Purification, crystallization and preliminary X-ray analysis of the membrane-bound [NiFe] hydrogenase from Allochromatium vinosum

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2008 Aug 1;64(Pt 8):719-22. doi: 10.1107/S1744309108019945. Epub 2008 Jul 5.

Abstract

The membrane-bound [NiFe] hydrogenase is a unique metalloprotein that is able to catalyze the reversible oxidation of hydrogen to protons and electrons during a complex reaction cycle. The [NiFe] hydrogenase was isolated from the photosynthetic purple sulfur bacterium Allochromatium vinosum and its crystallization and preliminary X-ray analysis are reported. It was crystallized by the hanging-drop vapour-diffusion method using sodium citrate and imidazole as crystallization agents. The crystals belong to space group P2(1)2(1)2, with unit-cell parameters a = 205.00, b = 217.42, c = 120.44 A. X-ray diffraction data have been collected to 2.5 A resolution.

MeSH terms

  • Chromatography, Gel
  • Crystallization
  • Crystallography, X-Ray
  • Electrophoresis, Polyacrylamide Gel
  • Hydrogenase / chemistry*
  • Hydrogenase / isolation & purification
  • Protein Conformation
  • Proteobacteria / enzymology*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • nickel-iron hydrogenase
  • Hydrogenase