Collén Anna, Persson Josefine, Linder Markus, Nakari-Setälä Tiina, Penttilä Merja, Tjerneld Folke, Sivars Ulf
Depqartment of Biochemistry, Center for Chemistry and Chemical Engineering, Lund University, Sweden.
Biochim Biophys Acta. 2002 Jan 15;1569(1-3):139-50. doi: 10.1016/s0304-4165(01)00244-6.
Extraction systems for hydrophobically tagged proteins have been developed based on phase separation in aqueous solutions of non-ionic detergents and polymers. The systems have earlier only been applied for separation of membrane proteins. Here, we examine the partitioning and purification of the amphiphilic fusion protein endoglucanase I(core)-hydrophobin I (EGI(core)-HFBI) from culture filtrate originating from a Trichoderma reesei fermentation. The micelle extraction system was formed by mixing the non-ionic detergent Triton X-114 or Triton X-100 with the hydroxypropyl starch polymer, Reppal PES100. The detergent/polymer aqueous two-phase systems resulted in both better separation characteristics and increased robustness compared to cloud point extraction in a Triton X-114/water system. Separation and robustness were characterized for the parameters: temperature, protein and salt additions. In the Triton X-114/Reppal PES100 detergent/polymer system EGI(core)-HFBI strongly partitioned into the micelle-rich phase with a partition coefficient (K) of 15 and was separated from hydrophilic proteins, which preferably partitioned to the polymer phase. After the primary recovery step, EGI(core)-HFBI was quantitatively back-extracted (K(EGIcore-HFBI)=150, yield=99%) into a water phase. In this second step, ethylene oxide-propylene oxide (EOPO) copolymers were added to the micelle-rich phase and temperature-induced phase separation at 55 degrees C was performed. Total recovery of EGI(core)-HFBI after the two separation steps was 90% with a volume reduction of six times. For thermolabile proteins, the back-extraction temperature could be decreased to room temperature by using a hydrophobically modified EOPO copolymer, with slightly lower yield. The addition of thermoseparating co-polymer is a novel approach to remove detergent and effectively releases the fusion protein EGI(core)-HFBI into a water phase.
基于非离子洗涤剂和聚合物水溶液中的相分离,已开发出用于疏水标记蛋白的提取系统。该系统早期仅用于膜蛋白的分离。在此,我们研究了来自里氏木霉发酵的培养滤液中两亲性融合蛋白内切葡聚糖酶I(核心)-疏水蛋白I(EGI(核心)-HFBI)的分配和纯化。通过将非离子洗涤剂Triton X-114或Triton X-100与羟丙基淀粉聚合物Reppal PES100混合形成胶束提取系统。与Triton X-114/水系统中的浊点萃取相比,洗涤剂/聚合物双水相系统具有更好的分离特性和更高的稳健性。对温度、蛋白质和盐添加等参数的分离和稳健性进行了表征。在Triton X-114/Reppal PES100洗涤剂/聚合物系统中,EGI(核心)-HFBI强烈分配到富含胶束的相中,分配系数(K)为15,并与亲水性蛋白分离,亲水性蛋白更倾向于分配到聚合物相中。在初步回收步骤之后,EGI(核心)-HFBI被定量反萃取(K(EGI核心-HFBI)=150,产率=99%)到水相中。在第二步中,将环氧乙烷-环氧丙烷(EOPO)共聚物添加到富含胶束的相中,并在55℃下进行温度诱导相分离。经过两步分离后,EGI(核心)-HFBI的总回收率为90%,体积减少了六倍。对于热不稳定蛋白,通过使用疏水改性的EOPO共聚物,可以将反萃取温度降低到室温,产率略低。添加热分离共聚物是一种去除洗涤剂并有效将融合蛋白EGI(核心)-HFBI释放到水相中的新方法。