Related Experiment Video
Updated: Apr 18, 2026

Author Spotlight: Employing Green-Chemistry Principles for Safe and Sustainable Synthesis of Biodiesels
Published on: April 19, 2024
Enzyme-assisted process for DAG synthesis in edible oils
Daniela von der Haar1, Andreas Stäbler1, Rolf Wichmann2
1Fraunhofer Institute for Process Engineering and Packaging, Department of Process Development for Plant Raw Materials, Giggenhauser Str. 35, 85354 Freising, Germany.
Abstract:
This study deals with the enzymatic synthesis of diacylglycerols in rapeseed oil by the esterification of free fatty acids and monoacylglycerols. As enzymatic reactions are influenced by many factors, a statistical design of experiments was conducted to investigate the enrichment of diacylglycerols, systematically. Simultaneously, the investigated method contributes to the refining process, as the amount of free fatty acids could be reduced significantly from 2% to 0.3%. Utilizing an immobilized lipase from Rhizomucormiehei, a maximum diacylglycerol content of 23% was obtained, after optimization. By washing with iso-propanol and hexane the immobilised lipase could be reused in 14 consecutive batches. In addition, glycerol was proven to be an alternative to MAG as acyl-group acceptor. However, the diacylglycerol enrichment was not accomplished in the same yields as for monoacylglycerols. Summarizing, the present study revealed the potential of an enzymatic diacylglycerol synthesis in edible oils as a suitable alternative to conventional processes also enabling the reduction of free fatty acids in crude oils.
Related Concept Videos
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...

