Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients

Problems derived from obesity and overweight have recently promoted the development of fat substitutes and other low-calorie foods. On the one hand, fats with short- and medium-chain fatty acids are a source of quick energy, easily hydrolyzable and hardly stored as fat. Furthermore, 1,3-diacylglycer...

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Published in:Frontiers in Bioengineering and Biotechnology
Main Authors: Vázquez de Frutos, Luis, González, N., Reglero Rada, Guillermo J., Torres Olivares, Carlos Fernando
Other Authors: UAM. Departamento de Química Física Aplicada, Ingredientes alimentarios funcionales (EXP C-064)
Format: Article in Journal/Newspaper
Language:English
Published: Frontiers Media 2017
Subjects:
Online Access:http://hdl.handle.net/10486/676547
https://doi.org/10.3389/fbioe.2016.00006
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author Vázquez de Frutos, Luis
González, N.
Reglero Rada, Guillermo J.
Torres Olivares, Carlos Fernando
author2 UAM. Departamento de Química Física Aplicada
Ingredientes alimentarios funcionales (EXP C-064)
author_facet Vázquez de Frutos, Luis
González, N.
Reglero Rada, Guillermo J.
Torres Olivares, Carlos Fernando
author_sort Vázquez de Frutos, Luis
collection Universidad Autónoma de Madrid (UAM): Biblos-e Archivo
container_title Frontiers in Bioengineering and Biotechnology
container_volume 4
description Problems derived from obesity and overweight have recently promoted the development of fat substitutes and other low-calorie foods. On the one hand, fats with short- and medium-chain fatty acids are a source of quick energy, easily hydrolyzable and hardly stored as fat. Furthermore, 1,3-diacylglycerols are not hydrolyzed to 2-monoacylglycerols in the gastrointestinal tract, reducing the formation of chylomicron and lowers the serum level of triacylglycerols by decreasing its resynthesis in the enterocyte. In this work, these two effects were combined to synthesize short- and medium-chain 1,3-diacylglycerols, leading to a product with great potential as for their low-calorie properties. Lipase-catalyzed transesterification reactions were performed between short- and medium-chain fatty acid ethyl esters and glycerol. Different variables were investigated, such as the type of biocatalyst, the molar ratio FAEE:glycerol, the adsorption of glycerol on silica gel, or the addition of lecithin. Best reaction conditions were evaluated considering the percentage of 1,3-DAG produced and the reaction rate. Except Novozym 435 (Candida antarctica), other lipases required the adsorption of glycerol on silica gel to form acylglycerols. Lipases that gave the best results with adsorption were Novozym 435 and Lipozyme RM IM (Rhizomucor miehei) with 52 and 60.7% DAG at 32 h, respectively. Because of its specificity for sn-1 and sn-3 positions, lipases leading to a higher proportion of 1,3-DAG vs. 1,2-DAG were Lipozyme RM IM (39.8 and 20.9%, respectively) and Lipase PLG (Alcaligenes sp.) (35.9 and 19.3%, respectively). By adding 1% (w/w) of lecithin to the reaction with Novozym 435 and raw glycerol, the reaction rate was considerably increased from 41.7 to 52.8% DAG at 24 h This work was supported by the Comunidad Autónoma de Madrid: ALIBIRD, project number S2013/ABI-2728
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Comunidad de Madrid. S2013/ABI-2728/ALIBIRD
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spelling ftuamadrid:oai:repositorio.uam.es:10486/676547 2025-04-13T14:08:37+00:00 Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients Vázquez de Frutos, Luis González, N. Reglero Rada, Guillermo J. Torres Olivares, Carlos Fernando UAM. Departamento de Química Física Aplicada Ingredientes alimentarios funcionales (EXP C-064) 2017-01-24T15:21:18Z application/pdf http://hdl.handle.net/10486/676547 https://doi.org/10.3389/fbioe.2016.00006 eng eng Frontiers Media Frontiers in Bioengineering and Biotechnology http://dx.doi.org/10.3389/fbioe.2016.00006 Comunidad de Madrid. S2013/ABI-2728/ALIBIRD Frontiers in Bioengineering and Biotechnology 4 (2016): 6 http://hdl.handle.net/10486/676547 doi:10.3389/fbioe.2016.00006 6 4 © 2016 Vázquez, González, Reglero and Torres Reconocimiento openAccess Diacylglycerol Fatty acid ethyl ester Lipase Medium-chain fatty acid Transesterification Química article info:eu-repo/semantics/publishedVersion 2017 ftuamadrid https://doi.org/10.3389/fbioe.2016.00006 2025-03-17T08:50:37Z Problems derived from obesity and overweight have recently promoted the development of fat substitutes and other low-calorie foods. On the one hand, fats with short- and medium-chain fatty acids are a source of quick energy, easily hydrolyzable and hardly stored as fat. Furthermore, 1,3-diacylglycerols are not hydrolyzed to 2-monoacylglycerols in the gastrointestinal tract, reducing the formation of chylomicron and lowers the serum level of triacylglycerols by decreasing its resynthesis in the enterocyte. In this work, these two effects were combined to synthesize short- and medium-chain 1,3-diacylglycerols, leading to a product with great potential as for their low-calorie properties. Lipase-catalyzed transesterification reactions were performed between short- and medium-chain fatty acid ethyl esters and glycerol. Different variables were investigated, such as the type of biocatalyst, the molar ratio FAEE:glycerol, the adsorption of glycerol on silica gel, or the addition of lecithin. Best reaction conditions were evaluated considering the percentage of 1,3-DAG produced and the reaction rate. Except Novozym 435 (Candida antarctica), other lipases required the adsorption of glycerol on silica gel to form acylglycerols. Lipases that gave the best results with adsorption were Novozym 435 and Lipozyme RM IM (Rhizomucor miehei) with 52 and 60.7% DAG at 32 h, respectively. Because of its specificity for sn-1 and sn-3 positions, lipases leading to a higher proportion of 1,3-DAG vs. 1,2-DAG were Lipozyme RM IM (39.8 and 20.9%, respectively) and Lipase PLG (Alcaligenes sp.) (35.9 and 19.3%, respectively). By adding 1% (w/w) of lecithin to the reaction with Novozym 435 and raw glycerol, the reaction rate was considerably increased from 41.7 to 52.8% DAG at 24 h This work was supported by the Comunidad Autónoma de Madrid: ALIBIRD, project number S2013/ABI-2728 Article in Journal/Newspaper Antarc* Antarctica Universidad Autónoma de Madrid (UAM): Biblos-e Archivo Frontiers in Bioengineering and Biotechnology 4
spellingShingle Diacylglycerol
Fatty acid ethyl ester
Lipase
Medium-chain fatty acid
Transesterification
Química
Vázquez de Frutos, Luis
González, N.
Reglero Rada, Guillermo J.
Torres Olivares, Carlos Fernando
Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients
title Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients
title_full Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients
title_fullStr Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients
title_full_unstemmed Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients
title_short Solvent-Free Lipase-Catalyzed Synthesis of Diacylgycerols as Low-Calorie Food Ingredients
title_sort solvent-free lipase-catalyzed synthesis of diacylgycerols as low-calorie food ingredients
topic Diacylglycerol
Fatty acid ethyl ester
Lipase
Medium-chain fatty acid
Transesterification
Química
topic_facet Diacylglycerol
Fatty acid ethyl ester
Lipase
Medium-chain fatty acid
Transesterification
Química
url http://hdl.handle.net/10486/676547
https://doi.org/10.3389/fbioe.2016.00006