Engineering the isobutanol biosynthetic pathway in Escherichia coli by comparison of three aldehyde reductase/alcohol dehydrogenase genes

Appl Microbiol Biotechnol. 2010 Jan;85(3):651-7. doi: 10.1007/s00253-009-2085-6. Epub 2009 Jul 16.

Abstract

Biofuels synthesized from renewable resources are of increasing interest because of global energy and environmental problems. We have previously demonstrated production of higher alcohols from Escherichia coli using a 2-keto acid-based pathway. Here, we have compared the effect of various alcohol dehydrogenases (ADH) for the last step of the isobutanol production. E. coli has the yqhD gene which encodes a broad-range ADH. Isobutanol production significantly decreased with the deletion of yqhD, suggesting that the yqhD gene on the genome contributed to isobutanol production. The adh genes of two bacteria and one yeast were also compared in E. coli harboring the isobutanol synthesis pathway. Overexpression of yqhD or adhA in E. coli showed better production than ADH2, a result confirmed by activity measurements with isobutyraldehyde.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Dehydrogenase / genetics*
  • Alcohol Dehydrogenase / metabolism
  • Aldehyde Reductase / genetics*
  • Aldehyde Reductase / metabolism
  • Biosynthetic Pathways / genetics*
  • Butanols / metabolism*
  • Cloning, Molecular
  • Escherichia coli / enzymology
  • Escherichia coli / genetics*
  • Escherichia coli / metabolism*
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Gene Deletion
  • Genetic Engineering*
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • Butanols
  • Escherichia coli Proteins
  • Fungal Proteins
  • Recombinant Proteins
  • isobutyl alcohol
  • Alcohol Dehydrogenase
  • Aldehyde Reductase