Identification and molecular characterization of novel peroxidase with structural protein-like properties

J Biol Chem. 1999 Sep 10;274(37):26192-8. doi: 10.1074/jbc.274.37.26192.

Abstract

Elicitor treatment or mechanical damage to Scutellaria baicalensis Georgi (skullcap plants) callus causes an immediate insolubilization of a 36-kDa protein into cell walls. The 36-kDa protein was identified as peroxidase 1 by analysis of its internal amino acid sequence and by immunoblotting using affinity-purified anti-peroxidase 1. Insolubilized peroxidase 1 is cross-linked to lignin through covalent bonds, and the cross-linking is catalyzed in the presence of H(2)O(2) by peroxidase 1 itself. The properties of insolubilized peroxidase 1 resemble those of defense-related structural proteins (extensins and proline-rich proteins) cross-linked to cell wall. Although the isozymes peroxidases 2 and 3 have enzyme activities similar to peroxidase 1, they are not insolubilized by stress treatment. Molecular characterization established that peroxidase 1 contains regions characteristic of structural proteins, but peroxidases 2 and 3 do not have such regions. These results suggest that among the three isozymes, only peroxidase 1 has a structural protein-like function as well as an enzymatic function.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cell Wall / enzymology
  • Cloning, Molecular
  • DNA, Complementary
  • Kinetics
  • Molecular Sequence Data
  • Peroxidase / chemistry
  • Peroxidase / genetics
  • Peroxidase / metabolism*
  • Plants / enzymology
  • Sequence Homology, Amino Acid
  • Solubility

Substances

  • DNA, Complementary
  • Peroxidase

Associated data

  • GENBANK/AB024437
  • GENBANK/AB024438
  • GENBANK/AB024439