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Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies
INTRODUCTION: Xanthophyllomyces dendrorhous is a non-conventional industrial yeast. It has the unique ability among yeasts to produce geranylgeranyl pyrophosphate derived terpenoids such as carotenoids and in particular the high value pigment astaxanthin. OBJECTIVE: In order to fully exploit the ind...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809543/ https://www.ncbi.nlm.nih.gov/pubmed/29479298 http://dx.doi.org/10.1007/s11306-017-1313-9 |
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author | Alcalde, Eugenio Fraser, Paul D. |
author_facet | Alcalde, Eugenio Fraser, Paul D. |
author_sort | Alcalde, Eugenio |
collection | PubMed |
description | INTRODUCTION: Xanthophyllomyces dendrorhous is a non-conventional industrial yeast. It has the unique ability among yeasts to produce geranylgeranyl pyrophosphate derived terpenoids such as carotenoids and in particular the high value pigment astaxanthin. OBJECTIVE: In order to fully exploit the industrial potential of Xanthophyllomyces using modern industrial biotechnology approaches the further development of “omic” resources in this organism are required to build on the now sequenced and annotated genome. To contribute to this goal, the present study has developed and implemented an efficient metabolite profiling system comprised of, quenching, extraction and associated GC–MS and UPLC analysis. METHOD: Four quenching methods and five extraction methods compatible with GC–MS and UPLC profiling were tested and validated by analysing steady state metabolite changes of Xanthophyllomyces cultivated at laboratory scale in liquid shake culture at lag, exponential and early and late stationary phases. RESULTS: A customised Automated Mass Spectral Deconvolution and Identification System (AMDIS) library has been created for Xanthophyllomyces, over 400 compounds are present in the library of which 78 are detected and quantified routinely in polar and non-polar derived extracts. A preliminary biochemical network has been constructed. Over a standardised laboratory growth cycle, changes in metabolite levels have been determined to create reference point for future strain improvement approaches and the initial biochemical network construction. Correlation analysis has illustrated that astaxanthin formation correlates positively with different sectors of intermediary metabolism (e.g. the TCA cycle intermediates and amino acid formation), “short” saturated fatty acids and β-carotene, while other metabolites are reduced in response to astaxanthin production. These sectors of intermediary metabolism offer potential future targets for the manipulation resulting in the generation of strains with improved titres of given terpenoids. DISCUSSION: In summary a robust metabolite profiling system for Xanthophyllomyces is in place to further our understanding and potential exploitation of this underutilised industrial yeast. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11306-017-1313-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5809543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-58095432018-02-22 Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies Alcalde, Eugenio Fraser, Paul D. Metabolomics Original Article INTRODUCTION: Xanthophyllomyces dendrorhous is a non-conventional industrial yeast. It has the unique ability among yeasts to produce geranylgeranyl pyrophosphate derived terpenoids such as carotenoids and in particular the high value pigment astaxanthin. OBJECTIVE: In order to fully exploit the industrial potential of Xanthophyllomyces using modern industrial biotechnology approaches the further development of “omic” resources in this organism are required to build on the now sequenced and annotated genome. To contribute to this goal, the present study has developed and implemented an efficient metabolite profiling system comprised of, quenching, extraction and associated GC–MS and UPLC analysis. METHOD: Four quenching methods and five extraction methods compatible with GC–MS and UPLC profiling were tested and validated by analysing steady state metabolite changes of Xanthophyllomyces cultivated at laboratory scale in liquid shake culture at lag, exponential and early and late stationary phases. RESULTS: A customised Automated Mass Spectral Deconvolution and Identification System (AMDIS) library has been created for Xanthophyllomyces, over 400 compounds are present in the library of which 78 are detected and quantified routinely in polar and non-polar derived extracts. A preliminary biochemical network has been constructed. Over a standardised laboratory growth cycle, changes in metabolite levels have been determined to create reference point for future strain improvement approaches and the initial biochemical network construction. Correlation analysis has illustrated that astaxanthin formation correlates positively with different sectors of intermediary metabolism (e.g. the TCA cycle intermediates and amino acid formation), “short” saturated fatty acids and β-carotene, while other metabolites are reduced in response to astaxanthin production. These sectors of intermediary metabolism offer potential future targets for the manipulation resulting in the generation of strains with improved titres of given terpenoids. DISCUSSION: In summary a robust metabolite profiling system for Xanthophyllomyces is in place to further our understanding and potential exploitation of this underutilised industrial yeast. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11306-017-1313-9) contains supplementary material, which is available to authorized users. Springer US 2018-02-12 2018 /pmc/articles/PMC5809543/ /pubmed/29479298 http://dx.doi.org/10.1007/s11306-017-1313-9 Text en © The Author(s) 2018 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 Alcalde, Eugenio Fraser, Paul D. Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies |
title | Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies |
title_full | Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies |
title_fullStr | Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies |
title_full_unstemmed | Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies |
title_short | Extending our tools and resources in the non-conventional industrial yeast Xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies |
title_sort | extending our tools and resources in the non-conventional industrial yeast xanthophyllomyces dendrorhous through the application of metabolite profiling methodologies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809543/ https://www.ncbi.nlm.nih.gov/pubmed/29479298 http://dx.doi.org/10.1007/s11306-017-1313-9 |
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