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Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade

Lipases are currently the subject of intensive studies due to their large range of industrial applications. The Lip2p lipase from the yeast Yarrowia lipolytica (YlLIP2) was recently shown to be a good candidate for different biotechnological applications. Using a combination of comparative genomics...

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Autores principales: Meunchan, Muchalin, Michely, Stéphanie, Devillers, Hugo, Nicaud, Jean-Marc, Marty, Alain, Neuvéglise, Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651352/
https://www.ncbi.nlm.nih.gov/pubmed/26580812
http://dx.doi.org/10.1371/journal.pone.0143096
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author Meunchan, Muchalin
Michely, Stéphanie
Devillers, Hugo
Nicaud, Jean-Marc
Marty, Alain
Neuvéglise, Cécile
author_facet Meunchan, Muchalin
Michely, Stéphanie
Devillers, Hugo
Nicaud, Jean-Marc
Marty, Alain
Neuvéglise, Cécile
author_sort Meunchan, Muchalin
collection PubMed
description Lipases are currently the subject of intensive studies due to their large range of industrial applications. The Lip2p lipase from the yeast Yarrowia lipolytica (YlLIP2) was recently shown to be a good candidate for different biotechnological applications. Using a combination of comparative genomics approaches based on sequence similarity, synteny conservation, and phylogeny, we constructed the evolutionary scenario of the lipase family for six species of the Yarrowia clade. RNA-seq based transcriptome analysis revealed the primary role of LIP2 homologues in the assimilation of different substrates. Once identified, these YlLIP2 homologues were expressed in Y. lipolytica. The lipase Lip2a from Candida phangngensis was shown to naturally present better activity and enantioselectivity than YlLip2. Enantioselectivity was further improved by site-directed mutagenesis targeted to the substrate binding site. The mono-substituted variant V232S displayed enantioselectivity greater than 200 and a 2.5 fold increase in velocity. A double-substituted variant 97A-V232F presented reversed enantioselectivity, with a total preference for the R-enantiomer.
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spelling pubmed-46513522015-11-25 Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade Meunchan, Muchalin Michely, Stéphanie Devillers, Hugo Nicaud, Jean-Marc Marty, Alain Neuvéglise, Cécile PLoS One Research Article Lipases are currently the subject of intensive studies due to their large range of industrial applications. The Lip2p lipase from the yeast Yarrowia lipolytica (YlLIP2) was recently shown to be a good candidate for different biotechnological applications. Using a combination of comparative genomics approaches based on sequence similarity, synteny conservation, and phylogeny, we constructed the evolutionary scenario of the lipase family for six species of the Yarrowia clade. RNA-seq based transcriptome analysis revealed the primary role of LIP2 homologues in the assimilation of different substrates. Once identified, these YlLIP2 homologues were expressed in Y. lipolytica. The lipase Lip2a from Candida phangngensis was shown to naturally present better activity and enantioselectivity than YlLip2. Enantioselectivity was further improved by site-directed mutagenesis targeted to the substrate binding site. The mono-substituted variant V232S displayed enantioselectivity greater than 200 and a 2.5 fold increase in velocity. A double-substituted variant 97A-V232F presented reversed enantioselectivity, with a total preference for the R-enantiomer. Public Library of Science 2015-11-18 /pmc/articles/PMC4651352/ /pubmed/26580812 http://dx.doi.org/10.1371/journal.pone.0143096 Text en © 2015 Meunchan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Meunchan, Muchalin
Michely, Stéphanie
Devillers, Hugo
Nicaud, Jean-Marc
Marty, Alain
Neuvéglise, Cécile
Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade
title Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade
title_full Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade
title_fullStr Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade
title_full_unstemmed Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade
title_short Comprehensive Analysis of a Yeast Lipase Family in the Yarrowia Clade
title_sort comprehensive analysis of a yeast lipase family in the yarrowia clade
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651352/
https://www.ncbi.nlm.nih.gov/pubmed/26580812
http://dx.doi.org/10.1371/journal.pone.0143096
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