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Covalent organic frameworks as emerging host platforms for enzyme immobilization and robust biocatalysis - A review.
Gan, JianSong; Bagheri, Ahmad Reza; Aramesh, Nahal; Gul, Ijaz; Franco, Marcelo; Almulaiky, Yaaser Q; Bilal, Muhammad.
Afiliación
  • Gan J; School of Food and Drug, Jiangsu Vocational College of Finance & Economics, Huaian 223003, China; Northeastern State University, United States of America. Electronic address: 19761120@jscj.edu.cn.
  • Bagheri AR; Chemistry Department, Yasouj University, Yasouj 75918-74831, Iran.
  • Aramesh N; Chemistry Department, Yasouj University, Yasouj 75918-74831, Iran.
  • Gul I; School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054, China.
  • Franco M; Department of Exact and Technological Sciences, State University of Santa Cruz, 45654-370 Ilhéus, Brazil.
  • Almulaiky YQ; University of Jeddah, College of Sciences and Arts at Khulais, Department of Chemistry, Jeddah, Saudi Arabia; Chemistry Department, Faculty of Applied Science, Taiz University, Taiz, Yemen.
  • Bilal M; School of Life Science and Food Engineering, Huaiyin Institute of Technology, Huaian 223003, China. Electronic address: bilaluaf@hotmail.com.
Int J Biol Macromol ; 167: 502-515, 2021 Jan 15.
Article en En | MEDLINE | ID: mdl-33279559
In recent years, the synthesis and application of green and sustainable products have become global ecological and societal issues. Based on the principles of green chemistry, the application of different biocatalysts not only produce target products and decreases side effects but also enhances the selectivity and activity. Enzyme-based biocatalysts are very interesting due to their high catalytic performance, eco-friendly reaction systems, and selectivity. Immobilization is demonstrated as a favorable approach to improve the stability and recyclability of enzymes. Among different supports, porous and crystalline materials, covalent organic frameworks (COFs), represent an interesting class of support matrices for the immobilization of different enzymes. Owing to tunable physicochemical characteristics, a high degree of crystallinity, large specific surface area, superior adsorption capacity, pre-designable structure and marked stability, COFs might consider as perfect host materials for improving the desirable properties of enzymes, such as poor stability, low operational range, lack of repeatability, and products/by-products inhibition for large-scale applications. The enzyme-incorporated COFs have emerged as one of the hopeful ways to constitute tailor-made biocatalytic systems, which can be employed in an array of reactions. Highly porous nature of many COFs led to increased process output in contrast to other micro/nanoparticles. The enzymes can be integrated into COFs through different techniques, including physical adsorption and direct covalent attachment between the enzyme molecules and COFs or through a cross-linking agent. Herein, we discuss and highlight the synthesis methods, properties, and functionalization of COFs and the recent literature for the application of these materials in enzymes immobilization. Main approaches for immobilization of enzymes into COFs and the catalytic applications of these materials are also presented. This study offers new avenues to address the limitations of traditional enzyme immobilization supports as well as delivers new possibilities to construct smart biocatalytic systems for diverse biotechnological applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enzimas Inmovilizadas / Estructuras Metalorgánicas Idioma: En Revista: Int J Biol Macromol Año: 2021 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enzimas Inmovilizadas / Estructuras Metalorgánicas Idioma: En Revista: Int J Biol Macromol Año: 2021 Tipo del documento: Article Pais de publicación: Países Bajos