Cargando…
A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates
BACKGROUND: Cellulose is the most abundant biological polymer on earth, making it an attractive substrate for the production of next-generation biofuels and commodity chemicals. However, the economics of cellulose utilization are currently unfavorable due to a lack of efficient methods for its hydro...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204037/ https://www.ncbi.nlm.nih.gov/pubmed/30386432 http://dx.doi.org/10.1186/s13068-018-1290-x |
_version_ | 1783365986438610944 |
---|---|
author | Neumann, Anthony P. Weimer, Paul J. Suen, Garret |
author_facet | Neumann, Anthony P. Weimer, Paul J. Suen, Garret |
author_sort | Neumann, Anthony P. |
collection | PubMed |
description | BACKGROUND: Cellulose is the most abundant biological polymer on earth, making it an attractive substrate for the production of next-generation biofuels and commodity chemicals. However, the economics of cellulose utilization are currently unfavorable due to a lack of efficient methods for its hydrolysis. Fibrobacter succinogenes strain S85, originally isolated from the bovine rumen, is among the most actively cellulolytic mesophilic bacteria known, producing succinate as its major fermentation product. In this study, we examined the transcriptome of F. succinogenes S85 grown in continuous culture at several dilution rates on cellulose, cellobiose, or glucose to gain a system-level understanding of cellulose degradation by this bacterium. RESULTS: Several patterns of gene expression were observed for the major cellulases produced by F. succinogenes S85. A large proportion of cellulase genes were constitutively expressed, including the gene encoding for Cel51A, the major cellulose-binding endoglucanase produced by this bacterium. Moreover, other cellulase genes displayed elevated expression during growth on cellulose relative to growth on soluble sugars. Growth rate had a strong effect on global gene expression, particularly with regard to genes predicted to encode carbohydrate-binding modules and glycoside hydrolases implicated in hemicellulose degradation. Expression of hemicellulase genes was tightly regulated, with these genes displaying elevated expression only during slow growth on soluble sugars. Clear differences in gene expression were also observed between adherent and planktonic populations within continuous cultures growing on cellulose. CONCLUSIONS: This work emphasizes the complexity of the fiber-degrading system utilized by F. succinogenes S85, and reinforces the complementary role of hemicellulases for accessing cellulose by these bacteria. We report for the first time evidence of global differences in gene expression between adherent and planktonic populations of an anaerobic bacterium growing on cellulose at steady state during continuous cultivation. Finally, our results also highlight the importance of controlling for growth rate in investigations of gene expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1290-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6204037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62040372018-11-01 A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates Neumann, Anthony P. Weimer, Paul J. Suen, Garret Biotechnol Biofuels Research BACKGROUND: Cellulose is the most abundant biological polymer on earth, making it an attractive substrate for the production of next-generation biofuels and commodity chemicals. However, the economics of cellulose utilization are currently unfavorable due to a lack of efficient methods for its hydrolysis. Fibrobacter succinogenes strain S85, originally isolated from the bovine rumen, is among the most actively cellulolytic mesophilic bacteria known, producing succinate as its major fermentation product. In this study, we examined the transcriptome of F. succinogenes S85 grown in continuous culture at several dilution rates on cellulose, cellobiose, or glucose to gain a system-level understanding of cellulose degradation by this bacterium. RESULTS: Several patterns of gene expression were observed for the major cellulases produced by F. succinogenes S85. A large proportion of cellulase genes were constitutively expressed, including the gene encoding for Cel51A, the major cellulose-binding endoglucanase produced by this bacterium. Moreover, other cellulase genes displayed elevated expression during growth on cellulose relative to growth on soluble sugars. Growth rate had a strong effect on global gene expression, particularly with regard to genes predicted to encode carbohydrate-binding modules and glycoside hydrolases implicated in hemicellulose degradation. Expression of hemicellulase genes was tightly regulated, with these genes displaying elevated expression only during slow growth on soluble sugars. Clear differences in gene expression were also observed between adherent and planktonic populations within continuous cultures growing on cellulose. CONCLUSIONS: This work emphasizes the complexity of the fiber-degrading system utilized by F. succinogenes S85, and reinforces the complementary role of hemicellulases for accessing cellulose by these bacteria. We report for the first time evidence of global differences in gene expression between adherent and planktonic populations of an anaerobic bacterium growing on cellulose at steady state during continuous cultivation. Finally, our results also highlight the importance of controlling for growth rate in investigations of gene expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1290-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-27 /pmc/articles/PMC6204037/ /pubmed/30386432 http://dx.doi.org/10.1186/s13068-018-1290-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Neumann, Anthony P. Weimer, Paul J. Suen, Garret A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates |
title | A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates |
title_full | A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates |
title_fullStr | A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates |
title_full_unstemmed | A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates |
title_short | A global analysis of gene expression in Fibrobacter succinogenes S85 grown on cellulose and soluble sugars at different growth rates |
title_sort | global analysis of gene expression in fibrobacter succinogenes s85 grown on cellulose and soluble sugars at different growth rates |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204037/ https://www.ncbi.nlm.nih.gov/pubmed/30386432 http://dx.doi.org/10.1186/s13068-018-1290-x |
work_keys_str_mv | AT neumannanthonyp aglobalanalysisofgeneexpressioninfibrobactersuccinogeness85grownoncelluloseandsolublesugarsatdifferentgrowthrates AT weimerpaulj aglobalanalysisofgeneexpressioninfibrobactersuccinogeness85grownoncelluloseandsolublesugarsatdifferentgrowthrates AT suengarret aglobalanalysisofgeneexpressioninfibrobactersuccinogeness85grownoncelluloseandsolublesugarsatdifferentgrowthrates AT neumannanthonyp globalanalysisofgeneexpressioninfibrobactersuccinogeness85grownoncelluloseandsolublesugarsatdifferentgrowthrates AT weimerpaulj globalanalysisofgeneexpressioninfibrobactersuccinogeness85grownoncelluloseandsolublesugarsatdifferentgrowthrates AT suengarret globalanalysisofgeneexpressioninfibrobactersuccinogeness85grownoncelluloseandsolublesugarsatdifferentgrowthrates |