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...
Autores principales: | , , , , , , , , , |
---|---|
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 |