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大肠杆菌中亚硝酰铁络合物的遗传信号转导

Genetic signal transduction by nitrosyl-iron complexes in Escherichia coli.

作者信息

Vasilieva S V, Moshkovskaya E Yu, Sanina N A, Aldoshin S M, Vanin A F

机构信息

Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Moscow, 117977, Russia.

出版信息

Biochemistry (Mosc). 2004 Aug;69(8):883-9. doi: 10.1023/b:biry.0000040220.13586.45.

Abstract

Nitrosyl-iron complexes used as aqueous preparations of binuclear dinitrosyl-iron complex with glutathione (DNICglu), initially polycrystalline preparations of binuclear tetranitrosyl-iron complex with thiosulfate (TNICthio), and also binuclear tetranitrosyl-iron complex with aminotriazole (TNICatria) and mononuclear dinitrosyl-iron complex with triazole (DNICtria) in the concentration to 0.1 mM activated expression of the soxS and sfiA genes in Escherichia coli. Higher concentrations of polycrystalline preparations of low stability in aqueous solutions were cytotoxic, whereas DNICglu, which is more stable in water (up to two days), increased the gene expression on increase in its concentration to 0.5 mM. The iron chelating agent o-phenanthroline completely inhibited the gene expression induced by all compounds studied. The genetic signal transduction seemed to be realized not by nitric oxide molecules and/or iron ions released in solutions but directly by the complexes themselves, which activate transcriptional proteins by transfer onto them of nitrosyl-iron groups [Fe+(NO+)2].

摘要

亚硝酰铁配合物用作双核二亚硝酰铁与谷胱甘肽(DNICglu)的水性制剂,最初是双核四亚硝酰铁与硫代硫酸盐(TNICthio)的多晶体制剂,还有双核四亚硝酰铁与氨基三唑(TNICatria)以及单核二亚硝酰铁与三唑(DNICtria),浓度达到0.1 mM时可激活大肠杆菌中soxS和sfiA基因的表达。在水溶液中稳定性低的多晶体制剂的较高浓度具有细胞毒性,而在水中更稳定(长达两天)的DNICglu,其浓度增加到0.5 mM时会增加基因表达。铁螯合剂邻菲罗啉完全抑制了所有研究化合物诱导的基因表达。遗传信号转导似乎不是通过溶液中释放的一氧化氮分子和/或铁离子实现的,而是直接由配合物本身实现的,这些配合物通过将亚硝酰铁基团[Fe+(NO+)2]转移到转录蛋白上来激活它们。

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