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Fractionation of Glycomacropeptide from Whey Using Positively Charged Ultrafiltration Membranes

机译:使用带正电的超滤膜分离乳清中的糖脂肽

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摘要

Fractionation of the bovine glycomacropeptide (GMP) from the other proteins in cheese whey was examined using ultrafiltration membranes surface modified to contain positively charged polymer brushes made of polyhexamethylene biguanide. By placing a strong positive charge on a 1000 kDa ultrafiltration membrane and adjusting the pH of whey close to the isoelectric point of GMP, a 14-fold increase in selectivity was observed compared to unmodified membranes. A one stage membrane system gave 90% pure GMP and a three-stage rectification system gave 97% pure GMP. The charged membrane was salt-tolerant up to 40 mS cm−1 conductivity, allowing fractionation of GMP directly from cheese whey without first lowering the whey conductivity by water dilution. Thus, similarly sized proteins that differed somewhat in isoelectric points and were 50–100 fold smaller than the membrane molecular weight cut-off (MWCO), were cleanly fractionated using charged ultrafiltration membranes without water addition. This is the first study to report on the use of salt-tolerant charged ultrafiltration membranes to produce chromatographically pure protein fractions from whey, making ultrafiltration an attractive alternative to chromatography for dairy protein fractionation.
机译:使用经表面改性以包含由聚六亚甲基双胍制成的带正电的聚合物刷的超滤膜,检查了干酪乳清中牛糖巨肽(GMP)与其他蛋白质的分离。通过在1000 kDa超滤膜上放置强正电荷并调节乳清的pH值使其接近GMP的等电点,与未修饰的膜相比,选择性提高了14倍。一阶段的膜系统给出了90%的纯GMP,三阶段的精馏系统给出了97%的纯GMP。带电的膜可耐受高达40 mS cm -1 的电导率,允许直接从干酪乳清中分离出GMP,而无需先通过水稀释降低乳清的电导率。因此,大小相同的蛋白质,其等电点略有不同,比膜分子量截留值(MWCO)小50-100倍,可以使用带电荷的超滤膜干净地分级分离,而无需加水。这是第一项报道使用耐盐带电超滤膜从乳清中生产色谱纯蛋白馏分的研究,这使超滤成为乳蛋白分离色谱法的有吸引力的替代方法。

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