A novel two-step extraction method with detergent/polymer systems for primary recovery of the fusion protein endoglucanase I-hydrophobin I

被引:41
作者
Collén, A
Persson, J
Linder, M
Nakari-Setälä, T
Penttilä, M
Tjerneld, F
Sivars, U
机构
[1] Lund Univ, Ctr Chem & Chem Engn, Dept Biochem, S-22100 Lund, Sweden
[2] VTT Biotechnol & Food Res, FIN-02044 Espoo, Finland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2002年 / 1569卷 / 1-3期
关键词
aqaeous two-phase system; detergent removal; extraction; fusion protein; hydrophobin; protein purification;
D O I
10.1016/S0304-4165(01)00244-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (KEGIcore-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 55degreesC 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. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:139 / 150
页数:12
相关论文
共 49 条
[1]  
Albertsson P.A., 1986, PARTITION CELL PARTI
[2]  
[Anonymous], 1994, AQUEOUS 2 PHASE SYST
[3]  
Berggren K, 1999, BIOTECHNOL BIOENG, V62, P135, DOI 10.1002/(SICI)1097-0290(19990120)62:2<135::AID-BIT2>3.0.CO
[4]  
2-1
[5]  
BORDIER C, 1981, J BIOL CHEM, V256, P1604
[6]  
Buchert J., 1998, TRICHODERMA GLIOCLAD, V2, P343
[7]   Extraction of endoglucanase I (Cel7B) fusion proteins from Trichoderma reesei culture filtrate in a poly(ethylene glycol)phosphate aqueous two-phase system [J].
Collén, A ;
Penttilä, M ;
Stålbrand, H ;
Tjerneld, F ;
Veide, A .
JOURNAL OF CHROMATOGRAPHY A, 2002, 943 (01) :55-62
[8]   Genetic engineering of the Trichoderma reesei endoglucanase I (Cel7B) for enhanced partitioning in aqueous two-phase systems containing thermoseparating ethylene oxide-propylene oxide copolymers [J].
Collén, A ;
Ward, M ;
Tjerneld, F ;
Stålbrand, H .
JOURNAL OF BIOTECHNOLOGY, 2001, 87 (02) :179-191
[9]   Genetically engineered peptide fusions for improved protein partitioning in aqueous two-phase systems -: Effect of fusion localization on endoglucanase I of Trichoderma reesei [J].
Collén, A ;
Ward, M ;
Tjerneld, F ;
Stålbrand, H .
JOURNAL OF CHROMATOGRAPHY A, 2001, 910 (02) :275-284
[10]  
COLLEN A, IN PRESS BIOTECHNOL