Abstract
The role of the lytic enzyme beta-(1,3)-glucanase in cell wall synthesis and its distribution in the mycelium of the fungus Sclerotium rolfsii were studied. Enzyme activity was determined after enzyme extraction with Triton X-100 from a cell wall preparation. Specific zones of immunofluorescence appeared in the hyphal tips, clamp connections, new septa, and lateral branching when a specific antiserum was used with the indirect method of the fluorescent antibody staining. Enzymatic activity in the cell wall preparation was inactivated by diethylpyrocarbonate. However, 69% of the total enzymatic activity was present in a latent form which was not affected by the ester. This result suggests that most of the beta-(1,3)-glucanase was present along the hyphal cell walls in a "masked" form. An active enzyme appeared only in those regions which showed immunofluorescence. The activity of glucan synthetase, an enzyme essential for wall formation, was higher in the branching funus grown on L-threonine-supplemented synthetic medium than in the synthetic medium-grown fungus.
MeSH Terms
Cell Wall/enzymology
Fluorescent Antibody Technique
Glucan Endo-1,3-beta-D-Glucosidase/analysis,metabolism
Glycoside Hydrolases/metabolism
Isoenzymes
Mitosporic Fungi/enzymology,ultrastructure
Starch Synthase/metabolism
Chemicals
Isoenzymes
Starch Synthase
Glycoside Hydrolases
Glucan Endo-1,3-beta-D-Glucosidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kritzman G
Chet I
Henis Y
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