Taxonomic group: fungi / Basidiomycota
(Phylum: Basidiomycota)
Organ / tissue: cell culture
The structure was elucidated in this paperNCBI PubMed ID: 24708983Publication DOI: 10.1016/j.carbpol.2014.01.064Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: de Assis SA <sandrinhaassis

yahoo.com.br>
Institutions: Laboratório de Enzimologia e Tecnologia de Fermentação, Departamento de Saúde, Universidade Estadual de Feira de Santana (UEFS), Bahia, Brazil, Departamento de Saúde, Universidade Estadual de Feira de Santana (UEFS), Bahia, Brazil, Departamento de Química Orgânica, Instituto de Química, Universidade Federal da Bahia, Campus Universitário de Ondina, Salvador, Brazil
β-D-glucans are polymers of d-glucose monomers found in the cell walls of many bacteria, plants, fungi and yeasts. A variety of β-D-glucans differing in structures have been isolated from various sources and their biological activity to be regulated by various structural factors, such as the primary structure, molecular weight, solubility, and conformation. This study investigated the effect of extraction time and temperature on the yield of β-D-glucan produced by Rhodotorula mucilaginosa. A statistical Doehlert design was applied to determine the important effects and interactions of these independent variables on the yield of β-D-glucan, the dependent variable. Significant models were obtained. The best yield was of 25% obtained after 128 min of extraction in a temperature of 72 C. The polysaccharides were characterized as (1→3)-β-D-glucan by methods spectroscopic (FT-IR, 1HNMR and 13CNMR). In addition, the antinociceptive effect was evaluated using different experimental tests (acetic acid-induced writhing test, formalin test and tail immersion test). The (1→3)-β-D-glucan showed a potent peripheral antinociceptive effect, possibly by the inhibition of inflammatory mediators.
optimization, response surface methodology, β-D-glucan, Rhodotorula mucilaginosa, Antinociceptive
Structure type: homopolymer ; 78200
Location inside paper: p.296, fig.4
Compound class: glucan
Contained glycoepitopes: IEDB_1397514,IEDB_142488,IEDB_146664,IEDB_153543,IEDB_158555,IEDB_161166,IEDB_2278476,IEDB_2278477,IEDB_558869,IEDB_857743,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, FTIR, HPSEC, extraction, biological assay, phenol-sulfuric acid assay
Biological activity: 30 mg/kg dose inhibited the acetic acid-induced writhing response significantly; treatment with (1−3)-β-D-glucan (30 mg/kg) 30 min before the formalin caused antinociceptive effect (P<0.005) in the late phase, but not early phase, of the formalin test
Comments, role: The best yield was of 25% obtained after 128 min of extraction in a temperature of 72 C
Related record ID(s): 4991, 46556, 46596
NCBI Taxonomy refs (TaxIDs): 5537Reference(s) to other database(s): GTC:G51056AN
Show glycosyltransferases
NMR conditions: in vol 86%D2O / vol 14%DMSO-d6
[as TSV]
13C NMR data:
Linkage Residue C1 C2 C3 C4 C5 C6
bDGlcp 105 74.0 86.1 72.0 76.4 61.5
1H NMR data:
missing...
13C NMR data:
| Linkage | Residue | C1 | C2 | C3 | C4 | C5 | C6 |
| | bDGlcp | 105 | 74.0 | 86.1 | 72.0 | 76.4 | 61.5 |
|
There is only one chemically distinct structure: