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Enzymatic synthesis of structured lipids: Transesterification of triolein and caprylic acid ethyl ester
Author(s) -
Huang KuanHsiang,
Akoh Casimir C.
Publication year - 1996
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/bf02523903
Subject(s) - triolein , transesterification , caprylic acid , lipase , chemistry , rhizomucor miehei , chromatography , organic chemistry , triacylglycerol lipase , fatty acid , enzyme , catalysis
Structured lipids were successfully synthesized by lipase‐catalyzed transesterification (ester interchange) of caprylic acid ethyl ester and triolein. The transesterification reaction was carried out in organic solvent as reaction media. Eight commercially‐available lipases (10% w/w substrates) were screened for their ability to synthesize structured lipid by incubating with 100 mg triolein and 78.0 mg caprylic acid ethyl ester in 3 mL hexane at 45°C for 24 h. The products were analyzed by reverse‐phase high‐performance liquid chromatography with evaporative light‐scattering detector. Immobilized lipase IM60 from Rhizomucor miehei converted most triolein into structured lipids (41.7% dicapryloolein, 46.0% monocapryloolein, and 12.3% unreacted triolein). However, lipase SP435 from Candida antarctica had a higher activity at higher temperature. The reaction catalyzed by lipase SP435 yielded 62.0% dicapryloolein, 33.5% monocapryloolein, and 4.5% unreacted triolein at 55°C. Time course, incubation media, added water, and substrate concentration were also investigated in this study. The results suggest that lipase‐catalyzed transesterification of long‐chain triglycerides and medium‐chain fatty acid ethyl ester is feasible to synthesize structured lipids.