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Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia

In nature, microorganisms often reside in symbiotic co‐existence providing nutrition, stability, and protection for each partner by applying “division of labor.” This principle may also be used for the overproduction of targeted compounds in bioprocesses. It requires the engineering of a synthetic c...

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Autores principales: Müller, Tobias, Schick, Simon, Beck, Jonathan, Sprenger, Georg, Takors, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815082/
https://www.ncbi.nlm.nih.gov/pubmed/36619882
http://dx.doi.org/10.1002/elsc.202100158
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author Müller, Tobias
Schick, Simon
Beck, Jonathan
Sprenger, Georg
Takors, Ralf
author_facet Müller, Tobias
Schick, Simon
Beck, Jonathan
Sprenger, Georg
Takors, Ralf
author_sort Müller, Tobias
collection PubMed
description In nature, microorganisms often reside in symbiotic co‐existence providing nutrition, stability, and protection for each partner by applying “division of labor.” This principle may also be used for the overproduction of targeted compounds in bioprocesses. It requires the engineering of a synthetic co‐culture with distributed tasks for each partner. Thereby, the competition on precursors, redox cofactors, and energy—which occurs in a single host—is prevented. Current applications often focus on unidirectional interactions, that is, the product of partner A is used for the completion of biosynthesis by partner B. Here, we present a synthetically engineered Escherichia coli co‐culture of two engineered mutant strains marked by the essential interaction of the partners which is achieved by implemented auxotrophies. The tryptophan auxotrophic strain E. coli ANT‐3, only requiring small amounts of the aromatic amino acid, provides the auxotrophic anthranilate for the tryptophan producer E. coli TRP‐3. The latter produces a surplus of tryptophan which is used to showcase the suitability of the co‐culture to access related products in future applications. Co‐culture characterization revealed that the microbial consortium is remarkably functionally stable for a broad range of inoculation ratios. The range of robust and functional interaction may even be extended by proper glucose feeding which was shown in a two‐compartment bioreactor setting with filtrate exchange. This system even enables the use of the co‐culture in a parallel two‐level temperature setting which opens the door to access temperature sensitive products via heterologous production in E. coli in a continuous manner.
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spelling pubmed-98150822023-01-05 Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia Müller, Tobias Schick, Simon Beck, Jonathan Sprenger, Georg Takors, Ralf Eng Life Sci Research Articles In nature, microorganisms often reside in symbiotic co‐existence providing nutrition, stability, and protection for each partner by applying “division of labor.” This principle may also be used for the overproduction of targeted compounds in bioprocesses. It requires the engineering of a synthetic co‐culture with distributed tasks for each partner. Thereby, the competition on precursors, redox cofactors, and energy—which occurs in a single host—is prevented. Current applications often focus on unidirectional interactions, that is, the product of partner A is used for the completion of biosynthesis by partner B. Here, we present a synthetically engineered Escherichia coli co‐culture of two engineered mutant strains marked by the essential interaction of the partners which is achieved by implemented auxotrophies. The tryptophan auxotrophic strain E. coli ANT‐3, only requiring small amounts of the aromatic amino acid, provides the auxotrophic anthranilate for the tryptophan producer E. coli TRP‐3. The latter produces a surplus of tryptophan which is used to showcase the suitability of the co‐culture to access related products in future applications. Co‐culture characterization revealed that the microbial consortium is remarkably functionally stable for a broad range of inoculation ratios. The range of robust and functional interaction may even be extended by proper glucose feeding which was shown in a two‐compartment bioreactor setting with filtrate exchange. This system even enables the use of the co‐culture in a parallel two‐level temperature setting which opens the door to access temperature sensitive products via heterologous production in E. coli in a continuous manner. John Wiley and Sons Inc. 2022-05-06 /pmc/articles/PMC9815082/ /pubmed/36619882 http://dx.doi.org/10.1002/elsc.202100158 Text en © 2022 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Müller, Tobias
Schick, Simon
Beck, Jonathan
Sprenger, Georg
Takors, Ralf
Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia
title Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia
title_full Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia
title_fullStr Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia
title_full_unstemmed Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia
title_short Synthetic mutualism in engineered E. coli mutant strains as functional basis for microbial production consortia
title_sort synthetic mutualism in engineered e. coli mutant strains as functional basis for microbial production consortia
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815082/
https://www.ncbi.nlm.nih.gov/pubmed/36619882
http://dx.doi.org/10.1002/elsc.202100158
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