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Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions

The budding yeast Saccharomyces cerevisiae has been used extensively in fermentative industrial processes, including biofuel production from sustainable plant-based hydrolysates. Myriad toxins and stressors found in hydrolysates inhibit microbial metabolism and product formation. Overcoming these st...

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Autores principales: Vanacloig-Pedros, Elena, Fisher, Kaitlin J, Liu, Lisa, Debrauske, Derek J, Young, Megan K M, Place, Michael, Hittinger, Chris Todd, Sato, Trey K, Gasch, Audrey P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508847/
https://www.ncbi.nlm.nih.gov/pubmed/35883225
http://dx.doi.org/10.1093/femsyr/foac036
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author Vanacloig-Pedros, Elena
Fisher, Kaitlin J
Liu, Lisa
Debrauske, Derek J
Young, Megan K M
Place, Michael
Hittinger, Chris Todd
Sato, Trey K
Gasch, Audrey P
author_facet Vanacloig-Pedros, Elena
Fisher, Kaitlin J
Liu, Lisa
Debrauske, Derek J
Young, Megan K M
Place, Michael
Hittinger, Chris Todd
Sato, Trey K
Gasch, Audrey P
author_sort Vanacloig-Pedros, Elena
collection PubMed
description The budding yeast Saccharomyces cerevisiae has been used extensively in fermentative industrial processes, including biofuel production from sustainable plant-based hydrolysates. Myriad toxins and stressors found in hydrolysates inhibit microbial metabolism and product formation. Overcoming these stresses requires mitigation strategies that include strain engineering. To identify shared and divergent mechanisms of toxicity and to implicate gene targets for genetic engineering, we used a chemical genomic approach to study fitness effects across a library of S. cerevisiae deletion mutants cultured anaerobically in dozens of individual compounds found in different types of hydrolysates. Relationships in chemical genomic profiles identified classes of toxins that provoked similar cellular responses, spanning inhibitor relationships that were not expected from chemical classification. Our results also revealed widespread antagonistic effects across inhibitors, such that the same gene deletions were beneficial for surviving some toxins but detrimental for others. This work presents a rich dataset relating gene function to chemical compounds, which both expands our understanding of plant-based hydrolysates and provides a useful resource to identify engineering targets.
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spelling pubmed-95088472022-09-26 Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions Vanacloig-Pedros, Elena Fisher, Kaitlin J Liu, Lisa Debrauske, Derek J Young, Megan K M Place, Michael Hittinger, Chris Todd Sato, Trey K Gasch, Audrey P FEMS Yeast Res Research Article The budding yeast Saccharomyces cerevisiae has been used extensively in fermentative industrial processes, including biofuel production from sustainable plant-based hydrolysates. Myriad toxins and stressors found in hydrolysates inhibit microbial metabolism and product formation. Overcoming these stresses requires mitigation strategies that include strain engineering. To identify shared and divergent mechanisms of toxicity and to implicate gene targets for genetic engineering, we used a chemical genomic approach to study fitness effects across a library of S. cerevisiae deletion mutants cultured anaerobically in dozens of individual compounds found in different types of hydrolysates. Relationships in chemical genomic profiles identified classes of toxins that provoked similar cellular responses, spanning inhibitor relationships that were not expected from chemical classification. Our results also revealed widespread antagonistic effects across inhibitors, such that the same gene deletions were beneficial for surviving some toxins but detrimental for others. This work presents a rich dataset relating gene function to chemical compounds, which both expands our understanding of plant-based hydrolysates and provides a useful resource to identify engineering targets. Oxford University Press 2022-07-26 /pmc/articles/PMC9508847/ /pubmed/35883225 http://dx.doi.org/10.1093/femsyr/foac036 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of FEMS. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vanacloig-Pedros, Elena
Fisher, Kaitlin J
Liu, Lisa
Debrauske, Derek J
Young, Megan K M
Place, Michael
Hittinger, Chris Todd
Sato, Trey K
Gasch, Audrey P
Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions
title Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions
title_full Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions
title_fullStr Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions
title_full_unstemmed Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions
title_short Comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions
title_sort comparative chemical genomic profiling across plant-based hydrolysate toxins reveals widespread antagonism in fitness contributions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508847/
https://www.ncbi.nlm.nih.gov/pubmed/35883225
http://dx.doi.org/10.1093/femsyr/foac036
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