Encapsulation of Immobilized β-Glucosidase with Calcium Metal–Organic Frameworks for Enhanced Stability in Hydrolysis of Cellobiose

纤维二糖 金属有机骨架 化学 水解 海藻酸钙 封装(网络) 金属 化学工程 有机化学 色谱法 无机化学 纤维素酶 吸附 计算机网络 工程类 计算机科学
作者
Lili Xu,Huanruo Liu,Xiaohan Wang,Qi Li,Suli Xu,Caizheng Sun,Hongbo Suo
出处
期刊:Langmuir [American Chemical Society]
卷期号:40 (35): 18727-18735 被引量:7
标识
DOI:10.1021/acs.langmuir.4c02436
摘要

β-Glucosidase (β-G) holds promising applications in various fields, such as biomass energy, food, pharmaceuticals, and environmental protection, yet its industrial application is still limited by issues of stability and recycling. Herein, we first immobilized β-G onto the surface of magnetic chitosan nanoparticles (MCS/β-G) through adsorption methods. Subsequently, utilizing the metal-organic framework (MOF), CaBDC, which possesses good stability under acidic conditions, we encapsulated MCS/β-G. The resulting biocatalyst (MCS/β-G@CaBDC) exhibited excellent activity and recyclability. MCS/β-G@CaBDC can convert 91.5% of cellobiose to glucose in 60 min and maintained 81.9% activity after 10 cycles. The apparent Km value of MCS/β-G@CaBDC was 0.148 mM, lower than free β-G (0.166 mM) and MCS/β-G (0.173 mM). The CaBDC layer increased the mass transfer resistance of the reaction but also triggered structural rearrangement of β-G during the encapsulation process. This resulted in the β-sheet content rising to 68.4%, which, in turn, contributed to enhancing the rigidity of β-G. Moreover, the saturated magnetic strength of this biocatalyst could reach 37.3 emu/g, facilitating its magnetic recovery. The biocatalyst prepared in this study exhibits promising application prospects, and the immobilization method can provide valuable insights into the field of enzyme immobilization.
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