幽门螺杆菌二硫还原酶:在甲硝唑还原中的作用

Nadeem O. Kaakoush, George L. Mendz
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引用次数: 10

摘要

二硫还原酶在维持细胞内氧化还原电位中起着重要作用。以二硫比-2-硝基苯甲酸、谷胱甘肽或l-胱氨酸和铁氧还蛋白为底物,在幽门螺杆菌中鉴定出3种二硫还原酶活性。测定了这些活性的动力学参数,证明了甲硝唑的存在抑制了还原酶的活性。底物竞争实验显示,在甲硝唑敏感和耐药配对菌株的裂解物中,二硫比-2-硝基苯甲酸、谷胱甘肽和铁氧还蛋白对甲硝唑还原的抑制作用。研究表明,甲硝唑的存在可调节三种二硫还原酶的活性,而二硫还原酶底物的存在可抑制甲硝唑还原。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Helicobacter pylori disulphide reductases: role in metronidazole reduction

Disulphide reductases play an important role in maintaining intracellular redox potential. Three disulphide reductase activities were identified in Helicobacter pylori, which used dithiobis-2-nitrobenzoic acid, glutathione or l-cystine and ferredoxin as substrates. The kinetic parameters of these activities were determined and it was demonstrated that the reductase activities were inhibited by the presence of metronidazole. Substrate competition experiments served to show inhibition of metronidazole reduction by dithiobis-2-nitrobenzoic acid, glutathione and ferredoxin in lysates from metronidazole susceptible and resistant matched pairs of strains. The study demonstrated that the activities of three disulphide reductases were modulated by the presence of metronidazole, and that metronidazole reduction was inhibited by the presence of disulphide reductase substrates.

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