Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/4243
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dc.contributor.authorNguyễn, Phú Cường-
dc.contributor.authorNguyễn, Minh Thủy-
dc.contributor.authorPark, Kwan-Hwa-
dc.contributor.authorPark, Jong-Tae-
dc.contributor.authorKim, Do-Gyun-
dc.contributor.authorOh, Il-Nam-
dc.contributor.authorLee, Wang-Hee-
dc.date.accessioned2018-09-14T07:52:42Z-
dc.date.available2018-09-14T07:52:42Z-
dc.date.issued2016-
dc.identifier.urihttp://dspace.ctu.edu.vn/jspui/handle/123456789/4243-
dc.description.abstractMaltodextrin in specific length is of great interest because of its wide industrial applications. Previously, we have proven that Pyrococcus furiosus thermostable amylase (PFTA) produces high purity maltoheptaose (G7) from ┐-cyclodextrin (CD) at early reaction time. In this study, an optimal continuous process for pure maltodextrin production from CDs using PFTA with immobilization in a packed-bed reactor (PBR) was developed. For testing PBR, ┐-CD was used as a substrate to produce G7. The activity of immobilized PFTA in PBR retained 85% of the initial activity after 6 cycles, and the product purity was unchanged. The optimal conditions for the maximized G7-purity of 96.3% were predicted at 4.7 mL/min of flow, 1.1% substrate and 48.7 ◦C. Maltohexaose and maltooctaose, 92% and 97% purity respectively, were produced from CDs at the similar condition as well. Through this study, we successfully demonstrated the possibility of large-scale continuous production of pure maltodextrins from CDs.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesProcess Biochemistry;51 .- p.282–287-
dc.subjectPure maltodextrinvi_VN
dc.subjectPacked-bed reactorvi_VN
dc.subjectContinuous productionvi_VN
dc.subjectPyrococcus furiosus thermostable amylasevi_VN
dc.subjectEnzyme immobilizationvi_VN
dc.subjectCyclodextrinvi_VN
dc.titleContinuous production of pure maltodextrin from cyclodextrin using immobilized Pyrococcus furiosus thermostable amylasevi_VN
dc.typeArticlevi_VN
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