Università di Verona, Dipartimento di Biotecnologie, Verona, Italy.
Food Chem. 2012 Dec 15;135(4):2643-9. doi: 10.1016/j.foodchem.2012.06.123. Epub 2012 Jul 14.
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.
本研究旨在对不同来源的α-淀粉酶抑制剂(αAIs)的表达进行分析,以开发更健康的基于二倍体小麦的功能性食品。采用 SDS-PAGE 和 Urea-PAGE 电泳后,利用针对面包小麦中表达的 0.19 和 0.28 αAIs 制备的多克隆抗体(PABs),对来自 53 个 Triticum monococcum subsp. monococcum(T.m.)、T. monococcum subsp. boeoticum(T.b.)和 Triticum urartu(T.u.)品种种子的盐溶性蛋白进行了免疫印迹分析。利用人唾液和黄粉虫α-淀粉酶进行反向酶谱分析,检测抑制活性。结果表明,T.b.和 T.u. PABs 中αAI 相关蛋白的表达存在很大差异,反向酶谱显示出不同的条带,这些条带通常与面包小麦中的条带不相关。通过二维电泳结合免疫印迹和质谱分析,鉴定出这些蛋白为αAIs。有趣的是,在 T.m. 品种中未观察到信号。这使得 T.m.成为生产新型功能性食品的重要候选品种。