Evidence map›Paper›PMID 25722742›Full record

ArticleBiotechnology for biofuels2015

Genome-wide transcriptional analysis suggests hydrogenase- and nitrogenase-mediated hydrogen production in Clostridium butyricum CWBI 1009.

Magdalena Calusinska, Christopher Hamilton, Pieter Monsieurs, Gregory Mathy, Natalie Leys, Fabrice Franck, Bernard Joris, Philippe Thonart, Serge Hiligsmann, Annick Wilmotte

Open access · goldAbstract read
In one paragraph

Article in Biotechnology for biofuels, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

10 citing papers in PubMed, 59 citations in OpenAlex.

  1. Comparative genomics ofMicrobial genomics · 2025
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  5. A Win-Loss Interaction on FeFrontiers in microbiology · 2021
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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

10 authors at 2 institutions in 1 country.

Magdalena Calusinska *Centre for Protein Engineering, Bacterial Physiology and Genetics, University of Liège, Allée de la Chimie 3, B-4000 Liège, Belgium.
Christopher Hamilton *Walloon Centre of Industrial Biology, University of Liège, Boulevard du Rectorat 29, B-4000 Liège, Belgium.
Pieter Monsieurs *Microbiology Unit, Expertise Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre (SCK-CEN), Boeretang 200, B-2400 Mol, Belgium.
Gregory MathyBioenergetics Laboratory, University of Liège, Boulevard du Rectorat 27, B-4000 Liège, Belgium.
Natalie LeysMicrobiology Unit, Expertise Group for Molecular and Cellular Biology, Institute for Environment, Health and Safety, Belgian Nuclear Research Centre (SCK-CEN), Boeretang 200, B-2400 Mol, Belgium.
Fabrice FranckBioenergetics Laboratory, University of Liège, Boulevard du Rectorat 27, B-4000 Liège, Belgium.
Bernard JorisCentre for Protein Engineering, Bacterial Physiology and Genetics, University of Liège, Allée de la Chimie 3, B-4000 Liège, Belgium.
Philippe ThonartWalloon Centre of Industrial Biology, University of Liège, Boulevard du Rectorat 29, B-4000 Liège, Belgium.
Serge HiligsmannWalloon Centre of Industrial Biology, University of Liège, Boulevard du Rectorat 29, B-4000 Liège, Belgium.
Annick WilmotteCentre for Protein Engineering, Bacterial Physiology and Genetics, University of Liège, Allée de la Chimie 3, B-4000 Liège, Belgium.
University of Liège · BEBelgian Nuclear Research Centre · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMolecular hydrogen, given its pollution-free combustion, has great potential to replace fossil fuels in future transportation and energy production. However, current industrial hydrogen production processes, such as steam reforming of methane, contribute significantly to the greenhouse effect. Therefore alternative methods, in particular the use of fermentative microorganisms, have attracted scientific interest in recent years. However the low overall yield obtained is a major challenge in biological H2 production. Thus, a thorough and detailed understanding of the relationships between genome content, gene expression patterns, pathway utilisation and metabolite synthesis is required to optimise the yield of biohydrogen production pathways.

resultsIn this study transcriptomic and proteomic analyses of the hydrogen-producing bacterium Clostridium butyricum CWBI 1009 were carried out to provide a biomolecular overview of the changes that occur when the metabolism shifts to H2 production. The growth, H2-production, and glucose-fermentation profiles were monitored in 20 L batch bioreactors under unregulated-pH and fixed-pH conditions (pH 7.3 and 5.2). Conspicuous differences were observed in the bioreactor performances and cellular metabolisms for all the tested metabolites, and they were pH dependent. During unregulated-pH glucose fermentation increased H2 production was associated with concurrent strong up-regulation of the nitrogenase coding genes. However, no such concurrent up-regulation of the [FeFe] hydrogenase genes was observed. During the fixed pH 5.2 fermentation, by contrast, the expression levels for the [FeFe] hydrogenase coding genes were higher than during the unregulated-pH fermentation, while the nitrogenase transcripts were less abundant. The overall results suggest, for the first time, that environmental factors may determine whether H2 production in C. butyricum CWBI 1009 is mediated by the hydrogenases and/or the nitrogenase.

conclusionsThis work, contributing to the field of dark fermentative hydrogen production, provides a multidisciplinary approach for the investigation of the processes involved in the molecular H2 metabolism of clostridia. In addition, it lays the groundwork for further optimisation of biohydrogen production pathways based on genetic engineering techniques.

Indexed as

2D-DIGEClostridium butyricumDark fermentation[FeFe] hydrogenaseNitrogenaseRNA-seq

Identifiers

PMID25722742
PMCPMC4342158
OpenAlexW2100219163

What OpenQuestion holds

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LicenceCC BY
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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.