English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/10873
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Exportar a otros formatos:


Immobilisation of fructosyltransferase from Aspergillus aculeatus on epoxy-activated Sepabeads EC for the synthesis of fructo-oligosaccharides

AuthorsGhazi, Iraj ; Gómez de Segura, María Aránzazu; Fernández Arrojo, Lucía ; Alcalde Galeote, Miguel ; Yates Buxcey, Malcolm ; Rojas-Cervantes, M. Luisa ; Plou Gasca, Francisco José ; Ballesteros Olmo, Antonio
Pectinex Ultra SP-L
Immobilized enzymes
Issue DateJun-2005
CitationJournal of Molecular Catalysis B: Enzymatic Volume 35, Issues 1–3, 1 August 2005, Pages 19–27
AbstractThe transfructosylating activity present in two commercial pectinase preparations (Pectinex Ultra SP-L, from Aspergillus aculeatus, and Rapidase TF, from Aspergillus niger) was studied. Pectinex Ultra SP-L, which has a high transferase/hydrolase ratio, was covalently immobilised on a polymethacrylate-based polymer (Sepabeads® EC) activated with epoxy groups. The influence of pore volume and average pore size on biocatalyst performance was studied for two of these carriers (Sepabeads EC-EP3 and EC-EP5). Several parameters that affect immobilisation such as buffer concentration, pH and amount (mg) of protein added per gram of support (varied over the range 30:1 to 200:1) were analysed. We found that Pectinex Ultra SP-L can be efficiently immobilised on these supports without adding any external salt or buffer. Using Sepabeads EC-EP5 –whose pore volume (1.67 cm3/g) and pore size (800 nm) are higher than those corresponding to Sepabeads EC-EP3– the activity towards sucrose reached 25.9 U/g biocatalyst. The immobilised fructosyltransferase was applied to the batch synthesis of fructo-oligosaccharides (FOS) using 630 g/l sucrose to shift activity towards transfructosylation in detriment of hydrolysis. The FOS concentration reached a maximum value of 387 g/l after 36 h (240 g/l 1-kestose, 144 g/l nystose and 3 g/l 1(F)-fructofuranosyl-nystose), which corresponds to 61.5% (w/w) of the total carbohydrates in the mixture. The features of these immobilised biocatalysts are very attractive for their application in batch and fixed-bed bioreactors.
Description9 pages, 7 figures.-- Printed version published Aug 1, 2005.
Publisher version (URL)http://dx.doi.org/10.1016/j.molcatb.2005.04.013
Appears in Collections:(ICP) Artículos
Files in This Item:
File Description SizeFormat 
postprint-GHAZIetal.pdf740,49 kBAdobe PDFThumbnail
Show full item record
Review this work

Related articles:

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.