Cargando…

Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity

Fungal Oligopeptide Transporters (Fot) Fot1, Fot2 and Fot3 have been found in Saccharomyces cerevisiae wine strains, but not in strains from other environments. In the S. cerevisiae wine strain EC1118, Fot1 and Fot2 are responsible for a broader range of oligopeptide utilization in comparison with s...

Descripción completa

Detalles Bibliográficos
Autores principales: Becerra-Rodríguez, Carmen, Taghouti, Géraldine, Portier, Perrine, Dequin, Sylvie, Casal, Margarida, Paiva, Sandra, Galeote, Virginie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625066/
https://www.ncbi.nlm.nih.gov/pubmed/34829250
http://dx.doi.org/10.3390/jof7110963
_version_ 1784606328283463680
author Becerra-Rodríguez, Carmen
Taghouti, Géraldine
Portier, Perrine
Dequin, Sylvie
Casal, Margarida
Paiva, Sandra
Galeote, Virginie
author_facet Becerra-Rodríguez, Carmen
Taghouti, Géraldine
Portier, Perrine
Dequin, Sylvie
Casal, Margarida
Paiva, Sandra
Galeote, Virginie
author_sort Becerra-Rodríguez, Carmen
collection PubMed
description Fungal Oligopeptide Transporters (Fot) Fot1, Fot2 and Fot3 have been found in Saccharomyces cerevisiae wine strains, but not in strains from other environments. In the S. cerevisiae wine strain EC1118, Fot1 and Fot2 are responsible for a broader range of oligopeptide utilization in comparison with strains not containing any Fot. This leads to better fermentation efficiency and an increased production of desirable organoleptic compounds in wine. Despite the benefits associated with Fot activity in S. cerevisiae within the wine environment, little is known about this family of transporters in yeast. The presence of Fot1, Fot2 and Fot3 in S. cerevisiae wine strains is due to horizontal gene transfer from the yeast Torulaspora microellipsoides, which harbors Fot2Tm, FotX and FotY proteins. Sequence analyses revealed that Fot family members have a high sequence identity in these yeast species. In this work, we aimed to further characterize the different Fot family members in terms of subcellular localization, gene expression in enological fermentation and substrate specificity. Using CRISPR/Cas9, we constructed S. cerevisiae wine strains containing each different Fot as the sole oligopeptide transporter to analyze their oligopeptide preferences by phenotype microarrays. The results of oligopeptide consumption show that Fot counterparts have different di-/tripeptide specificities, suggesting that punctual sequence divergence between FOT genes can be crucial for substrate recognition, binding and transport activity. FOT gene expression levels in different S. cerevisiae wine strains during enological fermentation, together with predicted binding motifs for transcriptional regulators in nitrogen metabolism, indicate that these transporters may be under the control of the Nitrogen Catabolite Repression (NCR) system. Finally, we demonstrated that Fot1 is located in the yeast plasma membrane. This work contributes to a better understanding of this family of oligopeptide transporters, which have demonstrated a key role in the utilization of oligopeptides by S. cerevisiae in enological fermentation.
format Online
Article
Text
id pubmed-8625066
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86250662021-11-27 Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity Becerra-Rodríguez, Carmen Taghouti, Géraldine Portier, Perrine Dequin, Sylvie Casal, Margarida Paiva, Sandra Galeote, Virginie J Fungi (Basel) Article Fungal Oligopeptide Transporters (Fot) Fot1, Fot2 and Fot3 have been found in Saccharomyces cerevisiae wine strains, but not in strains from other environments. In the S. cerevisiae wine strain EC1118, Fot1 and Fot2 are responsible for a broader range of oligopeptide utilization in comparison with strains not containing any Fot. This leads to better fermentation efficiency and an increased production of desirable organoleptic compounds in wine. Despite the benefits associated with Fot activity in S. cerevisiae within the wine environment, little is known about this family of transporters in yeast. The presence of Fot1, Fot2 and Fot3 in S. cerevisiae wine strains is due to horizontal gene transfer from the yeast Torulaspora microellipsoides, which harbors Fot2Tm, FotX and FotY proteins. Sequence analyses revealed that Fot family members have a high sequence identity in these yeast species. In this work, we aimed to further characterize the different Fot family members in terms of subcellular localization, gene expression in enological fermentation and substrate specificity. Using CRISPR/Cas9, we constructed S. cerevisiae wine strains containing each different Fot as the sole oligopeptide transporter to analyze their oligopeptide preferences by phenotype microarrays. The results of oligopeptide consumption show that Fot counterparts have different di-/tripeptide specificities, suggesting that punctual sequence divergence between FOT genes can be crucial for substrate recognition, binding and transport activity. FOT gene expression levels in different S. cerevisiae wine strains during enological fermentation, together with predicted binding motifs for transcriptional regulators in nitrogen metabolism, indicate that these transporters may be under the control of the Nitrogen Catabolite Repression (NCR) system. Finally, we demonstrated that Fot1 is located in the yeast plasma membrane. This work contributes to a better understanding of this family of oligopeptide transporters, which have demonstrated a key role in the utilization of oligopeptides by S. cerevisiae in enological fermentation. MDPI 2021-11-12 /pmc/articles/PMC8625066/ /pubmed/34829250 http://dx.doi.org/10.3390/jof7110963 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Becerra-Rodríguez, Carmen
Taghouti, Géraldine
Portier, Perrine
Dequin, Sylvie
Casal, Margarida
Paiva, Sandra
Galeote, Virginie
Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity
title Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity
title_full Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity
title_fullStr Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity
title_full_unstemmed Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity
title_short Yeast Plasma Membrane Fungal Oligopeptide Transporters Display Distinct Substrate Preferences despite Their High Sequence Identity
title_sort yeast plasma membrane fungal oligopeptide transporters display distinct substrate preferences despite their high sequence identity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625066/
https://www.ncbi.nlm.nih.gov/pubmed/34829250
http://dx.doi.org/10.3390/jof7110963
work_keys_str_mv AT becerrarodriguezcarmen yeastplasmamembranefungaloligopeptidetransportersdisplaydistinctsubstratepreferencesdespitetheirhighsequenceidentity
AT taghoutigeraldine yeastplasmamembranefungaloligopeptidetransportersdisplaydistinctsubstratepreferencesdespitetheirhighsequenceidentity
AT portierperrine yeastplasmamembranefungaloligopeptidetransportersdisplaydistinctsubstratepreferencesdespitetheirhighsequenceidentity
AT dequinsylvie yeastplasmamembranefungaloligopeptidetransportersdisplaydistinctsubstratepreferencesdespitetheirhighsequenceidentity
AT casalmargarida yeastplasmamembranefungaloligopeptidetransportersdisplaydistinctsubstratepreferencesdespitetheirhighsequenceidentity
AT paivasandra yeastplasmamembranefungaloligopeptidetransportersdisplaydistinctsubstratepreferencesdespitetheirhighsequenceidentity
AT galeotevirginie yeastplasmamembranefungaloligopeptidetransportersdisplaydistinctsubstratepreferencesdespitetheirhighsequenceidentity