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鼠伤寒沙门氏菌肠炎血清型的黄素血红蛋白(hmp)基因的多个调节因子包括RamA,一种赋予多药耐药表型的转录调节因子。

Multiple regulators of the Flavohaemoglobin (hmp) gene of Salmonella enterica serovar Typhimurium include RamA, a transcriptional regulator conferring the multidrug resistance phenotype.

作者信息

Hernández-Urzúa Elizabeth, Zamorano-Sánchez David S, Ponce-Coria José, Morett Enrique, Grogan Susan, Poole Robert K, Membrillo-Hernández Jorge

机构信息

Laboratorio de Microbiología y Genética Molecular, Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, PO Box 70-228, Coyoacán, Mexico City 04510, Mexico.

出版信息

Arch Microbiol. 2007 Jan;187(1):67-77. doi: 10.1007/s00203-006-0175-8. Epub 2006 Oct 6.

Abstract

Microbial flavohaemoglobins are proteins with homology to haemoglobins from higher organisms, but clearly linked to nitric oxide (NO) metabolism by bacteria and yeast. hmp mutant strains of several bacteria are hypersensitive to NO and related compounds and hmp genes are up-regulated by the presence of NO. The regulatory mechanisms involved in hmp induction by NO and the superoxide-generating agent, methyl viologen (paraquat; PQ), are complex, but progressively being resolved. Here we show for the first time that, in Salmonella enterica serovar Typhimurium, hmp transcription is increased on exposure to PQ and demonstrate that RamA, a homologue of MarA is responsible for most of the hmp paraquat regulation. In addition we demonstrate NO-dependent elevation of Salmonella hmp transcription and Hmp accumulation. In both Escherichia coli and Salmonella modest transcriptional repression of hmp is exerted by the iron responsive transcriptional repressor Fur. Finally, in contrast to previous reports, we show that in E. coli and Salmonella, hmp induction by both paraquat and sodium nitroprusside is further elevated in a fur mutant background, indicating that additional regulators are implicated in this control process.

摘要

微生物黄素血红蛋白是与高等生物的血红蛋白具有同源性的蛋白质,但显然与细菌和酵母的一氧化氮(NO)代谢有关。几种细菌的hmp突变株对NO及相关化合物高度敏感,并且hmp基因在有NO存在时会上调。由NO和超氧化物生成剂甲基紫精(百草枯;PQ)诱导hmp所涉及的调控机制很复杂,但正逐步得到解决。在此我们首次表明,在肠炎沙门氏菌血清型鼠伤寒沙门氏菌中,暴露于PQ时hmp转录增加,并证明MarA的同源物RamA负责大部分hmp百草枯调控。此外,我们证明了沙门氏菌hmp转录和Hmp积累的NO依赖性升高。在大肠杆菌和沙门氏菌中,铁响应转录阻遏物Fur对hmp都有适度的转录抑制作用。最后,与之前的报道相反,我们表明在大肠杆菌和沙门氏菌中,在fur突变背景下,百草枯和硝普钠对hmp的诱导作用进一步增强,这表明在此调控过程中还涉及其他调节因子。

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