Members of Glycosyl-Hydrolase Family 17 of A. fumigatus Differentially Affect Morphogenesis
Cell wall biosynthesis and remodeling are essential for fungal growth and development. In the fungal pathogen , the β(1,3)glucan is the major cell wall polysaccharide. This polymer is synthesized at the plasma membrane by a transmembrane complex, then released into the parietal space to be remodeled...
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Published in | Journal of fungi (Basel) Vol. 4; no. 1; p. 18 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
30.01.2018
MDPI |
Subjects | |
Online Access | Get full text |
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Summary: | Cell wall biosynthesis and remodeling are essential for fungal growth and development. In the fungal pathogen
, the β(1,3)glucan is the major cell wall polysaccharide. This polymer is synthesized at the plasma membrane by a transmembrane complex, then released into the parietal space to be remodeled by enzymes, and finally incorporated into the pre-existing cell wall. In the Glycosyl-Hydrolases family 17 (GH17) of
, two β(1,3)glucanosyltransferases, Bgt1p and Bgt2p, have been previously characterized. Disruption of
and
did not result in a phenotype, but sequence comparison and hydrophobic cluster analysis showed that three other genes in
belong to the GH17 family,
,
, and
. In constrast to
mutants, single and multiple deletion of
,
, and
showed a decrease in conidiation associated with a higher conidial mortality and an abnormal conidial shape. Moreover, mycelium was also affected with a slower growth, stronger sensitivity to cell wall disturbing agents, and altered cell wall composition. Finally, the synthetic interactions between Bgt1p, Bgt2p, and the three other members, which support a functional cooperation in cell-wall assembly, were analyzed. Our data suggest that Scw4p, Scw11p, and Bgt3p are essential for cell wall integrity and might have antagonistic and distinct functions to Bgt1p and Bgt2p. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 PMCID: PMC5872321 |
ISSN: | 2309-608X 2309-608X |
DOI: | 10.3390/jof4010018 |