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An enzyme formulation using customized enzyme activators (metal ions) to directly construct metal–organic frameworks (MOFs) as enzyme protective carriers is presented. These MOF carriers can also serve as the disintegrating agents to simultaneously release enzymes and their activators during biocatalysis with boosted activities. This highly efficient enzyme preparation combines enzyme immobilization (enhanced stability, easy operation) and homogeneous biocatalysis (fast diffusion, high activity). The MOF serves as an ion pump that continuously provides metal ion activators that greatly promote the enzymatic activities (up to 251 %). This MOF–enzyme composite demonstrated an excellent protective effect against various perturbation environments. A mechanistic investigation revealed that the spontaneous activator/enzyme release and ion pumping enable enzymes to sufficiently interact with their activators owing to the proximity effects, leading to a boost in biocatalytic performance. [ABSTRACT FROM AUTHOR]

An enzyme formulation using customized enzyme activators (metal ions) to directly construct metal–organic frameworks (MOFs) as enzyme protective carriers is presented. These MOF carriers can also serve as the disintegrating agents to simultaneously release enzymes and their activators during biocatalysis with boosted activities. This highly efficient enzyme preparation combines enzyme immobilization (enhanced stability, easy operation) and homogeneous biocatalysis (fast diffusion, high activity). The MOF serves as an ion pump that continuously provides metal ion activators that greatly promote the enzymatic activities (up to 251 %). This MOF–enzyme composite demonstrated an excellent protective effect against various perturbation environments. A mechanistic investigation revealed that the spontaneous activator/enzyme release and ion pumping enable enzymes to sufficiently interact with their activators owing to the proximity effects, leading to a boost in biocatalytic performance. [ABSTRACT FROM AUTHOR]

Abstract: Despite artificial nanozymes, as compared to natural enzymes, exhibit distinct superiorities of low cost, robustness against harsh environments, high stability and easy mass‐production, the relatively lower activity and efficiency still seriously restrict their application in high‐performance photometric chemosensing and biosensing. Promoting the activity and efficiency of nanozymes turns to be a significant yet challenging goal of the nanozyme community. Here we found, for the first time, that trace I− can dramatically boost the peroxidase‐like activity (over 50‐fold higher) of VOx at ppb‐concentration levels. It was deduced that the significant enhancement of nanozymatic activity mainly results from the synergetic modulation of surface redox and electronic structure of VOx. Based on this finding, ultrasensitive photometric detection of both H2O2 and I− (down to nM) was realized. [ABSTRACT FROM AUTHOR]