Expression of a heat-stable NADPH-dependent alcohol dehydrogenase from Thermoanaerobacter pseudethanolicus 39E in Clostridium thermocellum 1313 results in increased hydroxymethylfurfural resistance

  • Sun Ki Kim
  • , Joseph Groom
  • , Daehwan Chung
  • , James Elkins
  • , Janet Westpheling

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Background: Resistance to deconstruction is a major limitation to the use of lignocellulosic biomass as a substrate for the production of fuels and chemicals. Consolidated bioprocessing (CBP), the use of microbes for the simultaneous hydrolysis of lignocellulose into soluble sugars and fermentation of the resulting sugars to products of interest, is a potential solution to this obstacle. The pretreatment of plant biomass, however, releases compounds that are inhibitory to the growth of microbes used for CBP. Results: Heterologous expression of the Thermoanaerobacter pseudethanolicus 39E bdhA gene, that encodes an alcohol dehydrogenase, in Clostridium thermocellum significantly increased resistance to furan derivatives at concentrations found in acid-pretreated biomass. The mechanism of detoxification of hydroxymethylfurfural was shown to be primarily reduction using NADPH as the cofactor. In addition, we report the construction of new expression vectors for homologous and heterologous expression in C. thermocellum. These vectors use regulatory signals from both C. bescii (the S-layer promoter) and C. thermocellum (the enolase promoter) shown to efficiently drive expression of the BdhA enzyme. Conclusions: Toxic compounds present in lignocellulose hydrolysates that inhibit cell growth and product formation are obstacles to the commercialization of fuels and chemicals from biomass. Expression of genes that reduce the effect of these inhibitors, such as furan derivatives, will serve to enable commercial processes using plant biomass for the production of fuels and chemicals.

Original languageEnglish
Article number66
JournalBiotechnology for Biofuels
Volume10
Issue number1
DOIs
StatePublished - Mar 15 2017

Funding

This work was supported by the BioEnergy Science Center, US DOE Bioenergy Research Center supported by the Office of Biological and Environmental Research in the DOE Office of Science. Oak Ridge National Laboratory is man‑ aged by UT‑Battelle, LLC, for the US DOE under contract DE‑AC05‑00OR22725. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Keywords

  • 5-hydroxymethyl-2-furfural
  • Butanol dehydrogenase
  • Clostridium thermocellum
  • Consolidated bioprocessing
  • Furfural

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