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A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture

The complex changes in the life cycle of Clostridium acetobutylicum, a promising biofuel producer, are not well understood. During exponential growth, sugars are fermented to acetate and butyrate, and in the transition phase, the metabolism switches to the production of the solvents acetone and buta...

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Autores principales: Janssen, Holger, Döring, Christina, Ehrenreich, Armin, Voigt, Birgit, Hecker, Michael, Bahl, Hubert, Fischer, Ralf-Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227527/
https://www.ncbi.nlm.nih.gov/pubmed/20617312
http://dx.doi.org/10.1007/s00253-010-2741-x
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author Janssen, Holger
Döring, Christina
Ehrenreich, Armin
Voigt, Birgit
Hecker, Michael
Bahl, Hubert
Fischer, Ralf-Jörg
author_facet Janssen, Holger
Döring, Christina
Ehrenreich, Armin
Voigt, Birgit
Hecker, Michael
Bahl, Hubert
Fischer, Ralf-Jörg
author_sort Janssen, Holger
collection PubMed
description The complex changes in the life cycle of Clostridium acetobutylicum, a promising biofuel producer, are not well understood. During exponential growth, sugars are fermented to acetate and butyrate, and in the transition phase, the metabolism switches to the production of the solvents acetone and butanol accompanied by the initiation of endospore formation. Using phosphate-limited chemostat cultures at pH 5.7, C. acetobutylicum was kept at a steady state of acidogenic metabolism, whereas at pH 4.5, the cells showed stable solvent production without sporulation. Novel proteome reference maps of cytosolic proteins from both acidogenesis and solventogenesis with a high degree of reproducibility were generated. Yielding a 21% coverage, 15 protein spots were specifically assigned to the acidogenic phase, and 29 protein spots exhibited a significantly higher abundance in the solventogenic phase. Besides well-known metabolic proteins, unexpected proteins were also identified. Among these, the two proteins CAP0036 and CAP0037 of unknown function were found as major striking indicator proteins in acidogenic cells. Proteome data were confirmed by genome-wide DNA microarray analyses of the identical cultures. Thus, a first systematic study of acidogenic and solventogenic chemostat cultures is presented, and similarities as well as differences to previous studies of batch cultures are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-010-2741-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-32275272011-12-01 A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture Janssen, Holger Döring, Christina Ehrenreich, Armin Voigt, Birgit Hecker, Michael Bahl, Hubert Fischer, Ralf-Jörg Appl Microbiol Biotechnol Genomics, Transcriptomics, Proteomics The complex changes in the life cycle of Clostridium acetobutylicum, a promising biofuel producer, are not well understood. During exponential growth, sugars are fermented to acetate and butyrate, and in the transition phase, the metabolism switches to the production of the solvents acetone and butanol accompanied by the initiation of endospore formation. Using phosphate-limited chemostat cultures at pH 5.7, C. acetobutylicum was kept at a steady state of acidogenic metabolism, whereas at pH 4.5, the cells showed stable solvent production without sporulation. Novel proteome reference maps of cytosolic proteins from both acidogenesis and solventogenesis with a high degree of reproducibility were generated. Yielding a 21% coverage, 15 protein spots were specifically assigned to the acidogenic phase, and 29 protein spots exhibited a significantly higher abundance in the solventogenic phase. Besides well-known metabolic proteins, unexpected proteins were also identified. Among these, the two proteins CAP0036 and CAP0037 of unknown function were found as major striking indicator proteins in acidogenic cells. Proteome data were confirmed by genome-wide DNA microarray analyses of the identical cultures. Thus, a first systematic study of acidogenic and solventogenic chemostat cultures is presented, and similarities as well as differences to previous studies of batch cultures are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-010-2741-x) contains supplementary material, which is available to authorized users. Springer-Verlag 2010-07-09 2010-08 /pmc/articles/PMC3227527/ /pubmed/20617312 http://dx.doi.org/10.1007/s00253-010-2741-x Text en © Springer-Verlag 2010
spellingShingle Genomics, Transcriptomics, Proteomics
Janssen, Holger
Döring, Christina
Ehrenreich, Armin
Voigt, Birgit
Hecker, Michael
Bahl, Hubert
Fischer, Ralf-Jörg
A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture
title A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture
title_full A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture
title_fullStr A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture
title_full_unstemmed A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture
title_short A proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of Clostridium acetobutylicum in a chemostat culture
title_sort proteomic and transcriptional view of acidogenic and solventogenic steady-state cells of clostridium acetobutylicum in a chemostat culture
topic Genomics, Transcriptomics, Proteomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227527/
https://www.ncbi.nlm.nih.gov/pubmed/20617312
http://dx.doi.org/10.1007/s00253-010-2741-x
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