Crystallization and preliminary crystallographic analysis of the catechol 2,3-dioxygenase PheB from Bacillus stearothermophilus BR219

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2006 Feb 1;62(Pt 2):125-7. doi: 10.1107/S174430910504323X. Epub 2006 Jan 27.

Abstract

Class II extradiol-cleaving catecholic dioxygenase, a key enzyme of aromatic compound degradation in bacteria, cleaves the aromatic ring of catechol by adding two O atoms. PheB is one of the class II extradiol-cleaving catecholic dioxygenases and shows a high substrate specificity for catechol derivatives, which have one aromatic ring. In order to reveal the mechanism of the substrate specificity of PheB, PheB has been crystallized by the hanging-drop vapour-diffusion method using PEG 4000 as a precipitant. The space group of the obtained crystal was P2(1)2(1)2(1), with unit-cell parameters a = 65.5, b = 119.2, c = 158.7 A. The crystal diffracted to 2.3 A resolution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / classification
  • Bacterial Proteins / metabolism
  • Catechol 2,3-Dioxygenase / chemistry*
  • Catechol 2,3-Dioxygenase / classification
  • Catechol 2,3-Dioxygenase / metabolism
  • Crystallization
  • Crystallography, X-Ray
  • Geobacillus stearothermophilus / enzymology*
  • Substrate Specificity

Substances

  • Bacterial Proteins
  • Catechol 2,3-Dioxygenase