4.8 Article

Mesoporous Metal-Organic Framework with Well-Defined Cruciate Flower-Like Morphology for Enzyme Immobilization

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 9, Issue 12, Pages 10587-10594

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b00512

Keywords

metal organic frameworks; nanobiocatalysis; enzyme immobilization; morphological control; nanomaterials

Funding

  1. National Natural Science Foundation of China [21676069]
  2. Natural Science Foundation of Hebei Province, China [B2014208054]
  3. Open Foundation of Biomanufacturing Subject at Hebei University of Science and Technology
  4. Foundation of Key Laboratory of Industrial Fermentation Microbiology of Ministry of Education and Tianjin Key Lab of Industrial Microbiology (Tianjin University of Science Technology) [2016IM001]
  5. Science Foundation of Hebei University of Science and Technology [2016ZDYY26]

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Metal organic frameworks (MOFs) have recently emerged as a promising candidates for the immobilization of enzymes due to their diversified structures and porosity. However, a lack of good size and morphological control over the as-prepared MOFs has limited their practical applications in some cases. Herein, instead of zeolitic imidazolate framework-8 (ZIF-8) with the standard rhombic dodecahedral morphology, we successfully synthesize a novel mesoporous catalase@ZIF composite with cruciate flower-like morphology by embedding catalase molecules into uniformly sized ZIF crystals. With extraordinarily large mesopore size and high protein loading capacity, the catalase@ZIF composites with cruciate Enzyme flower-like morphology exhibit 400% higher activity than that of catalase@ZIF composites with conventional rhombic dodecahedral morphology, and show higher reusability than conventional rhombic dodecahedral morphology. More importantly, we demonstrate for the first time that the biomacromolecules (proteins) can not directly regulate the crystal size, morphology, and crystallinity of ZIF-8. Moreover,. the crystal morphology of ZIF has primary dependence on concentrations of 2-methylimidazole and Zn2+ ions, and can be directly controlled by adjusting, concentrations of Zn2+ ions while keeping the high concentration of 2-methylimidazole.

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