Enzymatic synthesis of high‐purity structured lipids with caprylic acid at 1,3‐positions and polyunsaturated fatty acid at 2‐position

Abstract

AbstractWe attempted to synthesize high‐purity structured triacylglycerols (TAG) with caprylic acid (CA) at the 1,3‐positions and a polyunsaturated fatty acid (PUFA) at the 2‐position by a two‐step enzymatic method. The first step was synthesis of TAG of PUFA (TriP), and the second step was acidolysis of TriP with CA. Candida antarctica lipase was effective for the first reaction. When a reaction medium of PUFA/glycerol (3∶1, mol/mol) and 5% immobilized Candida lipase was mixed for 24 h at 40°C and 15 mm Hg, syntheses of TAG of γ‐linolenic, arachidonic, eicosapentaenoic, and docosahexaenoic acids reached 89, 89, 88, and 83%, respectively. In these reactions, the lipase could be used for at least 10 cycles without significant loss of activity. In the second step, the resulting trieicosapentaenoin was acidolyzed at 30°C for 48h with 15 mol parts CA using 7% of immobilized Rhizopus delemar lipase. The CA content in the acylglycerol fraction reached 40 mol%. To increase the content further, the acylglycerols were extracted from the reaction mixture with n‐hexane and were allowed to react again with CA under conditions similar to those of the first acidolysis. After three successive acidolysis reactions, the CA content reached 66 mol%. The content of dicapryloyl‐eicosapentaenoyl‐glycerol reached 86 wt% of acylglycerols, and the ratio of 1,3‐dicapryloyl‐2‐eicosapentaenoyl‐glycerol to 1(3),2‐dicapryloyl‐3(1)‐eicosapentaenoyl‐glycerol was 98∶2 (w/w). In this reaction, the lipase could be used for at least 20 cycles without significant loss of activity. Repeated acidolysis of the other TriP with CA under similar conditions synthesized 1,3‐dicapryloyl‐2‐γ‐linolenoyl‐glycerol, 1,3‐dicapryloyl‐2‐arachidonoyl‐glycerol, and 1,3‐dicapryloyl‐2‐docosahexaenoyl‐glycerol in yields of 58, 87, and 19 wt%, respectively.