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在丙酮酸脱羧酶中,一个保守谷氨酸的双重作用:参与立体电子控制脱羧和新生碳负离子/烯胺中间体的质子化的证据。

Double duty for a conserved glutamate in pyruvate decarboxylase: evidence of the participation in stereoelectronically controlled decarboxylation and in protonation of the nascent carbanion/enamine intermediate .

机构信息

Albrecht-von-Haller-Institute for Plant Sciences and Göttingen Center for Molecular Biosciences, Georg-August-University Göttingen, Ernst-Caspari-Haus, Justus-von-Liebig-Weg 11, D-37077 Göttingen, Germany.

出版信息

Biochemistry. 2010 Sep 21;49(37):8197-212. doi: 10.1021/bi100828r.

Abstract

Pyruvate decarboxylase (PDC) catalyzes the nonoxidative decarboxylation of pyruvate into acetaldehyde and carbon dioxide and requires thiamin diphosphate (ThDP) and a divalent cation as cofactors. Recent studies have permitted the assignment of functional roles of active site residues; however, the underlying reaction mechanisms of elementary steps have remained hypothetical. Here, a kinetic and thermodynamic single-step analysis in conjunction with X-ray crystallographic studies of PDC from Zymomonas mobilis implicates active site residue Glu473 (located on the re-face of the ThDP thiazolium nucleus) in facilitating both decarboxylation of 2-lactyl-ThDP and protonation of the 2-hydroxyethyl-ThDP carbanion/enamine intermediate. Variants carrying either an isofunctional (Glu473Asp) or isosteric (Glu473Gln) substitution exhibit a residual catalytic activity of less than 0.1% but accumulate different intermediates at the steady state. Whereas the predecarboxylation intermediate 2-lactyl-ThDP is accumulated in Glu473Asp because of a 3000-fold slower decarboxylation compared to that of the wild-type enzyme, Glu473Gln is not impaired in decarboxylation but generates a long-lived 2-hydroxyethyl-ThDP carbanion/enamine postdecarboxylation intermediate. CD spectroscopic analysis of the protonic and tautomeric equilibria of the cocatalytic aminopyrimidine part of ThDP indicates that an acidic residue is required at position 473 for proper substrate binding. Wild-type PDC and the Glu473Asp variant bind the substrate analogue acetylphosphinate with the same affinity, implying a similar stabilization of the predecarboxylation intermediate analogue on the enzyme, whereas Glu473Gln fails to bind the analogue. The X-ray crystallographic structure of 2-lactyl-ThDP trapped in the decarboxylation-deficient variant Glu473Asp reveals a common stereochemistry of the intermediate C2α stereocenter; however, the scissile C2α-C(carboxylate) bond deviates by ∼25-30° from the perpendicular "maximum overlap" orientation relative to the thiazolium ring plane as commonly observed in ThDP enzymes. Because a reactant-state stabilization of the predecarboxylation intermediate can be excluded to account for the slower decarboxylation, the data suggest a strong stereoelectronic effect for the transition state of decarboxylation as supported by additional DFT studies on models. To the best of our knowledge, this is a very rare example in which the magnitude of a stereoelectronic effect could be experimentally estimated for an enzymatic system. Given that variant Glu473Gln is not decarboxylation-deficient, electrostatic stress can be excluded as a driving force for decarboxylation. The apparent dual function of Glu473 further suggests that decarboxylation and protonation of the incipient carbanion are committed and presumably proceed in the same transition state.

摘要

丙酮酸脱羧酶(PDC)催化丙酮酸的非氧化脱羧为乙醛和二氧化碳,需要硫胺素二磷酸(ThDP)和二价阳离子作为辅助因子。最近的研究允许对活性位点残基的功能角色进行分配;然而,基本步骤的潜在反应机制仍然是假设的。在这里,通过与来自运动发酵单胞菌的 PDC 的 X 射线晶体学研究相结合的动力学和热力学单步分析,表明活性位点残基Glu473(位于 ThDP 噻唑核的 re-面)有助于 2-乳酰-ThDP 的脱羧和 2-羟乙基-ThDP 碳阴离子/烯胺中间物的质子化。携带等效功能(Glu473Asp)或等排取代(Glu473Gln)的变体的残余催化活性低于 0.1%,但在稳定状态下积累不同的中间物。由于与野生型酶相比,前脱羧化中间物 2-乳酰-ThDP 的脱羧速度慢 3000 倍,因此 Glu473Asp 积累了 predecarboxylation 中间物,而 Glu473Gln 在脱羧方面没有受损,但生成了长寿命的 2-羟乙基-ThDP 碳阴离子/烯胺脱羧后中间物。ThDP 共催化的氨基嘧啶部分的质子和互变异构平衡的 CD 光谱分析表明,位置 473 需要一个酸性残基以正确结合底物。野生型 PDC 和 Glu473Asp 变体以相同的亲和力结合底物类似物乙酰膦酸盐,这意味着类似物在前脱羧化中间物上的类似稳定,而 Glu473Gln 不能结合类似物。在脱羧缺陷变体 Glu473Asp 中捕获的 2-乳酰-ThDP 的 X 射线晶体结构揭示了中间物 C2α 立体中心的共同立体化学;然而,与通常在 ThDP 酶中观察到的噻唑环平面垂直的“最大重叠”取向相比,裂解的 C2α-C(羧酸盐)键偏离约 25-30°。由于不能排除反应物状态对前脱羧化中间物的稳定作用来解释脱羧速度较慢的原因,因此数据表明过渡态存在强烈的立体电子效应,这得到了对模型进行的额外 DFT 研究的支持。据我们所知,这是一个非常罕见的例子,可以通过实验估计酶系统中立体电子效应的大小。鉴于变体 Glu473Gln 不是脱羧缺陷,静电应力可以排除为脱羧的驱动力。Glu473 的明显双重功能进一步表明,脱羧和初始碳阴离子的质子化是承诺的,并且可能在相同的过渡态中进行。

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