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一种用于在坚固的金属-有机骨架中高效固定酶的动态缺陷生成策略,用于催化水解和手性拆分。

A Dynamic Defect Generation Strategy for Efficient Enzyme Immobilization in Robust Metal-Organic Frameworks for Catalytic Hydrolysis and Chiral Resolution.

机构信息

State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University, Tianjin, 300071, China.

College of Chemistry, Nankai University, Tianjin, 300071, China.

出版信息

Angew Chem Int Ed Engl. 2023 May 8;62(20):e202302436. doi: 10.1002/anie.202302436. Epub 2023 Apr 7.

Abstract

Enzyme immobilization has been demonstrated to be a favorable protocol for promoting the industrialization of bioactive molecules, but still with formidable challenge. Addressing this challenge, we create a dynamic defect generation strategy for enzyme immobilization by using the dissociation equilibrium of metal-organic frameworks (MOFs) mediated by enzymes. Enzymes can act as "macro ligands" to generate competitive coordination against original ligands, along with the release of metal clusters of MOFs to generate defects, hence promoting the gradual transport of enzymes from the surface to inside. Various enzymes can be efficiently immobilized in MOFs to afford composites with good enzymatic activities, protective performances and exceptional reusabilities. Moreover, multienzyme bioreactors capable of efficient cascade reactions can also be generated. This study provides new opportunities to construct highly efficient biocatalysts incorporating different types of enzymes.

摘要

酶固定化已被证明是促进生物活性分子工业化的有利方案,但仍面临巨大挑战。为应对这一挑战,我们利用酶介导的金属有机框架(MOFs)的离解平衡,创建了一种用于酶固定化的动态缺陷生成策略。酶可以作为“大配体”与原始配体产生竞争配位,同时释放 MOFs 的金属簇以产生缺陷,从而促进酶从表面到内部的逐渐传输。各种酶可以有效地固定在 MOFs 中,得到具有良好酶活性、保护性能和出色可重复使用性的复合材料。此外,还可以生成能够进行高效级联反应的多酶生物反应器。这项研究为构建包含不同类型酶的高效生物催化剂提供了新的机会。

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