Assembling stable syntrophic Escherichia coli communities by comprehensively identifying beneficiaries of secreted goods
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UMass Chan Affiliations
Molecular, Cell and Cancer BiologyMorningside Graduate School of Biomedical Sciences
Program in Molecular Medicine
Systems Biology
Document Type
Journal ArticlePublication Date
2021-08-31Keywords
Escherichia coliauxotrophy
collaboration
cross-feeding
design principles
genetic screen
metabolism
microbial community
microbial consortium
mutualism
pooled genetic library
syntrophy
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Show full item recordAbstract
Metabolic cross-feeding frequently underlies mutualistic relationships in natural microbial communities and is often exploited to assemble synthetic microbial consortia. We systematically identified all single-gene knockouts suitable for imposing cross-feeding in Escherichia coli and used this information to assemble syntrophic communities. Most strains benefiting from shared goods were dysfunctional in biosynthesis of amino acids, nucleotides, and vitamins or mutants in central carbon metabolism. We tested cross-feeding potency in 1,444 strain pairs and mapped the interaction network between all functional groups of mutants. This network revealed that auxotrophs for vitamins are optimal cooperators. Lastly, we monitored how assemblies composed of dozens of auxotrophs change over time and observed that they rapidly and repeatedly coalesced to seven strain consortia composed primarily from vitamin auxotrophs. The composition of emerging consortia suggests that they were stabilized by multiple cross-feeding interactions. We conclude that vitamins are ideal shared goods since they optimize consortium growth while still imposing member co-dependence.Source
Noto Guillen M, Rosener B, Sayin S, Mitchell A. Assembling stable syntrophic Escherichia coli communities by comprehensively identifying beneficiaries of secreted goods. Cell Syst. 2021 Nov 17;12(11):1064-1078.e7. doi: 10.1016/j.cels.2021.08.002. Epub 2021 Aug 31. PMID: 34469744; PMCID: PMC8602757.DOI
10.1016/j.cels.2021.08.002Permanent Link to this Item
http://hdl.handle.net/20.500.14038/51725PubMed ID
34469744Rights
Copyright © 2021 Elsevier Inc. All rights reserved.ae974a485f413a2113503eed53cd6c53
10.1016/j.cels.2021.08.002