Evidence map›Paper›PMID 36201279›Full record

ArticleMolecular systems biology2022

Predictive evolution of metabolic phenotypes using model-designed environments.

Paula Jouhten, Dimitrios Konstantinidis, Filipa Pereira, Sergej Andrejev, Kristina Grkovska, Sandra Castillo, Payam Ghiachi, Gemma Beltran, Eivind Almaas, Albert Mas and 4 more

Erratum issuedAbstract read
In one paragraph

Article in Molecular systems biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. COmmunity and Single Microbe Optimisation System (COSMOS).NPJ systems biology and applications · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Plant and microbial sciences as key drivers in the development of metabolomics research.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Review
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Paula Jouhten *European Molecular Biology Laboratory, Heidelberg, Germany.ORCID 0000-0003-1075-7448
Dimitrios Konstantinidis *European Molecular Biology Laboratory, Heidelberg, Germany.
Filipa PereiraEuropean Molecular Biology Laboratory, Heidelberg, Germany.
Sergej AndrejevEuropean Molecular Biology Laboratory, Heidelberg, Germany.
Kristina GrkovskaEuropean Molecular Biology Laboratory, Heidelberg, Germany.
Sandra CastilloVTT Technical Research Centre of Finland Ltd, Espoo, Finland.
Payam GhiachiDepartment of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, Sweden.
Gemma BeltranDepartament Bioquímica i Biotecnologia, Facultat d'Enologia, Universitat Rovira i Virgili, Tarragona, Spain.
Eivind AlmaasDepartment of Biotechnology and Food Science, NTNU - Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0002-9125-326X
Albert MasDepartament Bioquímica i Biotecnologia, Facultat d'Enologia, Universitat Rovira i Virgili, Tarragona, Spain.ORCID 0000-0002-0763-1679
Jonas WarringerDepartment of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0001-6144-2740
Ramon GonzalezInstituto de Ciencias de la Vid y delVino (CSIC, Gobierno de la Rioja, Universidad de La Rioja) Finca La Grajera, Logroño, Spain.
Pilar MoralesInstituto de Ciencias de la Vid y delVino (CSIC, Gobierno de la Rioja, Universidad de La Rioja) Finca La Grajera, Logroño, Spain.ORCID 0000-0002-0130-6111
Kiran R PatilEuropean Molecular Biology Laboratory, Heidelberg, Germany.ORCID 0000-0002-6166-8640

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

ProteomicsSaccharomyces cerevisiaeGenomeGenomicsPhenotypeadaptive evolutiongenome-scale metabolic modelpredictive evolutionSaccharomyces cerevisiaewine aroma

Identifiers

PMID36201279
PMCPMC9536503

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.