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Appl Environ Microbiol, January 1998, p. 316-324, Vol. 64, No. 1
Department of Molecular Cell Biology and the Institute of
Biomembranes,
Received 15 October 1997/Accepted 29 October 1997
This study focuses on the different efficiencies of secretion of
two fungal cutinases by Saccharomyces cerevisiae,
a wild-type cutinase (CY000) and a hydrophobic mutant cutinase (CY028).
Both cutinases are placed under control of the GAL7
promoter, by which the expression levels can be regulated. Wild-type
cutinase was secreted at up to 25 mg per g (dry weight), while CY028
was secreted at a level of 2 mg per g (dry weight); this difference is
nearly independent of the expression level. Pulse-chase experiments
revealed that whereas CY000 cutinase is secreted, CY028 is irreversibly retained in the cell. Immunogold labelling followed by electron microscopy revealed colocalization of CY028 with immunoglobulin heavy-chain binding protein (BiP) in the endoplasmic reticulum (ER).
The increase of wild-type cutinase expression did not result in higher levels of the molecular chaperone BiP, but BiP levels are
raised by increased induction of the hydrophobic mutant
cutinase. Immunoprecipitation studies showed that in
contrast to the wild-type cutinase, the hydrophobic mutant
cutinase interacts with BiP. These results indicate that the
introduction of two exposed hydrophobic patches in cutinase
results in a higher affinity for BiP which might cause the retention of
this mutant cutinase in the ER.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Impaired Secretion of a Hydrophobic Cutinase by
Saccharomyces cerevisiae Correlates with an Increased
Association with Immunoglobulin Heavy-Chain Binding Protein
(BiP)
*
Corresponding author. Mailing address: Department of
Molecular Cell Biology and the Institute of Biomembranes, Utrecht
University, Padualaan 8, 3584 CH Utrecht, The Netherlands. Phone: 31 30 2532598. Fax: 31 30 2513655. E-mail:
cees{at}emsaserv.biol.ruu.nl.
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