Chromosomal integration of aldo-keto-reductase and short-chain dehydrogenase/reductase genes in Clostridium beijerinckii NCIMB 8052 enhanced tolerance to lignocellulose-derived microbial inhibitory compounds

Sci Rep. 2019 May 21;9(1):7634. doi: 10.1038/s41598-019-44061-1.

Abstract

In situ detoxification of lignocellulose-derived microbial inhibitory compounds is an economical strategy for the fermentation of lignocellulose-derived sugars to fuels and chemicals. In this study, we investigated homologous integration and constitutive expression of Cbei_3974 and Cbei_3904, which encode aldo-keto reductase and previously annotated short chain dehydrogenase/reductase, respectively, in Clostridium beijerinckii NCIMB 8052 (Cb), resulting in two strains: Cb_3974 and Cb_3904. Expression of Cbei_3974 led to 2-fold increase in furfural detoxification relative to Cb_3904 and Cb_wild type. Correspondingly, butanol production was up to 1.2-fold greater in furfural-challenged cultures of Cb_3974 relative to Cb_3904 and Cb_wild type. With 4-hydroxybezaldehyde and syringaldehyde supplementation, Cb_3974 showed up to 2.4-fold increase in butanol concentration when compared to Cb_3904 and Cb_wild type. Syringic and vanillic acids were considerably less deleterious to all three strains of Cb tested. Overall, Cb_3974 showed greater tolerance to furfural, 4-hydroxybezaldehyde, and syringaldehyde with improved capacity for butanol production. Hence, development of Cb_3974 represents a significant progress towards engineering solventogenic Clostridium species that are tolerant to lignocellulosic biomass hydrolysates as substrates for ABE fermentation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetone / metabolism
  • Aldo-Keto Reductases / genetics*
  • Aldo-Keto Reductases / metabolism
  • Benzaldehydes / pharmacology
  • Butanols / metabolism
  • Chromosomes, Fungal / genetics*
  • Clostridium beijerinckii / enzymology
  • Clostridium beijerinckii / genetics
  • Clostridium beijerinckii / metabolism*
  • Ethanol / metabolism
  • Fermentation*
  • Fungal Proteins / genetics*
  • Fungal Proteins / metabolism
  • Furaldehyde / metabolism
  • Gallic Acid / analogs & derivatives
  • Gallic Acid / metabolism
  • Industrial Microbiology / methods*
  • Lignin / metabolism*
  • Oxidoreductases / genetics*
  • Oxidoreductases / metabolism
  • Vanillic Acid / metabolism

Substances

  • Benzaldehydes
  • Butanols
  • Fungal Proteins
  • Acetone
  • syringaldehyde
  • Ethanol
  • Gallic Acid
  • Lignin
  • Furaldehyde
  • syringic acid
  • Oxidoreductases
  • Aldo-Keto Reductases
  • Vanillic Acid