Self-establishing communities enable cooperative metabolite exchange in a eukaryote

Metabolite exchange among co-growing cells is frequent by nature, however, is not necessarily occurring at growth-relevant quantities indicative of non-cell-autonomous metabolic function. Complementary auxotrophs of Saccharomyces cerevisiae amino acid and nucleotide metabolism regularly fail to comp...

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Main Authors: Kate Campbell, Jakob Vowinckel, Michael Mülleder, Silke Malmsheimer, Nicola Lawrence, Enrica Calvani, Leonor Miller-Fleming, Mohammad T Alam, Stefan Christen, Markus A Keller, Markus Ralser
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2015-10-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/09943
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spelling doaj-c95321687e0147c3ba882fb594c908d72021-05-05T00:05:03ZengeLife Sciences Publications LtdeLife2050-084X2015-10-01410.7554/eLife.09943Self-establishing communities enable cooperative metabolite exchange in a eukaryoteKate Campbell0Jakob Vowinckel1Michael Mülleder2Silke Malmsheimer3Nicola Lawrence4Enrica Calvani5Leonor Miller-Fleming6Mohammad T Alam7Stefan Christen8Markus A Keller9Markus Ralser10https://orcid.org/0000-0001-9535-7413Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomThe Wellcome Trust Gurdon Institute, University of Cambridge, Cambridge, United KingdomDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomInstitute of Molecular Systems Biology, ETH Zürich, Zurich, SwitzerlandDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United KingdomDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom; Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United Kingdom; Mill Hill Laboratory, The Francis Crick Institute, London, United KingdomMetabolite exchange among co-growing cells is frequent by nature, however, is not necessarily occurring at growth-relevant quantities indicative of non-cell-autonomous metabolic function. Complementary auxotrophs of Saccharomyces cerevisiae amino acid and nucleotide metabolism regularly fail to compensate for each other's deficiencies upon co-culturing, a situation which implied the absence of growth-relevant metabolite exchange interactions. Contrastingly, we find that yeast colonies maintain a rich exometabolome and that cells prefer the uptake of extracellular metabolites over self-synthesis, indicators of ongoing metabolite exchange. We conceived a system that circumvents co-culturing and begins with a self-supporting cell that grows autonomously into a heterogeneous community, only able to survive by exchanging histidine, leucine, uracil, and methionine. Compensating for the progressive loss of prototrophy, self-establishing communities successfully obtained an auxotrophic composition in a nutrition-dependent manner, maintaining a wild-type like exometabolome, growth parameters, and cell viability. Yeast, as a eukaryotic model, thus possesses extensive capacity for growth-relevant metabolite exchange and readily cooperates in metabolism within progressively establishing communities.https://elifesciences.org/articles/09943metabolismcooperativitycellular heterogeneity
collection DOAJ
language English
format Article
sources DOAJ
author Kate Campbell
Jakob Vowinckel
Michael Mülleder
Silke Malmsheimer
Nicola Lawrence
Enrica Calvani
Leonor Miller-Fleming
Mohammad T Alam
Stefan Christen
Markus A Keller
Markus Ralser
spellingShingle Kate Campbell
Jakob Vowinckel
Michael Mülleder
Silke Malmsheimer
Nicola Lawrence
Enrica Calvani
Leonor Miller-Fleming
Mohammad T Alam
Stefan Christen
Markus A Keller
Markus Ralser
Self-establishing communities enable cooperative metabolite exchange in a eukaryote
eLife
metabolism
cooperativity
cellular heterogeneity
author_facet Kate Campbell
Jakob Vowinckel
Michael Mülleder
Silke Malmsheimer
Nicola Lawrence
Enrica Calvani
Leonor Miller-Fleming
Mohammad T Alam
Stefan Christen
Markus A Keller
Markus Ralser
author_sort Kate Campbell
title Self-establishing communities enable cooperative metabolite exchange in a eukaryote
title_short Self-establishing communities enable cooperative metabolite exchange in a eukaryote
title_full Self-establishing communities enable cooperative metabolite exchange in a eukaryote
title_fullStr Self-establishing communities enable cooperative metabolite exchange in a eukaryote
title_full_unstemmed Self-establishing communities enable cooperative metabolite exchange in a eukaryote
title_sort self-establishing communities enable cooperative metabolite exchange in a eukaryote
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2015-10-01
description Metabolite exchange among co-growing cells is frequent by nature, however, is not necessarily occurring at growth-relevant quantities indicative of non-cell-autonomous metabolic function. Complementary auxotrophs of Saccharomyces cerevisiae amino acid and nucleotide metabolism regularly fail to compensate for each other's deficiencies upon co-culturing, a situation which implied the absence of growth-relevant metabolite exchange interactions. Contrastingly, we find that yeast colonies maintain a rich exometabolome and that cells prefer the uptake of extracellular metabolites over self-synthesis, indicators of ongoing metabolite exchange. We conceived a system that circumvents co-culturing and begins with a self-supporting cell that grows autonomously into a heterogeneous community, only able to survive by exchanging histidine, leucine, uracil, and methionine. Compensating for the progressive loss of prototrophy, self-establishing communities successfully obtained an auxotrophic composition in a nutrition-dependent manner, maintaining a wild-type like exometabolome, growth parameters, and cell viability. Yeast, as a eukaryotic model, thus possesses extensive capacity for growth-relevant metabolite exchange and readily cooperates in metabolism within progressively establishing communities.
topic metabolism
cooperativity
cellular heterogeneity
url https://elifesciences.org/articles/09943
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