The composition of the cell wall of Fusicoccum amygdali
- 1 November 1971
- journal article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 125 (2) , 461-471
- https://doi.org/10.1042/bj1250461
Abstract
1. The cell wall of Fusicoccum amygdali consisted of polysaccharides (85%), protein (4–6%), lipid (5%) and phosphorus (0.1%). 2. The main carbohydrate constituent was d-glucose; smaller amounts of d-glucosamine, d-galactose, d-mannose, l-rhamnose, xylose and arabinose were also identified, and 16 common amino acids were detected. 3. Chitin, which accounted for most of the cell-wall glucosamine, was isolated in an undegraded form by an enzymic method. Chitosan was not detected, but traces of glucosamine were found in alkali-soluble and water-soluble fractions. 4. Cell walls were stained dark blue by iodine and were attacked by α-amylase, with liberation of glucose, maltose and maltotriose, indicating the existence of chains of α-(1→4)-linked glucopyranose residues. 5. Glucose and gentiobiose were liberated from cell walls by the action of an exo-β-(1→3)-glucanase, giving evidence for both β-(1→3)- and β-(1→6)-glucopyranose linkages. 6. Incubation of cell walls with Helix pomatia digestive enzymes released glucose, N-acetyl-d-glucosamine and a non-diffusible fraction, containing most of the cell-wall galactose, mannose and rhamnose. Part of this fraction was released by incubating cell walls with Pronase; acid hydrolysis yielded galactose 6-phosphate and small amounts of mannose 6-phosphate and glucose 6-phosphate as well as other materials. Extracellular polysaccharides of a similar nature were isolated and may be formed by the action of lytic enzymes on the cell wall. 7. About 30% of the cell wall was resistant to the action of the H. pomatia digestive enzymes; the resistant fraction was shown to be a predominantly α-(1→3)-glucan. 8. Fractionation of the cell-wall complex with 1m-sodium hydroxide gave three principal glucan fractions: fraction BB had [α]D +236° (in 1m-sodium hydroxide) and showed two components on sedimentation analysis; fraction AA2 had [α]D −71° (in 1m-sodium hydroxide) and contained predominantly β-linkages; fraction AA1 had [α]D +40° (in 1m-sodium hydroxide) and may contain both α- and β-linkages.Keywords
This publication has 29 references indexed in Scilit:
- Characterization of two cell-wall polysaccharides from Fusicoccum amygdaliBiochemical Journal, 1971
- The Chemistry and Molecular Architecture of the Cell Walls of Penicillium chrysogenumJournal of Biological Chemistry, 1969
- Phosphoglycopeptides from yeast cell wallsBiochemical Journal, 1968
- Cell Wall Chemistry, Morphogenesis, and Taxonomy of FungiAnnual Review of Microbiology, 1968
- The occurrence of α(1–3)glucan in Cryptococcus, schizosaccharomyces and Polyporus species, and its hydrolysis by a Streptomyces culture filtrate lysing cell walls of CryptococcusBiochimica et Biophysica Acta (BBA) - General Subjects, 1968
- The composition of the cell wall of Aspergillus nigerBiochemical Journal, 1965
- The Oxidation of Glucose and Related Compounds by Glucose Oxidase from Aspergillus niger*Biochemistry, 1964
- Phosphorus Assay in Column ChromatographyJournal of Biological Chemistry, 1959
- METHOD FOR THE DETERMINATION OF HEXOSAMINES IN TISSUESJournal of Biological Chemistry, 1953
- A study of enzymes that can break down tobacco-leaf components. 1. Digestive juice of Helix on leaf fibreBiochemical Journal, 1950