Optimized Enzymatic Synthesis of Hesperidin Fatty Acid Esters in a Two-Phase System Containing Ionic Liquid
AbstractResponse surface methodology (RSM) based on a five-level, three-variable central composite design (CCD) was employed for modeling and optimizing the conversion yield of the enzymatic acylation of hesperidin with decanoic acid using immobilized Candida antarctica lipase B (CALB) in a two-phase system containing [bmim]BF4. The three variables studied (molar ratio of hesperidin to decanoic acid, [bmim]BF4/acetone ratio and lipase concentration) significantly affected the conversion yield of acylated hesperidin derivative. Verification experiments confirmed the validity of the predicted model. The lipase showed higher conversion degree in a two-phase system using [bmim]BF4 and acetone compared to that in pure acetone. Under the optimal reaction conditions carried out in a single-step biocatalytic process when the water content was kept lower than 200 ppm, the maximum acylation yield was 53.6%.
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Araújo, M.E.M.B.; Contesini, F.J.; Franco, Y.E.M.; Sawaya, A.C.F.; Alberto, T.G.; Dalfré, N.; Carvalho, P.O. Optimized Enzymatic Synthesis of Hesperidin Fatty Acid Esters in a Two-Phase System Containing Ionic Liquid. Molecules 2011, 16, 7171-7182.
Araújo MEMB, Contesini FJ, Franco YEM, Sawaya ACF, Alberto TG, Dalfré N, Carvalho PO. Optimized Enzymatic Synthesis of Hesperidin Fatty Acid Esters in a Two-Phase System Containing Ionic Liquid. Molecules. 2011; 16(8):7171-7182.Chicago/Turabian Style
Araújo, Maria Elisa Melo Branco de; Contesini, Fabiano Jares; Franco, Yollanda Edwirges Moreira; Sawaya, Alexandra C.H. Frankland; Alberto, Thiago Grando; Dalfré, Natália; Carvalho, Patrícia de Oliveira. 2011. "Optimized Enzymatic Synthesis of Hesperidin Fatty Acid Esters in a Two-Phase System Containing Ionic Liquid." Molecules 16, no. 8: 7171-7182.