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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...

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Autores principales: Zhou, Nerve, Swamy, Krishna B. S., Leu, Jun-Yi, McDonald, Michael J., Galafassi, Silvia, Compagno, Concetta, Piškur, Jure
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
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.
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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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