Cargando…
An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture
BACKGROUND: Soluble hydrogenases (SH) are enzymes that catalyse the oxidation of molecular hydrogen. The SH enzyme from Cupriavidus necator H16 is relatively oxygen tolerant and makes an attractive target for potential application in biochemical hydrogen fuel cells. Expression of the enzyme can be m...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377017/ https://www.ncbi.nlm.nih.gov/pubmed/25880663 http://dx.doi.org/10.1186/s12934-015-0226-4 |
_version_ | 1782363834461192192 |
---|---|
author | Jugder, Bat-Erdene Chen, Zhiliang Ping, Darren Tan Tek Lebhar, Helene Welch, Jeffrey Marquis, Christopher P |
author_facet | Jugder, Bat-Erdene Chen, Zhiliang Ping, Darren Tan Tek Lebhar, Helene Welch, Jeffrey Marquis, Christopher P |
author_sort | Jugder, Bat-Erdene |
collection | PubMed |
description | BACKGROUND: Soluble hydrogenases (SH) are enzymes that catalyse the oxidation of molecular hydrogen. The SH enzyme from Cupriavidus necator H16 is relatively oxygen tolerant and makes an attractive target for potential application in biochemical hydrogen fuel cells. Expression of the enzyme can be mediated by derepression of the hox promoter system under heterotrophic conditions. However, the overall impact of hox derepression, from a transcriptomic perspective, has never been previously reported. RESULTS: Derepression of hydrogenase gene expression upon fructose depletion was confirmed in replicate experiments. Using qRT-PCR, hoxF was 4.6-fold up-regulated, hypF2 was up-regulated in the cells grown 2.2-fold and the regulatory gene hoxA was up-regulated by a mean factor of 4.5. A full transcriptomic evaluation revealed a substantial shift in the global pattern of gene expression. In addition to up-regulation of genes associated with hydrogenase expression, significant changes were observed in genes associated with energy transduction, amino acid metabolism, transcription and translation (and regulation thereof), genes associated with cell stress, lipid and cell wall biogenesis and other functions, including cell motility. CONCLUSIONS: We report the first full transcriptome analysis of C. necator H16 grown heterotrophically on fructose and glycerol in diauxic batch culture, which permits expression of soluble hydrogenase under heterotrophic conditions. The data presented deepens our understanding of the changes in global gene expression patterns that occur during the switch to growth on glycerol and suggests that energy deficit is a key driver for induction of hydrogenase expression in this organism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0226-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4377017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43770172015-03-29 An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture Jugder, Bat-Erdene Chen, Zhiliang Ping, Darren Tan Tek Lebhar, Helene Welch, Jeffrey Marquis, Christopher P Microb Cell Fact Research BACKGROUND: Soluble hydrogenases (SH) are enzymes that catalyse the oxidation of molecular hydrogen. The SH enzyme from Cupriavidus necator H16 is relatively oxygen tolerant and makes an attractive target for potential application in biochemical hydrogen fuel cells. Expression of the enzyme can be mediated by derepression of the hox promoter system under heterotrophic conditions. However, the overall impact of hox derepression, from a transcriptomic perspective, has never been previously reported. RESULTS: Derepression of hydrogenase gene expression upon fructose depletion was confirmed in replicate experiments. Using qRT-PCR, hoxF was 4.6-fold up-regulated, hypF2 was up-regulated in the cells grown 2.2-fold and the regulatory gene hoxA was up-regulated by a mean factor of 4.5. A full transcriptomic evaluation revealed a substantial shift in the global pattern of gene expression. In addition to up-regulation of genes associated with hydrogenase expression, significant changes were observed in genes associated with energy transduction, amino acid metabolism, transcription and translation (and regulation thereof), genes associated with cell stress, lipid and cell wall biogenesis and other functions, including cell motility. CONCLUSIONS: We report the first full transcriptome analysis of C. necator H16 grown heterotrophically on fructose and glycerol in diauxic batch culture, which permits expression of soluble hydrogenase under heterotrophic conditions. The data presented deepens our understanding of the changes in global gene expression patterns that occur during the switch to growth on glycerol and suggests that energy deficit is a key driver for induction of hydrogenase expression in this organism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0226-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-25 /pmc/articles/PMC4377017/ /pubmed/25880663 http://dx.doi.org/10.1186/s12934-015-0226-4 Text en © Jugder et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Jugder, Bat-Erdene Chen, Zhiliang Ping, Darren Tan Tek Lebhar, Helene Welch, Jeffrey Marquis, Christopher P An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture |
title | An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture |
title_full | An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture |
title_fullStr | An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture |
title_full_unstemmed | An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture |
title_short | An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture |
title_sort | analysis of the changes in soluble hydrogenase and global gene expression in cupriavidus necator (ralstonia eutropha) h16 grown in heterotrophic diauxic batch culture |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377017/ https://www.ncbi.nlm.nih.gov/pubmed/25880663 http://dx.doi.org/10.1186/s12934-015-0226-4 |
work_keys_str_mv | AT jugderbaterdene ananalysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT chenzhiliang ananalysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT pingdarrentantek ananalysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT lebharhelene ananalysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT welchjeffrey ananalysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT marquischristopherp ananalysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT jugderbaterdene analysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT chenzhiliang analysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT pingdarrentantek analysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT lebharhelene analysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT welchjeffrey analysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture AT marquischristopherp analysisofthechangesinsolublehydrogenaseandglobalgeneexpressionincupriavidusnecatorralstoniaeutrophah16growninheterotrophicdiauxicbatchculture |