Evidence map›Paper›PMID 29666370›Full record

ArticleNature communications2018

Methanol-essential growth of Escherichia coli.

Fabian Meyer, Philipp Keller, Johannes Hartl, Olivier G Gröninger, Patrick Kiefer, Julia A Vorholt

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
7.3field-weighted citation impact, top 2% of its field
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

56 citing papers in PubMed, 155 citations in OpenAlex.

  1. Article
  2. Multi-omics analyses of evolvedSynthetic and systems biotechnology · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. A synthetic methylotrophicNature catalysis · 2024
    Article
  12. Review
  13. Perspectives for Using COBioengineering (Basel, Switzerland) · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Recent progress in adaptive laboratory evolution of industrial microorganisms.Journal of industrial microbiology & biotechnology · 2023
    Article
  20. OptimizingFrontiers in bioengineering and biotechnology · 2023
    Article
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

6 authors at 1 institution in 1 country.

Fabian MeyerInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, 8093, Switzerland.
Philipp KellerInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, 8093, Switzerland.
Johannes HartlInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, 8093, Switzerland.
Olivier G GröningerInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, 8093, Switzerland.
Patrick KieferInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, 8093, Switzerland.
Julia A VorholtInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, 8093, Switzerland. jvorholt@ethz.ch.
ETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methanol represents an attractive substrate for biotechnological applications. Utilization of reduced one-carbon compounds for growth is currently limited to methylotrophic organisms, and engineering synthetic methylotrophy remains a major challenge. Here we apply an in silico-guided multiple knockout approach to engineer a methanol-essential Escherichia coli strain, which contains the ribulose monophosphate cycle for methanol assimilation. Methanol conversion to biomass was stoichiometrically coupled to the metabolization of gluconate and the designed strain was subjected to laboratory evolution experiments. Evolved strains incorporate up to 24% methanol into core metabolites under a co-consumption regime and utilize methanol at rates comparable to natural methylotrophs. Genome sequencing reveals mutations in genes coding for glutathione-dependent formaldehyde oxidation (frmA), NAD(H) homeostasis/biosynthesis (nadR), phosphopentomutase (deoB), and gluconate metabolism (gntR). This study demonstrates a successful metabolic re-routing linked to a heterologous pathway to achieve methanol-dependent growth and represents a crucial step in generating a fully synthetic methylotrophic organism.

Indexed as

Metabolic EngineeringBacterial ProteinsComputer SimulationEscherichia coliGene Knockout TechniquesGenome, BacterialGluconatesMetabolic Networks and PathwaysMethanolBacterial ProteinsGluconatesgluconic acidMethanol

Identifiers

PMID29666370
PMCPMC5904121
OpenAlexW2801097103

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.