Clostridium thermocellum ATCC27405 transcriptomic, metabolomic and proteomic profiles after ethanol stress

Shihui Yang, Richard J. Giannone, Lezlee Dice, Zamin K. Yang, Nancy L. Engle, Timothy J. Tschaplinski, Robert L. Hettich, Steven D. Brown

Research output: Contribution to journalArticlepeer-review

64 Scopus citations

Abstract

Background: Clostridium thermocellum is a candidate consolidated bioprocessing biocatalyst, which is a microorganism that expresses enzymes for both cellulose hydrolysis and its fermentation to produce fuels such as lignocellulosic ethanol. However, C. thermocellum is relatively sensitive to ethanol compared to ethanologenic microorganisms such as yeast and Zymomonas mobilis that are used in industrial fermentations but do not possess native enzymes for industrial cellulose hydrolysis.Results: In this study, C. thermocellum was grown to mid-exponential phase and then treated with ethanol to a final concentration of 3.9 g/L to investigate its physiological and regulatory responses to ethanol stress. Samples were taken pre-shock and 2, 12, 30, 60, 120, and 240 min post-shock, and from untreated control fermentations for systems biology analyses. Cell growth was arrested by ethanol supplementation with intracellular accumulation of carbon sources such as cellobiose, and sugar phosphates, including fructose-6-phosphate and glucose-6-phosphate. The largest response of C. thermocellum to ethanol shock treatment was in genes and proteins related to nitrogen uptake and metabolism, which is likely important for redirecting the cells physiology to overcome inhibition and allow growth to resume.Conclusion: This study suggests possible avenues for metabolic engineering and provides comprehensive, integrated systems biology datasets that will be useful for future metabolic modeling and strain development endeavors.

Original languageEnglish
Article number336
JournalBMC Genomics
Volume13
Issue number1
DOIs
StatePublished - Jul 23 2012

Funding

The authors thank Choo Hamilton for technical assistance with HPLC analysis. We also thank Pin-Ching Maness for discussions on the hydrogenase data and Adam Guss for critical review during manuscript preparation. This work is sponsored by the BioEnergy Science Center, which is a U.S. Department of Energy Bioenergy Research Center supported by the Office of Biological and Environmental Research in the DOE Office of Science. This manuscript has been authored by UT-Battelle, LLC, under Contract No. DE-AC05-00OR22725 with the U.S. Department of Energy.

FundersFunder number
BioEnergy Science Center
U.S. Department of Energy Bioenergy Research Center
U.S. Department of Energy
Office of ScienceDE-AC05-00OR22725
Biological and Environmental Research

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