Fructose Laurate Enzymatic Synthesis by Resin D301 Immobilized Candida sp 99-125 Lipase

Sugar ester synthesis is catalyzed by the immobilized lipase of resin D301, which is obtained from immobilizing free Candida sp. lipase on the weakly basic anion exchange resin D301. This reaction requires butanone as a solvent, as well as fructose and lauric acid substrates. In this study, we designed and optimized an orthogonal immobilized enzyme catalyzed synthesis. The optimized reaction is incubated at 50 degrees C for 24 h with 20 mL of methyl ethyl ketone as a solvent and a rotation speed of 180 rpm. The optimal molecular sieve concentration was 75 g/L, the substrate ratio was 1.5:1 and the enzyme concentration was 10 g/L. Under these optimal conditions, the maximum relative per cent conversion of lauric acid was 60 % with the di-fructose laurate substrate. The products were analyzed by TLC and (13)C NMR and the resulting products were 1-beta-mono-D-fructopyranose laurate, which had an R(f) of 0.44 and 1,6-beta-di-D-fructopyranose laurate, which had an R(f) of 0.79. Compared to traditional reactions in solvents, the solvent-free system was easier to separate and purify, which made the procedure both more cost and time effective.