di Cagno Raffaella, de Angelis Maria, Alfonsi Giuditta, de Vincenzi Massimo, Silano Marco, Vincentini Olimpia, Gobbetti Marco
Department of Plant Protection and Applied Microbiology, University of Bari, 70126 Bari, Italy.
J Agric Food Chem. 2005 Jun 1;53(11):4393-402. doi: 10.1021/jf048341+.
A pool of selected lactic acid bacteria was used to ferment durum wheat semolina under liquid conditions. After fermentation, the dough was freeze-dried, mixed with buckwheat flour at a ratio of 3:7, and used to produce the "fusilli" type Italian pasta. Pasta without prefermentation was used as the control. Ingredients and pastas were characterized for compositional analysis. As shown by two-dimensional electrophoresis, 92 of the 130 durum wheat gliadin spots were hydrolyzed almost totally during fermentation by lactic acid bacteria. Mass spectrometry matrix-assisted laser desorption/ionization time-of-flight and reversed phase high-performance liquid chromatography analyses confirmed the hydrolysis of gliadins. As shown by immunological analysis by R5-Western blot, the concentration of gluten decreased from 6280 ppm in the control pasta to 1045 ppm in the pasta fermented with lactic acid bacteria. Gliadins were extracted from fermented and nonfermented durum wheat dough semolina and used to produce a peptic-tryptic (PT) digest for in vitro agglutination tests on cells of human origin. The whole PT digests did not cause agglutination. Affinity chromatography on Sepharose-6-B mannan column separated the PT digests in three fractions. Fraction C showed agglutination activity. The minimal agglutinating activity of fraction C from the PT digest of fermented durum wheat semolina was ca. 80 times higher than that of durum wheat semolina. Pasta was subjected to sensory analysis: The scores for stickiness and firmness were slightly lower than those found for the pasta control. Odor and flavor did not differ between the two types of pasta. These results showed that a pasta biotechnology that uses a prefermentation of durum wheat semolina by selected lactic acid bacteria and tolerated buckwheat flour could be considered as a novel tool to potentially decrease gluten intolerance and the risk of gluten contamination in gluten-free products.
使用一组精选的乳酸菌在液体条件下发酵硬质小麦粗粒粉。发酵后,将面团冷冻干燥,与荞麦粉按3:7的比例混合,并用于生产“螺旋面”类型的意大利面。未经预发酵的意大利面用作对照。对原料和意大利面进行成分分析表征。二维电泳结果显示,130个硬质小麦醇溶蛋白斑点中有92个在乳酸菌发酵过程中几乎完全被水解。基质辅助激光解吸/电离飞行时间质谱和反相高效液相色谱分析证实了醇溶蛋白的水解。R5-蛋白质免疫印迹免疫分析表明,面筋浓度从对照意大利面中的6280 ppm降至乳酸菌发酵意大利面中的1045 ppm。从发酵和未发酵的硬质小麦面团粗粒粉中提取醇溶蛋白,并用于制备胃蛋白酶-胰蛋白酶(PT)消化物,用于对人源细胞进行体外凝集试验。整个PT消化物未引起凝集。在琼脂糖-6-B甘露聚糖柱上进行亲和层析,将PT消化物分离为三个组分。组分C显示出凝集活性。发酵硬质小麦粗粒粉的PT消化物中组分C的最小凝集活性约为硬质小麦粗粒粉的80倍。对意大利面进行感官分析:粘性和硬度得分略低于对照意大利面。两种意大利面的气味和风味没有差异。这些结果表明,一种利用精选乳酸菌对硬质小麦粗粒粉进行预发酵并添加可耐受的荞麦粉的意大利面生物技术,可被视为一种潜在的新工具,用于降低麸质不耐受性以及无麸质产品中麸质污染的风险。