Evidence map›Paper›PMID 37553325›Full record

ArticleNature communications2023

Proteomics and constraint-based modelling reveal enzyme kinetic properties of Chlamydomonas reinhardtii on a genome scale.

Marius Arend, David Zimmer, Rudan Xu, Frederik Sommer, Timo Mühlhaus, Zoran Nikoloski

Abstract read
In one paragraph

Article in Nature communications, 2023. 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

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

16 citing papers in PubMed.

  1. A Low-DimensionalMolecules (Basel, Switzerland) · 2026
    Article
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  3. SAGA1 and SAGA2 localize the starch sheath to the pyrenoid inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  11. Integration of proteomic data with genome-scale metabolic models: A methodological overview.Protein science : a publication of the Protein Society · 2024
    Review
  12. Article
  13. Article
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  15. 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

6 authors.

Marius ArendBioinformatics, Institute of Biochemistry and Biology, University of Potsdam, 14476, Potsdam, Germany.ORCID http://orcid.org/0000-0002-9608-4960
David ZimmerComputational Systems Biology, TU Kaiserslautern, 67663, Kaiserslautern, Germany.
Rudan XuBioinformatics, Institute of Biochemistry and Biology, University of Potsdam, 14476, Potsdam, Germany.
Frederik SommerMolecular Biotechnology & Systems Biology, TU Kaiserslautern, 67663, Kaiserslautern, Germany.ORCID http://orcid.org/0000-0003-0247-4907
Timo MühlhausComputational Systems Biology, TU Kaiserslautern, 67663, Kaiserslautern, Germany.
Zoran NikoloskiBioinformatics, Institute of Biochemistry and Biology, University of Potsdam, 14476, Potsdam, Germany. nikoloski@mpimp-golm.mpg.de.ORCID http://orcid.org/0000-0003-2671-6763

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic engineering of microalgae offers a promising solution for sustainable biofuel production, and rational design of engineering strategies can be improved by employing metabolic models that integrate enzyme turnover numbers. However, the coverage of turnover numbers for Chlamydomonas reinhardtii, a model eukaryotic microalga accessible to metabolic engineering, is 17-fold smaller compared to the heterotrophic cell factory Saccharomyces cerevisiae. Here we generate quantitative protein abundance data of Chlamydomonas covering 2337 to 3708 proteins in various growth conditions to estimate in vivo maximum apparent turnover numbers. Using constrained-based modeling we provide proxies for in vivo turnover numbers of 568 reactions, representing a 10-fold increase over the in vitro data for Chlamydomonas. Integration of the in vivo estimates instead of in vitro values in a metabolic model of Chlamydomonas improved the accuracy of enzyme usage predictions. Our results help in extending the knowledge on uncharacterized enzymes and improve biotechnological applications of Chlamydomonas.

Indexed as

Chlamydomonas reinhardtiiBiotechnologyGenomeProteinsProteomicsSaccharomyces cerevisiaeProteins

Identifiers

PMID37553325
PMCPMC10409818

What OpenQuestion holds

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Registered trials

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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.