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Oligosaccharides production and purification from barley bran using sequential supercritical CO2 extraction, subcritical water hydrolysis and membrane filtration

  • Author / Creator
    Aghashahi, Azadeh
  • Barley bran is a by-product of the food industry, and a good source of lipid, protein and fiber. In this thesis research, fractionation of barley bran was carried out to remove lipid, starch and protein to obtain a sample enriched in fiber, specially arabinoxylan. Fiber concentrate was used for further hydrolysis, targeting the production of xylooligosaccharides (XOS) with degree of polymerization 2-4. Lipid was extracted using supercritical CO2, followed by enzymatic hydrolysis to remove starch. Defatted bran with 0.3% lipid was obtained. Defatted-destarched bran had 1% starch and 26.3% db arabinoxylan. Subcritical water (SCW) was used as an environmentally friendly approach to hydrolyse defatted-destarched bran. Temperature had a significant effect on the XOS production. The highest XOS content was produced at 180℃, where 112.5 mg of total XOS was obtained within 30 min, with no significant difference after 60 min hydrolysis. Deproteinized bran with 42.2% db arabinoxylan was hydrolyzed using SCW at 180℃/50 bar/30 min. Amounts of 100.9, 120.6, 112.4 and 334 mg of xylobiose, xylotriose, xylotetraose and total XOS were obtained in the hydrolysate. Deproteinized bran was also treated using enzymatic hydrolysis with endo-xylanase. Maximum amount of total XOS was 21.11 mg obtained using 10 U of enzyme at 40℃, pH of 4.5 after 4 h incubation. The recovery of total XOS from initial xylan of deproteinized bran was 78.4 and 45.1% for SCW and enzymatic hydrolysis, respectively. Purification of deproteinized bran SCW hydrolysate was performed using ultrafiltration with 1 kDa membrane to remove compounds with high molecular weight. In total, 68% of initial total XOS was recovered after passing through 1 kDa membrane. This permeate was treated by activated carbon adsorption (10% w/w) to remove monomers (arabinose and xylose) from XOS. Activated carbon was washed with aqueous ethanol solutions (15 and 30% v/v) to liberate the adsorbed XOS. Finally, 55% of xylose and 51% of arabinose were removed and 52% of total XOS was recovered in the ethanol fraction. The results suggest that SCW hydrolysis is a promising method to produce XOS from barley bran in a short time with higher recovery than the enzymatic hydrolysis. The obtained XOS has potential use in the functional food products as prebiotics.

  • Subjects / Keywords
  • Graduation date
    Spring 2020
  • Type of Item
    Thesis
  • Degree
    Master of Science
  • DOI
    https://doi.org/10.7939/r3-8fb7-2w30
  • License
    Permission is hereby granted to the University of Alberta Libraries to reproduce single copies of this thesis and to lend or sell such copies for private, scholarly or scientific research purposes only. Where the thesis is converted to, or otherwise made available in digital form, the University of Alberta will advise potential users of the thesis of these terms. The author reserves all other publication and other rights in association with the copyright in the thesis and, except as herein before provided, neither the thesis nor any substantial portion thereof may be printed or otherwise reproduced in any material form whatsoever without the author's prior written permission.