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“一氧化氮释放剂”S-亚硝基谷胱甘肽上调大肠杆菌K-12 hmp(黄素血红蛋白)基因的新机制:同型半胱氨酸的亚硝化作用以及MetR与glyA-hmp基因间区域结合的调节

A novel mechanism for upregulation of the Escherichia coli K-12 hmp (flavohaemoglobin) gene by the 'NO releaser', S-nitrosoglutathione: nitrosation of homocysteine and modulation of MetR binding to the glyA-hmp intergenic region.

作者信息

Membrillo-Hernández J, Coopamah M D, Channa A, Hughes M N, Poole R K

机构信息

The Krebs Institute for Biomolecular Research, Department of Molecular Biology & Biotechnology, The University of Sheffield, UK.

出版信息

Mol Microbiol. 1998 Aug;29(4):1101-12. doi: 10.1046/j.1365-2958.1998.01000.x.

Abstract

The flavohaemoglobin gene, hmp, of Escherichia coli is upregulated by nitric oxide (NO) in a SoxRS-independent manner. We now show that hmp expression is also upregulated by S-nitrosoglutathione (GSNO, widely used as an NO releaser) and sodium nitroprusside (SNP, which is a NO+ donor). Elevated homocysteine (Hcy) levels, achieved either by adding Hcy extracellularly or using metE mutants, decreased hmp expression. Conversely, metC mutants (defective in Hcy synthesis) had higher levels of hmp expression. Mutations in metR abolished hmp induction by GSNO and SNP, and hmp expression became insensitive to Hcy. We propose that the previously documented modulation by Hcy of MetR binding to the glyA-hmp intergenic regulatory region regulates hmp transcription. Although two MetR binding sites are present in this region, only the higher affinity site proximal to hmp is required for hmp induction by GSNO and SNP. GSNO and SNP react with Hcy in vitro under physiologically relevant conditions of pH and temperature generating S-nitrosohomocysteine, although in the latter case this would be co-ordinated to the Fe in SNP as a stable species. The free S-nitrosocysteine generated in the reaction with GSNO breaks down to release NO more readily than via homolysis of GSNO. As GSNO and SNP upregulate hmp similarly, the NO released in the former case on reaction with homocysteine cannot be involved in hmp regulation.

摘要

大肠杆菌的黄素血红蛋白基因hmp以不依赖SoxRS的方式被一氧化氮(NO)上调。我们现在表明,hmp的表达也被S-亚硝基谷胱甘肽(GSNO,广泛用作NO供体)和硝普钠(SNP,一种NO+供体)上调。通过细胞外添加同型半胱氨酸(Hcy)或使用metE突变体提高Hcy水平会降低hmp的表达。相反,metC突变体(Hcy合成有缺陷)的hmp表达水平更高。metR中的突变消除了GSNO和SNP对hmp的诱导作用,并且hmp的表达对Hcy变得不敏感。我们提出,先前记录的Hcy对MetR与glyA-hmp基因间调控区域结合的调节作用调控了hmp的转录。尽管该区域存在两个MetR结合位点,但GSNO和SNP诱导hmp仅需要靠近hmp的高亲和力位点。在生理相关的pH和温度条件下,GSNO和SNP在体外与Hcy反应生成S-亚硝基同型半胱氨酸,尽管在后一种情况下它会作为稳定物种与SNP中的铁配位。与GSNO反应生成的游离S-亚硝基半胱氨酸比通过GSNO的均裂更容易分解以释放NO。由于GSNO和SNP对hmp的上调作用相似,因此前者与同型半胱氨酸反应释放的NO不参与hmp的调控。

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