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Permanent link (DOI): https://doi.org/10.7939/R3JQ02

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Improved Approaches to Separate High-Value Phospholipids from Egg Yolk Open Access

Descriptions

Other title
Subject/Keyword
low denisty lipoprotein
emulsion
phosphatidylcholine
yolk
phospholipids
extraction
polysaccharide
supercritical carbon dioxide
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Navidghasemizad, Sahar
Supervisor and department
Wu, Jianping (Agricultural, Food and Nutritional Science)
Temelli, Feral (Agricultural, Food and Nutritional Science)
Examining committee member and department
Curtis, Jonathan (Agricultural, Food and Nutritional Science)
Li-Chan, Eunice (Land and Food Systems, the University of British Columbia)
Unsworth, Larry (Chemical and Materials Engineering)
Department
Department of Agricultural, Food, and Nutritional Science
Specialization
Food Science and Technology
Date accepted
2013-01-31T09:47:11Z
Graduation date
2013-06
Degree
Doctor of Philosophy
Degree level
Doctoral
Abstract
Egg yolk contains approximately 10% (w/w) phospholipids (PL), of which about 70% is phosphatidylcholine (PC). Conventional methods of PL extraction from egg yolk involve using hazardous organic solvents. Supercritical carbon dioxide (SC-CO2), as a "green" solvent, had been applied for the extraction of PL from egg yolk but resulted in limited success due to low recovery and purity of the final extracted PL. Hydrolysis of egg yolk after soluble proteins removal, referred to as pellet, by a combination of protease and Lipase AY30 reduced emulsion stability evident by larger oil droplets size and higher coalescence index. A cream fraction obtained from Protease P and Lipase AY30 treated egg yolk pellet was subjected to PL extraction using SC-CO2 in the presence of 8% ethanol as a co-solvent. The enzymatic treatment with Protease P and Lipase AY30 significantly improved the recovery of PC from 47% in dry yolk to 85%, 70% and 61% for dry, intermediate-moisture cream (20%), and “as is” cream (45% moisture), respectively, based on initial yolk weight. A higher purity of PC and PL (84% and 103%) was obtained by using hydrolysed pellet with the intermediate moisture content (20%), compared to dried egg yolk sample. Low-density lipoproteins (LDL) contain about 90% of PL from egg yolk. Possible interaction between egg yolk components and polysaccharides can be a potential technique for LDL separation. A simple method was proposed to isolate LDL from egg yolk using 0.2% to 0.6% xanthan gum at egg yolk natural pH. The mechanism of LDL separation with xanthan gum was suggested to be a combination of different interactions such initial electrostatic and hydrophobic forces and physical properties of the polysaccharide and its complex with egg yolk LDL such as shear thinning behaviour of xanthan gum solution and density difference of LDL-xanthan gum complexes. PL is a high-value component from egg yolk with potential applications in pharmaceutical and nutraceutical industries. Developing methods to improve the recovery and purity of PC and PL from egg yolk while eliminating hazardous organic solvents use will help to protect the environment and enhance food safety.
Language
English
DOI
doi:10.7939/R3JQ02
Rights
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.
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