Heterofunctional epoxy support development for immobilization of fructosyltransferase from Pectinex® Ultra SP-L: batch and continuous production of fructo-oligosaccharides. Issue 12 (26th August 2022)
- Record Type:
- Journal Article
- Title:
- Heterofunctional epoxy support development for immobilization of fructosyltransferase from Pectinex® Ultra SP-L: batch and continuous production of fructo-oligosaccharides. Issue 12 (26th August 2022)
- Main Title:
- Heterofunctional epoxy support development for immobilization of fructosyltransferase from Pectinex® Ultra SP-L: batch and continuous production of fructo-oligosaccharides
- Authors:
- Veljković, Milica
Simović, Milica
Banjanac, Katarina
Ćorović, Marija
Milivojević, Ana
Milivojević, Milan
Bezbradica, Dejan - Abstract:
- Abstract : The FTase from Pectinex® Ultra SP-L was immobilized using a newly developed epoxy-Purolite support with amino and epoxy groups. Continuous production of FOS in the air-lift reactor was established for 7 days (52.47% FOS of total carbohydrates). Abstract : In this study, a heterofunctional carrier was obtained by modification of a macroporous polystyrene ion exchange resin with primary amino groups (Purolite® A109) with epichlorohydrin, in view of achieving covalent immobilization of fructosyltransferase (FTase) from a complex enzyme mixture, Pectinex® Ultra SP-L, that is responsible for the synthesis of functionally active fructo-oligosaccharides (FOS). A two-step immobilization protocol, comprising the physical adsorption of FTase performed at pH 4 and subsequent buffer exchange to promote the establishment of covalent bonds at pH 9, was proposed for obtaining a highly active immobilized preparation (243 IU g −1 of support). Additionally, this protocol provided development of a preparation with 20 times more prominent expressed activity of FTase compared to the commercial preparation with predominant pectinase activity. The obtained immobilized preparation was further tested in batch and air-lift reactor systems for FOS synthesis, yielding 52.8% and 54.7% of FOS in total carbohydrates, respectively. Finally, the continuous production of FOS in the air-lift reactor was established for 7 days, with an average FOS yield of 52.5%. Accordingly, it is demonstrated thatAbstract : The FTase from Pectinex® Ultra SP-L was immobilized using a newly developed epoxy-Purolite support with amino and epoxy groups. Continuous production of FOS in the air-lift reactor was established for 7 days (52.47% FOS of total carbohydrates). Abstract : In this study, a heterofunctional carrier was obtained by modification of a macroporous polystyrene ion exchange resin with primary amino groups (Purolite® A109) with epichlorohydrin, in view of achieving covalent immobilization of fructosyltransferase (FTase) from a complex enzyme mixture, Pectinex® Ultra SP-L, that is responsible for the synthesis of functionally active fructo-oligosaccharides (FOS). A two-step immobilization protocol, comprising the physical adsorption of FTase performed at pH 4 and subsequent buffer exchange to promote the establishment of covalent bonds at pH 9, was proposed for obtaining a highly active immobilized preparation (243 IU g −1 of support). Additionally, this protocol provided development of a preparation with 20 times more prominent expressed activity of FTase compared to the commercial preparation with predominant pectinase activity. The obtained immobilized preparation was further tested in batch and air-lift reactor systems for FOS synthesis, yielding 52.8% and 54.7% of FOS in total carbohydrates, respectively. Finally, the continuous production of FOS in the air-lift reactor was established for 7 days, with an average FOS yield of 52.5%. Accordingly, it is demonstrated that the immobilization process enabled the development of preparations with exceptional potential for industrial implementation. … (more)
- Is Part Of:
- Reaction chemistry & engineering. Volume 7:Issue 12(2022)
- Journal:
- Reaction chemistry & engineering
- Issue:
- Volume 7:Issue 12(2022)
- Issue Display:
- Volume 7, Issue 12 (2022)
- Year:
- 2022
- Volume:
- 7
- Issue:
- 12
- Issue Sort Value:
- 2022-0007-0012-0000
- Page Start:
- 2518
- Page End:
- 2526
- Publication Date:
- 2022-08-26
- Subjects:
- Reaction mechanisms (Chemistry) -- Periodicals
Chemical engineering -- Periodicals
Chemical engineering
Reaction mechanisms (Chemistry)
Periodicals
547.705 - Journal URLs:
- http://pubs.rsc.org/en/content/articlelanding/2016/re/c6re90001a#!divAbstract ↗
http://pubs.rsc.org/en/journals/journalissues/re#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2re00182a ↗
- Languages:
- English
- ISSNs:
- 2058-9883
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7300.263610
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24358.xml