Abstract
The aim of this work was to modify the cell surface properties of
Saccharomyces cerevisiae by expression of the HFBI hydrophobin of the
filamentous fungus Trichoderma reesei on the yeast cell surface. The second
aim was to study the immobilization capacity of the modified cells. Fusion to
the Flo1p flocculin was used to target the HFBI moiety to the cell wall.
Determination of cell surface characteristics with contact angle and zeta
potential measurements indicated that HFBI-producing cells are more apolar
and slightly less negatively charged than the parent cells. Adsorption of the
yeast cells to different commercial supports was studied. A twofold
increase in the binding affinity of the hydrophobin-producing yeast to
hydrophobic silicone-based materials was observed, while no improvement in
the interaction with hydrophilic carriers could be seen compared to that of
the parent cells. Hydrophobic interactions between the yeast cells and the
support are suggested to play a major role in attachment. Also, a slight
increase in the initial adsorption rate of the hydrophobin yeast was
observed. Furthermore, due to the engineered cell surface,
hydrophobin-producing yeast cells were efficiently separated in an aqueous
two-phase system by using a nonionic polyoxyethylene detergent, C12-18EO5.
Original language | English |
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Pages (from-to) | 3385-3391 |
Journal | Applied and Environmental Microbiology |
Volume | 68 |
Issue number | 7 |
DOIs | |
Publication status | Published - 2002 |
MoE publication type | A1 Journal article-refereed |
Keywords
- hydrophobins
- Saccharomyces cerevisiae
- cell surface
- immobilization
- HFBI