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首页> 外文期刊>Poultry Science >Changes in the protein secondary structure of hen's egg yolk determined by Fourier transform infrared spectroscopy during the first eight days of incubation
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Changes in the protein secondary structure of hen's egg yolk determined by Fourier transform infrared spectroscopy during the first eight days of incubation

机译:在孵化的前八天,通过傅里叶变换红外光谱法测定的鸡蛋黄蛋白二级结构的变化

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In this study, incubation-induced alterations in the protein secondary structures of egg yolk and its major fractions (granules, plasma, and low-density lipoproteins [LDL]) were monitored during the first 8 d of embryogenesis using Fourier transform infrared spectroscopy (FTIR) and isoelectric focusing (IEF). Two factors potentially connected with egg yolk protein secondary structure changes were evaluated, i.e., the pH value of incubated egg yolk, and phosvitin, an important egg yolk protein assumed to play an important role in hematopoiesis as the iron carrier during early embryogenesis. However, neither the significant increase in pH value (6.07 to 6.92) of egg yolk during incubation of fertilized eggs, nor the release of iron from phosvitin were found to be directly related to the changes in protein secondary structure in egg yolk and its fractions. FTIR showed that the protein conformation in whole egg yolk, granules, and LDL was stable during incubation, but separate evaluation of the plasma fraction revealed consider-able changes in secondary structure. However, it is unlikely that these changes were provoked by structure changes of the proteins originally present in plasma; instead, the physiological influx of albumen into the yolk sac was expected to play an important role in the protein modifications of egg yolk, as was shown both by FTIR and IEF of the water-soluble egg yolk proteins. Moreover, FTIR was used to determine the naturally occurring proportions (%) of the secondary structure elements in egg yolk and its 3 fractions on d 0 of incubation. The granules fraction mainly consisted of a mixture of inter-and intramolecular beta-sheets (57.04% +/- 0.39%). The plasma fraction was found to consist mainly of alpha-helices (43.23% +/- 0.27%), whereas LDL was composed almost exclusively of intramolecular beta-sheets (67.36% +/- 0.56%) or beta-turns, or both. On the other hand, whole egg yolk was mainly composed of intermolecular beta-sheets (39.77% +/- 0.48%), potentially indicating molecular interchanges between the individual fractions.
机译:在这项研究中,使用傅里叶变换红外光谱法(FTIR)在胚胎发生的前8 d内对蛋黄及其主要部分(颗粒,血浆和低密度脂蛋白[LDL])的蛋白质二级结构的孵育诱导变化进行了监测。 )和等电聚焦(IEF)。评估了与蛋黄蛋白二级结构变化潜在相关的两个因素,即温育蛋黄的pH值和磷酸卵磷脂,一种重要的蛋黄蛋白被认为在早期胚胎形成过程中作为铁载体在造血中起着重要作用。然而,既没有发现卵黄在受精卵孵化过程中pH值的显着增加(6.07至6.92),也没有发现磷光体中铁的释放与卵黄及其部分蛋白质二级结构的变化直接相关。 FTIR显示,整个卵黄,颗粒和LDL中的蛋白质构象在孵育过程中是稳定的,但对血浆部分的单独评估显示二级结构发生了可观的变化。但是,这些变化不太可能是由血浆中最初存在的蛋白质的结构变化引起的。取而代之的是,预期蛋白的生理性流入卵黄囊在卵黄的蛋白质修饰中起重要作用,如水溶性卵黄蛋白的FTIR和IEF所显示的。此外,FTIR用于确定蛋黄中二级结构元素的天然存在比例(%)及其在孵化后d 0的3个组分。颗粒部分主要由分子间和分子内β-片层的混合物组成(57.04%+/- 0.39%)。发现血浆部分主要由α-螺旋(43.23%+ /-0.27%)组成,而LDL几乎仅由分子内β-折叠(67.36%+ /-0.56%)或β-转角或两者组成。另一方面,全蛋黄主要由分子间β-折叠构成(39.77%+/- 0.48%),可能表明各个部分之间存在分子互换。

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