介孔材料
生物催化
化学
甲基橙
催化作用
金属有机骨架
固定化酶
选择性
组合化学
金属
酶
有机化学
吸附
生物降解
反应机理
光催化
作者
Effrosyni Gkaniatsou,Clémence Sicard,Rémy Ricoux,Linda Benahmed,Flavien Bourdreux,Qi Zhang,Christian Serre,Jean‐Pierre Mahy,Nathalie Steunou
标识
DOI:10.1002/anie.201811327
摘要
Abstract Microperoxidase‐8, a small, peroxidase‐type enzyme was immobilized into nanoparticles of the mesoporous and ultra‐stable metal–organic framework (MOF) MIL‐101(Cr). The immobilized enzyme fully retained its catalytic activity and exhibited enhanced resistance to acidic conditions. The biocatalyst was reusable and showed a long‐term stability. By exploiting the properties of the MOF′s framework, we demonstrated, for the first time, that the MOF matrix could act in synergy with the enzyme (Microperoxidase‐8) and enhance selectivity the oxidation reaction of dyes. The oxidation rate of the harmful negatively charged dye (methyl orange) was significantly increased after enzyme immobilization, probably as a result of the pre‐concentration of the methyl orange reactant owing to a charge matching between this dye and the MOF.
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