Lipase-catalyzed synthesis of chiral triglycerides

• Published in: Journal of the American Oil Chemists' Society 1998-11, Vol.75 (11), p.1513-1517
• Main Authors: Chandler, I.C, Quinlan, P.T, McNeill, G.P
• Format: Article
• Language: English
• Subjects: Acidolysis; Bioconversions. Hemisynthesis; Biological and medical sciences; Biosynthesis; Biotechnology; Catalysis; chain length; Chemical reactions; Chemical synthesis; chiral; Composition effects; Enantiomers; Enzyme immobilization; Fatty acid composition; Fatty acids; free fatty acid; Fundamental and applied biological sciences. Psychology; Glycerol; High performance liquid chromatography; Lipase; Liquid chromatography; Mathematical models; Methods. Procedures. Technologies; Mixtures; NMR; Nuclear magnetic resonance; Nuclear magnetic resonance spectroscopy; Oleic acid; Reaction kinetics; Reaction products; Rhizomucor miehei; Selectivity; solvent type; Solvents; source organism; Stereoselectivity; triacylglycerol lipase; triglyceride; Triglycerides; Water activity
• ISSN: 0003-021X; 1558-9331
• DOI: 10.1007/s11746-998-0087-7

Under certain reaction conditions, the acidolysis of tripalmitin with oleic acid using immobilized lipase from Rhizomucor miehei resulted in a higher level of monosubstituted oleoyldipalmitoyl (OPP) triglycerides than had been predicted according to kinetic modeling. The reaction products were subjected to chiral analysis by high‐performance liquid chromatography (HPLC), which indicated that the enzyme was more active at the sn‐1 position of the triglyceride than at the sn‐3 position, resulting in synthesis of the chiral triglyceride 1‐oleoyl‐2,3‐dipalmitoyl‐sn‐glycerol. A kinetic model was developed and was correlated with the HPLC method to provide a simple means to predict the stereoselectivity of lipase‐catalyzed reactions. By using the model, the stereoselectivity of immobilized Rhizomucor miehei lipase was found to depend strongly on the initial water activity (aw) of the reaction mixture, with greater selectivity occurring at lower aw. The sn‐1 selectivity was essentially maintained using various solvents, or without solvent, when aw was kept constantly low. Variation in the fatty acid composition of the triglyceride indicated that shorter‐chain fatty acids result in greater stereoselectivity, while variation of the chainlength of the free fatty acid indicated an enhancement by the longest chainlength. The stereoselectivity of this lipase was confirmed using a new 13C nuclear magnetic resonance method. By using immobilized R. miehei lipase at low aw approximately 80% of the chiral triglyceride found in the reaction mixture was the sn‐1 enantiomer, at high reaction conversion.