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Potential inhibitors of the ascorbate-induced β-glucan degradation

机译:抗坏血酸诱导的β-葡聚糖降解的潜在抑制剂

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The effects of several radical scavengers and oxidation inhibitors on ascorbate-induced hydroxyl radicals, responsible for β-glucan oxidation, were studied by ESR spin trapping. The most effective compounds in decreasing the radical formation in β-glucan solutions were phytic acid, sulphite and enzymes (catalase and superoxide dismutase). Also phenolic compounds, sugars and organic acids demonstrated a high rad-ical-scavenging capacity, but they showed more variation within the group. The compounds showing a very high antioxidant capacity in 100 min monitoring were chosen for the viscosity measurements. Though able to reduce radical formation, phytic acid, potassium bisulphite and citric acid were inefficient in inhibiting viscosity loss. Sucrose, phenylalanine and hydroxybenzoic acid were able to significantly slow the viscosity decrease in a longer time frame. Catalase completely inhibited viscosity loss and thereby p-glucan degradation. These results show that the oxidative cleavage of β-glucan can be inhibited by radical scavengers and other oxidation inhibitors; however the effects are very much dependent on the compound, concentration and time of oxidation.
机译:通过ESR自旋捕集研究了几种自由基清除剂和氧化抑制剂对导致β-葡聚糖氧化的抗坏血酸诱导的羟基自由基的影响。减少β-葡聚糖溶液中自由基形成的最有效化合物是植酸,亚硫酸盐和酶(过氧化氢酶和超氧化物歧化酶)。酚类化合物,糖和有机酸也显示出较高的自由基清除能力,但它们在组内的变化更大。选择在100分钟监测中显示出极高抗氧化能力的化合物进行粘度测量。植酸,亚硫酸氢钾和柠檬酸虽然能够减少自由基的形成,但在抑制粘度损失方面效率低下。蔗糖,苯丙氨酸和羟基苯甲酸能够在更长的时间内显着减慢粘度的降低。过氧化氢酶完全抑制了粘度损失,从而抑制了对葡聚糖的降解。这些结果表明,β-葡聚糖的氧化裂解可被自由基清除剂和其他氧化抑制剂抑制。但是,效果很大程度上取决于化合物,浓度和氧化时间。

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