Biotechnology Letters, Vol.37, No.3, 691-696, 2015
Chemoenzymatic synthesis of 1,3-dioleoyl-2-palmitoylglycerol
We report the synthesis of 1,3-dioleoyl-2-palmitoylglycerol (OPO) by a three-step method. Vinyl oleate was first synthesized by transvinylation between vinyl acetate and oleic acid. This was further reacted with glycerol at 35 A degrees C for 8 h using 10 % (w/v) Novozym 435 to synthesize 1,3-diolein. The 1,3-diolein content in the crude reaction mixture was 90.8 % and was obtained at 82.3 % (w/w) yield with 98.6 % purity after purification. Finally, OPO was chemically synthesized by reacting purified 1,3-diolein with palmitic acid. 94.8 % OPO was produced in the crude reaction mixture and the regiopurity of OPO after purification was 98.7 % at 90.5 % yield based on positional distribution analysis. This is an innovative approach for the synthesis of 1,3-diolein in a solvent-free system as an alternative to previously presented studies that applied solvent system.
Keywords:Chemoenzymatic synthesis;Diolein;1,3-Dioleoyl-2-palmitoylglycerol;Purification;Vinyl oleate