沸石咪唑盐骨架
咪唑酯
化学
成核
化学工程
生物催化
酶
材料科学
固定化酶
有机溶剂
催化作用
纳米技术
酶催化
金属有机骨架
溶剂
有机化学
表面改性
表面能
纳米结构
封装(网络)
蛋白水解酶
比表面积
作者
Zefang Yu,Bernt Johannessen,Ming Zhang,Hongyu Shi,Yanhan Wang,Yu Wang,Jun Ge,Kang Liang,Jieying Liang
标识
DOI:10.1002/anie.202513501
摘要
Conventional enzymes immobilization strategies within metal-organic frameworks (MOF) typically require solvents and energy, resulting in solvent residues, environmental pollution, and high energy consumption. In this work, we present a solvent- and energy-free solid-state strategy for synthesizing enzyme-zeolitic imidazolate framework (ZIF) biocomposites. The nucleation of enzyme-ZIF is driven by acid-base interactions through the directly mixing of enzymes with ZIF precursors. The resulting biocomposites exhibit up to a four-fold enhancement in enzymatic activity compared to liquid-phase methods and a 1000-fold increase compared to free enzymes. This enhancement is attributed to the ZIF's multiphase crystalline structure, larger pore size, significantly higher surface area, and greater total pore volume, as well as a more favorable enzyme conformation (e.g., an open active-site pocket) achieved during synthesis followed by immobilization. Additionally, the synthesized enzyme-ZIF composites display excellent stability against organic solvents, proteolytic enzymes, and high temperatures, along with outstanding recyclability. This simple and sustainable approach to biocatalytic ZIF synthesis paves the way for the development of green, efficient, and robust biocatalysts for industrial applications.
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