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Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii

BACKGROUND: Saccharomycodes ludwigii belongs to the poorly characterized Saccharomycodeacea family and is known by its ability to spoil wines, a trait mostly attributable to its high tolerance to sulfur dioxide (SO(2)). To improve knowledge about Saccharomycodeacea our group determined whole-genome...

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Autores principales: Tavares, Maria J., Güldener, Ulrich, Mendes-Ferreira, Ana, Mira, Nuno P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903802/
https://www.ncbi.nlm.nih.gov/pubmed/33622260
http://dx.doi.org/10.1186/s12864-021-07438-z
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author Tavares, Maria J.
Güldener, Ulrich
Mendes-Ferreira, Ana
Mira, Nuno P.
author_facet Tavares, Maria J.
Güldener, Ulrich
Mendes-Ferreira, Ana
Mira, Nuno P.
author_sort Tavares, Maria J.
collection PubMed
description BACKGROUND: Saccharomycodes ludwigii belongs to the poorly characterized Saccharomycodeacea family and is known by its ability to spoil wines, a trait mostly attributable to its high tolerance to sulfur dioxide (SO(2)). To improve knowledge about Saccharomycodeacea our group determined whole-genome sequences of Hanseniaspora guilliermondii (UTAD222) and S. ludwigii (UTAD17), two members of this family. While in the case of H. guilliermondii the genomic information elucidated crucial aspects concerning the physiology of this species in the context of wine fermentation, the draft sequence obtained for S. ludwigii was distributed by more than 1000 contigs complicating extraction of biologically relevant information. In this work we describe the results obtained upon resequencing of S. ludwigii UTAD17 genome using PacBio as well as the insights gathered from the exploration of the annotation performed over the assembled genome. RESULTS: Resequencing of S. ludwigii UTAD17 genome with PacBio resulted in 20 contigs totaling 13 Mb of assembled DNA and corresponding to 95% of the DNA harbored by this strain. Annotation of the assembled UTAD17 genome predicts 4644 protein-encoding genes. Comparative analysis of the predicted S. ludwigii ORFeome with those encoded by other Saccharomycodeacea led to the identification of 213 proteins only found in this species. Among these were six enzymes required for catabolism of N-acetylglucosamine, four cell wall β-mannosyltransferases, several flocculins and three acetoin reductases. Different from its sister Hanseniaspora species, neoglucogenesis, glyoxylate cycle and thiamine biosynthetic pathways are functional in S. ludwigii. Four efflux pumps similar to the Ssu1 sulfite exporter, as well as robust orthologues for 65% of the S. cerevisiae SO(2)-tolerance genes, were identified in S. ludwigii genome. CONCLUSIONS: This work provides the first genome-wide picture of a S. ludwigii strain representing a step forward for a better understanding of the physiology and genetics of this species and of the Saccharomycodeacea family. The release of this genomic sequence and of the information extracted from it can contribute to guide the design of better wine preservation strategies to counteract spoilage prompted by S. ludwigii. It will also accelerate the exploration of this species as a cell factory, specially in production of fermented beverages where the use of Non-Saccharomyces species (including spoilage species) is booming. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07438-z.
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spelling pubmed-79038022021-02-25 Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii Tavares, Maria J. Güldener, Ulrich Mendes-Ferreira, Ana Mira, Nuno P. BMC Genomics Research Article BACKGROUND: Saccharomycodes ludwigii belongs to the poorly characterized Saccharomycodeacea family and is known by its ability to spoil wines, a trait mostly attributable to its high tolerance to sulfur dioxide (SO(2)). To improve knowledge about Saccharomycodeacea our group determined whole-genome sequences of Hanseniaspora guilliermondii (UTAD222) and S. ludwigii (UTAD17), two members of this family. While in the case of H. guilliermondii the genomic information elucidated crucial aspects concerning the physiology of this species in the context of wine fermentation, the draft sequence obtained for S. ludwigii was distributed by more than 1000 contigs complicating extraction of biologically relevant information. In this work we describe the results obtained upon resequencing of S. ludwigii UTAD17 genome using PacBio as well as the insights gathered from the exploration of the annotation performed over the assembled genome. RESULTS: Resequencing of S. ludwigii UTAD17 genome with PacBio resulted in 20 contigs totaling 13 Mb of assembled DNA and corresponding to 95% of the DNA harbored by this strain. Annotation of the assembled UTAD17 genome predicts 4644 protein-encoding genes. Comparative analysis of the predicted S. ludwigii ORFeome with those encoded by other Saccharomycodeacea led to the identification of 213 proteins only found in this species. Among these were six enzymes required for catabolism of N-acetylglucosamine, four cell wall β-mannosyltransferases, several flocculins and three acetoin reductases. Different from its sister Hanseniaspora species, neoglucogenesis, glyoxylate cycle and thiamine biosynthetic pathways are functional in S. ludwigii. Four efflux pumps similar to the Ssu1 sulfite exporter, as well as robust orthologues for 65% of the S. cerevisiae SO(2)-tolerance genes, were identified in S. ludwigii genome. CONCLUSIONS: This work provides the first genome-wide picture of a S. ludwigii strain representing a step forward for a better understanding of the physiology and genetics of this species and of the Saccharomycodeacea family. The release of this genomic sequence and of the information extracted from it can contribute to guide the design of better wine preservation strategies to counteract spoilage prompted by S. ludwigii. It will also accelerate the exploration of this species as a cell factory, specially in production of fermented beverages where the use of Non-Saccharomyces species (including spoilage species) is booming. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07438-z. BioMed Central 2021-02-23 /pmc/articles/PMC7903802/ /pubmed/33622260 http://dx.doi.org/10.1186/s12864-021-07438-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Tavares, Maria J.
Güldener, Ulrich
Mendes-Ferreira, Ana
Mira, Nuno P.
Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii
title Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii
title_full Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii
title_fullStr Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii
title_full_unstemmed Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii
title_short Genome sequencing, annotation and exploration of the SO(2)-tolerant non-conventional yeast Saccharomycodes ludwigii
title_sort genome sequencing, annotation and exploration of the so(2)-tolerant non-conventional yeast saccharomycodes ludwigii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903802/
https://www.ncbi.nlm.nih.gov/pubmed/33622260
http://dx.doi.org/10.1186/s12864-021-07438-z
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