Expression, purification, crystallization and preliminary X-ray diffraction data of methylmalonate-semialdehyde dehydrogenase from Bacillus subtilis

Acta Crystallogr D Biol Crystallogr. 2004 Aug;60(Pt 8):1435-7. doi: 10.1107/S0907444904012533. Epub 2004 Jul 21.

Abstract

Methylmalonate-semialdehyde dehydrogenase from Bacillus subtilis was cloned and overexpressed in Escherichia coli. Suitable crystals for X-ray diffraction experiments were obtained by the hanging-drop vapour-diffusion method using ammonium sulfate as precipitant. The crystals belong to space group P2(1)2(1)2(1), with unit-cell parameters a = 195.2, b = 192.5, c = 83.5 A, and contain one tetramer per asymmetric unit. X-ray diffraction data were collected to 2.5 A resolution using a synchrotron-radiation source. The crystal structure was solved by the molecular-replacement method.

MeSH terms

  • Aldehyde Oxidoreductases / biosynthesis
  • Aldehyde Oxidoreductases / chemistry*
  • Aldehyde Oxidoreductases / genetics
  • Aldehyde Oxidoreductases / isolation & purification*
  • Bacillus subtilis / enzymology*
  • Bacillus subtilis / genetics
  • Crystallization
  • Crystallography, X-Ray
  • Gene Expression
  • Methylmalonate-Semialdehyde Dehydrogenase (Acylating)

Substances

  • Aldehyde Oxidoreductases
  • Methylmalonate-Semialdehyde Dehydrogenase (Acylating)