Triglyceride Interesterification by Lipases: 2. Reaction parameters for the reduction of trisaturated impurities and diglycerides in batch reactions
- 1 January 1991
- journal article
- research article
- Published by Taylor & Francis in Biocatalysis
- Vol. 5 (2), 145-162
- https://doi.org/10.3109/10242429109014863
Abstract
A model system consisting of pure triolein and palmitic acid and LipozymeTM, an immobilized lipase (E.C. 3.1.1.3.). has been used to determine the effects of various reaction parameters on the reaction rate and the formation of by-products in the interesterification reaction. The goal was to minimize the level of diglycerides and eliminate trisaturated triglycerides at an endpoint chosen so that the results could be applied to the production of cocoa butter substitutes. The levels of diglycerides, which are essential reaction intermediates, and trisaturated glycerides, which are believed to be formed as a result of spontaneous acyl migration of mono- and diglyceride intermediates, were determined at a defined endpoint. A lag period was observed in which no tripalmitate was formed. The content of Lipozyme used was the most powerful factor in eliminating tripalmitate formation and reducing diglycerides; by using large quantities of Lipozyme, the reaction reached the endpoint before the tripalmitate formation became measurable and low levels of diglycerides were formed. The effects of varying the ratio of palmitic acid to triolein were investigated. A complex relationship between the ratio of substrate components emerged in which the diglyceride content increased with increasing triolein concentration and the tripalmitate content was lowest at a molar ratio of palmitic acid to triolein of 3.5. The reaction was run at 70, 80, and 90°C; best results were obtained at 70°. The water activity of the reaction was adjusted prior to catalysis and maintained during the reaction by equilibrating the reaction mixture and enzyme and running the reaction in an atmosphere of controlled water activity. A direct relationship between diglycerides and water activity was observed, and the level of tripalmitate formed corresponded to the time required to reach the endpoint. The reaction system was tested using ethyl palmitate instead of palmitic acid as acyl donor; the diglyceride content again increased with increasing water activity, but larger amounts of diglycerides were formed. Much shorter reaction times were required, with small quantities of tripalmitate formed.Keywords
This publication has 39 references indexed in Scilit:
- A serine protease triad forms the catalytic centre of a triacylglycerol lipaseNature, 1990
- Production of glycerides from glycerol and fatty acid by immobilized lipases in non‐aqueous mediaBiotechnology & Bioengineering, 1990
- Triglyceride interesterification by lipases. 1. Cocoa butter equivalents from a fraction of palm oilJournal of Oil & Fat Industries, 1990
- Solvent free triglyceride synthesis using lipozymeTM IM-20Biotechnology Letters, 1988
- Enzymatic transesterification of a triglyceride in microemulsionsColloid and Polymer Science, 1987
- Lipase‐catalyzed ester exchange reactions in organic media with controlled humidityBiotechnology & Bioengineering, 1987
- Humidity fixed points of binary saturated aqueous solutionsJournal of Research of the National Bureau of Standards Section A: Physics and Chemistry, 1977
- Mechanism of pancreatic lipase action. 1. Interfacial activation of pancreatic lipaseBiochemistry, 1976
- 152. Acyl migration in diglyceridesJournal of the Chemical Society, 1959
- Wanderung von Acyl bei den GlyceridenBerichte der deutschen chemischen Gesellschaft (A and B Series), 1920