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Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling

INTRODUCTION: Isoprenoids are amongst the most abundant and diverse biological molecules and are involved in a broad range of biological functions. Functional understanding of their biosynthesis is thus key in many fundamental and applicative fields, including systems biology, medicine and biotechno...

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Autores principales: Castaño-Cerezo, Sara, Kulyk-Barbier, Hanna, Millard, Pierre, Portais, Jean-Charles, Heux, Stéphanie, Truan, Gilles, Bellvert, Floriant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704079/
https://www.ncbi.nlm.nih.gov/pubmed/31435826
http://dx.doi.org/10.1007/s11306-019-1580-8
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author Castaño-Cerezo, Sara
Kulyk-Barbier, Hanna
Millard, Pierre
Portais, Jean-Charles
Heux, Stéphanie
Truan, Gilles
Bellvert, Floriant
author_facet Castaño-Cerezo, Sara
Kulyk-Barbier, Hanna
Millard, Pierre
Portais, Jean-Charles
Heux, Stéphanie
Truan, Gilles
Bellvert, Floriant
author_sort Castaño-Cerezo, Sara
collection PubMed
description INTRODUCTION: Isoprenoids are amongst the most abundant and diverse biological molecules and are involved in a broad range of biological functions. Functional understanding of their biosynthesis is thus key in many fundamental and applicative fields, including systems biology, medicine and biotechnology. However, available methods do not yet allow accurate quantification and tracing of stable isotopes incorporation for all the isoprenoids precursors. OBJECTIVES: We developed and validated a complete methodology for quantitative metabolomics and isotopologue profiling of isoprenoid precursors in the yeast Saccharomyces cerevisiae. METHODS: This workflow covers all the experimental and computational steps from sample collection and preparation to data acquisition and processing. It also includes a novel quantification method based on liquid chromatography coupled to high-resolution mass spectrometry. Method validation followed the Metabolomics Standards Initiative guidelines. RESULTS: This workflow ensures accurate absolute quantification (RSD < 20%) of all mevalonate and prenyl pyrophosphates intermediates with a high sensitivity over a large linear range (from 0.1 to 50 pmol). In addition, we demonstrate that this workflow brings crucial information to design more efficient phytoene producers. Results indicate stable turnover rates of prenyl pyrophosphate intermediates in the constructed strains and provide quantitative information on the change of the biosynthetic flux of phytoene precursors. CONCLUSION: This methodology fills one of the last technical gaps for functional studies of isoprenoids biosynthesis and should be applicable to other eukaryotic and prokaryotic (micro)organisms after adaptation of some organism-dependent steps. This methodology also opens the way to (13)C-metabolic flux analysis of isoprenoid biosynthesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11306-019-1580-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-67040792019-09-02 Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling Castaño-Cerezo, Sara Kulyk-Barbier, Hanna Millard, Pierre Portais, Jean-Charles Heux, Stéphanie Truan, Gilles Bellvert, Floriant Metabolomics Original Article INTRODUCTION: Isoprenoids are amongst the most abundant and diverse biological molecules and are involved in a broad range of biological functions. Functional understanding of their biosynthesis is thus key in many fundamental and applicative fields, including systems biology, medicine and biotechnology. However, available methods do not yet allow accurate quantification and tracing of stable isotopes incorporation for all the isoprenoids precursors. OBJECTIVES: We developed and validated a complete methodology for quantitative metabolomics and isotopologue profiling of isoprenoid precursors in the yeast Saccharomyces cerevisiae. METHODS: This workflow covers all the experimental and computational steps from sample collection and preparation to data acquisition and processing. It also includes a novel quantification method based on liquid chromatography coupled to high-resolution mass spectrometry. Method validation followed the Metabolomics Standards Initiative guidelines. RESULTS: This workflow ensures accurate absolute quantification (RSD < 20%) of all mevalonate and prenyl pyrophosphates intermediates with a high sensitivity over a large linear range (from 0.1 to 50 pmol). In addition, we demonstrate that this workflow brings crucial information to design more efficient phytoene producers. Results indicate stable turnover rates of prenyl pyrophosphate intermediates in the constructed strains and provide quantitative information on the change of the biosynthetic flux of phytoene precursors. CONCLUSION: This methodology fills one of the last technical gaps for functional studies of isoprenoids biosynthesis and should be applicable to other eukaryotic and prokaryotic (micro)organisms after adaptation of some organism-dependent steps. This methodology also opens the way to (13)C-metabolic flux analysis of isoprenoid biosynthesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11306-019-1580-8) contains supplementary material, which is available to authorized users. Springer US 2019-08-21 2019 /pmc/articles/PMC6704079/ /pubmed/31435826 http://dx.doi.org/10.1007/s11306-019-1580-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Castaño-Cerezo, Sara
Kulyk-Barbier, Hanna
Millard, Pierre
Portais, Jean-Charles
Heux, Stéphanie
Truan, Gilles
Bellvert, Floriant
Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling
title Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling
title_full Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling
title_fullStr Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling
title_full_unstemmed Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling
title_short Functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling
title_sort functional analysis of isoprenoid precursors biosynthesis by quantitative metabolomics and isotopologue profiling
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704079/
https://www.ncbi.nlm.nih.gov/pubmed/31435826
http://dx.doi.org/10.1007/s11306-019-1580-8
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