Stereoselective hydrolysis of triglycerides by animal and microbial lipases

Abstract In the present paper, a study on the stereoselectivity of 25 lipases of animal and microbial origin towards homogeneous prochiral triglycerides is presented. All the lipases tested catalyse the hydrolysis of the chemically alike but sterically nonequivalent ester groups in trioctanoin and t...

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Published in:Chirality
Main Authors: Rogalska, Ewa, Cudrey, Claire, Ferrato, Francine, Verger, Robert
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1993
Subjects:
Online Access:http://dx.doi.org/10.1002/chir.530050106
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spelling crwiley:10.1002/chir.530050106 2024-06-23T07:46:55+00:00 Stereoselective hydrolysis of triglycerides by animal and microbial lipases Rogalska, Ewa Cudrey, Claire Ferrato, Francine Verger, Robert 1993 http://dx.doi.org/10.1002/chir.530050106 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchir.530050106 https://onlinelibrary.wiley.com/doi/pdf/10.1002/chir.530050106 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Chirality volume 5, issue 1, page 24-30 ISSN 0899-0042 1520-636X journal-article 1993 crwiley https://doi.org/10.1002/chir.530050106 2024-06-04T06:47:38Z Abstract In the present paper, a study on the stereoselectivity of 25 lipases of animal and microbial origin towards homogeneous prochiral triglycerides is presented. All the lipases tested catalyse the hydrolysis of the chemically alike but sterically nonequivalent ester groups in trioctanoin and triolein with different degrees of stereobias, depending on the fatty acyl chain length of the substrate (Rogalska et al., J. Biol. Chem. 256:20271–20276, 1990). Hydrolysis of the sn ‐2 ester group is catalysed by very few lipases and only Candida antarctica A shows a clear preference for this position. Most of the lipases investigated (12 with trioctanoin and 16 with triolein) showed a preference for the sn ‐1 position. Using trioctanoin as substrate we observed a total stereoselectivity for position sn ‐1 with Pseudomonas sp. and Pseudomonas aeruginosa and for position sn ‐3 with Candida antarctica B. This was not the case with triolein as substrate. Among the 23 lipases studied here and the other two lipases described previously (Rogalska et al., J. Biol. Chem. 256:20271–20276, 1990), 17 show a higher stereoselectivity with trioctanoin than with triolein. With guinea pig pancreatic lipase and with three mold lipases ( Geotrichum candidum M, Geotrichum candidum A, and Candida antarctica B), the preference switches from sn ‐3 to sn ‐1 when the acyl chain length increases from eight to 18 carbon atoms. The main conclusion to emerge from the present study is that the specific stereopreference of each lipase for a given substrate under given lipolytic conditions can be said to be its fingerprint. © 1993 Wiley‐Liss, Inc. Article in Journal/Newspaper Antarc* Antarctica Wiley Online Library Chirality 5 1 24 30
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract In the present paper, a study on the stereoselectivity of 25 lipases of animal and microbial origin towards homogeneous prochiral triglycerides is presented. All the lipases tested catalyse the hydrolysis of the chemically alike but sterically nonequivalent ester groups in trioctanoin and triolein with different degrees of stereobias, depending on the fatty acyl chain length of the substrate (Rogalska et al., J. Biol. Chem. 256:20271–20276, 1990). Hydrolysis of the sn ‐2 ester group is catalysed by very few lipases and only Candida antarctica A shows a clear preference for this position. Most of the lipases investigated (12 with trioctanoin and 16 with triolein) showed a preference for the sn ‐1 position. Using trioctanoin as substrate we observed a total stereoselectivity for position sn ‐1 with Pseudomonas sp. and Pseudomonas aeruginosa and for position sn ‐3 with Candida antarctica B. This was not the case with triolein as substrate. Among the 23 lipases studied here and the other two lipases described previously (Rogalska et al., J. Biol. Chem. 256:20271–20276, 1990), 17 show a higher stereoselectivity with trioctanoin than with triolein. With guinea pig pancreatic lipase and with three mold lipases ( Geotrichum candidum M, Geotrichum candidum A, and Candida antarctica B), the preference switches from sn ‐3 to sn ‐1 when the acyl chain length increases from eight to 18 carbon atoms. The main conclusion to emerge from the present study is that the specific stereopreference of each lipase for a given substrate under given lipolytic conditions can be said to be its fingerprint. © 1993 Wiley‐Liss, Inc.
format Article in Journal/Newspaper
author Rogalska, Ewa
Cudrey, Claire
Ferrato, Francine
Verger, Robert
spellingShingle Rogalska, Ewa
Cudrey, Claire
Ferrato, Francine
Verger, Robert
Stereoselective hydrolysis of triglycerides by animal and microbial lipases
author_facet Rogalska, Ewa
Cudrey, Claire
Ferrato, Francine
Verger, Robert
author_sort Rogalska, Ewa
title Stereoselective hydrolysis of triglycerides by animal and microbial lipases
title_short Stereoselective hydrolysis of triglycerides by animal and microbial lipases
title_full Stereoselective hydrolysis of triglycerides by animal and microbial lipases
title_fullStr Stereoselective hydrolysis of triglycerides by animal and microbial lipases
title_full_unstemmed Stereoselective hydrolysis of triglycerides by animal and microbial lipases
title_sort stereoselective hydrolysis of triglycerides by animal and microbial lipases
publisher Wiley
publishDate 1993
url http://dx.doi.org/10.1002/chir.530050106
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchir.530050106
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chir.530050106
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volume 5, issue 1, page 24-30
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op_doi https://doi.org/10.1002/chir.530050106
container_title Chirality
container_volume 5
container_issue 1
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