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Increasing Soy Isoflavonoid Content and Diversity by Simultaneous Malting and Challenging by a Fungus to Modulate Estrogenicity

机译:通过同时发芽和挑战真菌调节雌激素来提高大豆异黄酮含量和多样性

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Soybeans were germinated on a kilogram-scale, by the application of malting technology used in the brewing industry, and concomitantly challenged with Rhizopus microsporus var. oryzae. In a time-course experiment, samples were taken every 24 h for 10 days, and the isoflavonoid profile was analyzed by RP-UHPLC-MS. Upon induction with R. microsporus, the isoflavonoid composition changed drastically with the formation of phytoalexins belonging to the subclasses of the pterocarpans and coumestans and by prenylation of the various isoflavonoids. The pterocarpan content stabilized at 2.24 mg of daidzein equivalents (DE) per g after ~9 days. The levels of the less common glyceofuran, glyceollin IV, and V/VI ranged from 0.18 to 0.35 mg DE/g and were comparable to those of the more commonly reported glyceollins I, II, and III (0.22—0.32 mg DE/g) and glycinol (0.42 mg DE/g). The content of prenylated isoflavones after the induction process was 0.30 mg DE/g. The total isoflavonoid content increased by a factor of 10—12 on DW basis after 9 days, which was suggested to be ascribable to de novo synthesis. These changes were accompanied by a gradual increase in agonistic activity of the extracts toward both the estrogen receptor a (ERa) and ERβ during the 10-day induction, with a more pronounced activity toward ERβ. Thus, the induction process yielded a completely different spectrum of isoflavonoids, with a much higher bioactivity toward the estrogen receptors. This, together with the over 10-fold increase in potential bioactives, offers promising perspectives for producing more, novel, and higher potency nutraceuticals by malting under stressed conditions.
机译:大豆通过酿造业中使用的麦芽技术发芽,千克规模发芽,并同时受到小根霉变种的挑战。水稻在时程实验中,每24小时取样10天,然后通过RP-UHPLC-MS分析异黄酮类。在用小孢子虫诱导后,异黄酮的组成发生了急剧变化,形成了翼龙类和香豆素亚类的植物抗毒素,并通过异戊二烯的异戊烯基化。约9天后,罗汉果皮含量稳定在每克2.24 mg大豆苷元当量(DE)。较少见的糖呋喃,甘油四酸酯和V / VI的含量范围为0.18至0.35 mg DE / g,可与较常见的糖蛋白I,II和III(0.22-0.32 mg DE / g)相媲美。和甘醇(0.42 mg DE / g)。诱导过程后异戊烯基异黄酮的含量为0.30 mg DE / g。 9天后,总异黄酮含量以DW为基础增加了10-12倍,这被认为是从头合成的缘故。这些变化伴随着在10天诱导过程中提取物对雌激素受体a(ERa)和ERβ的激动活性逐渐增加,对ERβ的活性更加明显。因此,诱导过程产生了完全不同的异黄酮谱,对雌激素受体具有更高的生物活性。这与潜在生物活性物质的10倍以上的增长相结合,为通过在压力条件下进行麦芽生产更多,新颖和更高效力的保健食品提供了广阔的前景。

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