Fagan T F, Mayhew S G
Department of Biochemistry, University College, Dublin, Ireland.
Biochem J. 1993 Jul 1;293 ( Pt 1)(Pt 1):237-41. doi: 10.1042/bj2930237.
The H2-oxidation, H2-production and H-3H-exchange activities of the periplasmic hydrogenase from Desulfovibrio vulgaris (Hildenborough) were almost completely abolished by Hg(II) and the organic mercurials p-chloromercuribenzoate (pCMB) and p-hydroxymercuriphenylsulphonate. The thiol-modifying reagents N-ethylmaleimide, iodoacetate, dithionitrobenzoate and 2-nitro-5-thiocyanobenzoate had no effect on the activities. Kinetic and spectroscopic measurements suggest that inactivation by pCMB involves at least two reactions; a rapid reaction that is reversed by thiols, and a second, slower and irreversible reaction that occurs at high concentrations of the mercurial. The irreversible reaction was associated with loss of visible absorbance, indicative of a disrupted iron sulphur cluster(s). The effects on the H-3H-exchange activity indicate that the reversible modification affects the H2-activating site. Enzyme that had lost activity due to pCMB treatment, or during long-term storage, was reactivated by thiols. This reactivation was followed by a slower irreversible inactivation, as also occurred with native enzyme; the inactivation was O2 dependent and it was partly prevented by catalase, suggesting that H2O2 may be involved.
普通脱硫弧菌(希登伯勒菌株)周质氢化酶的H₂氧化、H₂产生及H-³H交换活性几乎完全被Hg(II)以及有机汞化合物对氯汞苯甲酸(pCMB)和对羟基汞苯磺酸盐所抑制。硫醇修饰试剂N-乙基马来酰亚胺、碘乙酸盐、二硫代硝基苯甲酸盐和2-硝基-5-硫氰基苯甲酸盐对这些活性没有影响。动力学和光谱测量表明,pCMB导致的失活至少涉及两个反应:一个可被硫醇逆转的快速反应,以及在高浓度汞化合物存在时发生的第二个较慢且不可逆的反应。不可逆反应与可见吸光度的丧失有关,这表明铁硫簇被破坏。对H-³H交换活性的影响表明,可逆修饰影响H₂激活位点。因pCMB处理或长期储存而失去活性的酶可被硫醇重新激活。这种重新激活之后是较慢的不可逆失活,天然酶也会出现这种情况;失活依赖于O₂,过氧化氢酶可部分阻止这种失活,这表明可能涉及H₂O₂。