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Reduction of Technetium(VII) by Desulfovibrio fructosovorans Is Mediated by the Nickel-Iron Hydrogenase

机译:镍铁氢化酶介导果糖脱硫弧菌还原of(VII)

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摘要

Resting cells of the sulfate-reducing bacterium Desulfovibrio fructosovorans grown in the absence of sulfate had a very high Tc(VII)-reducing activity, which led to the formation of an insoluble black precipitate. The involvement of a periplasmic hydrogenase in Tc(VII) reduction was indicated (i) by the requirement for hydrogen as an electron donor, (ii) by the tolerance of this activity to oxygen, and (iii) by the inhibition of this activity by Cu(II). Moreover, a mutant carrying a deletion in the nickel-iron hydrogenase operon showed a dramatic decrease in the rate of Tc(VII) reduction. The restoration of Tc(VII) reduction by complementation of this mutation with nickel-iron hydrogenase genes demonstrated the specific involvement of the periplasmic nickel-iron hydrogenase in the mechanism in vivo. The Tc(VII)-reducing activity was also observed with cell extracts in the presence of hydrogen. Under these conditions, Tc(VII) was reduced enzymatically to soluble Tc(V) or precipitated to an insoluble black precipitate, depending on the chemical nature of the buffer used. The purified nickel-iron hydrogenase performed Tc(VII) reduction and precipitation at high rates. These series of genetic and biochemical approaches demonstrated that the periplasmic nickel-iron hydrogenase of sulfate-reducing bacteria functions as a Tc(VII) reductase. The role of cytochrome c3 in the mechanism is also discussed.
机译:在没有硫酸盐的情况下生长的硫酸盐还原细菌Desulfovibrio fructosovorans的静止细胞具有非常高的Tc(VII)还原活性,这导致形成了不溶的黑色沉淀物。 (i)要求氢作为电子供体,(ii)对该氧的耐受性,以及(iii)通过抑制该活性,表明了周质氢化酶参与Tc(VII)还原。铜(II)。此外,携带镍铁氢化酶操纵子缺失的突变体显示Tc(VII)还原速率显着降低。通过将该突变与镍铁氢化酶基因互补来恢复Tc(VII)还原,证明了周质镍铁氢化酶在体内机制中的特定参与。在氢存在下,用细胞提取物还观察到了降低Tc(VII)的活性。在这些条件下,取决于所用缓冲液的化学性质,将Tc(VII)酶法还原为可溶性Tc(V)或沉淀为不溶性黑色沉淀。纯化的镍铁氢化酶以高速率进行Tc(VII)还原和沉淀。这些系列的遗传和生化方法表明,硫酸盐还原细菌的周质镍铁氢化酶起着Tc(VII)还原酶的作用。还讨论了细胞色素c3在该机制中的作用。

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