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Hydrophobins line air channels in fruiting bodies of Schizophyllum commune and Agaricus bisporus

Published online by Cambridge University Press:  01 May 1999

LUIS G. LUGONES
Affiliation:
Molecular Plant Biology Laboratory, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
HAN A. B. WÖSTEN
Affiliation:
Molecular Plant Biology Laboratory, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
KIM U. BIRKENKAMP
Affiliation:
Molecular Plant Biology Laboratory, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
KLAAS A. SJOLLEMA
Affiliation:
Molecular Plant Biology Laboratory, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
JAN ZAGERS
Affiliation:
Molecular Plant Biology Laboratory, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
JOSEPH G. H. WESSELS
Affiliation:
Molecular Plant Biology Laboratory, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
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Abstract

The hydrophobin SC4 was isolated from the medium of a dikaryon from Schizophyllum commune with disrupted SC3 genes. Although not glycosylated, its biophysical properties were similar to those of SC3. As the hydrophobins SC3 from S. commune and ABH1 and ABH3 from Agaricus bisporus, SC4 self-assembled at hydrophilic-hydrophobic interfaces into an SDS insoluble amphipathic film with a typical rodlet structure at its hydrophobic face, and also proved to be a powerful surfactant. Similar rodlet structures were observed in the fruiting body plectenchyma. By immunodetection SC4 could be localized lining air channels within this tissue. A similar localization was found for the ABH1 hydrophobin in fruiting bodies of A. bisporus. Probably, these hydrophobin coatings prevent collapse of air channels allowing efficient gas exchange even under wet conditions.

Type
Research Article
Copyright
The British Mycological Society 1999

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