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首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >Quantitative measurement of protein digestion in simulated gastric fluid.
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Quantitative measurement of protein digestion in simulated gastric fluid.

机译:定量测量模拟胃液中蛋白质消化率。

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The digestibility of novel proteins in simulated gastric fluid is considered to be an indicator of reduced risk of allergenic potential in food, and estimates of digestibility for transgenic proteins expressed in crops are required for making a human-health risk assessment by regulatory authorities. The estimation of first-order rate constants for digestion under conditions of low substrate concentration was explored for two protein substrates (azocoll and DQ-ovalbumin). Data conformed to first-order kinetics, and half-lives were relatively insensitive to significant variations in both substrate and pepsin concentration when high purity pepsin preparations were used. Estimation of digestion efficiency using densitometric measurements of relative protein concentration based on SDS-PAGE corroborated digestion estimates based on measurements of dye or fluorescence release from the labeled substrates. The suitability of first-order rate constants for estimating the efficiency of the pepsin digestion of novel proteins is discussed. Results further support a kinetic approach as appropriate for comparing the digestibility of proteins in simulated gastric fluid.
机译:新型蛋白质在模拟胃液中的消化率被认为是降低食物中潜在致敏性风险的指标,对于监管机构进行人类健康风险评估,需要估计作物中表达的转基因蛋白的消化率。探索了在低底物浓度条件下消化的一级速率常数的估算值,用于两种蛋白质底物(偶氮唑和DQ-卵清蛋白)。数据符合一级动力学,当使用高纯度胃蛋白酶制剂时,半衰期对底物和胃蛋白酶浓度的显着变化相对不敏感。使用基于SDS-PAGE的相对蛋白质浓度的光密度测量法对消化效率进行估算,从而根据基于从标记底物上释放的染料或荧光的测量结果来确定消化率。讨论了一级速率常数对估计新蛋白的胃蛋白酶消化效率的适用性。结果进一步支持了适用于比较模拟胃液中蛋白质消化率的动力学方法。

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