Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1988 Apr;170(4):1950-4.
doi: 10.1128/jb.170.4.1950-1954.1988.

Isolation and characterization of Saccharomyces cerevisiae mutants resistant to Calcofluor white

Affiliations

Isolation and characterization of Saccharomyces cerevisiae mutants resistant to Calcofluor white

C Roncero et al. J Bacteriol. 1988 Apr.

Abstract

Calcofluor is a fluorochrome that exhibits antifungal activity and a high affinity for yeast cell wall chitin. We isolated Saccharomyces cerevisiae mutants resistant to Calcofluor. The resistance segregated in a Mendelian fashion and behaved as a recessive character in all the mutants analyzed. Five loci were defined by complementation analysis. The abnormally thick septa between mother and daughter cells caused by Calcofluor in wild-type cells were absent in the mutants. The Calcofluor-binding capacity, observed by fluorescence microscopy, in a S. cerevisiae wild-type cells during alpha-factor treatment was also absent in some mutants and reduced in others. Staining of cell walls with wheat germ agglutinin-fluorescein complex indicated that the chitin uniformly distributed over the whole cell wall in vegetative or in alpha-factor-treated cells was almost absent in three of the mutants and reduced in the two others. Cell wall analysis evidenced a five- to ninefold reduction in the amount of chitin in mutants compared with that in the wild-type strain. The total amounts of cell wall mannan and beta-glucan in wild-type and mutant strains were similar; however, the percentage of beta-glucan that remained insoluble after alkali extraction was considerably reduced in mutant cells. The susceptibilities of the mutants and the wild-type strains to a cell wall enzymic lytic complex were rather similar. The in vitro levels of chitin synthase 2 detected in all mutants were similar to that in the wild type. The significance of these results is discussed in connection with the mechanism of chitin synthesis and cell wall morphogenesis in S. cerevisiae.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Biol Chem. 1971 Jan 10;246(1):152-9 - PubMed
    1. Proc Natl Acad Sci U S A. 1971 Sep;68(9):2052-6 - PubMed
    1. Science. 1980 Nov 21;210(4472):903-6 - PubMed
    1. Biochem J. 1969 Sep;114(3):557-67 - PubMed
    1. Biochem J. 1973 Sep;135(1):31-6 - PubMed

Publication types

MeSH terms

LinkOut - more resources