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Obtaining monoglycerides by esterification of glycerol with palmitic acid using some high activity preparations of Candida antarctica lipase B
► Use of CLEA, PCMC and CLPCMC for monoglyceride synthesis. ► Monopalmitin with ≤10% diglyceride obtained. ► Process optimization resulted in 87% MG in 24h. Cross-linked enzyme aggregates (CLEAs), protein coated microcrystals (PCMCs), cross-linked protein coated microcrystals (CLPCMCs) of Candida an...
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Published in: | Process biochemistry (1991) 2012-03, Vol.47 (3), p.503-508 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► Use of CLEA, PCMC and CLPCMC for monoglyceride synthesis. ► Monopalmitin with ≤10% diglyceride obtained. ► Process optimization resulted in 87% MG in 24h.
Cross-linked enzyme aggregates (CLEAs), protein coated microcrystals (PCMCs), cross-linked protein coated microcrystals (CLPCMCs) of Candida antarctica lipase B (CALB) were used for esterification of glycerol with palmitic acid in acetone under low water condition. With CLEAs, 81% monoglyceride (MG) along with 4.5% diglyceride (DG) were produced at 1% (v/v) water content in 24h. The water content in the medium was managed by stepwise addition of the molecular sieves at appropriate time intervals. With PCMCs (potassium sulfate as a core material), 82% monoglyceride along with 4.0% diglyceride were obtained, with 0.5% water (v/v) added initially to anhydrous acetone with molecular sieves present in the reaction medium. With CLPCMC (prepared by cross-linking with 200mM glutaraldehyde), 87% monoglyceride and 3.3% diglyceride were produced in 24h in presence of 1% (v/v) water (added initially) and with appropriate amount of molecular sieves added in the reaction medium. The results offer a comparative study on the performance of three high activity preparations of CALB for preparation of monopalmitin with ≤10% of the diglyceride content. |
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ISSN: | 1359-5113 1873-3298 |
DOI: | 10.1016/j.procbio.2011.12.009 |