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Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms
Overflow metabolism is well known for yeast, bacteria and mammalian cells. It typically occurs under glucose excess conditions and is characterized by excretions of by-products such as ethanol, acetate or lactate. This phenomenon, also denoted the short-term Crabtree effect, has been extensively stu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526501/ https://www.ncbi.nlm.nih.gov/pubmed/22963408 http://dx.doi.org/10.1186/1475-2859-11-122 |
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author | Paczia, Nicole Nilgen, Anke Lehmann, Tobias Gätgens, Jochem Wiechert, Wolfgang Noack, Stephan |
author_facet | Paczia, Nicole Nilgen, Anke Lehmann, Tobias Gätgens, Jochem Wiechert, Wolfgang Noack, Stephan |
author_sort | Paczia, Nicole |
collection | PubMed |
description | Overflow metabolism is well known for yeast, bacteria and mammalian cells. It typically occurs under glucose excess conditions and is characterized by excretions of by-products such as ethanol, acetate or lactate. This phenomenon, also denoted the short-term Crabtree effect, has been extensively studied over the past few decades, however, its basic regulatory mechanism and functional role in metabolism is still unknown. Here we present a comprehensive quantitative and time-dependent analysis of the exometabolome of Escherichia coli, Corynebacterium glutamicum, Bacillus licheniformis, and Saccharomyces cerevisiae during well-controlled bioreactor cultivations. Most surprisingly, in all cases a great diversity of central metabolic intermediates and amino acids is found in the culture medium with extracellular concentrations varying in the micromolar range. Different hypotheses for these observations are formulated and experimentally tested. As a result, the intermediates in the culture medium during batch growth must originate from passive or active transportation due to a new phenomenon termed “extended” overflow metabolism. Moreover, we provide broad evidence that this could be a common feature of all microorganism species when cultivated under conditions of carbon excess and non-inhibited carbon uptake. In turn, this finding has consequences for metabolite balancing and, particularly, for intracellular metabolite quantification and (13)C-metabolic flux analysis. |
format | Online Article Text |
id | pubmed-3526501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35265012012-12-20 Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms Paczia, Nicole Nilgen, Anke Lehmann, Tobias Gätgens, Jochem Wiechert, Wolfgang Noack, Stephan Microb Cell Fact Research Overflow metabolism is well known for yeast, bacteria and mammalian cells. It typically occurs under glucose excess conditions and is characterized by excretions of by-products such as ethanol, acetate or lactate. This phenomenon, also denoted the short-term Crabtree effect, has been extensively studied over the past few decades, however, its basic regulatory mechanism and functional role in metabolism is still unknown. Here we present a comprehensive quantitative and time-dependent analysis of the exometabolome of Escherichia coli, Corynebacterium glutamicum, Bacillus licheniformis, and Saccharomyces cerevisiae during well-controlled bioreactor cultivations. Most surprisingly, in all cases a great diversity of central metabolic intermediates and amino acids is found in the culture medium with extracellular concentrations varying in the micromolar range. Different hypotheses for these observations are formulated and experimentally tested. As a result, the intermediates in the culture medium during batch growth must originate from passive or active transportation due to a new phenomenon termed “extended” overflow metabolism. Moreover, we provide broad evidence that this could be a common feature of all microorganism species when cultivated under conditions of carbon excess and non-inhibited carbon uptake. In turn, this finding has consequences for metabolite balancing and, particularly, for intracellular metabolite quantification and (13)C-metabolic flux analysis. BioMed Central 2012-09-11 /pmc/articles/PMC3526501/ /pubmed/22963408 http://dx.doi.org/10.1186/1475-2859-11-122 Text en Copyright ©2012 Paczia et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paczia, Nicole Nilgen, Anke Lehmann, Tobias Gätgens, Jochem Wiechert, Wolfgang Noack, Stephan Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms |
title | Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms |
title_full | Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms |
title_fullStr | Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms |
title_full_unstemmed | Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms |
title_short | Extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms |
title_sort | extensive exometabolome analysis reveals extended overflow metabolism in various microorganisms |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526501/ https://www.ncbi.nlm.nih.gov/pubmed/22963408 http://dx.doi.org/10.1186/1475-2859-11-122 |
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