Department of Animal Science, Iowa State University, Ames 50011-3150, USA. [corrected]
Poult Sci. 2011 May;90(5):1096-104. doi: 10.3382/ps.2010-01138.
The objective of this study was to develop a new protocol that could be used for large-scale separation of phosvitin from egg yolk using ethanol and salts. Yolk granules, which contain phosvitin, were precipitated after diluting egg yolk with 9 volumes of distilled water. The pH of the yolk solution was adjusted to pH 4.0 to 8.0 using 6 N HCl or NaOH, and then yolk granules containing phosvitin was separated by centrifugation at 3,220 × g for 30 min. Lipids and phospholipids were removed from the insoluble yolk granules using 85% ethanol. The optimal volumes and concentration of ethanol in removing lipids from the precipitants were determined. After centrifugation, the lipid-free precipitants were homogenized with 9 volumes of ammonium sulfate [(NH(4))(2)SO(4)] or NaCl to extract phosvitin. The optimal pH and concentration of (NH(4))(2)SO(4) or NaCl for the highest recovery rate and purity for phosvitin in final solution were determined. At pH 6.0, all the phosvitin in diluted egg yolk solution was precipitated. Among the (NH(4))(2)SO(4) and NaCl conditions tested, 10% (NH(4))(2)SO(4) or 10% NaCl at pH 4.0 yielded the greatest phosvitin extraction from the lipid-free precipitants. The recovery rates of phosvitin using (NH(4))(2)SO(4) and NaCl were 72 and 97%, respectively, and their purity was approximately 85%. Salt was removed from the extract using ultrafiltration. The salt-free phosvitin solution was concentrated using ultrafiltration, the impurities were removed by centrifugation, and the resulting solution was freeze-dried. The partially purified phosvitin was suitable for human use because ethanol was the only solvent used to remove lipids, (NH(4))(2)SO(4) or NaCl was used to extract phosvitin, and ultrafiltration was used to remove salt and concentrate the extract. The developed method was simple and suitable for a large-scale preparation of partially purified phosvitin.
本研究旨在开发一种新的方案,使用乙醇和盐从蛋黄中大规模分离卵黄磷蛋白。将蛋黄稀释至 9 倍蒸馏水后,蛋黄颗粒沉淀。使用 6 N HCl 或 NaOH 将蛋黄溶液的 pH 值调至 4.0 至 8.0,然后将含有卵黄磷蛋白的蛋黄颗粒在 3220×g 下离心 30 分钟以分离。使用 85%乙醇从不溶性蛋黄颗粒中去除脂质和磷脂。确定了从沉淀物中去除脂质的最佳乙醇体积和浓度。离心后,将无脂沉淀物与 9 倍体积的硫酸铵[(NH4)2SO4]或氯化钠混合以提取卵黄磷蛋白。确定了最终溶液中提取卵黄磷蛋白的最高回收率和纯度的最佳 pH 和 (NH4)2SO4 或 NaCl 浓度。在 pH 6.0 时,稀释蛋黄溶液中的所有卵黄磷蛋白都沉淀。在测试的 (NH4)2SO4 和 NaCl 条件下,在 pH 4.0 时,10% (NH4)2SO4 或 10% NaCl 从无脂沉淀物中提取了最大量的卵黄磷蛋白。使用 (NH4)2SO4 和 NaCl 提取卵黄磷蛋白的回收率分别为 72%和 97%,纯度约为 85%。使用超滤从提取物中去除盐。使用超滤浓缩无盐卵黄磷蛋白溶液,离心去除杂质,得到的溶液冻干。部分纯化的卵黄磷蛋白适合人体使用,因为乙醇是唯一用于去除脂质的溶剂,使用 (NH4)2SO4 或 NaCl 提取卵黄磷蛋白,超滤用于去除盐并浓缩提取物。所开发的方法简单,适合大规模制备部分纯化的卵黄磷蛋白。