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(Received for publication, May 8, 1996, and in revised form, September 4, 1996)
From the The formation of the ascospore wall of
Saccharomyces cerevisiae requires the coordinate activity
of enzymes involved in the biosynthesis of its components such as
chitosan, the deacetylated form of chitin. We have cloned the
CDA1 and CDA2 genes which together account for
the total chitin deacetylase activity of the organism. We have shown
that expression of these genes is restricted to a distinct time period
during sporulation. The two genes are functionally redundant, each
contributing equally to the total chitin deacetylase activity. Diploids
disrupted for both genes sporulate as efficiently as wild type cells,
and the resulting mutant spores are viable under standard laboratory
conditions. However, they fail to emit the natural fluorescence of
yeast spores imparted by the dityrosine residues of the outermost
ascospore wall layer. Moreover, mutant spores are relatively sensitive
to hydrolytic enzymes, ether, and heat shock, a fact that underscores
the importance of the CDA genes for the proper formation of
the ascospore wall.
Volume 271, Number 49,
Issue of December 6, 1996
pp. 31420-31425
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
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