Evidence map›Paper›PMID 27956602›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Pathway swapping: Toward modular engineering of essential cellular processes.

Niels G A Kuijpers, Daniel Solis-Escalante, Marijke A H Luttik, Markus M M Bisschops, Francine J Boonekamp, Marcel van den Broek, Jack T Pronk, Jean-Marc Daran, Pascale Daran-Lapujade

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Review
  3. The return of metabolism: biochemistry and physiology of glycolysis.Biological reviews of the Cambridge Philosophical Society · 2026
    Review
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  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
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  15. Article
  16. Article
  17. Article
  18. Selection of PofFrontiers in microbiology · 2018
    Article
  19. TheBiotechnology for biofuels · 2018
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Niels G A KuijpersDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Daniel Solis-EscalanteDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Marijke A H LuttikDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Markus M M BisschopsDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Francine J BoonekampDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Marcel van den BroekDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Jack T PronkDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Jean-Marc DaranDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Pascale Daran-LapujadeDepartment of Biotechnology, Delft University of Technology, 2629 HZ Delft, The Netherlands p.a.s.daran-lapujade@tudelft.nl.ORCID 0000-0002-4097-7831

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent developments in synthetic biology enable one-step implementation of entire metabolic pathways in industrial microorganisms. A similarly radical remodelling of central metabolism could greatly accelerate fundamental and applied research, but is impeded by the mosaic organization of microbial genomes. To eliminate this limitation, we propose and explore the concept of "pathway swapping," using yeast glycolysis as the experimental model. Construction of a "single-locus glycolysis" Saccharomyces cerevisiae platform enabled quick and easy replacement of this yeast's entire complement of 26 glycolytic isoenzymes by any alternative, functional glycolytic pathway configuration. The potential of this approach was demonstrated by the construction and characterization of S. cerevisiae strains whose growth depended on two nonnative glycolytic pathways: a complete glycolysis from the related yeast Saccharomyces kudriavzevii and a mosaic glycolysis consisting of yeast and human enzymes. This work demonstrates the feasibility and potential of modular, combinatorial approaches to engineering and analysis of core cellular processes.

Indexed as

Genome, FungalGlycolysisMetabolic EngineeringEthanolGene DosageGene Expression Regulation, FungalMetabolic Networks and PathwaysMultigene FamilyPhenotypeProtein EngineeringSaccharomyces cerevisiaeSynthetic BiologyEthanolglycolysismodular genomespathway swappingSaccharomyces cerevisiae

Identifiers

PMID27956602
PMCPMC5206561

What OpenQuestion holds

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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.