Di Zhengyi, Qi Yu, Yu Xin-Xin, Li Hai-Ruo, Zuo Meng-Xuan, Ren Tian-Tian, Li Cheng-Peng, Zhao Yanli
College of Chemistry, Tianjin Key Laboratory of Structure and Performance for Functional Molecules, Tianjin Normal University Tianjin 300387 China
School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University 21 Nanyang Link 637371 Singapore
Chem Sci. 2024 Sep 20;15(41):16987-96. doi: 10.1039/d4sc04619f.
Facile immobilization is essential for the wide application of enzymes in large-scale catalytic processes. However, exploration of suitable enzyme supports poses an unmet challenge, particularly in the context of scale-up biocatalyst fabrication. In this study, we present facile and scale-up syntheses of high-performance enzyme biocatalysts encapsulation of cytochrome c (Cyt-c) as mono-enzyme and glucose oxidase (GOx)-horseradish peroxidase (HRP) as dual-enzyme cascade (GOx&HRP) systems, respectively, into a stable mesoporous hydrogen-bonded organic framework (meso-HOF) matrix. encapsulation reactions occur under ambient conditions, and facilitate scale up (∼3 g per reaction) of enzyme@meso-HOF within a very short period (5-10 min). The resultant biocatalysts not only exhibit high enzyme loading (37.9 wt% for mono-enzyme and 22.8 wt% for dual-enzyme) with minimal leaching, but also demonstrate high catalytic activity, superior reusability, and durability. This study represents an example of scale-up fabrication of enzyme@meso-HOF biocatalysts on the gram level and highlights superior meso-HOFs as suitable host matrices for biomolecular entities.
简便的固定化对于酶在大规模催化过程中的广泛应用至关重要。然而,探索合适的酶载体是一项尚未解决的挑战,特别是在扩大生物催化剂制备规模的背景下。在本研究中,我们分别展示了将细胞色素c(Cyt-c)作为单酶以及葡萄糖氧化酶(GOx)-辣根过氧化物酶(HRP)作为双酶级联(GOx&HRP)系统简便且可扩大规模地合成高性能酶生物催化剂,即将它们封装到稳定的介孔氢键有机框架(meso-HOF)基质中。封装反应在环境条件下发生,并有助于在非常短的时间内(5-10分钟)扩大酶@meso-HOF的规模(每次反应约3克)。所得的生物催化剂不仅表现出高酶负载量(单酶为37.9重量%,双酶为22.8重量%)且浸出极少,还展示出高催化活性、卓越的可重复使用性和耐久性。本研究代表了在克级规模上扩大酶@meso-HOF生物催化剂制备的一个实例,并突出了优异的meso-HOF作为生物分子实体合适宿主基质的特点。