Co-immobilization of dextransucrase and dextranase in alginate

dc.contributor.authorOlcer, Zehra
dc.contributor.authorTanriseven, Aziz
dc.date.accessioned2025-10-29T11:23:31Z
dc.date.issued2010
dc.departmentFakülteler, Mühendislik Fakültesi, Biyomühendislik Bölümü
dc.description.abstractDextransucrase from Leuconostoc mesenteroides and dextranase from Penicillium lilacinum were co-immobilized and used to produce isomaltooligosaccharides from sucrose. The enzymes were co-immobilized by encapsulating soluble dextransucrase and dextranase covalently attached to Eupergit C in alginate (beads, fibers, and capsules). The alginate capsule co-immobilization was done in the presence of soluble starch and resulted in a high immobilization yield (71%), and the enzymes retained their activities during 20 repeated batch reactions and for a month in storage at 4 degrees C. The presence of starch was essential for the stability of dextransucrase in alginate capsules. Furthermore, it is important that the dextranase be pre-immobilized prior to alginate capsule co-immobilization to prevent dextranase leakage and inactivation of dextransucrase. The co-immobilized enzymes formed oligosaccharides from sucrose, which can be used as prebiotics. In addition, the oligosaccharides that were produced after the addition of sucrose reacted with the alginate fiber-encapsulted dextransucrase, thus increasing the amount of prebiotics. Co-immobilization in alginate fiber and beads also resulted in high yields (70 and 64%), but enzymatic activities decreased by 74 and 99%, respectively, after a month in storage at 4 C. The newly developed alginate capsule method for co-immobilization of dextransucrase and dextranase is simple yet effective and has the potential for industrial-scale production of isomaltooligosaccharides. (C) 2010 Elsevier Ltd. All rights reserved.
dc.description.sponsorshipScientific & Technological Research Council, Turkey [104M385]
dc.description.sponsorshipThis work was supported by a grant, 104M385, from The Scientific & Technological Research Council, Turkey. The authors acknowledge Novozyme (Bagsvaerd, Denmark) and Roehm GmbH & Co. KG (Darmstadt, Germany) for gifts of Dextranase 50 L and Eupergit C used in this work. The authors are also grateful to Dr. John F. Robyt for the genereous gift of Leuconostoc mesenteroides B-512 FMC-13 Glc strain.
dc.identifier.doi10.1016/j.procbio.2010.06.011
dc.identifier.endpage1651
dc.identifier.issn1359-5113
dc.identifier.issn1873-3298
dc.identifier.issue10
dc.identifier.scopus2-s2.0-77956180776
dc.identifier.scopusqualityQ1
dc.identifier.startpage1645
dc.identifier.urihttps://doi.org/10.1016/j.procbio.2010.06.011
dc.identifier.urihttps://hdl.handle.net/20.500.14854/9496
dc.identifier.volume45
dc.identifier.wosWOS:000282388800007
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier Sci Ltd
dc.relation.ispartofProcess Biochemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20251020
dc.subjectAlginate
dc.subjectCo-immobilization
dc.subjectDextranase
dc.subjectDextransucrase
dc.subjectEupergit C
dc.subjectIsomaltooligosaccharides
dc.titleCo-immobilization of dextransucrase and dextranase in alginate
dc.typeArticle

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