Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1983 Sep;155(3):1088–1093. doi: 10.1128/jb.155.3.1088-1093.1983

Two distinct classes of polyuronide from the cell walls of a dimorphic fungus, Mucor rouxii.

J M Dow, D W Darnall, V D Villa
PMCID: PMC217802  PMID: 6885716

Abstract

Polyuronides were extracted from purified yeast and mycelial walls of Mucor rouxii by sequential treatments with lithium chloride and potassium hydroxide and were fractionated by ion-exchange chromatography on DEAE-Sephadex. Two polymers (I and II) of different acidity were found in both wall types. Polymer I contained D-glucuronic acid, L-fucose, D-mannose, and much smaller amounts of D-galactose. Yeast and mycelial polymer I had similar uronic acid contents but differed in their neutral sugar compositions and molecular weights. Polymer II from both cell types contained largely D-glucuronic acid and had similar molecular weights. On partial acid hydrolysis, both polymers I and II gave rise to insoluble glucuronans which appeared to be homopolymeric. One-third of the total uronosyl residues of polymer I, and almost all of the uronosyl residues of polymer II, were present in homopolymeric segments. However, homopolymers derived from polymers I and II may not be identical.

Full text

PDF
1090

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aune K. C. Molecular weight measurements by sedimentation equilibrium: some common pitfalls and how to avoid them. Methods Enzymol. 1978;48:163–185. doi: 10.1016/s0076-6879(78)48009-7. [DOI] [PubMed] [Google Scholar]
  2. BARTNICKI-GARCIA S., NICKERSON W. J. Isolation, composition, and structure of cell walls of filamentous and yeast-like forms of Mucor rouxii. Biochim Biophys Acta. 1962 Mar 26;58:102–119. doi: 10.1016/0006-3002(62)90822-3. [DOI] [PubMed] [Google Scholar]
  3. BARTNICKI-GARCIA S., NICKERSON W. J. Nutrition, growth, and morphogenesis of Mucor rouxii. J Bacteriol. 1962 Oct;84:841–858. doi: 10.1128/jb.84.4.841-858.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BITTER T., MUIR H. M. A modified uronic acid carbazole reaction. Anal Biochem. 1962 Oct;4:330–334. doi: 10.1016/0003-2697(62)90095-7. [DOI] [PubMed] [Google Scholar]
  5. Bartnicki-Garcia S., Lindberg B. Partial characterization of mucoran: the glucuronomannan component. Carbohydr Res. 1972 Jun;23(1):75–85. doi: 10.1016/s0008-6215(00)81579-7. [DOI] [PubMed] [Google Scholar]
  6. Bartnicki-Garcia S., Lippman E. Fungal morphogenesis: cell wall construction in Mucor rouxii. Science. 1969 Jul 18;165(3890):302–304. doi: 10.1126/science.165.3890.302. [DOI] [PubMed] [Google Scholar]
  7. Bartnicki-Garcia S., Reyes E. Polyuronides in the cell walls of Mucor rouxii. Biochim Biophys Acta. 1968 Nov 12;170(1):54–62. doi: 10.1016/0304-4165(68)90160-8. [DOI] [PubMed] [Google Scholar]
  8. Datema R., van den Ende H., Wessels J. G. The hyphal wall of Mucor mucedo. 1. Polyanionic polymers. Eur J Biochem. 1977 Nov 1;80(2):611–619. doi: 10.1111/j.1432-1033.1977.tb11918.x. [DOI] [PubMed] [Google Scholar]
  9. Dow J. M., Villa V. D. Oligoglucuronide production in Mucor rouxii: evidence for a role for endohydrolases in hyphal extension. J Bacteriol. 1980 Jun;142(3):939–944. doi: 10.1128/jb.142.3.939-944.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kreger D. R. Polyuronides as structural components of cell walls of fungi and green algae. Nature. 1970 Jul 4;227(5253):81–82. doi: 10.1038/227081a0. [DOI] [PubMed] [Google Scholar]
  11. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  12. TREVELYAN W. E., PROCTER D. P., HARRISON J. S. Detection of sugars on paper chromatograms. Nature. 1950 Sep 9;166(4219):444–445. doi: 10.1038/166444b0. [DOI] [PubMed] [Google Scholar]
  13. Taylor R. L., Conrad H. E. Stoichiometric depolymerization of polyuronides and glycosaminoglycuronans to monosaccharides following reduction of their carbodiimide-activated carboxyl groups. Biochemistry. 1972 Apr 11;11(8):1383–1388. doi: 10.1021/bi00758a009. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES