Literature DB >> 11853968

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

Anna Collén1, Josefine Persson, Markus Linder, Tiina Nakari-Setälä, Merja Penttilä, Folke Tjerneld, Ulf Sivars.   

Abstract

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.

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Year:  2002        PMID: 11853968     DOI: 10.1016/s0304-4165(01)00244-6

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  6 in total

1.  Surface adhesion of fusion proteins containing the hydrophobins HFBI and HFBII from Trichoderma reesei.

Authors:  Markus Linder; Geza R Szilvay; Tiina Nakari-Setälä; Hans Söderlund; Merja Penttilä
Journal:  Protein Sci       Date:  2002-09       Impact factor: 6.725

Review 2.  Whole cell microbial transformation in cloud point system.

Authors:  Zhilong Wang; Jian-He Xu; Daijie Chen
Journal:  J Ind Microbiol Biotechnol       Date:  2008-04-08       Impact factor: 3.346

3.  The Adsorption Layer in the System: Carboxymethylcellulose/Surfactants/NaCl/MnO(2).

Authors:  Elżbieta Grządka
Journal:  J Surfactants Deterg       Date:  2012-03-14       Impact factor: 1.902

4.  Protein bodies in nature and biotechnology.

Authors:  Stefan R Schmidt
Journal:  Mol Biotechnol       Date:  2013-06       Impact factor: 2.860

5.  In-solution antibody harvesting with a plant-produced hydrophobin-Protein A fusion.

Authors:  Katri Kurppa; Lauri J Reuter; Anneli Ritala; Markus B Linder; Jussi J Joensuu
Journal:  Plant Biotechnol J       Date:  2017-08-01       Impact factor: 9.803

Review 6.  Making recombinant proteins in filamentous fungi- are we expecting too much?

Authors:  Helena Nevalainen; Robyn Peterson
Journal:  Front Microbiol       Date:  2014-02-27       Impact factor: 5.640

  6 in total

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