Rh. Barton et Cj. Oconnor, C-13 NUCLEAR-MAGNETIC-RESONANCE CHARACTERIZATION OF THE REACTION-PRODUCTS OF LAMB PREGASTRIC LIPASE-CATALYZED HYDROLYSIS OF TRIBUTYRYLGLYCEROL, Journal of the American Oil Chemists' Society, 75(8), 1998, pp. 967-976
Lamb pregastric lipase (LPGL), extracted from the tongue root and epig
lottis of suckling lamb, has been used to catalyze the hydrolysis of e
mulsified tributyrylglycerol. Reactions were generally carried out at
35 degrees C and initial pH 7.0. The speciation of the products of the
reaction has been examined by C-13 nuclear magnetic resonance spectro
scopy. Varying rates of reaction were produced by increasing the amoun
t of enzyme added relative to the amount of lipid. A system rate param
eter, Delta pH/Delta t, which is the change in pH (Delta pH) from time
zero to the time when the sample was removed (Delta t), has been deve
loped. 1,2(2,3)-Dibutyrylglycerol and 2-monobutyrylglyceroI have been
identified as products of LPGL-catalyzed hydrolysis, while 1,3-dibutyr
ylglycerol and 1 (3)-monobutyrylglycerol are products of uncatalyzed a
cyl transfer reactions.