The influence of congo red on the cell wall and (1----3)-beta-D-glucan microfibril biogenesis in Saccharomyces cerevisiae
Language English Country Germany Media print
Document type Journal Article
PubMed
1417414
DOI
10.1007/bf00245214
Knihovny.cz E-resources
- MeSH
- beta-Glucans * MeSH
- Cell Wall drug effects metabolism ultrastructure MeSH
- Cell Division drug effects MeSH
- Glucans biosynthesis MeSH
- Congo Red pharmacology MeSH
- Culture Media pharmacology MeSH
- Morphogenesis drug effects MeSH
- Protoplasts drug effects metabolism ultrastructure MeSH
- Plant Extracts pharmacology MeSH
- Saccharomyces cerevisiae drug effects growth & development ultrastructure MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- beta-1,3-glucan MeSH Browser
- beta-Glucans * MeSH
- Glucans MeSH
- Congo Red MeSH
- Culture Media MeSH
- Plant Extracts MeSH
Congo red was applied to growing yeast cells and regenerating protoplasts in order to study its effects on wall biogenesis and cell morphogenesis. In the presence of the dye, the whole yeast cells grew and divided to form chains of connected cells showing aberrant wall structures on both sides of the septum. The wall-less protoplasts in solid medium with the dye exhibited an abnormal increase in volume, regeneration of aberrant cell walls and inability to carry out cytokinesis or protoplast reversion to cells. In liquid medium, the protoplasts synthesized glucan nets composed mainly of thin fibrils orientated at random, whereas normally, in the absence of dye, the nets consist of rather thick fibrils, 10 to 20 nm in width, assembled into broad ribbons. These fibrils are known to consist of triple 6/1 helical strands of (1----3)-beta-D-glucan aggregated laterally in crystalline packing. The thin fibrils (c. 4 to 8 nm wide) can contain only a few triple helical strands (c. 1.6 nm wide) and are supposed to be prevented from further aggregation and crystallization by complexing with Congo red on their surfaces. Some loose triple 6/1 helical strands (native elementary fibrils) are also discernible. They represent the first native (1----3)-beta-D-glucan elementary fibrils depicted by electron microscopy. The effects of Congo red on growth and the wall structure in normal cells and regenerating protoplasts in solid medium can be explained by the presence of a complex which the dye forms with (helical) chain parts of the glucan network and which results in a loss of rigidity by a blocked lateral interaction between the helices.
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J Cell Biol. 1980 Nov;87(2 Pt 1):442-50 PubMed
J Cell Biol. 1991 Jul;114(1):111-23 PubMed
J Gen Microbiol. 1976 Jan;92 (1):207-20 PubMed
J Cell Biol. 1963 Jun 1;17(3):609-28 PubMed
Science. 1975 Oct 3;190(4209):54-6 PubMed
Science. 1980 Nov 21;210(4472):903-6 PubMed
Proc Natl Acad Sci U S A. 1977 Oct;74(10):4351-5 PubMed
Nature. 1961 Nov 11;192:580-1 PubMed
Proc Natl Acad Sci U S A. 1988 Jul;85(13):4735-9 PubMed
J Bacteriol. 1974 Aug;119(2):564-75 PubMed
J Basic Microbiol. 1985;25(3):161-74 PubMed
Curr Top Cell Regul. 1974;8(0):1-32 PubMed
Arch Microbiol. 1986 Jan;143(4):387-95 PubMed
Microbiol Sci. 1988 Dec;5(12):370-5 PubMed
Antonie Van Leeuwenhoek. 1953;19(1):1-24 PubMed
Carbohydr Res. 1975 Aug;43(1):200-3 PubMed
J Cell Biol. 1974 Jul;62(1):66-76 PubMed
J Bacteriol. 1967 Jul;94(1):192-5 PubMed
J Gen Microbiol. 1983 May;129(5):1577-82 PubMed
Cytobios. 1987;49(197):89-97 PubMed
Biochem J. 1966 Nov;101(2):36C-38C PubMed
Acta Physiol Acad Sci Hung. 1954;5(1-2):213-40 PubMed
Biochemistry. 1977 Mar 8;16(5):908-14 PubMed
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6678-82 PubMed