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Environmental Topology and Water Availability Modulates the Catalytic Activity of β-Galactosidase Entrapped in a Nanosporous Silicate Matrix

机译:环境拓扑结构和水的可利用性调节纳米多孔硅酸盐基质中捕获的β-半乳糖苷酶的催化活性。

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摘要

In the present work we studied the catalytic activity of E. coli β-Gal confined in a nanoporous silicate matrix (Eβ-Gal) at different times after the beginning of the sol-gel polymerization process. Enzyme kinetic experiments with two substrates (ONPG and PNPG) that differed in the rate-limiting steps of the reaction mechanism for their β-Gal-catalyzed hydrolysis, measurements of transverse relaxation times (T2) of water protons through 1H-NMR, and scanning electron microscopy analysis of the gel nanostructure, were performed. In conjunction, results provided evidence that water availability is crucial for the modulation observed in the catalytic activity of β-Gal as long as water participate in the rate limiting step of the reaction (only with ONPG). In this case, a biphasic rate vs. substrate concentration was obtained exhibiting one phase with catalytic rate constant (kcA), similar to that observed in solution, and another phase with a higher and aging-dependent catalytic rate constant (kcB). More structured water populations (lower T2) correlates with higher catalytic rate constants (kcB). The T2-kcB negative correlation observed along the aging of gels within the 15-days period assayed reinforces the coupling between water structure and the hydrolysis catalysis inside gels.
机译:在目前的工作中,我们研究了溶胶-凝胶聚合过程开始后不同时间封闭在纳米多孔硅酸盐基质(Eβ-Gal)中的大肠杆菌β-Gal的催化活性。用两种底物(ONPG和PNPG)进行酶动力学实验,这两种底物在其β-Gal催化水解的反应机理的限速步骤中有所不同,并通过 1测量水质子的横向弛豫时间(T2)。进行了H-NMR和凝胶纳米结构的扫描电子显微镜分析。结合起来,结果提供了证据,证明水的可用性对于β-Gal催化活性中观察到的调节至关重要,只要水参与了反应的限速步骤(仅使用ONPG)。在这种情况下,获得了双相速率与底物浓度的关系,显示出一个具有催化速率常数(kcA)的相,与在溶液中观察到的相类似,而另一相具有更高的且取决于老化的催化速率常数(kcB)​​。更多的结构化水种群(较低的T2)与较高的催化速率常数(kcB)​​相关。在测定的15天之内沿着凝胶老化观察到的T2-kcB负相关关系增强了水结构与凝胶内部水解催化之间的耦合。

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