Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xylose

<p>Abstract</p> <p>Background</p> <p>The concerted effects of changes in gene expression due to changes in the environment are ultimately reflected in the metabolome. Dynamics of metabolite concentrations under a certain condition can therefore give a description of the...

Full description

Bibliographic Details
Main Authors: Bergdahl Basti, Heer Dominik, Sauer Uwe, Hahn-Hägerdal Bärbel, van Niel Ed WJ
Format: Article
Language:English
Published: BMC 2012-05-01
Series:Biotechnology for Biofuels
Subjects:
Online Access:http://www.biotechnologyforbiofuels.com/content/5/1/34
_version_ 1828531180983549952
author Bergdahl Basti
Heer Dominik
Sauer Uwe
Hahn-Hägerdal Bärbel
van Niel Ed WJ
author_facet Bergdahl Basti
Heer Dominik
Sauer Uwe
Hahn-Hägerdal Bärbel
van Niel Ed WJ
author_sort Bergdahl Basti
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The concerted effects of changes in gene expression due to changes in the environment are ultimately reflected in the metabolome. Dynamics of metabolite concentrations under a certain condition can therefore give a description of the cellular state with a high degree of functional information. We used this potential to evaluate the metabolic status of two recombinant strains of <it>Saccharomyces cerevisiae</it> during anaerobic batch fermentation of a glucose/xylose mixture. Two isogenic strains were studied, differing only in the pathways used for xylose assimilation: the oxidoreductive pathway with xylose reductase (XR) and xylitol dehydrogenase (XDH) or the isomerization pathway with xylose isomerase (XI). The isogenic relationship between the two strains ascertains that the observed responses are a result of the particular xylose pathway and not due to unknown changes in regulatory systems. An increased understanding of the physiological state of these strains is important for further development of efficient pentose-utilizing strains for bioethanol production.</p> <p>Results</p> <p>Using LC-MS/MS we determined the dynamics in the concentrations of intracellular metabolites in central carbon metabolism, nine amino acids, the purine nucleotides and redox cofactors. The general response to the transition from glucose to xylose was increased concentrations of amino acids and TCA-cycle intermediates, and decreased concentrations of sugar phosphates and redox cofactors. The two strains investigated had significantly different uptake rates of xylose which led to an enhanced response in the XI-strain. Despite the difference in xylose uptake rate, the adenylate energy charge remained high and stable around 0.8 in both strains. In contrast to the adenylate pool, large changes were observed in the guanylate pool.</p> <p>Conclusions</p> <p>The low uptake of xylose by the XI-strain led to several distinguished responses: depletion of key metabolites in glycolysis and NADPH, a reduced GTP/GDP ratio and accumulation of PEP and aromatic amino acids. These changes are strong indicators of carbon starvation. The XR/XDH-strain displayed few such traits. The coexistence of these traits and a stable adenylate charge indicates that xylose supplies energy to the cells but does not suppress a response similar to carbon starvation. Particular signals may play a role in the latter, of which the GTP/GMP ratio could be a candidate as it decreased significantly in both strains.</p>
first_indexed 2024-12-11T22:34:00Z
format Article
id doaj.art-6c446a85fd424ddfbecbc0624bca346f
institution Directory Open Access Journal
issn 1754-6834
language English
last_indexed 2024-12-11T22:34:00Z
publishDate 2012-05-01
publisher BMC
record_format Article
series Biotechnology for Biofuels
spelling doaj.art-6c446a85fd424ddfbecbc0624bca346f2022-12-22T00:48:02ZengBMCBiotechnology for Biofuels1754-68342012-05-01513410.1186/1754-6834-5-34Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xyloseBergdahl BastiHeer DominikSauer UweHahn-Hägerdal Bärbelvan Niel Ed WJ<p>Abstract</p> <p>Background</p> <p>The concerted effects of changes in gene expression due to changes in the environment are ultimately reflected in the metabolome. Dynamics of metabolite concentrations under a certain condition can therefore give a description of the cellular state with a high degree of functional information. We used this potential to evaluate the metabolic status of two recombinant strains of <it>Saccharomyces cerevisiae</it> during anaerobic batch fermentation of a glucose/xylose mixture. Two isogenic strains were studied, differing only in the pathways used for xylose assimilation: the oxidoreductive pathway with xylose reductase (XR) and xylitol dehydrogenase (XDH) or the isomerization pathway with xylose isomerase (XI). The isogenic relationship between the two strains ascertains that the observed responses are a result of the particular xylose pathway and not due to unknown changes in regulatory systems. An increased understanding of the physiological state of these strains is important for further development of efficient pentose-utilizing strains for bioethanol production.</p> <p>Results</p> <p>Using LC-MS/MS we determined the dynamics in the concentrations of intracellular metabolites in central carbon metabolism, nine amino acids, the purine nucleotides and redox cofactors. The general response to the transition from glucose to xylose was increased concentrations of amino acids and TCA-cycle intermediates, and decreased concentrations of sugar phosphates and redox cofactors. The two strains investigated had significantly different uptake rates of xylose which led to an enhanced response in the XI-strain. Despite the difference in xylose uptake rate, the adenylate energy charge remained high and stable around 0.8 in both strains. In contrast to the adenylate pool, large changes were observed in the guanylate pool.</p> <p>Conclusions</p> <p>The low uptake of xylose by the XI-strain led to several distinguished responses: depletion of key metabolites in glycolysis and NADPH, a reduced GTP/GDP ratio and accumulation of PEP and aromatic amino acids. These changes are strong indicators of carbon starvation. The XR/XDH-strain displayed few such traits. The coexistence of these traits and a stable adenylate charge indicates that xylose supplies energy to the cells but does not suppress a response similar to carbon starvation. Particular signals may play a role in the latter, of which the GTP/GMP ratio could be a candidate as it decreased significantly in both strains.</p>http://www.biotechnologyforbiofuels.com/content/5/1/34MetabolomicsYeast metabolismXylose fermentationMetabolic statusStarvationBioethanol
spellingShingle Bergdahl Basti
Heer Dominik
Sauer Uwe
Hahn-Hägerdal Bärbel
van Niel Ed WJ
Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xylose
Biotechnology for Biofuels
Metabolomics
Yeast metabolism
Xylose fermentation
Metabolic status
Starvation
Bioethanol
title Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xylose
title_full Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xylose
title_fullStr Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xylose
title_full_unstemmed Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xylose
title_short Dynamic metabolomics differentiates between carbon and energy starvation in recombinant <it>Saccharomyces cerevisiae</it> fermenting xylose
title_sort dynamic metabolomics differentiates between carbon and energy starvation in recombinant it saccharomyces cerevisiae it fermenting xylose
topic Metabolomics
Yeast metabolism
Xylose fermentation
Metabolic status
Starvation
Bioethanol
url http://www.biotechnologyforbiofuels.com/content/5/1/34
work_keys_str_mv AT bergdahlbasti dynamicmetabolomicsdifferentiatesbetweencarbonandenergystarvationinrecombinantitsaccharomycescerevisiaeitfermentingxylose
AT heerdominik dynamicmetabolomicsdifferentiatesbetweencarbonandenergystarvationinrecombinantitsaccharomycescerevisiaeitfermentingxylose
AT saueruwe dynamicmetabolomicsdifferentiatesbetweencarbonandenergystarvationinrecombinantitsaccharomycescerevisiaeitfermentingxylose
AT hahnhagerdalbarbel dynamicmetabolomicsdifferentiatesbetweencarbonandenergystarvationinrecombinantitsaccharomycescerevisiaeitfermentingxylose
AT vannieledwj dynamicmetabolomicsdifferentiatesbetweencarbonandenergystarvationinrecombinantitsaccharomycescerevisiaeitfermentingxylose