首页> 外文期刊>Journal of Food Measurement and Characterization >Kunitz trypsin inhibitor in soybean: contribution to total trypsin inhibitor activity as a function of genotype and fate during processing
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Kunitz trypsin inhibitor in soybean: contribution to total trypsin inhibitor activity as a function of genotype and fate during processing

机译:大豆中Kunitz胰蛋白酶抑制剂:作为在加工过程中作为基因型和命运的函数的胰蛋白酶抑制剂活性的贡献

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摘要

Detrimental effects of trypsin inhibitor activity (TIA) in soybean on human health have been attributed to Kunitz trypsin inhibitor (KTI) polypeptide. Literature is replete with reports pertaining to TIA in soybean seeds, however, the studies on the contribution of KTI polypeptide to total TIA have not been carried out. Further, very limited information is available on the quantitative changes occurring in this polypeptide due to different processing methods. In the present investigation, KTI polypeptide in soybean seeds was resolved by native polyacrylamide gel electrophoresis (PAGE) and substantiated by western blotting. Densitometry was employed to quantify KTI polypeptide in 102 soybean genotypes and assess the inactivation of this polypeptide due to boiling, autoclaving, microwave irradiation and sprouting. KTI concentration exhibited wide genetic variation, ranging from 0.07 to 15.9 mg/g soy flour, which corresponded to 1.0–79.8% of total TIA. Boiling and autoclaving for 15 min both resultedin complete inactivation of KTI. Microwave irradiation induced significantly higher reduction for KTI in soaked than dry seeds. Sprouting for 4 days caused 71.4% inactivation of KTI. The study showed that KTI contribution to total TIA was genotype-dependent and the inactivation of this polypeptide was a function of processing methods.
机译:胰蛋白酶抑制剂活性(TIA)在大豆对人体健康中的不利影响归因于Kunitz胰蛋白酶抑制剂(KTI)多肽。文献与大豆种子有关TIA的报道,然而,对KTI多肽对总TIA的贡献的研究尚未进行。此外,由于不同的处理方法,在该多肽中发生的定量变化非常有限。在本研究中,通过天然聚丙烯酰胺凝胶电泳(PAGE)分解大豆种子中的KTI多肽,并通过Western印迹证实。使用密度测定法在102只大豆基因型中量化KTI多肽,并评估由于沸腾,高压灭菌,微波辐射和发芽而导致这种多肽的灭活。 KTI浓度表现出广泛的遗传变异,范围为0.07至15.9mg / g大豆面粉,其占总TIA的1.0-79.8%。煮沸和高压灭菌15分钟,均为KTI的完全失活。微波辐射诱导浸湿的KTI比干燥种子显着更高。萌芽4天导致KTI的71.4%失活。该研究表明,KTI对总TIA的贡献是基因型依赖性,并且该多肽的失活是加工方法的函数。

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