Overexpression, purification, crystallization and preliminary X-ray crystal analysis of Bacillus pallidusD-arabinose isomerase

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2008 Oct 1;64(Pt 10):945-8. doi: 10.1107/S1744309108028352. Epub 2008 Sep 30.

Abstract

D-Arabinose isomerase catalyzes the isomerization of D-arabinose to D-ribulose. Bacillus pallidus D-arabinose isomerase has broad substrate specificity and can catalyze the isomerization of D-arabinose, L-fucose, L-xylose, L-galactose and D-altrose. Recombinant B. pallidus D-arabinose isomerase was overexpressed, purified and crystallized. A crystal of the enzyme was obtained by the sitting-drop method at room temperature and belonged to the orthorhombic space group P2(1)2(1)2, with unit-cell parameters a = 144.9, b = 127.9, c = 109.5 A. Diffraction data were collected to 2.3 A resolution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldose-Ketose Isomerases / chemistry
  • Aldose-Ketose Isomerases / genetics*
  • Aldose-Ketose Isomerases / isolation & purification
  • Aldose-Ketose Isomerases / metabolism
  • Bacillus / enzymology*
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / isolation & purification
  • Crystallography, X-Ray / methods
  • DNA Primers
  • Pentoses / metabolism
  • Polymerase Chain Reaction

Substances

  • Bacterial Proteins
  • DNA Primers
  • Pentoses
  • ribulose
  • Aldose-Ketose Isomerases
  • D-arabinose isomerase