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Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff
Maximizing growth and survival in the face of a complex, time-varying environment is a common problem for single-celled organisms in the wild. When offered two different sugars as carbon sources, microorganisms first consume the preferred sugar, then undergo a transient growth delay, the “diauxic la...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4308108/ https://www.ncbi.nlm.nih.gov/pubmed/25626068 http://dx.doi.org/10.1371/journal.pbio.1002041 |
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author | Wang, Jue Atolia, Esha Hua, Bo Savir, Yonatan Escalante-Chong, Renan Springer, Michael |
author_facet | Wang, Jue Atolia, Esha Hua, Bo Savir, Yonatan Escalante-Chong, Renan Springer, Michael |
author_sort | Wang, Jue |
collection | PubMed |
description | Maximizing growth and survival in the face of a complex, time-varying environment is a common problem for single-celled organisms in the wild. When offered two different sugars as carbon sources, microorganisms first consume the preferred sugar, then undergo a transient growth delay, the “diauxic lag,” while inducing genes to metabolize the less preferred sugar. This delay is commonly assumed to be an inevitable consequence of selection to maximize use of the preferred sugar. Contrary to this view, we found that many natural isolates of Saccharomyces cerevisiae display short or nonexistent diauxic lags when grown in mixtures of glucose (preferred) and galactose. These strains induce galactose utilization (GAL) genes hours before glucose exhaustion, thereby “preparing” for the transition from glucose to galactose metabolism. The extent of preparation varies across strains, and seems to be determined by the steady-state response of GAL genes to mixtures of glucose and galactose rather than by induction kinetics. Although early GAL gene induction gives strains a competitive advantage once glucose runs out, it comes at a cost while glucose is still present. Costs and benefits correlate with the degree of preparation: strains with higher expression of GAL genes prior to glucose exhaustion experience a larger upfront growth cost but also a shorter diauxic lag. Our results show that classical diauxic growth is only one extreme on a continuum of growth strategies constrained by a cost–benefit tradeoff. This type of continuum is likely to be common in nature, as similar tradeoffs can arise whenever cells evolve to use mixtures of nutrients. |
format | Online Article Text |
id | pubmed-4308108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43081082015-02-06 Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff Wang, Jue Atolia, Esha Hua, Bo Savir, Yonatan Escalante-Chong, Renan Springer, Michael PLoS Biol Research Article Maximizing growth and survival in the face of a complex, time-varying environment is a common problem for single-celled organisms in the wild. When offered two different sugars as carbon sources, microorganisms first consume the preferred sugar, then undergo a transient growth delay, the “diauxic lag,” while inducing genes to metabolize the less preferred sugar. This delay is commonly assumed to be an inevitable consequence of selection to maximize use of the preferred sugar. Contrary to this view, we found that many natural isolates of Saccharomyces cerevisiae display short or nonexistent diauxic lags when grown in mixtures of glucose (preferred) and galactose. These strains induce galactose utilization (GAL) genes hours before glucose exhaustion, thereby “preparing” for the transition from glucose to galactose metabolism. The extent of preparation varies across strains, and seems to be determined by the steady-state response of GAL genes to mixtures of glucose and galactose rather than by induction kinetics. Although early GAL gene induction gives strains a competitive advantage once glucose runs out, it comes at a cost while glucose is still present. Costs and benefits correlate with the degree of preparation: strains with higher expression of GAL genes prior to glucose exhaustion experience a larger upfront growth cost but also a shorter diauxic lag. Our results show that classical diauxic growth is only one extreme on a continuum of growth strategies constrained by a cost–benefit tradeoff. This type of continuum is likely to be common in nature, as similar tradeoffs can arise whenever cells evolve to use mixtures of nutrients. Public Library of Science 2015-01-27 /pmc/articles/PMC4308108/ /pubmed/25626068 http://dx.doi.org/10.1371/journal.pbio.1002041 Text en © 2015 Wang 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wang, Jue Atolia, Esha Hua, Bo Savir, Yonatan Escalante-Chong, Renan Springer, Michael Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff |
title | Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff |
title_full | Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff |
title_fullStr | Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff |
title_full_unstemmed | Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff |
title_short | Natural Variation in Preparation for Nutrient Depletion Reveals a Cost–Benefit Tradeoff |
title_sort | natural variation in preparation for nutrient depletion reveals a cost–benefit tradeoff |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4308108/ https://www.ncbi.nlm.nih.gov/pubmed/25626068 http://dx.doi.org/10.1371/journal.pbio.1002041 |
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