Complete genome analysis of Clostridium bornimense strain M2/40T: A new acidogenic Clostridium species isolated from a mesophilic two-phase laboratory-scale biogas reactor

•Presentation of the genome sequence for the new type strain Clostridium bornimense M2/40T.•Strain C. bornimense M2/40T harbors a chromid encoding active glycoside hydrolase enzymes.•Reconstruction of fermentation pathways with importance for biofuel production from the genome sequence. Taxonomic an...

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Veröffentlicht in:Journal of biotechnology 2016-08, Vol.232, p.38-49
Hauptverfasser: Tomazetto, Geizecler, Hahnke, Sarah, Koeck, Daniela E., Wibberg, Daniel, Maus, Irena, Pühler, Alfred, Klocke, Michael, Schlüter, Andreas
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Sprache:eng
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Zusammenfassung:•Presentation of the genome sequence for the new type strain Clostridium bornimense M2/40T.•Strain C. bornimense M2/40T harbors a chromid encoding active glycoside hydrolase enzymes.•Reconstruction of fermentation pathways with importance for biofuel production from the genome sequence. Taxonomic and functional profiling based on metagenome analyses frequently revealed that members of the class Clostridia dominate biogas reactor communities and perform different essential metabolic pathways in the biogas fermentation process. Clostridium bornimense strain M2/40T was recently isolated from a mesophilic two-phase lab-scale biogas reactor continuously fed with maize silage and wheat straw. The genome of the strain was completely sequenced and manually annotated to reconstruct its metabolic potential regarding carbohydrate active enzyme production and fermentation of organic compounds for consolidated biofuel production from biomass. The C. bornimense M2/40T genome consists of a chromosome (2,917,864bp in size) containing 2613 protein coding sequences, and a 699,161bp chromid (secondary replicon) harboring 680 coding sequences. Both replicons feature very similar GC-contents of approximately 29%. The complex genome comprises three prophage regions, two CRISPR-cas systems and a putative cellulosomal gene cluster that is located on the second replicon (chromid) of the strain. The overexpressed glycosyl hydrolases (GH) CelK (GH9) and CelA (GH48) encoded in the cellulosomal gene cluster were shown to be active on the substrates xylan and xyloglucan whereas XghA (GH74) is highly active on xyloglucan. Reconstruction of fermentation pathways from genome sequence data revealed that strain M2/40T encodes all enzymes for hydrogen, acetate, formate, lactate, butyrate, and ethanol production, leading to the classification of the isolate as acidogenic bacterium. Phylogenetic analyses uncovered that the closest characterized relative of C. bornimense is C. cellulovorans. Comparative analyses of the C. bornimense and C. cellulovorans genomes revealed considerable rearrangements within their chromosomes suggesting that both species evolved separately for a relatively long period of time and adapted to specific tasks within microbial consortia responsible for anaerobic digestion.
ISSN:0168-1656
1873-4863
DOI:10.1016/j.jbiotec.2015.08.001