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Role of hydrogen in the activation and regulation of hydrogen oxidation by the soluble hydrogenase from Alcaligenes eutrophus H16.

机译:氢在来自拟南芥H16的可溶性氢化酶激活和调节氢氧化中的作用。

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摘要

The activation kinetics of the H2-oxidizing activity of the soluble hydrogenase from Alcaligenes eutrophus H16 were investigated. Activation with Na2S2O4 plus 101 kPa H2 resulted in a rapid increase in activity over 1 h and constant activity after 3 h incubation. Less-stable activations were achieved if enzyme was incubated with Na2S2O4 under 1 kPa H2 or 101 kPa N2. The enzyme could also be partly activated either with NADH alone or with H2 alone. The level of activity obtained with both 101 kPa H2 and NADH present was greater than that obtained with either 101 kPa H2 or NADH alone. Activation with H2 plus NADH was virtually independent of NADH concentration but highly dependent on H2 concentration. The effects of various concentrations of H2 and constant concentration of NADH on the level of activation were the same whether H2 oxidation was assayed by H2-dependent Methylene Blue or NAD+ reduction. Diaphorase activity did not require activation and was little affected by the treatments that activated H2-oxidizing activity. The results suggest that H2 plays an important role in regulating the level of H2-oxidizing activity in this soluble hydrogenase.
机译:研究了嗜碱产碱杆菌H16的可溶性氢化酶H2-氧化活性的活化动力学。用Na2S2O4加101 kPa H2活化可在1小时内迅速增加活性,并在3小时孵育后保持恒定活性。如果将酶与Na2S2O4在1 kPa H2或101 kPa N2下温育,则激活的稳定性较差。该酶也可以被单独的NADH或单独的H2部分活化。同时存在101 kPa H2和NADH所获得的活性水平高于单独使用101 kPa H2或NADH所获得的活性水平。用H2和NADH激活实际上与NADH浓度无关,但高度依赖于H2浓度。无论通过依赖H2的亚甲基蓝或NAD +还原法检测H2氧化,各种浓度的H2和恒定浓度的NADH对活化水平的影响都是相同的。心肌黄酶活性不需要激活,并且几乎不受激活H2氧化活性的处理的影响。结果表明,H2在调节该可溶性氢化酶中H2氧化活性的水平中起着重要作用。

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