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内源性活性氧的产生:还原活性化合物产生超氧自由基和过氧化氢。

Reprint of: Intracellular Production of Superoxide Radical and of Hydrogen Peroxide by Redox Active Compounds.

机构信息

Department of Biochemistry, Duke University Medical Center, Durham, North Carolina, 27710.

出版信息

Arch Biochem Biophys. 2022 Sep 15;726:109229. doi: 10.1016/j.abb.2022.109229. Epub 2022 Jun 2.

Abstract

Several compounds have been found capable of diverting the electron flow in Escherichia coli and thus causing increased intracellular production of O and HO. One indication of this electron-shunting action was increased cyanide-resistant respiration and one cellular response was increased biosynthesis of the manganese-containing superoxide dismutase and of catalase. Blocking cytochrome oxidase with cyanide or azide increased the electron flow available for reduction of paraquat and presumably of the other exogenous compounds tested and thus increased their biological effects. Paraquat, pyocyanine, phenazine methosulfate, streptonigrin, juglone, menadione, plumbagin, methylene blue, and azure C were all effective in elevating intracellular production of O and HO. The effect of alloxan appeared paradoxical in that it increased cyanide-resistant respiration without significantly increasing the cell content of the manganese-superoxide dismutase and with only a small effect on the level of catalase. The alloxan effect on cyanide-resistant respiration was artifactual and was due to an oxygen-consuming reaction between alloxan and cyanide, rather than to a diversion of the intracellular electron flow. With paraquat as a representative electron-shunting compound, the increase in biosynthesis of the manganese-superoxide dismutase was prevented by inhibitors of transcription or of translation, but not by an inhibitor of replication. The increase in this enzyme activity, caused by paraquat and presumably by the other compounds, was thus due to de novo enzyme synthesis activated or derepressed at the level of transcription.

摘要

已经发现了几种能够转移大肠杆菌中电子流的化合物,从而导致细胞内 O 和 HO 的产量增加。这种电子转移作用的一个迹象是氰化物抗性呼吸增加,细胞的一个反应是锰过氧化物酶和过氧化氢酶的生物合成增加。用氰化物或叠氮化钠阻断细胞色素氧化酶会增加可用于还原百草枯和其他测试的外源化合物的电子流,从而增加它们的生物学效应。百草枯、绿脓菌素、吩嗪甲硫酸盐、斯特雷酮、胡桃醌、维生素 K3、扁柏醌、亚甲蓝和 Azure C 都能有效地提高细胞内 O 和 HO 的产量。所有唑烷的作用似乎是矛盾的,因为它增加了氰化物抗性呼吸,而没有显著增加细胞内锰过氧化物酶的含量,对过氧化氢酶的水平只有很小的影响。所有唑烷对氰化物抗性呼吸的影响是人为的,是由于所有唑烷和氰化物之间的耗氧反应,而不是由于细胞内电子流的转移。以百草枯作为代表性的电子转移化合物,转录或翻译抑制剂可以阻止锰过氧化物酶生物合成的增加,但不能阻止复制抑制剂的增加。因此,百草枯和其他化合物引起的这种酶活性的增加是由于转录水平上新酶的合成被激活或去阻遏。

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