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A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s
BACKGROUND: (Pro)anthocyanidins are synthesized by the flavonoid biosynthesis pathway with multi-layered regulatory control. Methods for the analysis of the flavonoid composition in plants are well established for different purposes. However, they typically compromise either on speed or on depth of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007998/ https://www.ncbi.nlm.nih.gov/pubmed/27586417 http://dx.doi.org/10.1186/s12870-016-0880-7 |
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author | Jaegle, Benjamin Uroic, Miran Kalle Holtkotte, Xu Lucas, Christina Termath, Andreas Ole Schmalz, Hans-Günther Bucher, Marcel Hoecker, Ute Hülskamp, Martin Schrader, Andrea |
author_facet | Jaegle, Benjamin Uroic, Miran Kalle Holtkotte, Xu Lucas, Christina Termath, Andreas Ole Schmalz, Hans-Günther Bucher, Marcel Hoecker, Ute Hülskamp, Martin Schrader, Andrea |
author_sort | Jaegle, Benjamin |
collection | PubMed |
description | BACKGROUND: (Pro)anthocyanidins are synthesized by the flavonoid biosynthesis pathway with multi-layered regulatory control. Methods for the analysis of the flavonoid composition in plants are well established for different purposes. However, they typically compromise either on speed or on depth of analysis. RESULTS: In this work we combined and optimized different protocols to enable the analysis of the flavonoid biosynthesis pathway with as little as possible biological material. We chose core substances of this metabolic pathway that serve as a fingerprint to recognize alterations in the main branches of the pathway. We used a simplified sample preparation, two deuterated internal standards, a short and efficient LC separation, highly sensitive detection with tandem MS in multiple reaction monitoring (MRM) mode and hydrolytic release of the core substances to reduce complexity. The method was optimized for Arabidopsis thaliana seeds and seedlings. We demonstrate that one Col-0 seed/seedling is sufficient to obtain a fingerprint of the core substances of the flavonoid biosynthesis pathway. For comparative analysis of different genotypes, we suggest the use of 10 seed(lings). The analysis of Arabidopsis thaliana mutants affecting steps in the pathway revealed foreseen and unexpected alterations of the pathway. For example, HY5 was found to differentially regulate kaempferol in seeds vs. seedlings. Furthermore, our results suggest that COP1 is a master regulator of flavonoid biosynthesis in seedlings but not of flavonoid deposition in seeds. CONCLUSIONS: When sample numbers are high and the plant material is limited, this method effectively facilitates metabolic fingerprinting with one seed(ling), revealing shifts and differences in the pathway. Moreover the combination of extracted non-hydrolysed, extracted hydrolysed and non-extracted hydrolysed samples proved useful to deduce the class of derivative from which the individual flavonoids have been released. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-016-0880-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5007998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50079982016-09-02 A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s Jaegle, Benjamin Uroic, Miran Kalle Holtkotte, Xu Lucas, Christina Termath, Andreas Ole Schmalz, Hans-Günther Bucher, Marcel Hoecker, Ute Hülskamp, Martin Schrader, Andrea BMC Plant Biol Methodology Article BACKGROUND: (Pro)anthocyanidins are synthesized by the flavonoid biosynthesis pathway with multi-layered regulatory control. Methods for the analysis of the flavonoid composition in plants are well established for different purposes. However, they typically compromise either on speed or on depth of analysis. RESULTS: In this work we combined and optimized different protocols to enable the analysis of the flavonoid biosynthesis pathway with as little as possible biological material. We chose core substances of this metabolic pathway that serve as a fingerprint to recognize alterations in the main branches of the pathway. We used a simplified sample preparation, two deuterated internal standards, a short and efficient LC separation, highly sensitive detection with tandem MS in multiple reaction monitoring (MRM) mode and hydrolytic release of the core substances to reduce complexity. The method was optimized for Arabidopsis thaliana seeds and seedlings. We demonstrate that one Col-0 seed/seedling is sufficient to obtain a fingerprint of the core substances of the flavonoid biosynthesis pathway. For comparative analysis of different genotypes, we suggest the use of 10 seed(lings). The analysis of Arabidopsis thaliana mutants affecting steps in the pathway revealed foreseen and unexpected alterations of the pathway. For example, HY5 was found to differentially regulate kaempferol in seeds vs. seedlings. Furthermore, our results suggest that COP1 is a master regulator of flavonoid biosynthesis in seedlings but not of flavonoid deposition in seeds. CONCLUSIONS: When sample numbers are high and the plant material is limited, this method effectively facilitates metabolic fingerprinting with one seed(ling), revealing shifts and differences in the pathway. Moreover the combination of extracted non-hydrolysed, extracted hydrolysed and non-extracted hydrolysed samples proved useful to deduce the class of derivative from which the individual flavonoids have been released. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-016-0880-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-01 /pmc/articles/PMC5007998/ /pubmed/27586417 http://dx.doi.org/10.1186/s12870-016-0880-7 Text en © The Author(s). 2016 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Jaegle, Benjamin Uroic, Miran Kalle Holtkotte, Xu Lucas, Christina Termath, Andreas Ole Schmalz, Hans-Günther Bucher, Marcel Hoecker, Ute Hülskamp, Martin Schrader, Andrea A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s |
title | A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s |
title_full | A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s |
title_fullStr | A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s |
title_full_unstemmed | A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s |
title_short | A fast and simple LC-MS-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s |
title_sort | fast and simple lc-ms-based characterization of the flavonoid biosynthesis pathway for few seed(ling)s |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007998/ https://www.ncbi.nlm.nih.gov/pubmed/27586417 http://dx.doi.org/10.1186/s12870-016-0880-7 |
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