Cargando…
Predictive evolution of metabolic phenotypes using model‐designed environments
Adaptive evolution under controlled laboratory conditions has been highly effective in selecting organisms with beneficial phenotypes such as stress tolerance. The evolution route is particularly attractive when the organisms are either difficult to engineer or the genetic basis of the phenotype is...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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/PMC9536503/ https://www.ncbi.nlm.nih.gov/pubmed/36201279 http://dx.doi.org/10.15252/msb.202210980 |
_version_ | 1784802995364429824 |
---|---|
author | Jouhten, Paula Konstantinidis, Dimitrios Pereira, Filipa Andrejev, Sergej Grkovska, Kristina Castillo, Sandra Ghiachi, Payam Beltran, Gemma Almaas, Eivind Mas, Albert Warringer, Jonas Gonzalez, Ramon Morales, Pilar Patil, Kiran R |
author_facet | Jouhten, Paula Konstantinidis, Dimitrios Pereira, Filipa Andrejev, Sergej Grkovska, Kristina Castillo, Sandra Ghiachi, Payam Beltran, Gemma Almaas, Eivind Mas, Albert Warringer, Jonas Gonzalez, Ramon Morales, Pilar Patil, Kiran R |
author_sort | Jouhten, Paula |
collection | PubMed |
description | Adaptive evolution under controlled laboratory conditions has been highly effective in selecting organisms with beneficial phenotypes such as stress tolerance. The evolution route is particularly attractive when the organisms are either difficult to engineer or the genetic basis of the phenotype is complex. However, many desired traits, like metabolite secretion, have been inaccessible to adaptive selection due to their trade‐off with cell growth. Here, we utilize genome‐scale metabolic models to design nutrient environments for selecting lineages with enhanced metabolite secretion. To overcome the growth‐secretion trade‐off, we identify environments wherein growth becomes correlated with a secondary trait termed tacking trait. The latter is selected to be coupled with the desired trait in the application environment where the trait manifestation is required. Thus, adaptive evolution in the model‐designed selection environment and subsequent return to the application environment is predicted to enhance the desired trait. We experimentally validate this strategy by evolving Saccharomyces cerevisiae for increased secretion of aroma compounds, and confirm the predicted flux‐rerouting using genomic, transcriptomic, and proteomic analyses. Overall, model‐designed selection environments open new opportunities for predictive evolution. |
format | Online Article Text |
id | pubmed-9536503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95365032022-10-16 Predictive evolution of metabolic phenotypes using model‐designed environments Jouhten, Paula Konstantinidis, Dimitrios Pereira, Filipa Andrejev, Sergej Grkovska, Kristina Castillo, Sandra Ghiachi, Payam Beltran, Gemma Almaas, Eivind Mas, Albert Warringer, Jonas Gonzalez, Ramon Morales, Pilar Patil, Kiran R Mol Syst Biol Articles Adaptive evolution under controlled laboratory conditions has been highly effective in selecting organisms with beneficial phenotypes such as stress tolerance. The evolution route is particularly attractive when the organisms are either difficult to engineer or the genetic basis of the phenotype is complex. However, many desired traits, like metabolite secretion, have been inaccessible to adaptive selection due to their trade‐off with cell growth. Here, we utilize genome‐scale metabolic models to design nutrient environments for selecting lineages with enhanced metabolite secretion. To overcome the growth‐secretion trade‐off, we identify environments wherein growth becomes correlated with a secondary trait termed tacking trait. The latter is selected to be coupled with the desired trait in the application environment where the trait manifestation is required. Thus, adaptive evolution in the model‐designed selection environment and subsequent return to the application environment is predicted to enhance the desired trait. We experimentally validate this strategy by evolving Saccharomyces cerevisiae for increased secretion of aroma compounds, and confirm the predicted flux‐rerouting using genomic, transcriptomic, and proteomic analyses. Overall, model‐designed selection environments open new opportunities for predictive evolution. John Wiley and Sons Inc. 2022-10-06 /pmc/articles/PMC9536503/ /pubmed/36201279 http://dx.doi.org/10.15252/msb.202210980 Text en © 2022 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 Jouhten, Paula Konstantinidis, Dimitrios Pereira, Filipa Andrejev, Sergej Grkovska, Kristina Castillo, Sandra Ghiachi, Payam Beltran, Gemma Almaas, Eivind Mas, Albert Warringer, Jonas Gonzalez, Ramon Morales, Pilar Patil, Kiran R Predictive evolution of metabolic phenotypes using model‐designed environments |
title | Predictive evolution of metabolic phenotypes using model‐designed environments |
title_full | Predictive evolution of metabolic phenotypes using model‐designed environments |
title_fullStr | Predictive evolution of metabolic phenotypes using model‐designed environments |
title_full_unstemmed | Predictive evolution of metabolic phenotypes using model‐designed environments |
title_short | Predictive evolution of metabolic phenotypes using model‐designed environments |
title_sort | predictive evolution of metabolic phenotypes using model‐designed environments |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536503/ https://www.ncbi.nlm.nih.gov/pubmed/36201279 http://dx.doi.org/10.15252/msb.202210980 |
work_keys_str_mv | AT jouhtenpaula predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT konstantinidisdimitrios predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT pereirafilipa predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT andrejevsergej predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT grkovskakristina predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT castillosandra predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT ghiachipayam predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT beltrangemma predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT almaaseivind predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT masalbert predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT warringerjonas predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT gonzalezramon predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT moralespilar predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments AT patilkiranr predictiveevolutionofmetabolicphenotypesusingmodeldesignedenvironments |