Cell wall and cytoskeleton reorganization as the response to hyperosmotic shock in Saccharomyces cerevisiae
Language English Country Germany Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
10816042
DOI
10.1007/s002030000136
Knihovny.cz E-resources
- MeSH
- Cell Wall metabolism ultrastructure MeSH
- Cytoskeleton metabolism ultrastructure MeSH
- Microscopy, Electron MeSH
- Fluorescence MeSH
- Culture Media MeSH
- Mitogen-Activated Protein Kinase Kinases genetics metabolism MeSH
- Mitogen-Activated Protein Kinases genetics metabolism MeSH
- Freeze Fracturing MeSH
- Osmolar Concentration MeSH
- Osmotic Pressure MeSH
- Saccharomyces cerevisiae Proteins * MeSH
- Saccharomyces cerevisiae genetics growth & development ultrastructure MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- HOG1 protein, S cerevisiae MeSH Browser
- Culture Media MeSH
- Mitogen-Activated Protein Kinase Kinases MeSH
- Mitogen-Activated Protein Kinases MeSH
- PBS2 protein, S cerevisiae MeSH Browser
- Saccharomyces cerevisiae Proteins * MeSH
Transfer of exponentially growing cells of the yeast Saccharomyces cerevisiae to hyperosmotic growth medium containing 0.7-1 M KCl, 1 M mannitol, and/or 1 M glycerol caused cessation of yeast growth for about 2 h; thereafter, growth resumed at almost the original rate. During this time, formation of fluorescent patches on the inner surface of cell walls stained with Primulin or Calcofluor white was observed. The fluorescent patches also formed in solutions of KCl or when synthesis of the cell wall was blocked with cycloheximide and/or 2-deoxyglucose. The patches gradually disappeared as the cells resumed growth, and the new buds had smooth cell walls. Electron microscopy of freeze-etched replicas of osmotically stressed cells revealed deep plasma membrane invaginations filled from the periplasmic side with an amorphous cell wall material that appeared to correspond to the fluorescent patches on the cell surface. The rate of incorporation of D-[U-14C]glucose from the growth medium into the individual cell wall polysaccharides during osmotic shock followed the growth kinetics. No differences in cell wall composition between osmotically stressed yeast and control cells were found. Hyperosmotic shock caused changes in cytoskeletal elements, as demonstrated by the disappearance of microtubules and actin microfilaments. After 2-3 h in hyperosmotic medium, both microtubules and microfilaments regenerated to their original polarized forms and the actin patches resumed their positions at the apices of growing buds. The response of S. cerevisiae strains with mutations in the osmosensing pathway genes hog1 and pbs2 to hyperosmotic shock was similar to that of the wild-type strain. We conclude that, besides causing a temporary disassembling of the cytoskeleton, hyperosmotic shock induces a change in the organization of the cell wall, apparently resulting from the displacement of periplasmic and cell wall matrix material into invaginations of the plasma membrane created by the plasmolysis.
References provided by Crossref.org
Structure and biosynthesis of fungal cell walls: methodological approaches