Expression of α-amylase inhibitors in diploid Triticum species

Food Chem. 2012 Dec 15;135(4):2643-9. doi: 10.1016/j.foodchem.2012.06.123. Epub 2012 Jul 14.

Abstract

The aim of the work was to characterize the expression of various α-amylase inhibitors (αAIs), well known anti-nutritional compounds, for the development of healthier diploid wheat-based functional foods. The salt-soluble protein fractions from the seeds of 53 accessions among Triticum monococcum subsp. monococcum (T.m.), T. monococcum subsp. boeoticum (T.b.) and Triticum urartu (T.u.) were analyzed by immunoblotting after SDS-PAGE and Urea-PAGE using polyclonal antibodies (PABs) raised against 0.19 and 0.28 αAIs expressed in bread-wheat. Reverse zymography with human saliva and Tenebrio molitor α-amylases was used to assay inhibition activity. A great variability of the expression of αAI-related proteins was observed among T.b. and T.u. PABs, and reverse zymography revealed different bands, often not correlating with those present in bread-wheat. Two-dimensional electrophoresis followed by immunoblotting and mass spectrometric analysis identified these proteins as αAIs. Interestingly, no signal was observed within T.m. accessions. This makes T.m. an important candidate for the production of novel functional foods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diploidy
  • Electrophoresis, Polyacrylamide Gel
  • Gene Expression
  • Humans
  • Plant Proteins / chemistry*
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism
  • Seeds / chemistry
  • Seeds / genetics
  • Seeds / metabolism
  • Triticum / chemistry
  • Triticum / classification
  • Triticum / genetics
  • Triticum / metabolism*
  • alpha-Amylases / antagonists & inhibitors*

Substances

  • Plant Proteins
  • alpha-Amylases