U. Bornscheuer et al., A COMPARISON OF DIFFERENT STRATEGIES FOR LIPASE-CATALYZED SYNTHESIS OF PARTIAL GLYCERIDES, Biotechnology letters, 16(7), 1994, pp. 697-702
Four different approaches for the synthesis of monolaurylglycerol (MLG
) by non specific Pseudomonas cepacia lipase in a crude and purified f
orm have been studied: a. The direct esterification of glycerol by lau
ric acid in bis-(2-ethylhexyl)sulfosuccinate sodium salt (AOT)/isoocta
ne microemulsion systems; b. the transesterification of glycerol by vi
nyl laurate in the presence or not of any solvent; c. solid-phase glyc
erolysis of trilaurin; and, d. transesterification of protected glycer
ol, 1,2-O-isopropylidene glycerol, by vinyl laurate, in the presence o
r not of any solvent. It was found that in the two latter cases (d and
c) the formation of pure MLG was occurred, while in the first two cas
es (a and b) apart of MLG the formation of DLG was also observed.