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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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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. |
format | Online Article Text |
id | pubmed-4651352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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