Crawford M J, Goldberg D E
Howard Hughes Medical Institute, Departments of Medicine and Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Biol Chem. 1998 Dec 18;273(51):34028-32. doi: 10.1074/jbc.273.51.34028.
Flavohemoglobins, a family of two-domain proteins with homology to vertebrate hemoglobins, are found in a variety of prokaryotic and eukaryotic microorganisms. Recent studies suggest a role for these proteins in nitrogen oxide metabolism. We now show that nitric oxide donors positively regulate a chromosomal flavohemoglobin (hmp)/lacZ operon fusion in Salmonella typhimurium. hmp gene expression in the presence of NO. is independent of the SoxS, OxyR, and FNR transcription factors and instead relies on inactivation of the iron-dependent Fur repressor. Other Fur-repressed promoters in S. typhimurium are also activated by an NO. donor. In contrast to the wild-type strain, an hmp- mutant requires markedly lower concentrations of NO to induce the hmp/lacZ fusion, whereas its response to iron chelation is equivalent to wild type. These data unveil a new pathway for NO-dependent gene expression in S. typhimurium.
黄素血红蛋白是一类与脊椎动物血红蛋白具有同源性的双结构域蛋白质家族,存在于多种原核和真核微生物中。最近的研究表明这些蛋白质在一氧化氮代谢中发挥作用。我们现在发现一氧化氮供体可正向调节鼠伤寒沙门氏菌中的染色体黄素血红蛋白(hmp)/lacZ操纵子融合。在有一氧化氮存在的情况下,hmp基因的表达不依赖于SoxS、OxyR和FNR转录因子,而是依赖于铁依赖性Fur阻遏物的失活。鼠伤寒沙门氏菌中其他受Fur阻遏的启动子也可被一氧化氮供体激活。与野生型菌株相比,hmp突变体诱导hmp/lacZ融合所需的一氧化氮浓度明显更低,而其对铁螯合的反应与野生型相当。这些数据揭示了鼠伤寒沙门氏菌中一氧化氮依赖性基因表达的新途径。