Affiliation:
1. Lehrstuhl für Zellbiologie und Pflanzenphysiologie, Universität Regensburg, 93040 Regensburg, Germany
Abstract
ABSTRACT
Biotinylation of intact
Saccharomyces cerevisiae
cells with a nonpermeant reagent (Sulfo-NHS-LC-Biotin) allowed the identification of seven cell wall proteins that were released from intact cells by dithiothreitol (DTT). By N-terminal sequencing, three of these proteins were identified as the known proteins β-exoglucanase 1 (Exg1p), β-endoglucanase (Bgl2p), and chitinase (Cts1p). One protein was related to the PIR protein family, whereas the remaining three (Scw3p, Scw4p, and Scw10p [for soluble cell wall proteins]) were found to be related to glucanases. Single knockouts of these three potential glucanases did not result in dramatic phenotypes. The double knockout of
SCW4
and the homologous gene
SCW10
resulted in slower growth, significantly increased release of proteins from intact cells by DTT, and highly decreased mating efficiency when these two genes were disrupted in both mating types. The synergistic behavior of the disruption of
SCW4
and
SCW10
was partly antagonized by the disruption of
BGL2
. The data are discussed in terms of a possible counterplay of transglucosidase and glucosidase activities.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
187 articles.
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