Fan Wenqing, Yu Zefang, Appadoo Dominique, Liang Kang, Liang Jieying
School of Chemical Engineering, Australian Centre for NanoMedicine, The University of New South Wales, Sydney, NSW, 2052, Australia.
Australian Synchrotron-ANSTO, Clayton, VIC, 3168, Australia.
Small. 2025 Jun;21(22):e2503059. doi: 10.1002/smll.202503059. Epub 2025 Apr 8.
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.
为了将多酶定位在核壳结构中,通常采用传统的层层组装方法。然而,这种方法耗时且复杂,需要多个步骤并且在每个阶段都要分离中间体。为了应对这一挑战,引入了一种顺序策略,用于在金属有机框架(MOF)中对多酶进行可控封装,无需分离中间体即可实现核壳结构。采用同步辐射太赫兹-远红外(THz-Far-IR)光谱来监测这种封装过程。结果表明,第一种酶在MOF中共沉淀,随后在加入第二种酶后发生生物矿化,从而实现了不同酶的定位。这种方法适用于双酶和三酶级联系统。结果表明,与传统的一锅法和层层组装方法相比,多酶级联活性显著提高,这归因于最佳的空间排列、增加的表面积和改善的酶构象。此外,封装的酶对高温、蛋白水解和有机溶剂具有很强的抗性,并且具有出色的可重复使用性,使得这种方法在工业生物催化应用中极具前景。