征。

Identification and characterization of narQ, a second nitrate sensor for nitrate-dependent gene regulation in Escherichia coli.

作者信息

Chiang R C, Cavicchioli R, Gunsalus R P

机构信息

Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90024.

出版信息

Mol Microbiol. 1992 Jul;6(14):1913-23. doi: 10.1111/j.1365-2958.1992.tb01364.x.

Abstract

In response to nitrate availability, Escherichia coli regulates the synthesis of a number of enzymes involved in anaerobic respiration and fermentation. When nitrate is present, nitrate reductase (narGHJI) gene expression is induced, while expression of the DMSO/TMAO reductase (dmsABC), fumarate reductase (frdABCD) and fermentation related genes are repressed. The narL and narX gene products are required for this nitrate-dependent control, and apparently function as members of a two-component regulatory system. NarX is a presumed sensor-transmitter for nitrate and possibly molybdenum detection. The presumed response-regulator, NarL, when activated by NarX then binds at the regulatory DNA sites of genes to modulate their expression. In this study a third nitrate regulatory gene, narQ, was identified that also participates in nitrate-dependent gene regulation. Strains defective in either narQ or narX alone exhibited no nitrate-dependent phenotype whereas mutants defective in both narQ and narX were fully inactive for nitrate-dependent repression or activation. In all conditions tested, this regulation required a functional narL gene product. These findings suggest that the narX and narQ products have complementary sensor-transmitter functions for nitrate detection, and can work independently to activate NarL, for eliciting nitrate-dependent regulation of anaerobic electron transport and fermentation functions. The narQ gene was cloned, sequenced, and compared with the narX gene. Both gene products are similar in size, hydrophobicity, and sequence, and contain a highly conserved histidine residue common to sensor-transmitter proteins.

摘要

为响应硝酸盐的可利用性,大肠杆菌会调节许多参与厌氧呼吸和发酵的酶的合成。当存在硝酸盐时,硝酸盐还原酶(narGHJI)基因的表达被诱导,而二甲基亚砜/三甲胺氧化物还原酶(dmsABC)、延胡索酸还原酶(frdABCD)以及与发酵相关基因的表达则受到抑制。这种硝酸盐依赖性调控需要narL和narX基因产物,它们显然作为双组分调控系统的成员发挥作用。NarX被认为是用于检测硝酸盐以及可能还有钼的传感器传递蛋白。假定的应答调节因子NarL在被NarX激活后,会结合到基因的调控DNA位点上以调节其表达。在本研究中,鉴定出了第三个硝酸盐调控基因narQ,它也参与硝酸盐依赖性基因调控。单独缺失narQ或narX的菌株没有表现出硝酸盐依赖性表型,而同时缺失narQ和narX的突变体对于硝酸盐依赖性抑制或激活则完全没有活性。在所有测试条件下,这种调控都需要功能性的narL基因产物。这些发现表明,narX和narQ产物在检测硝酸盐方面具有互补的传感器传递功能,并且可以独立发挥作用来激活NarL,以引发对厌氧电子传递和发酵功能的硝酸盐依赖性调控。narQ基因被克隆、测序,并与narX基因进行了比较。这两种基因产物在大小、疏水性和序列方面相似,并且都含有传感器传递蛋白共有的高度保守的组氨酸残基。

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