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通过固定化来修饰酶的活性和选择性。

Modifying enzyme activity and selectivity by immobilization.

机构信息

Biocatalysis and Enzyme Technology Lab, Institute of Food Science and Technology, Federal University of Rio Grande do Sul, Av. Bento Gonçalves, 9500, P.O. Box 15090, ZC 91501-970, Porto Alegre, RS, Brazil.

出版信息

Chem Soc Rev. 2013 Aug 7;42(15):6290-307. doi: 10.1039/c2cs35231a.

Abstract

Immobilization of enzymes may produce alterations in their observed activity, specificity or selectivity. Although in many cases an impoverishment of the enzyme properties is observed upon immobilization (caused by the distortion of the enzyme due to the interaction with the support) in some instances such properties may be enhanced by this immobilization. These alterations in enzyme properties are sometimes associated with changes in the enzyme structure. Occasionally, these variations will be positive. For example, they may be related to the stabilization of a hyperactivated form of the enzyme, like in the case of lipases immobilized on hydrophobic supports via interfacial activation. In some other instances, these improvements will be just a consequence of random modifications in the enzyme properties that in some reactions will be positive while in others may be negative. For this reason, the preparation of a library of biocatalysts as broad as possible may be a key turning point to find an immobilized biocatalyst with improved properties when compared to the free enzyme. Immobilized enzymes will be dispersed on the support surface and aggregation will no longer be possible, while the free enzyme may suffer aggregation, which greatly decreases enzyme activity. Moreover, enzyme rigidification may lead to preservation of the enzyme properties under drastic conditions in which the enzyme tends to become distorted thus decreasing its activity. Furthermore, immobilization of enzymes on a support, mainly on a porous support, may in many cases also have a positive impact on the observed enzyme behavior, not really related to structural changes. For example, the promotion of diffusional problems (e.g., pH gradients, substrate or product gradients), partition (towards or away from the enzyme environment, for substrate or products), or the blocking of some areas (e.g., reducing inhibitions) may greatly improve enzyme performance. Thus, in this tutorial review, we will try to list and explain some of the main reasons that may produce an improvement in enzyme activity, specificity or selectivity, either real or apparent, due to immobilization.

摘要

酶的固定化可能会导致其观察到的活性、特异性或选择性发生变化。虽然在许多情况下,固定化会导致酶性质的贫化(由于与载体的相互作用导致酶的变形),但在某些情况下,这些性质可能会通过固定化得到增强。这些酶性质的变化有时与酶结构的变化有关。偶尔,这些变化是积极的。例如,它们可能与酶的超活化形式的稳定有关,例如在通过界面活化固定在疏水性载体上的脂肪酶的情况下。在其他一些情况下,这些改进只是酶性质随机变化的结果,在某些反应中是积极的,而在其他反应中可能是消极的。因此,尽可能广泛地制备生物催化剂文库可能是找到与游离酶相比具有改进性质的固定化生物催化剂的关键转折点。固定化酶将分散在载体表面上,不再可能发生聚集,而游离酶可能会发生聚集,这会大大降低酶活性。此外,酶的刚性化可能会导致在酶倾向于变形从而降低其活性的剧烈条件下保留酶的性质。此外,酶在载体上的固定化,主要是在多孔载体上的固定化,在许多情况下也可能对观察到的酶行为产生积极影响,而与结构变化无关。例如,促进扩散问题(例如 pH 梯度、底物或产物梯度)、分配(朝向或远离酶环境,对于底物或产物)或阻断某些区域(例如,减少抑制)可能会大大提高酶的性能。因此,在本教程综述中,我们将尝试列出并解释一些主要原因,这些原因可能会由于固定化而导致酶活性、特异性或选择性的真正或表观改善。

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