可重用性
材料科学
酶
金属有机骨架
级联
封装(网络)
纳米技术
化学
组合化学
化学工程
色谱法
有机化学
计算机科学
吸附
软件
程序设计语言
工程类
计算机网络
作者
Wenqing Fan,Zefang Yu,Dominique Appadoo,Kang Liang,Jieying Liang
出处
期刊:Small
[Wiley]
日期:2025-04-08
标识
DOI:10.1002/smll.202503059
摘要
Abstract To position multi‐enzymes in a core‐shell structure, the conventional layer‐by‐layer approach is often used. However, this method is time‐consuming and complex, requiring multiple steps and the isolation of intermediates at each stage. To address this challenge, a sequential strategy is introduced for the controlled encapsulation of multi‐enzymes within metal‐organic frameworks (MOFs), achieving a core‐shell structure without the need for intermediate isolation. Synchrotron Terahertz‐Far‐Infrared (THz‐Far‐IR) spectroscopy is employed to monitor this encapsulation process. The results revealed that the first enzyme is co‐precipitated within the MOFs, followed by biomineralization upon the addition of a second enzyme, achieving distinct enzyme positioning. This approach is applicable to both two‐enzyme and three‐enzyme cascade systems. The results demonstrate that multi‐enzyme cascade activity is significantly enhanced compared to conventional one‐pot and layer‐by‐layer approaches, owing to optimal spatial arrangement, increased surface area, and improved enzyme conformation. Furthermore, the encapsulated enzymes exhibit strong resistance to high temperatures, proteolysis, and organic solvents, along with excellent reusability, making this method highly promising for industrial biocatalytic applications.
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