Purification and characterization of a thermostable class II fumarase from Thermus thermophilus

Arch Biochem Biophys. 1998 Jul 1;355(1):49-55. doi: 10.1006/abbi.1998.0693.

Abstract

A thermostable fumarase was purified from a strain of Thermus thermophilus isolated from a Japanese hot spring. The maximum specific activity of the purified enzyme was 1740 units/mg at pH 8.0 and 85 degreesC. The enzyme was composed of four identical subunits with a molecular weight of 46,000 and displayed other enzymatic characteristics which are common to the class II fumarases. The thermal stability of the purified enzyme was remarkable, with over 80% of the activity remaining after a 24-h incubation at 90 degreesC. The enzyme was also resistant to chemical denaturants; 50% of the initial specific activity was detected in assay mixtures containing 0.8 M guanidine hydrochloride. The purified enzyme shared an extremely high sequence homology with Thermus aquaticus fumarase and Bacillus subtilis fumarase in the first 43 amino acid residues.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Enzyme Stability
  • Fumarate Hydratase / classification*
  • Fumarate Hydratase / genetics
  • Fumarate Hydratase / isolation & purification*
  • Hot Temperature
  • Humans
  • Hydrogen-Ion Concentration
  • Kinetics
  • Molecular Sequence Data
  • Molecular Weight
  • Protein Conformation
  • Sequence Homology, Amino Acid
  • Thermus thermophilus / enzymology*
  • Thermus thermophilus / genetics

Substances

  • Fumarate Hydratase