Diversity of wheat anti-microbial peptides

Peptides. 2005 Nov;26(11):2064-73. doi: 10.1016/j.peptides.2005.03.007. Epub 2005 Apr 19.

Abstract

From seeds of Triticum kiharae Dorof. et Migusch., 24 novel anti-microbial peptides were isolated and characterized by a combination of three-step HPLC (affinity, size-exclusion and reversed-phase) with matrix-assisted laser-desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry and Edman degradation. Based on sequence similarity and cysteine motifs, partially sequenced peptides were assigned to 7 families: defensins, thionins, lipid-transfer proteins, hevein-like peptides, knottin-like peptides, glycine-rich peptides, and MBP-1 homologs. A novel subfamily of defensins consisting of 6 peptides and a new family of glycine-rich (8 peptides with different repeat motifs) were identified. Three 6-cysteine knottin-like peptides represented by N- and C-terminally truncated variants revealed no sequence homology to any known plant anti-microbial peptides. A new 8-cysteine hevein-like peptide and three 4-cysteine peptides homologous to MBP-1 from maize were isolated. This is the first communication on the occurrence of nearly all families of plant anti-microbial peptides in a single species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Infective Agents / chemistry*
  • Anti-Infective Agents / classification
  • Anti-Infective Agents / isolation & purification
  • Chromatography, High Pressure Liquid
  • Peptides / chemistry*
  • Peptides / classification
  • Peptides / isolation & purification
  • Plant Proteins / chemistry*
  • Plant Proteins / isolation & purification
  • Plant Proteins / pharmacology
  • Seeds / chemistry*
  • Sequence Analysis, Protein
  • Sequence Homology, Amino Acid
  • Triticum / chemistry*

Substances

  • Anti-Infective Agents
  • Peptides
  • Plant Proteins