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Facile Construction of Synergistic β-Glucosidase and Cellulase Sequential Co-immobilization System for Enhanced Biomass Conversion
Ist Teil von
Chinese journal of polymer science, 2020-12, Vol.38 (12), p.1277-1285
Ort / Verlag
Beijing: Chinese Chemical Society and Institute of Chemistry, CAS
Erscheinungsjahr
2020
Quelle
SpringerLink
Beschreibungen/Notizen
Converting renewable cellulose into glucose
via
cellulase catalysis for further production of biofuel has been recognized as one of the most promising ways for solving energy crisis. However, the hydrolysis performance of immobilized cellulase was not satisfactory for practical application due to the reduced catalytic efficiency and lack of
β
-glucosidase (BG) component in cellulase. Here, a facile method was developed to sequentially co-immobilize BG and cellulase by polymeric microparticles with hierarchical structure. In this strategy, BG was firstly entrapped into the cross-linked poly(ethylene glycol) (PEG) microparticles
via
inverse emulsion polymerization initiated by isopropyl thioxanthone (ITX) under the irradiation of visible light, leaving the formed ITX semi-pinacol (ITXSP) dormant groups on surface of BG-loaded microparticles, which could be further activated by visible light irradiation and initiated a graft polymerization to introduce poly(acrylic acid) (PAA) brush on the PEG core. After that, cellulase was covalently bonded on the PAA chains
via
carbodiimide reaction. The synergic effect of BG and cellulase was verified in the dual enzyme immobilization system, which led to a better stability at a wide range of temperature and pH than free enzymes. The dual enzymes system exhibited excellent reusability, which could retain 75% and 57% of the initial activity after 10 cycles of hydrolysis of carboxyl methyl cellulose and 5 cycles of hydrolysis of filter paper, respectively, indicative of the potential in biofuel areas in a cost-effective manner.