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使用由阴离子表面活性剂AOT产生的胶体气体泡沫(CGA)从甜乳清中回收乳铁蛋白和乳过氧化物酶。

Recovery of lactoferrin and lactoperoxidase from sweet whey using colloidal gas aphrons (CGAs) generated from an anionic surfactant, AOT.

作者信息

Fuda Elisabeth, Jauregi Paula, Pyle D L

机构信息

School of Food Biosciences, The University of Reading, Whiteknights Campus, P.O. Box 226, Reading RG6 6AP, UK.

出版信息

Biotechnol Prog. 2004 Mar-Apr;20(2):514-25. doi: 10.1021/bp034198d.

Abstract

The recovery of lactoferrin and lactoperoxidase from sweet whey was studied using colloidal gas aphrons (CGAs), which are surfactant-stabilized microbubbles (10-100 microm). CGAs are generated by intense stirring (8000 rpm for 10 min) of the anionic surfactant AOT (sodium bis-2-ethylhexyl sulfosuccinate). A volume of CGAs (10-30 mL) is mixed with a given volume of whey (1-10 mL), and the mixture is allowed to separate into two phases: the aphron (top) phase and the liquid (bottom) phase. Each of the phases is analyzed by SDS-PAGE and surfactant colorimetric assay. A statistical experimental design has been developed to assess the effect of different process parameters including pH, ionic strength, the concentration of surfactant in the CGAs generating solution, the volume of CGAs and the volume of whey on separation efficiency. As expected pH, ionic strength and the volume of whey (i.e. the amount of total protein in the starting material) are the main factors influencing the partitioning of the Lf.Lp fraction into the aphron phase. Moreover, it has been demonstrated that best separation performance was achieved at pH = 4 and ionic strength = 0.1 mol/L i.e., with conditions favoring electrostatic interactions between target proteins and CGAs (recovery was 90% and the concentration of lactoferrin and lactoperoxidase in the aphron phase was 25 times higher than that in the liquid phase), whereas conditions favoring hydrophobic interactions (pH close to pI and high ionic strength) led to lower performance. However, under these conditions, as confirmed by zeta potential measurements, the adsorption of both target proteins and contaminant proteins is favored. Thus, low selectivity is achieved at all of the studied conditions. These results confirm the initial hypothesis that CGAs act as ion exchangers and that the selectivity of the process can be manipulated by changing main operating parameters such as type of surfactant, pH and ionic strength.

摘要

使用胶体气体泡沫(CGA)研究了从甜乳清中回收乳铁蛋白和乳过氧化物酶的方法,胶体气体泡沫是由表面活性剂稳定的微泡(10 - 100微米)。通过对阴离子表面活性剂AOT(二(2 - 乙基己基)磺基琥珀酸钠)进行剧烈搅拌(8000转/分钟,持续10分钟)来产生胶体气体泡沫。将一定体积(10 - 30毫升)的胶体气体泡沫与给定体积(1 - 10毫升)的乳清混合,然后使混合物分离成两相:泡沫(上层)相和液体(下层)相。通过SDS - PAGE和表面活性剂比色法对每个相进行分析。已经开发了一种统计实验设计来评估不同工艺参数的影响,这些参数包括pH值、离子强度、在产生胶体气体泡沫的溶液中表面活性剂的浓度、胶体气体泡沫的体积以及乳清的体积对分离效率的影响。正如预期的那样,pH值、离子强度和乳清的体积(即起始原料中总蛋白的量)是影响乳铁蛋白 - 乳过氧化物酶组分分配到泡沫相的主要因素。此外,已经证明在pH = 4和离子强度 = 0.1摩尔/升的条件下实现了最佳分离性能,即在有利于目标蛋白与胶体气体泡沫之间静电相互作用的条件下(回收率为90%,泡沫相中乳铁蛋白和乳过氧化物酶的浓度比液相中高25倍),而有利于疏水相互作用的条件(pH接近蛋白质的等电点且离子强度高)导致性能较低。然而,在这些条件下,正如通过zeta电位测量所证实的,目标蛋白和污染蛋白的吸附都受到促进。因此,在所有研究条件下选择性都较低。这些结果证实了最初的假设,即胶体气体泡沫充当离子交换剂,并且可以通过改变主要操作参数(如表面活性剂类型、pH值和离子强度)来控制该过程的选择性。

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