2011
DOI: 10.1016/j.biortech.2010.08.095
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Kinetically controlled synthesis of monoglyceryl esters from chiral and prochiral acids methyl esters catalyzed by immobilized Rhizomucor miehei lipase

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Cited by 23 publications
(15 citation statements)
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“…Higher yield of enantioselective product is obtained in final 37 step when pure monoacetylated product is used as substrate. 38 Lipases are the most important group of biocatalysts in non-39 aqueous enzymology; they do not need cofactors for assisting the 40 reaction, are capable of differentiating the chiral centers and have 41 extensive substrate specificity [23][24][25][26][27][28][29][30][31][32]. Lipases are widely 42 present in different sources which include bacteria and fungi 43 and hence can be readily available for biotransformation of 44 interest.…”
mentioning
confidence: 99%
“…Higher yield of enantioselective product is obtained in final 37 step when pure monoacetylated product is used as substrate. 38 Lipases are the most important group of biocatalysts in non-39 aqueous enzymology; they do not need cofactors for assisting the 40 reaction, are capable of differentiating the chiral centers and have 41 extensive substrate specificity [23][24][25][26][27][28][29][30][31][32]. Lipases are widely 42 present in different sources which include bacteria and fungi 43 and hence can be readily available for biotransformation of 44 interest.…”
mentioning
confidence: 99%
“…The two diastereoisomeric leucine derivatives 16 and 17 were subjected to lipase‐catalysed esterification under identical experimental conditions and quantification showed similar conversions (55–60 % conversion; Scheme ). This last experiment clearly demonstrated that lipozyme ® is not diastereoselective for these transesterification reactions, contrary to the results obtained with monoacylglycerol 17. If diastereoselectivity is not responsible for the difference in the conversion of 3‐[(β‐cyclodextrinyl)succinamido]propane‐1,2‐diol, it can be hypothesized that the difference is due to the spatial configurations of the R and S substrates.…”
Section: Resultsmentioning
confidence: 56%
“…For example, PS lipase from Amano was reported to give a higher diastereoisomeric excess ( de ) than AK lipase (62 % < de < 96 %) 16. Finally, Mucor miehei lipase, which was used in this study, successfully catalysed the synthesis of monoacylglycerol with a diastereoisomeric excess superior to 99 % 17. As shown in this report, this diastereoselectivity depends on the enzyme and substrate.…”
Section: Introductionmentioning
confidence: 53%
“…The extra cellular and the intracellular lipases are also able to catalyze the transesterification of triglycerides effectively (Andreina et al, 2011;Giovana et al, 2011;Ríos et al, 2011;Junmin et al, 2011;Shiva and Patrick, 2011).…”
Section: Discussionmentioning
confidence: 99%