Crystallization and preliminary X-ray analysis of the molybdenum-dependent pyrogallol-phloroglucinol transhydroxylase of Pelobacter acidigallici

Acta Crystallogr D Biol Crystallogr. 2002 Feb;58(Pt 2):343-5. doi: 10.1107/s0907444901020443. Epub 2002 Jan 24.

Abstract

Crystals of the molybdo-/iron-sulfur protein pyrogallol:phloroglucinol hydroxyltransferase (transhydroxylase; EC 1.97.1.2) from Pelobacter acidigallici were grown by vapour diffusion in an N(2)/H(2) atmosphere using polyethylene glycol as a precipitant. In this microorganism, transhydroxylase converts pyrogallol to phloroglucinol in a unique reaction without oxygen transfer from water. Growth of crystals suitable for X-ray analysis was strongly dependent on the presence of dithionite as a reducing agent. The crystals belonged to space group P1 and MAD data were collected on the iron K edge to resolutions higher than 2.5 A.

MeSH terms

  • Crystallization
  • Crystallography, X-Ray
  • Molybdenum / chemistry
  • Molybdenum / metabolism*
  • Oxidoreductases / chemistry*
  • Oxidoreductases / metabolism
  • Protein Conformation
  • Proteobacteria / enzymology*

Substances

  • Molybdenum
  • Oxidoreductases
  • pyrogallol hydroxyltransferase