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  4. Immobilization of piromyces rhizinflata β-glucanase on poly(dimethylsiloxane) and Si wafer and prediction of optimum reaction for enzyme activity
 
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Immobilization of piromyces rhizinflata β-glucanase on poly(dimethylsiloxane) and Si wafer and prediction of optimum reaction for enzyme activity

Journal
Preparative Biochemistry and Biotechnology
Journal Volume
45
Journal Issue
1
Pages
42-55
Date Issued
2015
Author(s)
Tseng, C.-W.
Yeh, D.-J.
Chuang, F.-T.
Lee, S.-C.
JE-RUEI LIU  
DOI
10.1080/10826068.2014.887579
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-84906057285&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/393643
Abstract
EglA, a β-1,4-glucanase isolated from the ruminal fungus Piromyces rhizinflata, shows promise in a wide range of industrial applications because of its broad substrate specificity. In this study, EglA was immobilized on different supporting materials including poly(dimethylsiloxane) (PDMS), Si wafer, textured Si wafer, and indium tin oxide-coated (ITO-coated) glass. The binding abilities of PDMS and Si wafer toward EglA were significantly higher than those of the other supporting materials. The optimized temperature and pH conditions for EglA immobilized on PDMS and on Si wafer were further determined by a response surface methodology (RSM) combined with a central composite design (CCD). The results indicated that the optimum pH and temperature values as well as the specific β-glucanase activity of EglA on PDMS were higher than those of free-form EglA. In addition, EglA immobilized on PDMS could be reused up to six times with detectable enzyme activity, while the enzyme activity of Eg1A on Si wafer was undetectable after three cycles of enzyme reaction. The results demonstrate that PDMS is an attractive supporting material for EglA immobilization and could be developed into an enzyme chip or enzyme tube for potential industrial applications.
SDGs

[SDGs]SDG9

Type
journal article

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