Rapid mechanochemical encapsulation of biocatalysts into robust metal-organic frameworks

被引:162
|
作者
Wei, Tz-Han [1 ,2 ]
Wu, Shi-Hong [2 ]
Huang, Yi-Da [2 ]
Lo, Wei-Shang [3 ]
Williams, Benjamin P. [3 ]
Chen, Sheng-Yu [1 ]
Yang, Hsun-Chih [2 ]
Hsu, Yu-Shen [2 ]
Lin, Zih-Yin [2 ]
Chen, Xin-Hua [2 ]
Kuo, Pei-En [2 ]
Chou, Lien-Yang [1 ]
Tsung, Chia-Kuang [3 ]
Shieh, Fa-Kuen [2 ]
机构
[1] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[2] Natl Cent Univ, Dept Chem, Taoyuan 32001, Taiwan
[3] Boston Coll, Merkert Chem Ctr, Dept Chem, Chestnut Hill, MA 02467 USA
关键词
IN-SITU; EMBEDDING ENZYMES; BETA-GLUCOSIDASE; IMMOBILIZATION; FUNCTIONALITY; CHEMISTRY; MECHANISM; CELLULOSE; UIO-66; GREEN;
D O I
10.1038/s41467-019-12966-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metal-organic frameworks (MOFs) have recently garnered consideration as an attractive solid substrate because the highly tunable MOF framework can not only serve as an inert host but also enhance the selectivity, stability, and/or activity of the enzymes. Herein, we demonstrate the advantages of using a mechanochemical strategy to encapsulate enzymes into robust MOFs. A range of enzymes, namely beta-glucosidase, invertase, beta-galactosidase, and catalase, are encapsulated in ZIF-8, UiO-66-NH2, or Zn-MOF-74 via a ball milling process. The solid-state mechanochemical strategy is rapid and minimizes the use of organic solvents and strong acids during synthesis, allowing the encapsulation of enzymes into three prototypical robust MOFs while maintaining enzymatic biological activity. The activity of encapsulated enzyme is demonstrated and shows increased resistance to proteases, even under acidic conditions. This work represents a step toward the creation of a suite of biomolecule-in-MOF composites for application in a variety of industrial processes.
引用
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页数:8
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