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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...

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Autores principales: 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
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
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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.
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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
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