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紫外线或荧光灯照射后全脂和脱脂牛奶中的蛋白质氧化变化。

Protein oxidative changes in whole and skim milk after ultraviolet or fluorescent light exposure.

机构信息

Departamento de Química Biológica-CIQUIBIC, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.

出版信息

J Dairy Sci. 2010 Nov;93(11):5101-9. doi: 10.3168/jds.2010-3513.

Abstract

We investigated how protein changes occur, at the primary or higher structural levels, when proteins are exposed to UV or fluorescent (FL) light while in the complex matrix, milk. Whole milk (WM) or skim milk (SM) samples were exposed to FL or UV light from 0 to 24h at 4°C. Protein oxidation was evaluated by the formation of protein carbonyls (PC), dityrosine bond (DiTyr), and changes in molecular weight (protein fragmentation and polymerization). Oxidative changes in AA residues were measured by PC. Dityrosine and N'-formylkynurenine (NFK), a carbonylation derivative of Trp, were measured by fluorometry. Protein carbonyls increased as a function of irradiation time for both WM and SM. The initial rate for PC formation by exposure to FL light (0.25 or 0.27 nmol/h for WM and SM, respectively) was slower than that following exposure to UV light (1.95 or 1.20 nmol/h, respectively). The time course of NFK formation resembled that of PC. After 24h of UV exposure, SM had significantly higher levels of NFK than did WM. In contrast, WM samples irradiated with UV had higher levels of DiTyr than did SM samples, indicating different molecular pathways. The formation of intra- or intermolecular DiTyr bonds could be indicative of changes in the tertiary structure or oligomerization of proteins. The existence of NFK suggests the occurrence of protein fragmentation. Thus, proteolysis and oligomerization were analyzed by sodium dodecyl sulfate-PAGE. After 24h of exposing WM to UV or FL light, all the proteins were affected by both types of light, as evidenced by loss of material in most of the bands. Aggregates were produced only by UV irradiation. Hydrolysis by pepsin and enzyme-induced coagulation by rennet were performed to evaluate altered biological properties of the oxidized proteins. No effect on pepsin digestion or rennet coagulation was found in irradiated SM or WM. The oxidative status of proteins in milk and dairy products is of interest to the dairy industry and consumers. These findings provide knowledge that could be useful in determining the optimal lighting conditions in the dairy industry in general and in cheese making in particular.

摘要

我们研究了当蛋白质在复杂基质牛奶中暴露于紫外或荧光(FL)光时,其在一级或更高结构水平上如何发生变化。全脂牛奶(WM)或脱脂牛奶(SM)样品在 4°C 下分别暴露于 FL 或 UV 光 0 至 24 小时。通过形成蛋白质羰基(PC)、二酪氨酸键(DiTyr)和分子量变化(蛋白质片段化和聚合)来评估蛋白质氧化。通过 PC 测量 AA 残基的氧化变化。通过荧光法测量二酪氨酸和 N'-甲酰基犬尿氨酸(NFK),色氨酸的羰基衍生物。PC 形成的辐照时间依赖性增加适用于 WM 和 SM。暴露于 FL 光时 PC 形成的初始速率(WM 和 SM 分别为 0.25 或 0.27 nmol/h)比暴露于 UV 光时慢(WM 和 SM 分别为 1.95 或 1.20 nmol/h)。NFK 形成的时间过程类似于 PC。暴露于 UV 24 小时后,SM 中的 NFK 水平明显高于 WM。相比之下,经 UV 照射的 WM 样品中 DiTyr 的水平高于 SM 样品,表明存在不同的分子途径。形成内或二酪氨酸键可能表明蛋白质三级结构或寡聚化的变化。NFK 的存在表明蛋白质片段化的发生。因此,通过十二烷基硫酸钠-PAGE 分析蛋白质的降解和寡聚化。暴露于 UV 或 FL 光 24 小时后,WM 中的所有蛋白质都受到两种类型光的影响,这从大多数条带中物质的损失中可以得到证明。只有在 UV 照射下才会产生聚集体。通过胃蛋白酶水解和凝乳酶诱导的酶凝结进行蛋白质氧化的生物性质改变的评估。未发现辐照 SM 或 WM 对胃蛋白酶消化或凝乳酶凝结的影响。蛋白质在牛奶和乳制品中的氧化状态引起了乳制品行业和消费者的关注。这些发现为确定乳制品行业特别是奶酪生产的最佳照明条件提供了有用的知识。

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