Differential inhibition of chitin synthetases 1 and 2 from Saccharomyces cerevisiae by polyoxin D and nikkomycins

Author:

Cabib E1

Affiliation:

1. Laboratory of Biochemistry and Metabolism, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.

Abstract

Polyoxin D, nikkomycin X, and nikkomycin Z are all competitive inhibitors of chitin synthetase 2 (Chs2), the essential enzyme for primary septum formation in Saccharomyces cerevisiae, and of Chs1, a repair enzyme. However, Chs2 is more resistant to these antibiotics than Chs1. When Co2+, the best stimulator of Chs2, was used in the assay for this enzyme, the differences in the Ki values for nikkomycins between the two isozymes reached 3 orders of magnitude. These results point to differences in the active sites of the two isozymes. Polyoxin D was much more effective than nikkomycin Z in inhibiting cell growth. This underlines the importance of the choice of enzyme and of assay conditions when cell wall-synthesizing enzymes are used in screens for possible antifungal agents.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference21 articles.

1. Isolation of a chitin synthase gene (CHSI) from Candida albicans by expression in Saccharomyces cerevisiae;Au-Young J.;Mol. Microbiol.,1990

2. Effect of polyoxin D on chitin synthesis and septum formation in Saccharomyces cerevisiae;Bowers B.;J. Bacteriol.,1974

3. Chitin synthesis in Candida albicans: comparison of yeast and hyphal forms;Braun P. C.;J. Bacteriol.,1978

4. The synthesis and degradation of chitin;Cabib E.;Adv. Enzymol. Relat. Areas Mol. Biol.,1987

5. Fungal cell wall synthesis: the construction of a biological structure;Cabib E.;Microbiol. Sci.,1988

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