沸石咪唑盐骨架
生物矿化
微型多孔材料
生物传感器
材料科学
咪唑酯
金属有机骨架
生物催化
生物相容性
酪氨酸酶
纳米技术
化学工程
电化学
组合化学
酶
化学
有机化学
吸附
电极
冶金
复合材料
物理化学
工程类
作者
Jun Xiong,Bin Chen,Zhixian Li,Shuli Liu,Min‐Hua Zong,Xiaoling Wu,Wen‐Yong Lou
标识
DOI:10.1021/acsami.4c16880
摘要
Biomineralization of enzymes inside rigid metal-organic frameworks (MOFs) is appealing due to its biocompatibility and simplicity. However, this strategy has hitherto been limited to microporous MOFs, leading to low apparent enzymatic activity. In this study, polysaccharide sodium alginate is introduced during the biomineralization of enzymes in zeolitic imidazolate frameworks (ZIFs) to competitively coordinate with metal ions, which endows the encapsulated enzyme with a 7-fold higher activity than that in microporous ZIFs. Mechanism investigation showed that the introduction of alginate generates hierarchical porous structures and enhances the hydrophilicity, which contributes to the enhanced activity of the enzyme. Moreover, the porous ZIFs protect the embedded tyrosinase under detrimental conditions, which allows for the fast detection of phenol, with the limit of detection of 0.03 mM (S/N = 3). Engineering the enzyme with MOFs to enhance its activity and stability is anticipated to extend its application in biocatalysis and biosensors.
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