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RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum

The strictly anaerobic bacterium Clostridium acetobutylicum is well known for its ability to convert sugars into organic acids and solvents, most notably the potential biofuel butanol. However, the regulation of its fermentation metabolism, in particular the shift from acid to solvent production, re...

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Autores principales: Kotte, Ann-Kathrin, Severn, Oliver, Bean, Zak, Schwarz, Katrin, Minton, Nigel P., Winzer, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376267/
https://www.ncbi.nlm.nih.gov/pubmed/32375981
http://dx.doi.org/10.1099/mic.0.000916
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author Kotte, Ann-Kathrin
Severn, Oliver
Bean, Zak
Schwarz, Katrin
Minton, Nigel P.
Winzer, Klaus
author_facet Kotte, Ann-Kathrin
Severn, Oliver
Bean, Zak
Schwarz, Katrin
Minton, Nigel P.
Winzer, Klaus
author_sort Kotte, Ann-Kathrin
collection PubMed
description The strictly anaerobic bacterium Clostridium acetobutylicum is well known for its ability to convert sugars into organic acids and solvents, most notably the potential biofuel butanol. However, the regulation of its fermentation metabolism, in particular the shift from acid to solvent production, remains poorly understood. The aim of this study was to investigate whether cell–cell communication plays a role in controlling the timing of this shift or the extent of solvent formation. Analysis of the available C. acetobutylicum genome sequences revealed the presence of eight putative RRNPP-type quorum-sensing systems, here designated qssA to qssH, each consisting of an RRNPP-type regulator gene followed by a small open reading frame encoding a putative signalling peptide precursor. The identified regulator and signal peptide precursor genes were designated qsrA to qsrH and qspA to qspH, respectively. Triplicate regulator mutants were generated in strain ATCC 824 for each of the eight systems and screened for phenotypic changes. The qsrB mutants showed increased solvent formation during early solventogenesis and hence the QssB system was selected for further characterization. Overexpression of qsrB severely reduced solvent and endospore formation and this effect could be overcome by adding short synthetic peptides to the culture medium representing a specific region of the QspB signalling peptide precursor. In addition, overexpression of qspB increased the production of acetone and butanol and the initial (48 h) titre of heat-resistant endospores. Together, these findings establish a role for QssB quorum sensing in the regulation of early solventogenesis and sporulation in C. acetobutylicum .
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spelling pubmed-73762672020-07-24 RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum Kotte, Ann-Kathrin Severn, Oliver Bean, Zak Schwarz, Katrin Minton, Nigel P. Winzer, Klaus Microbiology (Reading) Research Article The strictly anaerobic bacterium Clostridium acetobutylicum is well known for its ability to convert sugars into organic acids and solvents, most notably the potential biofuel butanol. However, the regulation of its fermentation metabolism, in particular the shift from acid to solvent production, remains poorly understood. The aim of this study was to investigate whether cell–cell communication plays a role in controlling the timing of this shift or the extent of solvent formation. Analysis of the available C. acetobutylicum genome sequences revealed the presence of eight putative RRNPP-type quorum-sensing systems, here designated qssA to qssH, each consisting of an RRNPP-type regulator gene followed by a small open reading frame encoding a putative signalling peptide precursor. The identified regulator and signal peptide precursor genes were designated qsrA to qsrH and qspA to qspH, respectively. Triplicate regulator mutants were generated in strain ATCC 824 for each of the eight systems and screened for phenotypic changes. The qsrB mutants showed increased solvent formation during early solventogenesis and hence the QssB system was selected for further characterization. Overexpression of qsrB severely reduced solvent and endospore formation and this effect could be overcome by adding short synthetic peptides to the culture medium representing a specific region of the QspB signalling peptide precursor. In addition, overexpression of qspB increased the production of acetone and butanol and the initial (48 h) titre of heat-resistant endospores. Together, these findings establish a role for QssB quorum sensing in the regulation of early solventogenesis and sporulation in C. acetobutylicum . Microbiology Society 2020-07 2020-04-28 /pmc/articles/PMC7376267/ /pubmed/32375981 http://dx.doi.org/10.1099/mic.0.000916 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
spellingShingle Research Article
Kotte, Ann-Kathrin
Severn, Oliver
Bean, Zak
Schwarz, Katrin
Minton, Nigel P.
Winzer, Klaus
RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum
title RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum
title_full RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum
title_fullStr RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum
title_full_unstemmed RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum
title_short RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum
title_sort rrnpp-type quorum sensing affects solvent formation and sporulation in clostridium acetobutylicum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376267/
https://www.ncbi.nlm.nih.gov/pubmed/32375981
http://dx.doi.org/10.1099/mic.0.000916
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