Evidence map›Paper›PMID 33971881›Full record

ArticleMicrobial cell factories2021

Adaptive laboratory evolution accelerated glutarate production by Corynebacterium glutamicum.

Carina Prell, Tobias Busche, Christian Rückert, Lea Nolte, Christoph Brandenbusch, Volker F Wendisch

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  9. Recent progress in adaptive laboratory evolution of industrial microorganisms.Journal of industrial microbiology & biotechnology · 2023
    Article
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  11. Review
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  14. Metabolic Engineering ofMicroorganisms · 2022
    Article
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  17. Review
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  19. Utilization of a Wheat Sidestream for 5-Aminovalerate Production inFrontiers in bioengineering and biotechnology · 2021
    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 2 institutions in 1 country.

Carina PrellGenetics of Prokaryotes, Faculty of Biology & CeBiTec, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany.
Tobias BuscheTechnology Platform Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Sequenz 1, 33615, Bielefeld, Germany.
Christian RückertTechnology Platform Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Sequenz 1, 33615, Bielefeld, Germany.
Lea NolteLaboratory of Thermodynamics, Department of Biochemical and Chemical Engineering, TU Dortmund University, Emil-Figge-Str. 70, 44227, Dortmund, Germany.
Christoph BrandenbuschLaboratory of Thermodynamics, Department of Biochemical and Chemical Engineering, TU Dortmund University, Emil-Figge-Str. 70, 44227, Dortmund, Germany.
Volker F WendischGenetics of Prokaryotes, Faculty of Biology & CeBiTec, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany. volker.wendisch@uni-bielefeld.de.ORCID http://orcid.org/0000-0003-3473-0012
Bielefeld University · DETU Dortmund University · DE

Funding

Deutsche Forschungsgemeinschaft Open Acces Publication FundEuropean Regional Development Fund (ERDF) and the Ministry of Economic Affairs, Innovation, Digitalization and Energy of the State of North Rhine-Westphalia 34.EFRE-0300095/1703FI04Universität Bielefeld Open Acces Publication Fund
6 · The paper itself

Abstract

backgroundThe demand for biobased polymers is increasing steadily worldwide. Microbial hosts for production of their monomeric precursors such as glutarate are developed. To meet the market demand, production hosts have to be improved constantly with respect to product titers and yields, but also shortening bioprocess duration is important.

resultsIn this study, adaptive laboratory evolution was used to improve a C. glutamicum strain engineered for production of the C

conclusionFlux enforcement to couple growth to operation of a product biosynthesis pathway provides a basis to select strains growing and producing faster by adaptive laboratory evolution. After identifying candidate mutations by genome sequencing causal mutations can be identified by reverse genetics. As exemplified here for glutarate production by C. glutamicum, this approach allowed deducing rational metabolic engineering strategies.

Indexed as

Directed Molecular EvolutionBioreactorsCorynebacterium glutamicumCulture MediaFermentationGlutaratesMetabolic EngineeringMetabolic Flux AnalysisMutationReverse GeneticsCulture MediaGlutaratesAdaptive laboratory evolutionCorynebacterium glutamicumGlutarateMetabolic engineeringReactive extractionReverse geneticsVolumetric productivity

Identifiers

PMID33971881
PMCPMC8112011
OpenAlexW3162338105

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.