Rex in Caldicellulosiruptor bescii: Novel regulon members and its effect on the production of ethanol and overflow metabolites

Kyle Sander, Daehwan Chung, Doug Hyatt, Janet Westpheling, Dawn M. Klingeman, Miguel Rodriguez, Nancy L. Engle, Timothy J. Tschaplinski, Brian H. Davison, Steven D. Brown

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Rex is a global redox-sensing transcription factor that senses and responds to the intracellular [NADH]/[NAD+] ratio to regulate genes for central metabolism, and a variety of metabolic processes in Gram-positive bacteria. We decipher and validate four new members of the Rex regulon in Caldicellulosiruptor bescii; a gene encoding a class V aminotransferase, the HydG FeFe Hydrogenase maturation protein, an oxidoreductase, and a gene encoding a hypothetical protein. Structural genes for the NiFe and FeFe hydrogenases, pyruvate:ferredoxin oxidoreductase, as well as the rex gene itself are also members of this regulon, as has been predicted previously in different organisms. A C. bescii rex deletion strain constructed in an ethanol-producing strain made 54% more ethanol (0.16 mmol/L) than its genetic parent after 36 hr of fermentation, though only under nitrogen limited conditions. Metabolomic interrogation shows this rex-deficient ethanol-producing strain synthesizes other reduced overflow metabolism products likely in response to more reduced intracellular redox conditions and the accumulation of pyruvate. These results suggest ethanol production is strongly dependent on the native intracellular redox state in C. bescii, and highlight the combined promise of using this gene and manipulation of culture conditions to yield strains capable of producing ethanol at higher yields and final titer.

Original languageEnglish
Article numbere00639
JournalMicrobiologyOpen
Volume8
Issue number2
DOIs
StatePublished - Feb 2019

Funding

The authors acknowledge and thank Charlotte Wilson, Chia-Wei Wu, and Geoff Christensen for thoughtful and critical discussion and assistance in troubleshooting, and optimizing protocols used in this study. The authors thank Dr. Joseph Groom for his suggestions during strain generation Sanger sequencing support was provided by the DNA Sequencing Lab at the University of Tennessee Genomics Core Facility and Illumina data was generated by The Genomic Services Lab at Hudson Alpha Institute for Biotechnology. The publisher, by accepting the article for publication, acknowledges that the United States Government retains a nonexclusive, paid-up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan). This work is supported by the BioEnergy Science Center (BESC), 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. The manuscript has been authored by UT-Battelle, LLC, under contract no. DE-AC05-00OR22725 with the U.S. Department of Energy. The funders had no role in study design, data collection and interpretation, preparation of the manuscript, or the decision to submit the work for publication.

Keywords

  • Caldicellulosiruptor bescii
  • Rex
  • consolidated bioprocessing
  • ethanol

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