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13C nuclear magnetic resonance characterization of the reaction products of lamb pregastric lipase-catalyzed hydrolysis of tributyrylglycerol

Authors :
Charmian J. O'Connor
Richard H. Barton
Source :
Journal of the American Oil Chemists' Society. 75:967-976
Publication Year :
1998
Publisher :
Wiley, 1998.

Abstract

Lamb pregastric lipase (LPGL), extracted from the tongue root and epiglottis of suckling lamb, has been used to catalyze the hydrolysis of emulsified tributyrylglycerol. Reactions were generally carried out at 35°C and initial pH 7.0. The speciation of the products of the reaction has been examined by 13C nuclear magnetic resonance spectroscopy. Varying rates of reaction were produced by increasing the amount of enzyme added relative to the amount of lipid. A system rate parameter, ΔpH/Δt, which is the change in pH (ΔpH) from time zero to the time when the sample was removed (Δt), has been developed. 1,2(2,3)-Dibutyrylglycerol and 2-monobutyrylglycerol have been identified as products of LPGL-catalyzed hydrolysis, while 1,3-dibutyrylglycerol and 1(3)-monobutyrylglycerol are products of uncatalyzed acyl transfer reactions.

Details

ISSN :
15589331 and 0003021X
Volume :
75
Database :
OpenAIRE
Journal :
Journal of the American Oil Chemists' Society
Accession number :
edsair.doi...........90ffc005b55b1ad345da73cdf4b747c4