Cargando…

A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species

Yeasts are increasingly employed in synthetic biology as chassis strains, including conventional and non-conventional species. It is still unclear how genomic evolution determines metabolic diversity among various yeast species and strains. In this study, we constructed draft GEMs for 332 yeast spec...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Hongzhong, Kerkhoven, Eduard J., Nielsen, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687678/
https://www.ncbi.nlm.nih.gov/pubmed/36358981
http://dx.doi.org/10.3390/biom12111632
_version_ 1784836068699275264
author Lu, Hongzhong
Kerkhoven, Eduard J.
Nielsen, Jens
author_facet Lu, Hongzhong
Kerkhoven, Eduard J.
Nielsen, Jens
author_sort Lu, Hongzhong
collection PubMed
description Yeasts are increasingly employed in synthetic biology as chassis strains, including conventional and non-conventional species. It is still unclear how genomic evolution determines metabolic diversity among various yeast species and strains. In this study, we constructed draft GEMs for 332 yeast species using two alternative procedures from the toolbox RAVEN v 2.0. We found that draft GEMs could reflect the difference in yeast metabolic potentials, and therefore, could be utilized to probe the evolutionary trend of metabolism among 332 yeast species. We created a pan-draft metabolic model to account for the metabolic capacity of every sequenced yeast species by merging all draft GEMs. Further analysis showed that the pan-reactome of yeast has a “closed” property, which confirmed the great conservatism that exists in yeast metabolic evolution. Lastly, the quantitative correlations among trait similarity, evolutionary distances, genotype, and model similarity were thoroughly investigated. The results suggest that the evolutionary distance and genotype, to some extent, determine model similarity, but not trait similarity, indicating that multiple mechanisms shape yeast trait evolution. A large-scale reconstruction and integrative analysis of yeast draft GEMs would be a valuable resource to probe the evolutionary mechanism behind yeast trait variety and to further refine the existing yeast species-specific GEMs for the community.
format Online
Article
Text
id pubmed-9687678
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96876782022-11-25 A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species Lu, Hongzhong Kerkhoven, Eduard J. Nielsen, Jens Biomolecules Article Yeasts are increasingly employed in synthetic biology as chassis strains, including conventional and non-conventional species. It is still unclear how genomic evolution determines metabolic diversity among various yeast species and strains. In this study, we constructed draft GEMs for 332 yeast species using two alternative procedures from the toolbox RAVEN v 2.0. We found that draft GEMs could reflect the difference in yeast metabolic potentials, and therefore, could be utilized to probe the evolutionary trend of metabolism among 332 yeast species. We created a pan-draft metabolic model to account for the metabolic capacity of every sequenced yeast species by merging all draft GEMs. Further analysis showed that the pan-reactome of yeast has a “closed” property, which confirmed the great conservatism that exists in yeast metabolic evolution. Lastly, the quantitative correlations among trait similarity, evolutionary distances, genotype, and model similarity were thoroughly investigated. The results suggest that the evolutionary distance and genotype, to some extent, determine model similarity, but not trait similarity, indicating that multiple mechanisms shape yeast trait evolution. A large-scale reconstruction and integrative analysis of yeast draft GEMs would be a valuable resource to probe the evolutionary mechanism behind yeast trait variety and to further refine the existing yeast species-specific GEMs for the community. MDPI 2022-11-03 /pmc/articles/PMC9687678/ /pubmed/36358981 http://dx.doi.org/10.3390/biom12111632 Text en © 2022 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
Lu, Hongzhong
Kerkhoven, Eduard J.
Nielsen, Jens
A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species
title A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species
title_full A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species
title_fullStr A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species
title_full_unstemmed A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species
title_short A Pan-Draft Metabolic Model Reflects Evolutionary Diversity across 332 Yeast Species
title_sort pan-draft metabolic model reflects evolutionary diversity across 332 yeast species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687678/
https://www.ncbi.nlm.nih.gov/pubmed/36358981
http://dx.doi.org/10.3390/biom12111632
work_keys_str_mv AT luhongzhong apandraftmetabolicmodelreflectsevolutionarydiversityacross332yeastspecies
AT kerkhoveneduardj apandraftmetabolicmodelreflectsevolutionarydiversityacross332yeastspecies
AT nielsenjens apandraftmetabolicmodelreflectsevolutionarydiversityacross332yeastspecies
AT luhongzhong pandraftmetabolicmodelreflectsevolutionarydiversityacross332yeastspecies
AT kerkhoveneduardj pandraftmetabolicmodelreflectsevolutionarydiversityacross332yeastspecies
AT nielsenjens pandraftmetabolicmodelreflectsevolutionarydiversityacross332yeastspecies