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Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging

Optimal metabolic trade-offs between growth and productivity are key constraints in strain optimization by metabolic engineering; however, how cellular noise impacts these trade-offs and drives the emergence of subpopulations with distinct resource allocation strategies, remains largely unknown. Her...

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Autores principales: Vasdekis, A. E., Alanazi, H., Silverman, A. M., Williams, C. J., Canul, A. J., Cliff, J. B., Dohnalkova, A. C., Stephanopoulos, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381102/
https://www.ncbi.nlm.nih.gov/pubmed/30783105
http://dx.doi.org/10.1038/s41467-019-08717-w
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author Vasdekis, A. E.
Alanazi, H.
Silverman, A. M.
Williams, C. J.
Canul, A. J.
Cliff, J. B.
Dohnalkova, A. C.
Stephanopoulos, G.
author_facet Vasdekis, A. E.
Alanazi, H.
Silverman, A. M.
Williams, C. J.
Canul, A. J.
Cliff, J. B.
Dohnalkova, A. C.
Stephanopoulos, G.
author_sort Vasdekis, A. E.
collection PubMed
description Optimal metabolic trade-offs between growth and productivity are key constraints in strain optimization by metabolic engineering; however, how cellular noise impacts these trade-offs and drives the emergence of subpopulations with distinct resource allocation strategies, remains largely unknown. Here, we introduce a single-cell strategy for quantifying the trade-offs between triacylglycerol production and growth in the oleaginous microorganism Yarrowia lipolytica. The strategy relies on high-throughput quantitative-phase imaging and, enabled by nanoscale secondary ion mass spectrometry analyses and dedicated image processing, allows us to image how resources are partitioned between growth and productivity. Enhanced precision over population-averaging biotechnologies and conventional microscopy demonstrates how cellular noise impacts growth and productivity differently. As such, subpopulations with distinct metabolic trade-offs emerge, with notable impacts on strain performance and robustness. By quantifying the self-degradation of cytosolic macromolecules under nutrient-limiting conditions, we discover the cell-to-cell heterogeneity in protein and fatty-acid recycling, unmasking a potential bet-hedging strategy under starvation.
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spelling pubmed-63811022019-02-21 Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging Vasdekis, A. E. Alanazi, H. Silverman, A. M. Williams, C. J. Canul, A. J. Cliff, J. B. Dohnalkova, A. C. Stephanopoulos, G. Nat Commun Article Optimal metabolic trade-offs between growth and productivity are key constraints in strain optimization by metabolic engineering; however, how cellular noise impacts these trade-offs and drives the emergence of subpopulations with distinct resource allocation strategies, remains largely unknown. Here, we introduce a single-cell strategy for quantifying the trade-offs between triacylglycerol production and growth in the oleaginous microorganism Yarrowia lipolytica. The strategy relies on high-throughput quantitative-phase imaging and, enabled by nanoscale secondary ion mass spectrometry analyses and dedicated image processing, allows us to image how resources are partitioned between growth and productivity. Enhanced precision over population-averaging biotechnologies and conventional microscopy demonstrates how cellular noise impacts growth and productivity differently. As such, subpopulations with distinct metabolic trade-offs emerge, with notable impacts on strain performance and robustness. By quantifying the self-degradation of cytosolic macromolecules under nutrient-limiting conditions, we discover the cell-to-cell heterogeneity in protein and fatty-acid recycling, unmasking a potential bet-hedging strategy under starvation. Nature Publishing Group UK 2019-02-19 /pmc/articles/PMC6381102/ /pubmed/30783105 http://dx.doi.org/10.1038/s41467-019-08717-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Vasdekis, A. E.
Alanazi, H.
Silverman, A. M.
Williams, C. J.
Canul, A. J.
Cliff, J. B.
Dohnalkova, A. C.
Stephanopoulos, G.
Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging
title Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging
title_full Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging
title_fullStr Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging
title_full_unstemmed Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging
title_short Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging
title_sort eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381102/
https://www.ncbi.nlm.nih.gov/pubmed/30783105
http://dx.doi.org/10.1038/s41467-019-08717-w
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