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http://dx.doi.org/10.5658/WOOD.2010.38.3.251

Immobilization of Cellulases from Fomitopsis pinicola and Their Changes of Enzymatic Characteristics  

Shin, Keum (Department of Forest Products and Biotechnology, College of Forest Science, Kookmin University)
Kim, Tae-Jong (Department of Forest Products and Biotechnology, College of Forest Science, Kookmin University)
Kim, Young-Kyoon (Department of Forest Products and Biotechnology, College of Forest Science, Kookmin University)
Kim, Yeong-Suk (Department of Forest Products and Biotechnology, College of Forest Science, Kookmin University)
Publication Information
Journal of the Korean Wood Science and Technology / v.38, no.3, 2010 , pp. 251-261 More about this Journal
Abstract
Cellulase from Formiptosis pinicola KMJ812 is an efficient cellulose degradation enzyme complex, especially with a high ${\beta}$-glucosidase activity. In this study, the change in enzymatic characteristics by immobilization and the reduction of immobilized enzyme activity by repeated usages were evaluated using cellulases from F. pinicola KMJ812. Among tested four resins, Duolite A568 resin had the best enzyme activity yield with 61.7% cellulase activity and 64.4% ${\beta}$- glucosidase activity during the cellulase immobilization. The best reaction temperature was $55^{\circ}C$ for both cellulase and ${\beta}$-glucosidase activities which were higher than the unimmobilized soluble cellulases. The best reaction pH was 4.0 for cellulase activity which was a little more basic than a soluble form and 4.5 for ${\beta}$-glucosidase activity. The immobilized cellulase activity was remained 98% of the beginning activity after 72 h incubation at $50^{\circ}C$ and 50% of the beginning activity after eight times usage at $50^{\circ}C$.
Keywords
immobilization; Duolite A568; cellulase; ${\beta}$-glucosidase;
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