Evidence map›Paper›PMID 32471427›Full record

ArticleMicrobial cell factories2020

Escherichia coli metabolism under short-term repetitive substrate dynamics: adaptation and trade-offs.

Eleni Vasilakou, Mark C M van Loosdrecht, S Aljoscha Wahl

Abstract read
In one paragraph

Article in Microbial cell factories, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
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  5. Glyceraldehyde-3-phosphate dehydrogenase homologs as bifunctional gatekeepers of metabolic segregation inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Scale-down bioreactors-comparative analysis of configurations.Bioprocess and biosystems engineering · 2025
    Review
  7. Article
  8. Article
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  14. Review
  15. Minimizing acetate formation from overflow metabolism inFrontiers in bioengineering and biotechnology · 2024
    Article
  16. A Unique Response Behavior in the Dissolved Oxygen Tension inBioengineering (Basel, Switzerland) · 2023
    Article
  17. Article
  18. Article
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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

3 authors.

Eleni VasilakouDepartment of Biotechnology, Delft University of Technology, Van der Maasweg, 2629 HZ, Delft, The Netherlands. elenvasil16@gmail.com.ORCID http://orcid.org/0000-0003-1220-1099
Mark C M van LoosdrechtDepartment of Biotechnology, Delft University of Technology, Van der Maasweg, 2629 HZ, Delft, The Netherlands.
S Aljoscha WahlDepartment of Biotechnology, Delft University of Technology, Van der Maasweg, 2629 HZ, Delft, The Netherlands. s.a.wahl@tudelft.nl.

Funding

European Research Area ERA-IB-14-081Nederlandse Organisatie voor Wetenschappelijk Onderzoek 053.80.724
6 · The paper itself

Abstract

backgroundMicrobial metabolism is highly dependent on the environmental conditions. Especially, the substrate concentration, as well as oxygen availability, determine the metabolic rates. In large-scale bioreactors, microorganisms encounter dynamic conditions in substrate and oxygen availability (mixing limitations), which influence their metabolism and subsequently their physiology. Earlier, single substrate pulse experiments were not able to explain the observed physiological changes generated under large-scale industrial fermentation conditions.

resultsIn this study we applied a repetitive feast-famine regime in an aerobic Escherichia coli culture in a time-scale of seconds. The regime was applied for several generations, allowing cells to adapt to the (repetitive) dynamic environment. The observed response was highly reproducible over the cycles, indicating that cells were indeed fully adapted to the regime. We observed an increase of the specific substrate and oxygen consumption (average) rates during the feast-famine regime, compared to a steady-state (chemostat) reference environment. The increased rates at same (average) growth rate led to a reduced biomass yield (30% lower). Interestingly, this drop was not followed by increased by-product formation, pointing to the existence of energy-spilling reactions. During the feast-famine cycle, the cells rapidly increased their uptake rate. Within 10 s after the beginning of the feeding, the substrate uptake rate was higher (4.68 μmol/g

conclusionsThe adaptation of the physiology and metabolism of E. coli under substrate dynamics, representative for large-scale fermenters, revealed the existence of several cellular mechanisms coping with stress. Changes in the substrate uptake system, storage potential and energy-spilling processes resulted to be of great importance. These metabolic strategies consist a meaningful step to further tackle reduced microbial performance, observed under large-scale cultivations.

Indexed as

Batch Cell Culture TechniquesBioreactorsEscherichia coliFermentationGlucoseOxygenGlucoseOxygenDynamic metabolic responsesEnergy homeostasisEscherichia coliFeast–famineSubstrate dynamics

Identifiers

PMID32471427
PMCPMC7260802

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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.