Abstract
Previously, we showed that chitin synthase 2 (Chs2) is required for septum formation in Saccharomyces cerevisiae, whereas chitin synthase 1 (Chs1) does not appear to be an essential enzyme. However, in strains carrying a disrupted CHS1 gene, frequent lysis of buds is observed. Lysis occurs after nuclear separation and appears to result from damage to the cell wall, as indicated by osmotic stabilization and by a approximately 50-nm orifice at the center of the birth scar. Lysis occurs at a low pH and is prevented by buffering the medium above pH 5. A likely candidate for the lytic system is a previously described chitinase that is probably involved in cell separation. The chitinase has a very acidic pH optimum and a location in the periplasmic space that exposes it to external pH. Accordingly, allosamidin, a specific chitinase inhibitor, substantially reduced the number of lysed cells. Because the presence of Chs1 in the cell abolishes lysis, it is concluded that damage to the cell wall is caused by excessive chitinase activity at acidic pH, which can normally be repaired through chitin synthesis by Chs1. The latter emerges as an auxiliary or emergency enzyme. Other experiments suggest that both Chs1 and Chs2 collaborate in the repair synthesis of chitin, whereas Chs1 cannot substitute for Chs2 in septum formation.
MeSH Terms
Acetylglucosamine/analogs & derivatives,pharmacology
Antifungal Agents/pharmacology
Cell Cycle
Chitin/biosynthesis
Chitin Synthase/metabolism
Chitinases/antagonists & inhibitors
Glucosyltransferases/metabolism
Hydrogen-Ion Concentration
Kinetics
Pyrimidine Nucleosides/pharmacology
Saccharomyces cerevisiae/drug effects,enzymology,growth & development
Trisaccharides
Chemicals
Antifungal Agents
Pyrimidine Nucleosides
Trisaccharides
allosamidin
Chitin
polyoxorim
Glucosyltransferases
Chitin Synthase
Chitinases
Acetylglucosamine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Cabib E
Laboratory of Biochemistry and Metabolism, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.
Sburlati A
Bowers B
Silverman S J
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