Abstract

In this investigation, we reported the production of prototype breads from the processed flours of three specific Triticum turgidum wheat genotypes that were selected in our previous investigation for their potential low toxic/immunogenic activity for celiac disease (CD) patients. The flours were subjected to sourdough fermentation with a mixture of selected Lactobacillus strains, and in presence of fungal endoproteases. The breads were characterized by R5 competitive enzyme linked immunosorbent assay in order to quantify the residual gluten, and the differential efficacy in gluten degradation was assessed. In particular, two of them were classified as gluten-free (<20 ppm) and very low-gluten content (<100 ppm) breads, respectively, whereas the third monovarietal prototype retained a gluten content that was well above the safety threshold prescribed for direct consumption by CD patients. In order to investigate such a genotype-dependent efficiency of the detoxification method applied, an advanced proteomic characterization by high-resolution tandem mass spectrometry was performed. Notably, to the best of our knowledge, this is the first proteomic investigation which benefitted, for protein identification, from the full sequencing of the Triticum turgidum ssp. durum genome. The differences of the proteins’ primary structures affecting their susceptibility to hydrolysis were investigated. As a confirmation of the previous immunoassay-based results, two out of the three breads made with the processed flours presented an exhaustive degradation of the epitopic sequences that are relevant for CD immune stimulatory activity. The list of the detected epitopes was analyzed and critically discussed in light of their susceptibility to the detoxification strategy applied. Finally, in-vitro experiments of human gastroduodenal digestion were carried out in order to assess, in-silico, the toxicity risk of the prototype breads under investigation for direct consumption by CD patients. This approach allowed us to confirm the total degradation of the epitopic sequences upon gastro-duodenal digestion.

Highlights

  • The wheat varietal selection undertaken by breeders in the last decades was tailored mainly to improve its technological and productivity-related traits; the latter resulted in a considerable impoverishment of the genetic diversity of wheat-based products available on the market

  • It was assessed that there is a great variability in the immunogenic level of wheat genotypes and, none of them can be considered safe for direct consumption by celiac disease (CD) patients, there is an undeniable potential to select lines with lower toxicity for newly-tailored breeding programs [9,10,11]

  • We reported the production of prototype GF breads from processed flours of specific Triticum turgidum wheat genotypes, which were subjected to sourdough fermentation with a mixture of selected Lactobacillus strains and fungal endoproteases

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Summary

Introduction

The wheat varietal selection undertaken by breeders in the last decades was tailored mainly to improve its technological and productivity-related traits; the latter resulted in a considerable impoverishment of the genetic diversity of wheat-based products available on the market. It was assessed that there is a great variability in the immunogenic level of wheat genotypes and, none of them can be considered safe for direct consumption by CD patients, there is an undeniable potential to select lines with lower toxicity for newly-tailored breeding programs [9,10,11]. Such variability was investigated in old, landraces, and modern genotypes, reporting no correlation with the year of release, meaning that the past breeding programs did not cause an increase for immunostimulatory epitopes, as was originally speculated [1]. The genetic improvement of wheat by breeders was mostly focused on the glutenin fraction, which is the main factor that is responsible for the dough’s strength and baking characteristics [12,13]

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