Meyer Andrea, Hansen Dennis B, Gomes Cláudia S G, Hobley Timothy J, Thomas Owen R T, Franzreb Matthias
Institute for Technical Chemistry, Water- and Geotechnology Division, Forschungszentrum Karlsruhe, Hermann v. Helmholtz Platz 1, 76344 Eggenstein-Leopoldshafen, Germany.
Biotechnol Prog. 2005 Jan-Feb;21(1):244-54. doi: 10.1021/bp049656c.
A systematic approach for the design of a bioproduct recovery process employing magnetic supports and the technique of high-gradient magnetic fishing (HGMF) is described. The approach is illustrated for the separation of superoxide dismutase (SOD), an antioxidant protein present in low concentrations (ca. 0.15-0.6 mg L(-1)) in whey. The first part of the process design consisted of ligand screening in which metal chelate supports charged with copper(II) ions were found to be the most suitable. The second stage involved systematic and sequential optimization of conditions for the following steps: product adsorption, support washing, and product elution. Next, the capacity of a novel high-gradient magnetic separator (designed for biotechnological applications) for trapping and holding magnetic supports was determined. Finally, all of the above elements were assembled to deliver a HGMF process for the isolation of SOD from crude sweet whey, which consisted of (i) binding SOD using Cu2+ -charged magnetic metal chelator particles in a batch reactor with whey; (ii) recovery of the "SOD-loaded" supports by high-gradient magnetic separation (HGMS); (iii) washing out loosely bound and entrained proteins and solids; (iv) elution of the target protein; and (v) recovery of the eluted supports from the HGMF rig. Efficient recovery of SOD was demonstrated at approximately 50-fold increased scale (cf magnetic rack studies) in three separate HGMF experiments, and in the best of these (run 3) an SOD yield of >85% and purification factor of approximately 21 were obtained.
本文描述了一种采用磁性载体和高梯度磁捕获技术(HGMF)设计生物产品回收工艺的系统方法。以从乳清中分离超氧化物歧化酶(SOD)为例说明了该方法,SOD是一种抗氧化蛋白,在乳清中的浓度较低(约0.15 - 0.6 mg L⁻¹)。工艺设计的第一部分包括配体筛选,结果发现负载铜(II)离子的金属螯合载体是最合适的。第二阶段涉及对以下步骤的条件进行系统且有序的优化:产物吸附、载体洗涤和产物洗脱。接下来,测定了一种新型高梯度磁分离器(专为生物技术应用设计)捕获和固定磁性载体的能力。最后,将上述所有要素整合在一起,构建了一个从粗甜乳清中分离SOD的HGMF工艺,该工艺包括:(i)在间歇反应器中使用负载Cu²⁺的磁性金属螯合颗粒与乳清结合SOD;(ii)通过高梯度磁分离(HGMS)回收“负载SOD”的载体;(iii)洗去松散结合和夹带的蛋白质及固体;(iv)洗脱目标蛋白;(v)从HGMF装置中回收洗脱后的载体。在三个独立的HGMF实验中,以约50倍的规模(对比磁架研究)证明了SOD的高效回收,其中最佳实验(实验3)的SOD产率>85%,纯化倍数约为21。