Discrimination against diacylglycerol ethers in lipase-catalysed ethanolysis of shark liver oil

This is the author’s version of a work that was accepted for publication in Food Chemistry. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have be...

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Bibliographic Details
Published in:Food Chemistry
Main Authors: Fernández, Óscar, Vázquez, Luis Nuñez, Reglero, Guillermo, Torres, Carlos F.
Other Authors: UAM. Departamento de Química Física Aplicada
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier B.V 2014
Subjects:
Online Access:http://hdl.handle.net/10486/660729
https://doi.org/10.1016/j.foodchem.2012.08.004
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Summary:This is the author’s version of a work that was accepted for publication in Food Chemistry. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Food Chemistry, 136 (2013): 464–471. DOI:10.1016/j.foodchem.2012.08.004 Lipase-catalysed ethanolysis of squalene-free shark liver oil was investigated. The mentioned shark liver oil was comprised mainly of diacylglycerol ether and triacylglycerols. In order to test discrimination against diacylglycerol ether, up to 10 different lipases were compared. The ratio of oil to ethanol and lipase stability were also evaluated. Surprisingly, lipase from Pseudomonas stutzeri was the fastest biocatalyst among all assayed, although poor discrimination against diacylglycerol ether was observed. The best results in terms of selectivity and stability were obtained with immobilised lipase from Candida antarctica (Novozym 435). Ethanolysis reaction after 24 h in the presence of Novozym 435 produced total disappearance of triacylglycerol and a final reaction mixture comprised mainly of diacylglycerol ethers (10.6%), monoacylglycerol ethers (32.9%) and fatty acid ethyl esters (46.0%). In addition, when an excess of ethanol was used, diacylglycerol ethers completely disappeared after 15 h, giving a final product mainly composed of monoacylglycerol ethers (36.6%) and fatty acid ethyl esters (46.4%). This work was supported by Comunidad Autónoma de Madrid (ALIBIRD, Project No. S2009/AGR-1469) and Consolider-Ingenio FUN-C-FOOD (CSD2007-00063).