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首页> 外文期刊>Food Chemistry >Effects of o-phenylenediamine on methylglyoxal generation from monosaccharide: Comment on 'correlation of methylglyoxal with acrylamide formation in fructose/asparagine Maillard reaction model system'
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Effects of o-phenylenediamine on methylglyoxal generation from monosaccharide: Comment on 'correlation of methylglyoxal with acrylamide formation in fructose/asparagine Maillard reaction model system'

机译:邻苯二胺对单糖生成甲基乙二醛的影响:评述“果糖/天冬酰胺美拉德反应模型系统中甲基乙二醛与丙烯酰胺形成的相关性”

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Methylglyoxal (MG), a reactive carbonyl compound, has recently garnered much attention because of its ability to modify proteins over time and yield advanced glycation end products (AGEs) that are thought to contribute to the development of diabetes mellitus and its complications. In a recent paper published in Food Chemistry by Yuan et al. [Yuan, Y., Zhao, G. H., Hu, X. S., Wu, J. H., Liu, J., & Chen, F. (2007a). Correlation of methylglyoxal with acrylamide formation in fructose/asparagines Maillard reaction model system. Food Chemistry, 108(3), 885-890] authors showed a high correlation between methylglyoxal formation and acrylamide formation. However, in their study, model systems of aqueous fructose/asparagines (Fru/Asn) and fructose/asparagines/o-phenylenediamine (Fru/Asn/OPD) heating at 150 ℃ were used. The validity of these models relies on the assumption that OPD will only serve the role of a trapping agent for MG. In this short communication, we would like to call to attention that MG can also have a strong catalytic effect in the generation of MG from fructose. Therefore, it is concluded that the concentration of MG obtained in Fru/Asn/OPD model system cannot correspond to the total amount of MG formed by Maillard reaction of Fru and Asn as claimed by Yuan et al. [Yuan, Y., Zhao, G. H., Hu, X. S., Wu, J. H., Liu, J., & Chen, F. (2007a). Correlation of methylglyoxal with acrylamide formation in fructose/asparagines Maillard reaction model system. Food Chemistry, 108(3), 885-890, Yuan, Y., Zhao, G. H., Hu X. S., Wu, J. H., Liu, J., & Chen. F. (2007b). High correlation of methylglyoxal with acrylamide formation in glucose/asparagine Maillardreaction model. European Food Research and Technology. doi:10.1007/s00217-007-0658-0].
机译:甲基乙二醛(MG)是一种反应性羰基化合物,由于其随着时间的推移修饰蛋白质并产生先进的糖基化终产物(AGEs)的能力而受到了广泛的关注,据认为,糖化终产物(AGEs)有助于糖尿病的发展及其并发症。 Yuan等人在《食品化学》上发表的最新论文中。 [Yuan Y.,Zhao G. H.,Hu,X。S.,Wu,J。H.,Liu,J。,&Chen,F.(2007a)。果糖/天冬酰胺美拉德反应模型系统中甲基乙二醛与丙烯酰胺形成的相关性。 Food Chemistry,108(3),885-890]的作者显示甲基乙二醛形成与丙烯酰胺形成之间高度相关。然而,在他们的研究中,使用了在150℃下加热的果糖/天冬酰胺水溶液(Fru / Asn)和果糖/天冬酰胺/邻苯二胺(Fru / Asn / OPD)的模型系统。这些模型的有效性依赖于这样的假设,即OPD将仅充当MG的诱捕剂。在此简短的交流中,我们要提请注意MG在由果糖生成MG方面也具有强大的催化作用。因此,可以得出结论,在Fru / Asn / OPD模型系统中获得的MG浓度不能与Yuan等人提出的Fru和Asn的美拉德反应形成的MG总量相对应。 [Yuan Y.,Zhao G. H.,Hu,X。S.,Wu,J。H.,Liu,J。,&Chen,F.(2007a)。果糖/天冬酰胺美拉德反应模型系统中甲基乙二醛与丙烯酰胺形成的相关性。食品化学,108(3),885-890,袁Y,赵国华,胡新书,吴建华,刘建民,陈。 F.(2007b)。在葡萄糖/天冬酰胺美拉德反应模型中甲基乙二醛与丙烯酰胺形成高度相关。欧洲食品研究与技术。 doi:10.1007 / s00217-007-0658-0]。

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