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Aromatic inhibitors derived from ammonia-pretreated lignocellulose hinder bacterial ethanologenesis by activating regulatory circuits controlling inhibitor efflux and detoxification.
Keating, David H; Zhang, Yaoping; Ong, Irene M; McIlwain, Sean; Morales, Eduardo H; Grass, Jeffrey A; Tremaine, Mary; Bothfeld, William; Higbee, Alan; Ulbrich, Arne; Balloon, Allison J; Westphall, Michael S; Aldrich, Josh; Lipton, Mary S; Kim, Joonhoon; Moskvin, Oleg V; Bukhman, Yury V; Coon, Joshua J; Kiley, Patricia J; Bates, Donna M; Landick, Robert.
Afiliação
  • Keating DH; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Zhang Y; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Ong IM; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • McIlwain S; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Morales EH; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA ; Department of Biomolecular Chemistry, University of Wisconsin-Madison Madison, WI, USA.
  • Grass JA; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA ; Department of Biochemistry, University of Wisconsin-Madison Madison, WI, USA.
  • Tremaine M; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Bothfeld W; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Higbee A; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Ulbrich A; Department of Chemistry, University of Wisconsin-Madison Madison, WI, USA.
  • Balloon AJ; Department of Chemistry, University of Wisconsin-Madison Madison, WI, USA.
  • Westphall MS; Department of Biomolecular Chemistry, University of Wisconsin-Madison Madison, WI, USA ; Department of Chemistry, University of Wisconsin-Madison Madison, WI, USA.
  • Aldrich J; Pacific Northwest National Laboratory Richland, WA, USA.
  • Lipton MS; Pacific Northwest National Laboratory Richland, WA, USA.
  • Kim J; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA ; Department of Chemical and Biological Engineering, University of Wisconsin-Madison Madison, WI, USA.
  • Moskvin OV; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Bukhman YV; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Coon JJ; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA ; Department of Biomolecular Chemistry, University of Wisconsin-Madison Madison, WI, USA ; Department of Chemistry, University of Wisconsin-Madison Madison, WI, USA.
  • Kiley PJ; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA ; Department of Biomolecular Chemistry, University of Wisconsin-Madison Madison, WI, USA.
  • Bates DM; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA.
  • Landick R; Great Lakes Bioenergy Research Center, University of Wisconsin-Madison Madison, WI, USA ; Department of Biochemistry, University of Wisconsin-Madison Madison, WI, USA ; Department of Bacteriology, University of Wisconsin-Madison Madison, WI, USA.
Front Microbiol ; 5: 402, 2014.
Article em En | MEDLINE | ID: mdl-25177315
ABSTRACT
Efficient microbial conversion of lignocellulosic hydrolysates to biofuels is a key barrier to the economically viable deployment of lignocellulosic biofuels. A chief contributor to this barrier is the impact on microbial processes and energy metabolism of lignocellulose-derived inhibitors, including phenolic carboxylates, phenolic amides (for ammonia-pretreated biomass), phenolic aldehydes, and furfurals. To understand the bacterial pathways induced by inhibitors present in ammonia-pretreated biomass hydrolysates, which are less well studied than acid-pretreated biomass hydrolysates, we developed and exploited synthetic mimics of ammonia-pretreated corn stover hydrolysate (ACSH). To determine regulatory responses to the inhibitors normally present in ACSH, we measured transcript and protein levels in an Escherichia coli ethanologen using RNA-seq and quantitative proteomics during fermentation to ethanol of synthetic hydrolysates containing or lacking the inhibitors. Our study identified four major regulators mediating these responses, the MarA/SoxS/Rob network, AaeR, FrmR, and YqhC. Induction of these regulons was correlated with a reduced rate of ethanol production, buildup of pyruvate, depletion of ATP and NAD(P)H, and an inhibition of xylose conversion. The aromatic aldehyde inhibitor 5-hydroxymethylfurfural appeared to be reduced to its alcohol form by the ethanologen during fermentation, whereas phenolic acid and amide inhibitors were not metabolized. Together, our findings establish that the major regulatory responses to lignocellulose-derived inhibitors are mediated by transcriptional rather than translational regulators, suggest that energy consumed for inhibitor efflux and detoxification may limit biofuel production, and identify a network of regulators for future synthetic biology efforts.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Microbiol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Microbiol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos