首页> 外文期刊>Journal of Agricultural and Food Chemistry >Novel Maillard Pigment, Furpenthiazinate, Having Furan and Cyclopentathiazine Rings Formed by Acid Hydrolysis of Protein in the Presence of Xylose or by Reaction between Cysteine and Furfural under Strongly Acidic Conditions
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Novel Maillard Pigment, Furpenthiazinate, Having Furan and Cyclopentathiazine Rings Formed by Acid Hydrolysis of Protein in the Presence of Xylose or by Reaction between Cysteine and Furfural under Strongly Acidic Conditions

机译:小说美丽的颜料,Furpenthiazinate,具有在木糖存在下通过酸性水解的呋喃和环戊羟肟环,或通过在强酸性条件下通过半胱氨酸和糠醛的反应形成

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摘要

A novel Maillard pigment having partial structures of furan and cyclopentathiazine, named furpenthiazinate, was isolated and identified. Although this pigment was found in an acid hydrolysate of a Maillard reaction solution between soy protein and xylose, the same pigment was also formed by the Maillard reaction under strongly acidic conditions between soy protein and xylose and cysteine and furfural. The structure of its reduced form by NaBH4 was determined by MS, NMR, and X-ray analysis and identified as 7-(2-furany1)-2,3,4,4a,5,6-hexahydrocyclopenta[b][1,4]thiazin-4-ium-3-carboxylate, indicating that the chemical structure of furpenthiazinate is 7-(2-furanyl)-2,3,5,6-tetrahydrocyclopenta[b][1,4]thiazine-3-carboxylic acid. Furpenthiazinate showed an absorption maximum at 400 nm and strong yellow color under acidic and neutral conditions. The color contribution of furpenthiazinate was estimated to be more than 60% in a reaction solution prepared from cysteine and furfural.
机译:分离并鉴定出具有呋喃和环戊硫嗪的部分结构的新型美丽色素,并鉴定出来。 虽然在大豆蛋白和木糖之间的美丽反应溶液的酸水解产物中发现该颜料,但在大豆蛋白和木糖和半胱氨酸和糠醛和糠醛和糠醛之间的强酸性条件下也形成了相同的颜料。 通过NaBH 4的其减少形式的结构由MS,NMR和X射线分析测定,并鉴定为7-(2-Furany1)-2,3,4,4a,5,6-六氢环戊基[1, 4]噻嗪-4-IuM-3-羧酸盐,表明Furpenthiazinate的化学结构是7-(2-呋喃基)-2,3,5,6-四氢环戊酰基[B] [1,4]噻嗪-3-羧酸 酸。 Furpenthiazinate在酸性和中性条件下显示出至少400nm的最大吸收和强烈的黄色。 在半胱氨酸和糠醛制备的反应溶液中估计Furpenthiazinate的颜色贡献估计超过60%。

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