Federal Centre for Cereal, Potato and Lipid Research, Institute for Biochemistry and Technology of Lipids, H. P. Kaufmann-Institute, Piusallee 68, D-48147 Münster, Germany
Abstract:
Ethyl esters (EE) of C2 to C14 saturated acids were interesterified with tripalmitin using papaya (Carica papaya) lipase to produce structured triacylglycerols (TG) with palmitoyl moieties in the secondary (sn-2), and short-chain or medium-chain acyl moieties in the primary (sn-1,3) positions. It was found that the incorporation of the acyl moieties rose with time and chain length of the ethyl ester. Little reaction occurred with ethyl acetate. The positional analysis of the structured TG formed revealed an increase in preference of the lipase for the primary positions as compared to the secondary position with increasing chain length of the acyl donor from C2 to C14.