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High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics

Identifying metabolites in model organisms is critical for many areas of biology, including unravelling disease aetiology or elucidating functions of putative enzymes. Even now, hundreds of predicted metabolic genes in Saccharomyces cerevisiae remain uncharacterized, indicating that our understandin...

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Autores principales: Favilli, Lorenzo, Griffith, Corey M., Schymanski, Emma L., Linster, Carole L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289995/
https://www.ncbi.nlm.nih.gov/pubmed/37212869
http://dx.doi.org/10.1007/s00216-023-04724-5
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author Favilli, Lorenzo
Griffith, Corey M.
Schymanski, Emma L.
Linster, Carole L.
author_facet Favilli, Lorenzo
Griffith, Corey M.
Schymanski, Emma L.
Linster, Carole L.
author_sort Favilli, Lorenzo
collection PubMed
description Identifying metabolites in model organisms is critical for many areas of biology, including unravelling disease aetiology or elucidating functions of putative enzymes. Even now, hundreds of predicted metabolic genes in Saccharomyces cerevisiae remain uncharacterized, indicating that our understanding of metabolism is far from complete even in well-characterized organisms. While untargeted high-resolution mass spectrometry (HRMS) enables the detection of thousands of features per analysis, many of these have a non-biological origin. Stable isotope labelling (SIL) approaches can serve as credentialing strategies to distinguish biologically relevant features from background signals, but implementing these experiments at large scale remains challenging. Here, we developed a SIL-based approach for high-throughput untargeted metabolomics in S. cerevisiae, including deep-48 well format-based cultivation and metabolite extraction, building on the peak annotation and verification engine (PAVE) tool. Aqueous and nonpolar extracts were analysed using HILIC and RP liquid chromatography, respectively, coupled to Orbitrap Q Exactive HF mass spectrometry. Of the approximately 37,000 total detected features, only 3–7% of the features were credentialed and used for data analysis with open-source software such as MS-DIAL, MetFrag, Shinyscreen, SIRIUS CSI:FingerID, and MetaboAnalyst, leading to the successful annotation of 198 metabolites using MS(2) database matching. Comparable metabolic profiles were observed for wild-type and sdh1Δ yeast strains grown in deep-48 well plates versus the classical shake flask format, including the expected increase in intracellular succinate concentration in the sdh1Δ strain. The described approach enables high-throughput yeast cultivation and credentialing-based untargeted metabolomics, providing a means to efficiently perform molecular phenotypic screens and help complete metabolic networks. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-023-04724-5.
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spelling pubmed-102899952023-06-25 High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics Favilli, Lorenzo Griffith, Corey M. Schymanski, Emma L. Linster, Carole L. Anal Bioanal Chem Research Paper Identifying metabolites in model organisms is critical for many areas of biology, including unravelling disease aetiology or elucidating functions of putative enzymes. Even now, hundreds of predicted metabolic genes in Saccharomyces cerevisiae remain uncharacterized, indicating that our understanding of metabolism is far from complete even in well-characterized organisms. While untargeted high-resolution mass spectrometry (HRMS) enables the detection of thousands of features per analysis, many of these have a non-biological origin. Stable isotope labelling (SIL) approaches can serve as credentialing strategies to distinguish biologically relevant features from background signals, but implementing these experiments at large scale remains challenging. Here, we developed a SIL-based approach for high-throughput untargeted metabolomics in S. cerevisiae, including deep-48 well format-based cultivation and metabolite extraction, building on the peak annotation and verification engine (PAVE) tool. Aqueous and nonpolar extracts were analysed using HILIC and RP liquid chromatography, respectively, coupled to Orbitrap Q Exactive HF mass spectrometry. Of the approximately 37,000 total detected features, only 3–7% of the features were credentialed and used for data analysis with open-source software such as MS-DIAL, MetFrag, Shinyscreen, SIRIUS CSI:FingerID, and MetaboAnalyst, leading to the successful annotation of 198 metabolites using MS(2) database matching. Comparable metabolic profiles were observed for wild-type and sdh1Δ yeast strains grown in deep-48 well plates versus the classical shake flask format, including the expected increase in intracellular succinate concentration in the sdh1Δ strain. The described approach enables high-throughput yeast cultivation and credentialing-based untargeted metabolomics, providing a means to efficiently perform molecular phenotypic screens and help complete metabolic networks. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-023-04724-5. Springer Berlin Heidelberg 2023-05-22 2023 /pmc/articles/PMC10289995/ /pubmed/37212869 http://dx.doi.org/10.1007/s00216-023-04724-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Paper
Favilli, Lorenzo
Griffith, Corey M.
Schymanski, Emma L.
Linster, Carole L.
High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics
title High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics
title_full High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics
title_fullStr High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics
title_full_unstemmed High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics
title_short High-throughput Saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics
title_sort high-throughput saccharomyces cerevisiae cultivation method for credentialing-based untargeted metabolomics
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289995/
https://www.ncbi.nlm.nih.gov/pubmed/37212869
http://dx.doi.org/10.1007/s00216-023-04724-5
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