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Glycerol suppresses glucose consumption in trypanosomes through metabolic contest
Microorganisms must make the right choice for nutrient consumption to adapt to their changing environment. As a consequence, bacteria and yeasts have developed regulatory mechanisms involving nutrient sensing and signaling, known as “catabolite repression,” allowing redirection of cell metabolism to...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386887/ https://www.ncbi.nlm.nih.gov/pubmed/34388147 http://dx.doi.org/10.1371/journal.pbio.3001359 |
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author | Allmann, Stefan Wargnies, Marion Plazolles, Nicolas Cahoreau, Edern Biran, Marc Morand, Pauline Pineda, Erika Kulyk, Hanna Asencio, Corinne Villafraz, Oriana Rivière, Loïc Tetaud, Emmanuel Rotureau, Brice Mourier, Arnaud Portais, Jean-Charles Bringaud, Frédéric |
author_facet | Allmann, Stefan Wargnies, Marion Plazolles, Nicolas Cahoreau, Edern Biran, Marc Morand, Pauline Pineda, Erika Kulyk, Hanna Asencio, Corinne Villafraz, Oriana Rivière, Loïc Tetaud, Emmanuel Rotureau, Brice Mourier, Arnaud Portais, Jean-Charles Bringaud, Frédéric |
author_sort | Allmann, Stefan |
collection | PubMed |
description | Microorganisms must make the right choice for nutrient consumption to adapt to their changing environment. As a consequence, bacteria and yeasts have developed regulatory mechanisms involving nutrient sensing and signaling, known as “catabolite repression,” allowing redirection of cell metabolism to maximize the consumption of an energy-efficient carbon source. Here, we report a new mechanism named “metabolic contest” for regulating the use of carbon sources without nutrient sensing and signaling. Trypanosoma brucei is a unicellular eukaryote transmitted by tsetse flies and causing human African trypanosomiasis, or sleeping sickness. We showed that, in contrast to most microorganisms, the insect stages of this parasite developed a preference for glycerol over glucose, with glucose consumption beginning after the depletion of glycerol present in the medium. This “metabolic contest” depends on the combination of 3 conditions: (i) the sequestration of both metabolic pathways in the same subcellular compartment, here in the peroxisomal-related organelles named glycosomes; (ii) the competition for the same substrate, here ATP, with the first enzymatic step of the glycerol and glucose metabolic pathways both being ATP-dependent (glycerol kinase and hexokinase, respectively); and (iii) an unbalanced activity between the competing enzymes, here the glycerol kinase activity being approximately 80-fold higher than the hexokinase activity. As predicted by our model, an approximately 50-fold down-regulation of the GK expression abolished the preference for glycerol over glucose, with glucose and glycerol being metabolized concomitantly. In theory, a metabolic contest could be found in any organism provided that the 3 conditions listed above are met. |
format | Online Article Text |
id | pubmed-8386887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83868872021-08-26 Glycerol suppresses glucose consumption in trypanosomes through metabolic contest Allmann, Stefan Wargnies, Marion Plazolles, Nicolas Cahoreau, Edern Biran, Marc Morand, Pauline Pineda, Erika Kulyk, Hanna Asencio, Corinne Villafraz, Oriana Rivière, Loïc Tetaud, Emmanuel Rotureau, Brice Mourier, Arnaud Portais, Jean-Charles Bringaud, Frédéric PLoS Biol Research Article Microorganisms must make the right choice for nutrient consumption to adapt to their changing environment. As a consequence, bacteria and yeasts have developed regulatory mechanisms involving nutrient sensing and signaling, known as “catabolite repression,” allowing redirection of cell metabolism to maximize the consumption of an energy-efficient carbon source. Here, we report a new mechanism named “metabolic contest” for regulating the use of carbon sources without nutrient sensing and signaling. Trypanosoma brucei is a unicellular eukaryote transmitted by tsetse flies and causing human African trypanosomiasis, or sleeping sickness. We showed that, in contrast to most microorganisms, the insect stages of this parasite developed a preference for glycerol over glucose, with glucose consumption beginning after the depletion of glycerol present in the medium. This “metabolic contest” depends on the combination of 3 conditions: (i) the sequestration of both metabolic pathways in the same subcellular compartment, here in the peroxisomal-related organelles named glycosomes; (ii) the competition for the same substrate, here ATP, with the first enzymatic step of the glycerol and glucose metabolic pathways both being ATP-dependent (glycerol kinase and hexokinase, respectively); and (iii) an unbalanced activity between the competing enzymes, here the glycerol kinase activity being approximately 80-fold higher than the hexokinase activity. As predicted by our model, an approximately 50-fold down-regulation of the GK expression abolished the preference for glycerol over glucose, with glucose and glycerol being metabolized concomitantly. In theory, a metabolic contest could be found in any organism provided that the 3 conditions listed above are met. Public Library of Science 2021-08-13 /pmc/articles/PMC8386887/ /pubmed/34388147 http://dx.doi.org/10.1371/journal.pbio.3001359 Text en © 2021 Allmann et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Allmann, Stefan Wargnies, Marion Plazolles, Nicolas Cahoreau, Edern Biran, Marc Morand, Pauline Pineda, Erika Kulyk, Hanna Asencio, Corinne Villafraz, Oriana Rivière, Loïc Tetaud, Emmanuel Rotureau, Brice Mourier, Arnaud Portais, Jean-Charles Bringaud, Frédéric Glycerol suppresses glucose consumption in trypanosomes through metabolic contest |
title | Glycerol suppresses glucose consumption in trypanosomes through metabolic contest |
title_full | Glycerol suppresses glucose consumption in trypanosomes through metabolic contest |
title_fullStr | Glycerol suppresses glucose consumption in trypanosomes through metabolic contest |
title_full_unstemmed | Glycerol suppresses glucose consumption in trypanosomes through metabolic contest |
title_short | Glycerol suppresses glucose consumption in trypanosomes through metabolic contest |
title_sort | glycerol suppresses glucose consumption in trypanosomes through metabolic contest |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386887/ https://www.ncbi.nlm.nih.gov/pubmed/34388147 http://dx.doi.org/10.1371/journal.pbio.3001359 |
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