Literature DB >> 603339

Glycogen and other soluble glucans from chytridiomycete and oomycete species.

D B Coulter, J M Aronson.   

Abstract

Dry weight, protein, lipid, and glycogen were determined at various times during cultivation of the Chytridiomycetes, Rhizophydium sphaerotheca and Monoblepharella elongata. M. elongata had relatively stable levels of glycogen, but, in R. sphaerotheca, glycogen levels showed significant changes, particularly in older cultures in which a depletion of glycogen was accompanied by a marked thickening of the cell walls. Glycogen was a significant cellular constituent in both chytridiomycete species. In R. sphaerotheca and M. elongata, respectively, glycogen accounted for as much as 6% and 8.1% of the dry weight. In purified glycogens of both species, only alpha-1,4- and alpha-1,6-linked glucosyl residues were detected and the absorbance spectra of I2-complexes were similar to those of other well characterized glycogens. Purified Rhizophydium glycogen had a beta-amylolysis limit of 43%, and a CL of approximately 12. For the Monoblepharella polysaccharide, the respective values were 45% and 11. In extracts of the Oomycetes, Pythium debaryanum, Mindeniella spinospora, and Apodachlya sp., only beta-1,3- and beta-1,6-linked glucosyl residues were detected. These glucans were not iodophilic nor were they sensitive to alpha-amylase and beta-amylase. The properties of the oomycete polysaccharides suggested that they were similar to the mycolaminarans of Phytophthora spp. Although both investigated chytridiomycete species produced glycogen with typical properties, glycogen was apparently absent in the investigated Oomycetes.

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Year:  1977        PMID: 603339     DOI: 10.1007/bf00446458

Source DB:  PubMed          Journal:  Arch Microbiol        ISSN: 0302-8933            Impact factor:   2.552


  17 in total

1.  Enzymatic determination of the unit chain length of glycogen and related polysaccharides.

Authors:  Z Ggunja-Smith; J J. Marshall; E E. Smith
Journal:  FEBS Lett       Date:  1971-03-22       Impact factor: 4.124

2.  Variation in average unit chain length of glycogen in relation to developmental stage in Blastocladiella emersonii.

Authors:  J Norrman; G Wöber; E C Cantino
Journal:  Mol Cell Biochem       Date:  1975-12-31       Impact factor: 3.396

3.  Detection of sugars on paper chromatograms.

Authors:  W E TREVELYAN; D P PROCTER; J S HARRISON
Journal:  Nature       Date:  1950-09-09       Impact factor: 49.962

4.  Notes on sugar determination.

Authors:  M SMOGYI
Journal:  J Biol Chem       Date:  1952-03       Impact factor: 5.157

5.  Characterization of the -D-glucan from the plastids of Cecropia peltata as a glycogen-type polysaccharide.

Authors:  J J Marshall; F R Rickson
Journal:  Carbohydr Res       Date:  1973-05       Impact factor: 2.104

6.  Physiological studies on Phymatotrichum omnivorum. II. Physicochemical properties of glycogen.

Authors:  M Gunasekaran
Journal:  Arch Mikrobiol       Date:  1972

7.  The preparation of two insoluble forms of the phytohemagglutinin, concanavalin A, and their interactions with polysaccharides and glycoproteins.

Authors:  K O Lloyd
Journal:  Arch Biochem Biophys       Date:  1970-04       Impact factor: 4.013

8.  Composition of cellulin, the unique chitin-glucan granules of the fungus, Apodachlya sp.

Authors:  H Y Lee; J M Aronson
Journal:  Arch Microbiol       Date:  1975-03-10       Impact factor: 2.552

9.  Glucans of oomycete cell walls.

Authors:  J M Aronson; B A Cooper; M S Fuller
Journal:  Science       Date:  1967-01-20       Impact factor: 47.728

10.  Rabbit skeletal muscle glycogen. A morphological and biochemical study of glycogen beta-particles isolated by the precipitation-centrifugation method.

Authors:  J C Wanson; P Drochmans
Journal:  J Cell Biol       Date:  1968-07       Impact factor: 10.539

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  2 in total

1.  Carbohydrate Storage in the Entomopathogenic Fungus Beauveria bassiana.

Authors:  M J Bidochka; N H Low; G G Khachatourians
Journal:  Appl Environ Microbiol       Date:  1990-10       Impact factor: 4.792

2.  Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia).

Authors:  Ramsy Agha; Manja Saebelfeld; Christin Manthey; Thomas Rohrlack; Justyna Wolinska
Journal:  Sci Rep       Date:  2016-10-13       Impact factor: 4.379

  2 in total

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