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Bioprocess Biosyst Eng ; 40(1): 9-22, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27534411

ABSTRACT

In the present study, Trichoderma reesei cellulase was covalently immobilized on chitosan-coated magnetic nanoparticles using glutaraldehyde as a coupling agent. The average diameter of magnetic nanoparticles before and after enzyme immobilization was about 8 and 10 nm, respectively. The immobilized enzyme retained about 37 % of its initial activity, and also showed better thermal and storage stability than free enzyme. Immobilized cellulase retained about 80 % of its activity after 15 cycles of carboxymethylcellulose hydrolysis and was easily separated with the application of an external magnetic field. However, in this reaction, K m was increased eight times. The immobilized enzyme was able to hydrolyze lignocellulosic material from Agave atrovirens leaves with yield close to the amount detected with free enzyme and it was re-used in vegetal material conversion up to four cycles with 50 % of activity decrease. This provides an opportunity to reduce the enzyme consumption during lignocellulosic material saccharification for bioethanol production.


Subject(s)
Agave/chemistry , Biomass , Cellulases/chemistry , Chitosan/chemistry , Fungal Proteins/chemistry , Lignin/chemistry , Magnetite Nanoparticles/chemistry , Trichoderma/enzymology , Enzymes, Immobilized/chemistry , Hydrolysis
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