Vanadium haloperoxidases from brown algae of the Laminariaceae family

Phytochemistry. 2001 Jul;57(5):633-42. doi: 10.1016/s0031-9422(01)00094-2.


Vanadium haloperoxidases were extracted, purified and characterized from three different species of Laminariaceae--Laminaria saccharina (Linné) Lamouroux, Laminaria hyperborea (Gunner) Foslie and Laminaria ochroleuca de la Pylaie. Two different forms of the vanadium haloperoxidases were purified from L. saccharina and L. hyperborea and one form from L. ochroleuca species. Reconstitution experiments in the presence of several metal ions showed that only vanadium(V) completely restored the enzymes activity. The stability of some enzymes in mixtures of buffer solution and several organic solvents such as acetone, ethanol, methanol and 1-propanol was noteworthy; for instance, after 30 days at least 40% of the initial activity for some isoforms remained in mixtures of 3:1 buffer solution/organic solvent. The enzymes were also moderately thermostable, keeping full activity up to 40 degrees C. Some preliminary steady-state kinetic studies were performed and apparent Michaelis-Menten kinetic parameters were determined for the substrates iodide and hydrogen peroxide. Histochemical studies were also performed in fresh tissue sections from stipe and blade of L. hyperborea and L. saccharina, showing that haloperoxidase activity was concentrated in the external cortex near the cuticle, although some activity was also observed in the inner cortical region.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, Ion Exchange
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Stability
  • Iodide Peroxidase / chemistry
  • Iodide Peroxidase / isolation & purification*
  • Iodide Peroxidase / metabolism
  • Kinetics
  • Molecular Weight
  • Peroxidases / chemistry
  • Peroxidases / isolation & purification*
  • Peroxidases / metabolism
  • Phaeophyta / enzymology*
  • Solvents


  • Solvents
  • Peroxidases
  • bromide peroxidase
  • vanadium iodoperoxidase
  • Iodide Peroxidase