Kinetic properties of triose-phosphate isomerase from Trypanosoma brucei brucei. A comparison with the rabbit muscle and yeast enzymes

Eur J Biochem. 1987 Oct 1;168(1):69-74. doi: 10.1111/j.1432-1033.1987.tb13388.x.

Abstract

The kinetic properties of Trypanosoma brucei brucei triose-phosphate isomerase are compared with those of the commercially available rabbit muscle and yeast enzymes and with published data on the chicken muscle enzyme. With glyceraldehyde 3-phosphate as substrate Km = 0.25 +/- 0.05 mM and kcat = 3.7 X 10(5) min-1. With dihydroxyacetone phosphate as substrate Km = 1.2 +/- 0.1 mM and kcat = 6.5 X 10(4) min-1. The pH dependence of Km and Vmax at 0.1 M ionic strength is in agreement with the results published for the yeast and chicken muscle enzymes. At ionic strength below 0.05 M the effect of a charged group specific for the trypanosomal enzyme and absent from the yeast and rabbit muscle enzymes becomes detectable. This effect significantly increases Km whereas Vmax becomes slightly higher. Trypanosomal triose-phosphate isomerase is inhibited by sulphate, phosphate and arsenate ions, by 2-phosphoglycolate and a number of documented inhibitors in the same concentration range as are the other triose-phosphate isomerases. The trypanocidal drug, Suramin inhibits T. brucei and rabbit muscle triose-phosphate isomerase to the same extent while leaving the yeast enzyme relatively unaffected.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Carbohydrate Epimerases / metabolism*
  • Chickens
  • Hydrogen-Ion Concentration
  • Kinetics
  • Mathematics
  • Muscles / enzymology*
  • Rabbits
  • Saccharomyces cerevisiae / enzymology*
  • Suramin / pharmacology
  • Triose-Phosphate Isomerase / antagonists & inhibitors
  • Triose-Phosphate Isomerase / metabolism*
  • Trypanosoma brucei brucei / enzymology*

Substances

  • Suramin
  • Carbohydrate Epimerases
  • Triose-Phosphate Isomerase