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首页> 外文期刊>Biochemistry >Regulation of Methane Monooxygenase Catalysis Based on Size Exclusion and Quantum Tunneling
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Regulation of Methane Monooxygenase Catalysis Based on Size Exclusion and Quantum Tunneling

机译:基于尺寸排阻和量子隧穿的甲烷单加氧酶催化反应调控

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The hydroxylase component (MMOH) of the soluble form of methane monooxygenase (sMMO) isolated from Methylosinus trichosporium OB3b catalyzes both the O_2 activation and the CH_4 oxidation reactions at the oxygen-bridged dinuclear iron cluster present in its buried active site.During the reaction cycle,the diiron cluster forms a bis-mu-oxo-(Fe(IV))_2 intermediate termed compound Q (Q) that reacts directly with methane.Many adventitious substrates also react with Q,most at a relatively slow rate.We have proposed that Q reacts preferentially with CH_4 because the sMMO regulatory component MMOB induces a size selective pore into the MMOH active site as the two components form a complex.Support for this proposal has come through the observation of a nonlinear Arrhenius plot for the CH_4 oxidation,presumably due to a shift in rate-limiting step from substrate binding at low temperature to C-H bond cleavage at high temperature.Reactions of all substrates other than CH_4 fail to exhibit a break in the Arrhenius plot because binding is always rate limiting in the temperature range explored.Here we show that it is possible to induce a break in the Arrhenius plot for the ethane reaction with Q by using an MMOB mutant termed DBL2 (S109 A/T111A) in which residues at the MMOH-MMOB interface are reduced in size.We hypothesize that this increases the ethane binding rate and shifts the Arrhenius breakpoint into the observable temperature range.As a result of this shift,the kinetic and activation parameters of the C-H bond breaking reaction for both methane and ethane can be observed using the DBL2 mutant.A ~2H-KIE is observed for both substrate oxidation reactions when using DBL2,whereas only CH_4 oxidation exhibits an effect when using wild type MMOB,consistent with the C-H bond cleaving reaction becoming at least partially rate limiting for ethane.Analysis of the temperature dependence of the ~2H-KIE for ethane and methane for reactions using both mutant and wild type forms of MMOB suggests that quantum tunneling plays a significant role in methane oxidation but not ethane oxidation.
机译:从甲烷单孢菌OB3b中分离出的甲烷单加氧酶(sMMO)的可溶形式的羟化酶组分(MMOH)在其掩埋的活性位点中存在的氧桥联双核铁簇上催化O_2活化和CH_4氧化反应。 ,二铁簇形成了一个双-mu-oxo-(Fe(IV))_ 2中间化合物Q(Q),它直接与甲烷反应。许多不定形底物也与Q反应,速度相对较慢。 Q优先与CH_4反应,因为sMMO调节成分MMOB会在这两个成分形成复合物时在MMOH活性位点诱导一个大小选择性的孔。该建议的支持来自观察到CH_4氧化的非线性阿伦尼乌斯图。由于限速步骤从低温下的底物结合转变为高温下的CH键断裂,因此CH_4以外的所有底物的反应均未显示出断裂因为在研究的温度范围内结合总是限制速率,所以在Arrhenius图中显示了k。在这里我们表明,通过使用称为DBL2的MMOB突变体(S109 A / T111A ),其中MMOH-MMOB界面上的残基尺寸减小。我们假设这会增加乙烷键合速率,并将Arrhenius断裂点移动到可观察的温度范围内。由于这种移动,CH的动力学和激活参数使用DBL2突变体可以观察到甲烷和乙烷的键断裂反应。使用DBL2时,两个底物氧化反应均观察到〜2H-KIE,而使用野生型MMOB时只有CH_4氧化才起作用,与CH键一致裂解反应至少部分限制了乙烷的速率。〜2H-KIE对乙烷和甲烷的温度依赖性分析,涉及使用突变型和野生型MMO的反应B表明量子隧穿在甲烷氧化中起重要作用,而在乙烷氧化中不起作用。

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