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Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus
BACKGROUND: UDP-glucose pyrophosphorylase (UGPase) is a sugar-metabolizing enzyme (E.C. 2.7.7.9) that catalyzes a reversible reaction of UDP-glucose and pyrophosphate from glucose-1-phosphate and UTP. UDP-glucose is a key intermediate sugar that is channeled to multiple metabolic pathways. The funct...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197241/ https://www.ncbi.nlm.nih.gov/pubmed/25287590 http://dx.doi.org/10.1186/s12870-014-0265-8 |
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author | Payyavula, Raja S Tschaplinski, Timothy J Jawdy, Sara S Sykes, Robert W Tuskan, Gerald A Kalluri, Udaya C |
author_facet | Payyavula, Raja S Tschaplinski, Timothy J Jawdy, Sara S Sykes, Robert W Tuskan, Gerald A Kalluri, Udaya C |
author_sort | Payyavula, Raja S |
collection | PubMed |
description | BACKGROUND: UDP-glucose pyrophosphorylase (UGPase) is a sugar-metabolizing enzyme (E.C. 2.7.7.9) that catalyzes a reversible reaction of UDP-glucose and pyrophosphate from glucose-1-phosphate and UTP. UDP-glucose is a key intermediate sugar that is channeled to multiple metabolic pathways. The functional role of UGPase in perennial woody plants is poorly understood. RESULTS: We characterized the functional role of a UGPase gene in Populus deltoides, PdUGPase2. Overexpression of the native gene resulted in increased leaf area and leaf-to-shoot biomass ratio but decreased shoot and root growth. Metabolomic analyses showed that manipulation of PdUGPase2 results in perturbations in primary, as well as secondary metabolism, resulting in reduced sugar and starch levels and increased phenolics, such as caffeoyl and feruloyl conjugates. While cellulose and lignin levels in the cell walls were not significantly altered, the syringyl-to-guaiacyl ratio was significantly reduced. CONCLUSIONS: These results demonstrate that PdUGPase2 plays a key role in the tightly coupled primary and secondary metabolic pathways and perturbation in its function results in pronounced effects on growth and metabolism beyond cell wall biosynthesis of Populus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0265-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4197241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41972412014-10-16 Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus Payyavula, Raja S Tschaplinski, Timothy J Jawdy, Sara S Sykes, Robert W Tuskan, Gerald A Kalluri, Udaya C BMC Plant Biol Research Article BACKGROUND: UDP-glucose pyrophosphorylase (UGPase) is a sugar-metabolizing enzyme (E.C. 2.7.7.9) that catalyzes a reversible reaction of UDP-glucose and pyrophosphate from glucose-1-phosphate and UTP. UDP-glucose is a key intermediate sugar that is channeled to multiple metabolic pathways. The functional role of UGPase in perennial woody plants is poorly understood. RESULTS: We characterized the functional role of a UGPase gene in Populus deltoides, PdUGPase2. Overexpression of the native gene resulted in increased leaf area and leaf-to-shoot biomass ratio but decreased shoot and root growth. Metabolomic analyses showed that manipulation of PdUGPase2 results in perturbations in primary, as well as secondary metabolism, resulting in reduced sugar and starch levels and increased phenolics, such as caffeoyl and feruloyl conjugates. While cellulose and lignin levels in the cell walls were not significantly altered, the syringyl-to-guaiacyl ratio was significantly reduced. CONCLUSIONS: These results demonstrate that PdUGPase2 plays a key role in the tightly coupled primary and secondary metabolic pathways and perturbation in its function results in pronounced effects on growth and metabolism beyond cell wall biosynthesis of Populus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0265-8) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-07 /pmc/articles/PMC4197241/ /pubmed/25287590 http://dx.doi.org/10.1186/s12870-014-0265-8 Text en © Payyavula et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Research Article Payyavula, Raja S Tschaplinski, Timothy J Jawdy, Sara S Sykes, Robert W Tuskan, Gerald A Kalluri, Udaya C Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus |
title | Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus |
title_full | Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus |
title_fullStr | Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus |
title_full_unstemmed | Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus |
title_short | Metabolic profiling reveals altered sugar and secondary metabolism in response to UGPase overexpression in Populus |
title_sort | metabolic profiling reveals altered sugar and secondary metabolism in response to ugpase overexpression in populus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197241/ https://www.ncbi.nlm.nih.gov/pubmed/25287590 http://dx.doi.org/10.1186/s12870-014-0265-8 |
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