| Literature DB >> 25598311 |
Dawei Feng1, Tian-Fu Liu1, Jie Su2, Mathieu Bosch1, Zhangwen Wei1, Wei Wan2, Daqiang Yuan3, Ying-Pin Chen4, Xuan Wang1, Kecheng Wang1, Xizhen Lian1, Zhi-Yuan Gu1, Jihye Park1, Xiaodong Zou2, Hong-Cai Zhou4.
Abstract
Enzymatic catalytic processes possess great potential in chemical manufacturing, including pharmaceuticals, fuel production and food processing. However, the engineering of enzymes is severely hampered due to their low operational stability and difficulty of reuse. Here, we develop a series of stable metal-organic frameworks with rationally designed ultra-large mesoporous cages as single-molecule traps (SMTs) for enzyme encapsulation. With a high concentration of mesoporous cages as SMTs, PCN-333(Al) encapsulates three enzymes with record-high loadings and recyclability. Immobilized enzymes that most likely undergo single-enzyme encapsulation (SEE) show smaller Km than free enzymes while maintaining comparable catalytic efficiency. Under harsh conditions, the enzyme in SEE exhibits better performance than free enzyme, showing the effectiveness of SEE in preventing enzyme aggregation or denaturation. With extraordinarily large pore size and excellent chemical stability, PCN-333 may be of interest not only for enzyme encapsulation, but also for entrapment of other nanoscaled functional moieties.Entities:
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Year: 2015 PMID: 25598311 DOI: 10.1038/ncomms6979
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919