Evidence map›Paper›PMID 32434546›Full record

ArticleBMC microbiology2020

New perspectives on butyrate assimilation in Rhodospirillum rubrum S1H under photoheterotrophic conditions.

Quentin De Meur, Adam Deutschbauer, Matthias Koch, Guillaume Bayon-Vicente, Paloma Cabecas Segura, Ruddy Wattiez, Baptiste Leroy

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  10. Study of the Production of Poly(Hydroxybutyrate-Applied and environmental microbiology · 2022
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  11. Review
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  15. Review
  16. Article
  17. 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

7 authors at 2 institutions in 2 countries.

Quentin De MeurLaboratory of Proteomics and Microbiology, Research Institute for Biosciences, University of Mons, Avenue du champs de Mars, 6 (Pentagone 3B), 7000, Mons, Belgium.
Adam DeutschbauerEnvironmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA.
Matthias KochLaboratory of Proteomics and Microbiology, Research Institute for Biosciences, University of Mons, Avenue du champs de Mars, 6 (Pentagone 3B), 7000, Mons, Belgium.
Guillaume Bayon-VicenteLaboratory of Proteomics and Microbiology, Research Institute for Biosciences, University of Mons, Avenue du champs de Mars, 6 (Pentagone 3B), 7000, Mons, Belgium.
Paloma Cabecas SeguraLaboratory of Proteomics and Microbiology, Research Institute for Biosciences, University of Mons, Avenue du champs de Mars, 6 (Pentagone 3B), 7000, Mons, Belgium.
Ruddy WattiezLaboratory of Proteomics and Microbiology, Research Institute for Biosciences, University of Mons, Avenue du champs de Mars, 6 (Pentagone 3B), 7000, Mons, Belgium.
Baptiste LeroyLaboratory of Proteomics and Microbiology, Research Institute for Biosciences, University of Mons, Avenue du champs de Mars, 6 (Pentagone 3B), 7000, Mons, Belgium. baptiste.leroy@umons.ac.be.
University of Mons · BELawrence Berkeley National Laboratory · US

Funding

Belgian Scientific policy ProdexEuropean Space Agency MELiSSAFonds De La Recherche Scientifique - FNRS 2877824
6 · The paper itself

Abstract

backgroundThe great metabolic versatility of the purple non-sulfur bacteria is of particular interest in green technology. Rhodospirillum rubrum S1H is an α-proteobacterium that is capable of photoheterotrophic assimilation of volatile fatty acids (VFAs). Butyrate is one of the most abundant VFAs produced during fermentative biodegradation of crude organic wastes in various applications. While there is a growing understanding of the photoassimilation of acetate, another abundantly produced VFA, the mechanisms involved in the photoheterotrophic metabolism of butyrate remain poorly studied.

resultsIn this work, we used proteomic and functional genomic analyses to determine potential metabolic pathways involved in the photoassimilation of butyrate. We propose that a fraction of butyrate is converted to acetyl-CoA, a reaction shared with polyhydroxybutyrate metabolism, while the other fraction supplies the ethylmalonyl-CoA (EMC) pathway used as an anaplerotic pathway to replenish the TCA cycle. Surprisingly, we also highlighted a potential assimilation pathway, through isoleucine synthesis and degradation, allowing the conversion of acetyl-CoA to propionyl-CoA. We tentatively named this pathway the methylbutanoyl-CoA pathway (MBC). An increase in isoleucine abundance was observed during the early growth phase under butyrate condition. Nevertheless, while the EMC and MBC pathways appeared to be concomitantly used, a genome-wide mutant fitness assay highlighted the EMC pathway as the only pathway strictly required for the assimilation of butyrate.

conclusionPhotoheterotrophic growth of Rs. rubrum with butyrate as sole carbon source requires a functional EMC pathway. In addition, a new assimilation pathway involving isoleucine synthesis and degradation, named the methylbutanoyl-CoA (MBC) pathway, could also be involved in the assimilation of this volatile fatty acid by Rs. rubrum.

Indexed as

Acyl Coenzyme ABacterial ProteinsButyratesFermentationGenetic FitnessIsoleucineMetabolic Networks and PathwaysMutationPentanolsProteomicsRhodospirillum rubrumAcyl Coenzyme ABacterial ProteinsButyratesethylmalonyl-coenzyme AIsoleucinePentanolsAnaplerosisButyrate assimilationEthylmalonyl-CoAPhotoheterotrophyPolyhydroxybutyrate

Identifiers

PMID32434546
PMCPMC7238569
OpenAlexW3022602298

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.