Haloquadratum walsbyi Yields a Versatile, NAD+/NADP+ Dual Affinity, Thermostable, Alcohol Dehydrogenase (HwADH)

Mol Biotechnol. 2018 Jun;60(6):420-426. doi: 10.1007/s12033-018-0083-6.

Abstract

This study presents the first example of an alcohol dehydrogenase (ADH) from the halophilic archaeum Haloquadratum walsbyi (HwADH). A hexahistidine-tagged recombinant HwADH was heterologously overexpressed in Haloferax volcanii. HwADH was purified in one step and was found to be thermophilic with optimal activity at 65 °C. HwADH was active in the presence of 10% (v/v) organic solvent. The enzyme displayed dual cofactor specificity and a broad substrate scope, and maximum activity was detected with benzyl alcohol and 2-phenyl-1-propanol. HwADH accepted aromatic ketones, acetophenone and phenylacetone as substrates. The enzyme also accepted cyclohexanol and aromatic secondary alcohols, 1-phenylethanol and 4-phenyl-2-butanol. H. walsbyi may offer an excellent alternative to other archaeal sources to expand the toolbox of halophilic biocatalysts.

Keywords: Alcohol dehydrogenase; Dual cofactor specificity; Haloquadratum walsbyi; Thermoactivity.

MeSH terms

  • Alcohol Dehydrogenase / genetics
  • Alcohol Dehydrogenase / isolation & purification
  • Alcohol Dehydrogenase / metabolism*
  • Alcohols / metabolism*
  • Archaeal Proteins / genetics
  • Archaeal Proteins / isolation & purification
  • Archaeal Proteins / metabolism*
  • Benzyl Alcohol / metabolism
  • Cloning, Molecular
  • Enzyme Stability
  • Genes, Archaeal
  • Halobacteriaceae / enzymology*
  • Haloferax volcanii / genetics
  • Hot Temperature
  • Kinetics
  • NAD / metabolism
  • NADP / metabolism
  • Propanols / metabolism
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Substrate Specificity

Substances

  • Alcohols
  • Archaeal Proteins
  • Propanols
  • Recombinant Proteins
  • NAD
  • 2-phenylpropanol-1
  • NADP
  • Alcohol Dehydrogenase
  • Benzyl Alcohol

Supplementary concepts

  • Haloquadratum