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Spontaneously established syntrophic yeast communities improve bioproduction

Nutritional codependence (syntrophy) has underexplored potential to improve biotechnological processes by using cooperating cell types. So far, design of yeast syntrophic communities has required extensive genetic manipulation, as the co-inoculation of most eukaryotic microbial auxotrophs does not r...

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Autores principales: Aulakh, Simran Kaur, Sellés Vidal, Lara, South, Eric J., Peng, Huadong, Varma, Sreejith Jayasree, Herrera-Dominguez, Lucia, Ralser, Markus, Ledesma-Amaro, Rodrigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374442/
https://www.ncbi.nlm.nih.gov/pubmed/37248413
http://dx.doi.org/10.1038/s41589-023-01341-2
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author Aulakh, Simran Kaur
Sellés Vidal, Lara
South, Eric J.
Peng, Huadong
Varma, Sreejith Jayasree
Herrera-Dominguez, Lucia
Ralser, Markus
Ledesma-Amaro, Rodrigo
author_facet Aulakh, Simran Kaur
Sellés Vidal, Lara
South, Eric J.
Peng, Huadong
Varma, Sreejith Jayasree
Herrera-Dominguez, Lucia
Ralser, Markus
Ledesma-Amaro, Rodrigo
author_sort Aulakh, Simran Kaur
collection PubMed
description Nutritional codependence (syntrophy) has underexplored potential to improve biotechnological processes by using cooperating cell types. So far, design of yeast syntrophic communities has required extensive genetic manipulation, as the co-inoculation of most eukaryotic microbial auxotrophs does not result in cooperative growth. Here we employ high-throughput phenotypic screening to systematically test pairwise combinations of auxotrophic Saccharomyces cerevisiae deletion mutants. Although most coculture pairs do not enter syntrophic growth, we identify 49 pairs that spontaneously form syntrophic, synergistic communities. We characterized the stability and growth dynamics of nine cocultures and demonstrated that a pair of tryptophan auxotrophs grow by exchanging a pathway intermediate rather than end products. We then introduced a malonic semialdehyde biosynthesis pathway split between different pairs of auxotrophs, which resulted in increased production. Our results report the spontaneous formation of stable syntrophy in S. cerevisiae auxotrophs and illustrate the biotechnological potential of dividing labor in a cooperating intraspecies community. [Image: see text]
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spelling pubmed-103744422023-07-29 Spontaneously established syntrophic yeast communities improve bioproduction Aulakh, Simran Kaur Sellés Vidal, Lara South, Eric J. Peng, Huadong Varma, Sreejith Jayasree Herrera-Dominguez, Lucia Ralser, Markus Ledesma-Amaro, Rodrigo Nat Chem Biol Article Nutritional codependence (syntrophy) has underexplored potential to improve biotechnological processes by using cooperating cell types. So far, design of yeast syntrophic communities has required extensive genetic manipulation, as the co-inoculation of most eukaryotic microbial auxotrophs does not result in cooperative growth. Here we employ high-throughput phenotypic screening to systematically test pairwise combinations of auxotrophic Saccharomyces cerevisiae deletion mutants. Although most coculture pairs do not enter syntrophic growth, we identify 49 pairs that spontaneously form syntrophic, synergistic communities. We characterized the stability and growth dynamics of nine cocultures and demonstrated that a pair of tryptophan auxotrophs grow by exchanging a pathway intermediate rather than end products. We then introduced a malonic semialdehyde biosynthesis pathway split between different pairs of auxotrophs, which resulted in increased production. Our results report the spontaneous formation of stable syntrophy in S. cerevisiae auxotrophs and illustrate the biotechnological potential of dividing labor in a cooperating intraspecies community. [Image: see text] Nature Publishing Group US 2023-05-29 2023 /pmc/articles/PMC10374442/ /pubmed/37248413 http://dx.doi.org/10.1038/s41589-023-01341-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Aulakh, Simran Kaur
Sellés Vidal, Lara
South, Eric J.
Peng, Huadong
Varma, Sreejith Jayasree
Herrera-Dominguez, Lucia
Ralser, Markus
Ledesma-Amaro, Rodrigo
Spontaneously established syntrophic yeast communities improve bioproduction
title Spontaneously established syntrophic yeast communities improve bioproduction
title_full Spontaneously established syntrophic yeast communities improve bioproduction
title_fullStr Spontaneously established syntrophic yeast communities improve bioproduction
title_full_unstemmed Spontaneously established syntrophic yeast communities improve bioproduction
title_short Spontaneously established syntrophic yeast communities improve bioproduction
title_sort spontaneously established syntrophic yeast communities improve bioproduction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374442/
https://www.ncbi.nlm.nih.gov/pubmed/37248413
http://dx.doi.org/10.1038/s41589-023-01341-2
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