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Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri
The Crabtree positive yeasts, such as Saccharomyces cerevisiae, prefer fermentation to respiration, even under fully aerobic conditions. The selective pressures that drove the evolution of this trait remain controversial because of the low ATP yield of fermentation compared to respiration. Here we p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345805/ https://www.ncbi.nlm.nih.gov/pubmed/28282411 http://dx.doi.org/10.1371/journal.pone.0173318 |
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author | Zhou, Nerve Swamy, Krishna B. S. Leu, Jun-Yi McDonald, Michael J. Galafassi, Silvia Compagno, Concetta Piškur, Jure |
author_facet | Zhou, Nerve Swamy, Krishna B. S. Leu, Jun-Yi McDonald, Michael J. Galafassi, Silvia Compagno, Concetta Piškur, Jure |
author_sort | Zhou, Nerve |
collection | PubMed |
description | The Crabtree positive yeasts, such as Saccharomyces cerevisiae, prefer fermentation to respiration, even under fully aerobic conditions. The selective pressures that drove the evolution of this trait remain controversial because of the low ATP yield of fermentation compared to respiration. Here we propagate experimental populations of the weak-Crabtree yeast Lachancea kluyveri, in competitive co-culture with bacteria. We find that L. kluyveri adapts by producing quantities of ethanol lethal to bacteria and evolves several of the defining characteristics of Crabtree positive yeasts. We use precise quantitative analysis to show that the rate advantage of fermentation over aerobic respiration is insufficient to provide an overall growth advantage. Thus, the rapid consumption of glucose and the utilization of ethanol are essential for the success of the aerobic fermentation strategy. These results corroborate that selection derived from competition with bacteria could have provided the impetus for the evolution of the Crabtree positive trait. |
format | Online Article Text |
id | pubmed-5345805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53458052017-03-30 Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri Zhou, Nerve Swamy, Krishna B. S. Leu, Jun-Yi McDonald, Michael J. Galafassi, Silvia Compagno, Concetta Piškur, Jure PLoS One Research Article The Crabtree positive yeasts, such as Saccharomyces cerevisiae, prefer fermentation to respiration, even under fully aerobic conditions. The selective pressures that drove the evolution of this trait remain controversial because of the low ATP yield of fermentation compared to respiration. Here we propagate experimental populations of the weak-Crabtree yeast Lachancea kluyveri, in competitive co-culture with bacteria. We find that L. kluyveri adapts by producing quantities of ethanol lethal to bacteria and evolves several of the defining characteristics of Crabtree positive yeasts. We use precise quantitative analysis to show that the rate advantage of fermentation over aerobic respiration is insufficient to provide an overall growth advantage. Thus, the rapid consumption of glucose and the utilization of ethanol are essential for the success of the aerobic fermentation strategy. These results corroborate that selection derived from competition with bacteria could have provided the impetus for the evolution of the Crabtree positive trait. Public Library of Science 2017-03-10 /pmc/articles/PMC5345805/ /pubmed/28282411 http://dx.doi.org/10.1371/journal.pone.0173318 Text en © 2017 Zhou 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 (http://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 Zhou, Nerve Swamy, Krishna B. S. Leu, Jun-Yi McDonald, Michael J. Galafassi, Silvia Compagno, Concetta Piškur, Jure Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri |
title | Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri |
title_full | Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri |
title_fullStr | Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri |
title_full_unstemmed | Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri |
title_short | Coevolution with bacteria drives the evolution of aerobic fermentation in Lachancea kluyveri |
title_sort | coevolution with bacteria drives the evolution of aerobic fermentation in lachancea kluyveri |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345805/ https://www.ncbi.nlm.nih.gov/pubmed/28282411 http://dx.doi.org/10.1371/journal.pone.0173318 |
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