Cargando…

Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion

Adaptive laboratory evolution has proven highly effective for obtaining microorganisms with enhanced capabilities. Yet, this method is inherently restricted to the traits that are positively linked to cell fitness, such as nutrient utilization. Here, we introduce coevolution of obligatory mutualisti...

Descripción completa

Detalles Bibliográficos
Autores principales: Konstantinidis, Dimitrios, Pereira, Filipa, Geissen, Eva‐Maria, Grkovska, Kristina, Kafkia, Eleni, Jouhten, Paula, Kim, Yongkyu, Devendran, Saravanan, Zimmermann, Michael, Patil, Kiran Raosaheb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351387/
https://www.ncbi.nlm.nih.gov/pubmed/34370382
http://dx.doi.org/10.15252/msb.202010189
_version_ 1783735963921416192
author Konstantinidis, Dimitrios
Pereira, Filipa
Geissen, Eva‐Maria
Grkovska, Kristina
Kafkia, Eleni
Jouhten, Paula
Kim, Yongkyu
Devendran, Saravanan
Zimmermann, Michael
Patil, Kiran Raosaheb
author_facet Konstantinidis, Dimitrios
Pereira, Filipa
Geissen, Eva‐Maria
Grkovska, Kristina
Kafkia, Eleni
Jouhten, Paula
Kim, Yongkyu
Devendran, Saravanan
Zimmermann, Michael
Patil, Kiran Raosaheb
author_sort Konstantinidis, Dimitrios
collection PubMed
description Adaptive laboratory evolution has proven highly effective for obtaining microorganisms with enhanced capabilities. Yet, this method is inherently restricted to the traits that are positively linked to cell fitness, such as nutrient utilization. Here, we introduce coevolution of obligatory mutualistic communities for improving secretion of fitness‐costly metabolites through natural selection. In this strategy, metabolic cross‐feeding connects secretion of the target metabolite, despite its cost to the secretor, to the survival and proliferation of the entire community. We thus co‐evolved wild‐type lactic acid bacteria and engineered auxotrophic Saccharomyces cerevisiae in a synthetic growth medium leading to bacterial isolates with enhanced secretion of two B‐group vitamins, viz., riboflavin and folate. The increased production was specific to the targeted vitamin, and evident also in milk, a more complex nutrient environment that naturally contains vitamins. Genomic, proteomic and metabolomic analyses of the evolved lactic acid bacteria, in combination with flux balance analysis, showed altered metabolic regulation towards increased supply of the vitamin precursors. Together, our findings demonstrate how microbial metabolism adapts to mutualistic lifestyle through enhanced metabolite exchange.
format Online
Article
Text
id pubmed-8351387
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-83513872021-08-15 Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion Konstantinidis, Dimitrios Pereira, Filipa Geissen, Eva‐Maria Grkovska, Kristina Kafkia, Eleni Jouhten, Paula Kim, Yongkyu Devendran, Saravanan Zimmermann, Michael Patil, Kiran Raosaheb Mol Syst Biol Articles Adaptive laboratory evolution has proven highly effective for obtaining microorganisms with enhanced capabilities. Yet, this method is inherently restricted to the traits that are positively linked to cell fitness, such as nutrient utilization. Here, we introduce coevolution of obligatory mutualistic communities for improving secretion of fitness‐costly metabolites through natural selection. In this strategy, metabolic cross‐feeding connects secretion of the target metabolite, despite its cost to the secretor, to the survival and proliferation of the entire community. We thus co‐evolved wild‐type lactic acid bacteria and engineered auxotrophic Saccharomyces cerevisiae in a synthetic growth medium leading to bacterial isolates with enhanced secretion of two B‐group vitamins, viz., riboflavin and folate. The increased production was specific to the targeted vitamin, and evident also in milk, a more complex nutrient environment that naturally contains vitamins. Genomic, proteomic and metabolomic analyses of the evolved lactic acid bacteria, in combination with flux balance analysis, showed altered metabolic regulation towards increased supply of the vitamin precursors. Together, our findings demonstrate how microbial metabolism adapts to mutualistic lifestyle through enhanced metabolite exchange. John Wiley and Sons Inc. 2021-08-09 /pmc/articles/PMC8351387/ /pubmed/34370382 http://dx.doi.org/10.15252/msb.202010189 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license 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 Articles
Konstantinidis, Dimitrios
Pereira, Filipa
Geissen, Eva‐Maria
Grkovska, Kristina
Kafkia, Eleni
Jouhten, Paula
Kim, Yongkyu
Devendran, Saravanan
Zimmermann, Michael
Patil, Kiran Raosaheb
Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion
title Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion
title_full Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion
title_fullStr Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion
title_full_unstemmed Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion
title_short Adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion
title_sort adaptive laboratory evolution of microbial co‐cultures for improved metabolite secretion
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351387/
https://www.ncbi.nlm.nih.gov/pubmed/34370382
http://dx.doi.org/10.15252/msb.202010189
work_keys_str_mv AT konstantinidisdimitrios adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT pereirafilipa adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT geissenevamaria adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT grkovskakristina adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT kafkiaeleni adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT jouhtenpaula adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT kimyongkyu adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT devendransaravanan adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT zimmermannmichael adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion
AT patilkiranraosaheb adaptivelaboratoryevolutionofmicrobialcoculturesforimprovedmetabolitesecretion