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Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis

BACKGROUND: Recent studies using transcript and metabolite profiles of wild-type and gene deletion mutants revealed that photorespiratory pathways are essential for the growth of Synechocystis sp. PCC 6803 under atmospheric conditions. Pool size changes of primary metabolites, such as glycine and gl...

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Autores principales: Huege, Jan, Goetze, Jan, Schwarz, Doreen, Bauwe, Hermann, Hagemann, Martin, Kopka, Joachim
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025020/
https://www.ncbi.nlm.nih.gov/pubmed/21283704
http://dx.doi.org/10.1371/journal.pone.0016278
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author Huege, Jan
Goetze, Jan
Schwarz, Doreen
Bauwe, Hermann
Hagemann, Martin
Kopka, Joachim
author_facet Huege, Jan
Goetze, Jan
Schwarz, Doreen
Bauwe, Hermann
Hagemann, Martin
Kopka, Joachim
author_sort Huege, Jan
collection PubMed
description BACKGROUND: Recent studies using transcript and metabolite profiles of wild-type and gene deletion mutants revealed that photorespiratory pathways are essential for the growth of Synechocystis sp. PCC 6803 under atmospheric conditions. Pool size changes of primary metabolites, such as glycine and glycolate, indicated a link to photorespiration. METHODOLOGY/PRINCIPAL FINDINGS: The (13)C labelling kinetics of primary metabolites were analysed in photoautotrophically grown cultures of Synechocystis sp. PCC 6803 by gas chromatography-mass spectrometry (GC-MS) to demonstrate the link with photorespiration. Cells pre-acclimated to high CO(2) (5%, HC) or limited CO(2) (0.035%, LC) conditions were pulse-labelled under very high (2% w/w) (13)C-NaHCO(3) (VHC) conditions followed by treatment with ambient (12)C at HC and LC conditions, respectively. The (13)C enrichment, relative changes in pool size, and (13)C flux of selected metabolites were evaluated. We demonstrate two major paths of CO(2) assimilation via Rubisco in Synechocystis, i.e., from 3PGA via PEP to aspartate, malate and citrate or, to a lesser extent, from 3PGA via glucose-6-phosphate to sucrose. The results reveal evidence of carbon channelling from 3PGA to the PEP pool. Furthermore, (13)C labelling of glycolate was observed under conditions thought to suppress photorespiration. Using the glycolate-accumulating ΔglcD1 mutant, we demonstrate enhanced (13)C partitioning into the glycolate pool under conditions favouring photorespiration and enhanced (13)C partitioning into the glycine pool of the glycine-accumulating ΔgcvT mutant. Under LC conditions, the photorespiratory mutants ΔglcD1 and ΔgcvT showed enhanced activity of the additional carbon-fixing PEP carboxylase pathway. CONCLUSIONS/SIGNIFICANCE: With our approach of non-steady-state (13)C labelling and analysis of metabolite pool sizes with respective (13)C enrichments, we identify the use and modulation of major pathways of carbon assimilation in Synechocystis in the presence of high and low inorganic carbon supplies.
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spelling pubmed-30250202011-01-31 Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis Huege, Jan Goetze, Jan Schwarz, Doreen Bauwe, Hermann Hagemann, Martin Kopka, Joachim PLoS One Research Article BACKGROUND: Recent studies using transcript and metabolite profiles of wild-type and gene deletion mutants revealed that photorespiratory pathways are essential for the growth of Synechocystis sp. PCC 6803 under atmospheric conditions. Pool size changes of primary metabolites, such as glycine and glycolate, indicated a link to photorespiration. METHODOLOGY/PRINCIPAL FINDINGS: The (13)C labelling kinetics of primary metabolites were analysed in photoautotrophically grown cultures of Synechocystis sp. PCC 6803 by gas chromatography-mass spectrometry (GC-MS) to demonstrate the link with photorespiration. Cells pre-acclimated to high CO(2) (5%, HC) or limited CO(2) (0.035%, LC) conditions were pulse-labelled under very high (2% w/w) (13)C-NaHCO(3) (VHC) conditions followed by treatment with ambient (12)C at HC and LC conditions, respectively. The (13)C enrichment, relative changes in pool size, and (13)C flux of selected metabolites were evaluated. We demonstrate two major paths of CO(2) assimilation via Rubisco in Synechocystis, i.e., from 3PGA via PEP to aspartate, malate and citrate or, to a lesser extent, from 3PGA via glucose-6-phosphate to sucrose. The results reveal evidence of carbon channelling from 3PGA to the PEP pool. Furthermore, (13)C labelling of glycolate was observed under conditions thought to suppress photorespiration. Using the glycolate-accumulating ΔglcD1 mutant, we demonstrate enhanced (13)C partitioning into the glycolate pool under conditions favouring photorespiration and enhanced (13)C partitioning into the glycine pool of the glycine-accumulating ΔgcvT mutant. Under LC conditions, the photorespiratory mutants ΔglcD1 and ΔgcvT showed enhanced activity of the additional carbon-fixing PEP carboxylase pathway. CONCLUSIONS/SIGNIFICANCE: With our approach of non-steady-state (13)C labelling and analysis of metabolite pool sizes with respective (13)C enrichments, we identify the use and modulation of major pathways of carbon assimilation in Synechocystis in the presence of high and low inorganic carbon supplies. Public Library of Science 2011-01-21 /pmc/articles/PMC3025020/ /pubmed/21283704 http://dx.doi.org/10.1371/journal.pone.0016278 Text en Huege et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Huege, Jan
Goetze, Jan
Schwarz, Doreen
Bauwe, Hermann
Hagemann, Martin
Kopka, Joachim
Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis
title Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis
title_full Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis
title_fullStr Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis
title_full_unstemmed Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis
title_short Modulation of the Major Paths of Carbon in Photorespiratory Mutants of Synechocystis
title_sort modulation of the major paths of carbon in photorespiratory mutants of synechocystis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025020/
https://www.ncbi.nlm.nih.gov/pubmed/21283704
http://dx.doi.org/10.1371/journal.pone.0016278
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