Crystallization and preliminary X-ray diffraction studies of methyl-coenzyme M reductase from methanobacterium thermoautotrophicum

J Biochem. 1997 May;121(5):829-30. doi: 10.1093/oxfordjournals.jbchem.a021660.

Abstract

Methyl-coenzyme M reductase isoenzyme I from the methanogenic Archaeon, Methanobacterium thermoautotrophicum (strain Marburg), was crystallized by vapor diffusion methods. Crystal form M obtained with 2-methyl-2,4-pentanediol as the precipitant displayed space group P2(1), with unit cell parameters of a=83.2 A, b=117.4 A, c=125.1 A, and beta= 92.6 degrees, and diffracted at better than 2.8 A resolution. Crystal form P grown from polyethylene glycol 400 belonged to space group P2(1), and had unit cell parameters of a=83.1 A, b=120.2 A, c=123.1 A, and beta=91.7 degrees, diffracting at least to 1.7 A resolution. Both crystal forms have one molecule per asymmetric unit and are suitable for X-ray structure analysis.

MeSH terms

  • Crystallization
  • Crystallography, X-Ray
  • Methanobacterium / enzymology*
  • Molecular Structure
  • Oxidoreductases / chemistry*

Substances

  • Oxidoreductases
  • methyl coenzyme M reductase