Evidence map›Paper›PMID 25754258›Full record

ArticleScientific reports2015

Metabolomics integrated elementary flux mode analysis in large metabolic networks.

Matthias P Gerstl, David E Ruckerbauer, Diethard Mattanovich, Christian Jungreuthmayer, Jürgen Zanghellini

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

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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

16 citing papers in PubMed.

  1. Article
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  4. Review
  5. Article
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  8. Article
  9. Metabolomics in Plant Priming Research: The Way Forward?International journal of molecular sciences · 2018
    Review
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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

5 authors.

Matthias P Gerstl1] Austrian Centre of Industrial Biotechnology, Vienna, Austria, EU [2] Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria, EU.
David E Ruckerbauer1] Austrian Centre of Industrial Biotechnology, Vienna, Austria, EU [2] Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria, EU.
Diethard Mattanovich1] Austrian Centre of Industrial Biotechnology, Vienna, Austria, EU [2] Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria, EU.
Christian Jungreuthmayer1] Austrian Centre of Industrial Biotechnology, Vienna, Austria, EU [2] Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria, EU.
Jürgen Zanghellini1] Austrian Centre of Industrial Biotechnology, Vienna, Austria, EU [2] Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria, EU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elementary flux modes (EFMs) are non-decomposable steady-state pathways in metabolic networks. They characterize phenotypes, quantify robustness or identify engineering targets. An EFM analysis (EFMA) is currently restricted to medium-scale models, as the number of EFMs explodes with the network's size. However, many topologically feasible EFMs are biologically irrelevant. We present thermodynamic EFMA (tEFMA), which calculates only the small(er) subset of thermodynamically feasible EFMs. We integrate network embedded thermodynamics into EFMA and show that we can use the metabolome to identify and remove thermodynamically infeasible EFMs during an EFMA without losing biologically relevant EFMs. Calculating only the thermodynamically feasible EFMs strongly reduces memory consumption and program runtime, allowing the analysis of larger networks. We apply tEFMA to study the central carbon metabolism of E. coli and find that up to 80% of its EFMs are thermodynamically infeasible. Moreover, we identify glutamate dehydrogenase as a bottleneck, when E. coli is grown on glucose and explain its inactivity as a consequence of network embedded thermodynamics. We implemented tEFMA as a Java package which is available for download at https://github.com/mpgerstl/tEFMA.

Indexed as

Metabolic Networks and PathwaysMetabolomicsThermodynamicsAlgorithmsComputational BiologyEscherichia coliGlucoseGlutamate DehydrogenaseModels, BiologicalGlucoseGlutamate Dehydrogenase

Identifiers

PMID25754258
PMCPMC4354105

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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.