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吡嗪形成的结构多样性和浓度依赖性:l-丙氨酰-l-谷氨酰胺美拉德化合物热加工过程中外源氨基酸底物和反应参数。

Structural diversity and concentration dependence of pyrazine formation: Exogenous amino substrates and reaction parameters during thermal processing of l-alanyl-l-glutamine Amadori compound.

机构信息

State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province, Jiangnan University, 1800 Lihu Avenue, Wuxi 214122, Jiangsu, PR China.

Department of Kinesiology, Nutrition, and Health, Miami University, Oxford, OH 45056, USA.

出版信息

Food Chem. 2022 Oct 1;390:133144. doi: 10.1016/j.foodchem.2022.133144. Epub 2022 May 6.

Abstract

The Amadori compound of glucose and l-alanyl-l-glutamine (Ala-Gln-ARP) was prepared and characterized by UPLC-MS/MS and NMR. There were no pyrazines produced by heated Ala-Gln-ARP alone due to the asynchronicity of regenerated l-alanyl-l-glutamine and α-dicarbonyl compounds. High temperature (130 °C) and long reaction time could facilitate the 2,5-dimethylpyrazine formation at a small concentration (33.4 ± 3.47 μg/L). The exogenous amino substrates would lower the formation temperature of pyrazines and make it to be generated effectively. Extra supplied l-alanyl-l-glutamine could generate 2,5-dimethylpyrazine at 110 °C, while higher temperature of 140 °C could strengthen the formation of 2,5-dimethylpyrazine (793 ± 119 μg/L) and stimulate the generation of other pyrazines, including methylpyrazine and 2,6-dimethylpyrazine. The exogenous alanine, glutamic acid, and glutamine was also beneficial to enhance the pyrazines formation, especially the glutamic acid. Furthermore, alkaline pH of thermal reaction made pyrazines increase significantly than in neutral medium and further enriched their species such as unsubstituted pyrazine and trimethylpyrazine.

摘要

葡萄糖和 l-丙氨酰-l-谷氨酰胺(Ala-Gln-ARP)的 Amadori 化合物通过 UPLC-MS/MS 和 NMR 进行了制备和表征。由于再生的 l-丙氨酰-l-谷氨酰胺和α-二羰基化合物的异步性,单独加热 Ala-Gln-ARP 不会产生吡嗪。高温(130°C)和长反应时间可以在较小浓度(33.4±3.47μg/L)下促进 2,5-二甲基吡嗪的形成。外源性氨基酸底物会降低吡嗪的形成温度,并使其有效地生成。额外提供的 l-丙氨酰-l-谷氨酰胺可以在 110°C 下生成 2,5-二甲基吡嗪,而 140°C 的更高温度可以加强 2,5-二甲基吡嗪的形成(793±119μg/L)并刺激其他吡嗪的生成,包括甲基吡嗪和 2,6-二甲基吡嗪。外源性的丙氨酸、谷氨酸和谷氨酰胺也有利于增强吡嗪的形成,特别是谷氨酸。此外,热反应的碱性 pH 值使吡嗪显著增加,比在中性介质中增加更多,并且进一步丰富了它们的种类,如未取代的吡嗪和三甲基吡嗪。

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