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Reduction of Cupric Ions with Elemental Sulfur by Thiobacillus ferrooxidans

机译:亚铁氧化硫杆菌还原元素硫中的铜离子

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In anaerobic or aerobic conditions in the presence of 5 mM sodium cyanide, an inhibitor of iron oxidase, cupric ion (Cu2+) was reduced enzymatically with elemental sulfur (S0) by washed intact cells of Thiobacillus ferrooxidans AP19-3 to give cuprous ion (Cu+). The rate of Cu2+ reduction was proportional to the concentrations of S0 and Cu2+ added to the reaction mixture. The pH optimum for the cupric ion-reducing system was 5.0, and the activity was completely destroyed by 10-min incubation of cells at 70°C. The activity of Cu2+ reduction with S0 by this strain was strongly inhibited by inhibitors of hydrogen sulfide: ferric ion oxidoreductase (SFORase), such as α,α′-dipyridyl, 4,5-dihydroxy-m-benzene disulfonic acid disodium salts, and diazine dicarboxylic acid bis-(N, N-dimethylamide). A SFORase purified from this strain, which catalyzes oxidation of both hydrogen sulfide and S0 with Fe3+ or Mo6+ as an electron acceptor in the presence of glutathione, catalyzed a reduction of Cu2+ by S0, and the Michaelis constant of SFORase for Cu2+ was 7.2 mM, indicating that a SFORase catalyzes the reduction of not only Fe3+ and Mo6+ but also Cu2+.
机译:在5 mM氰化钠存在下的厌氧或好氧条件下,洗涤过的氧化亚铁硫杆菌AP19-3的完整细胞会用元素硫(S0)将铁氧化酶抑制剂铜离子(Cu2 +)酶促还原,得到亚铜离子(Cu + )。 Cu 2+的还原速率与添加到反应混合物中的SO和Cu2 +的浓度成比例。铜离子还原体系的最适pH为5.0,在70°C下孵育10分钟可完全破坏活性。硫化氢抑制剂:三价铁离子氧化还原酶(SFORase),如α,α'-二吡啶基,4,5-二羟基-间苯二磺酸二钠盐,和二嗪二羧酸双-(N,N-二甲基酰胺)。从该菌株中纯化出的SFORase可在谷胱甘肽存在下用Fe3 +或Mo6 +作为电子受体催化硫化氢和S0的氧化,通过S0催化Cu2 +的还原,SFORase对Cu2 +的米氏常数为7.2 mM,这表明SFORase不仅催化Fe3 +和Mo6 +的还原,而且还催化Cu2 +的还原。

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