Preliminary crystallographic studies of glucose dehydrogenase from the promiscuous Entner-Doudoroff pathway in the hyperthermophilic archaeon Sulfolobus solfataricus

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2005 Jan 1;61(Pt 1):112-5. doi: 10.1107/S174430910403101X. Epub 2004 Dec 24.

Abstract

The hyperthermophilic archaeon Sulfolobus solfataricus grows optimally above 353 K and can metabolize glucose and its C4 epimer galactose via a non-phosphorylative variant of the Entner-Doudoroff pathway involving catalytically promiscuous enzymes that can operate with both sugars. The initial oxidation step is catalysed by glucose dehydrogenase (SsGDH), which can utilize both NAD and NADP as cofactors. The enzyme operates with glucose and galactose at similar catalytic efficiency, while its substrate profile also includes a range of other five- and six-carbon sugars. Crystals of the 164 kDa SsGDH homotetramer have been grown under a variety of conditions. The best crystals to date diffract to 1.8 A on a synchrotron source, have orthorhombic symmetry and belong to space group P2(1)2(1)2. Attempts are being made to solve the structure by MAD and MR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Archaeal Proteins / chemistry
  • Archaeal Proteins / isolation & purification
  • Archaeal Proteins / metabolism
  • Cloning, Molecular
  • Crystallization
  • Escherichia coli / enzymology
  • Glucose 1-Dehydrogenase / chemistry*
  • Glucose 1-Dehydrogenase / isolation & purification
  • Glucose 1-Dehydrogenase / metabolism
  • Hot Temperature
  • Models, Molecular
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Substrate Specificity
  • Sulfolobus solfataricus / enzymology*
  • Synchrotrons
  • Thermodynamics
  • X-Ray Diffraction

Substances

  • Archaeal Proteins
  • Recombinant Proteins
  • Glucose 1-Dehydrogenase