Taxonomic group: fungi / Basidiomycota
(Phylum: Basidiomycota)
Organ / tissue: fruiting bodies
The structure was elucidated in this paperNCBI PubMed ID: 37839837Publication DOI: 10.1016/j.carbpol.2023.121367Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: C.F. Ellefsen <c.f.ellefsen

farmasi.uio.no>
Institutions: Department of Pharmacy, University of Oslo, Sem S?lands vei 3, 1068 Blindern, NO-0371 Oslo, Norway, Department of Biotechnology and Food Science, NTNU Norwegian University of Science and Technology, Sem S?lands vei 6/8, NO-7491 Trondheim, Norway
Fungal β-glucans have received a lot of interest due to their proinflammatory activity towards cells of the innate immune system. Although commonly described as (1➔3)-β-glucans with varying degree of (1➔6)-branching, the fungal β-glucans constitute a diverse polysaccharide class. In this study, the alkali-soluble β-glucans from the edible mushroom Pleurotus eryngii were extracted and characterized by GC, GC-MS and 2D NMR analyses. The extracts contain several structurally different polysaccharides, including a (1➔3)-β-d-glucan with single glucose units attached at O-6, and a (1➔6)-β-d-glucan, possibly branched at O-3. The immunomodulatory activities of the P. eryngii extracts were assessed by investigating their ability to bind to the receptor dectin-1, and their ability to induce production of the proinflammatory cytokines TNF-α, IL-6 and IL-1β in LPS-differentiated THP-1 cells. Although the samples were able to bind to the dectin-1a receptor, they did not induce production of significant levels of cytokines in the THP-1 cells. Positive controls of yeast-derived (1➔3)-β-d-glucans with branches at O-6 induced cytokine production in the cells. Thus, it appears that the P. eryngii β-glucans are unable to induce production of proinflammatory cytokines in LPS-differentiated THP-1 cells, despite being able to activate the human dectin-1a receptor.
NMR, THP-1, Dectin-1, dispersion, mushroom glucans
Structure type: fragment of a bigger structure
Location inside paper: Fig. 2C, table 4, structure 4
Trivial name: pustulan, 1-6-β-glucan, alkali-soluble β-glucan (PeA3)
Compound class: EPS, O-polysaccharide, cell wall polysaccharide, glucan, b-glucan
Contained glycoepitopes: IEDB_135614,IEDB_141806,IEDB_142488,IEDB_146664,IEDB_241101,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, NMR-2D, GC-MS, sugar analysis, GC, cytokine analysis, extraction, statistical analysis, elemental analysis, cell viability assay, DEPT, DLS, bioassays, dispersion method
Related record ID(s): 41035, 41405, 41406
NCBI Taxonomy refs (TaxIDs): 5323Reference(s) to other database(s): GTC:G26777BZ
Show glycosyltransferases
NMR conditions: in DMSO-d6 at 333 K
[as TSV]
13C NMR data:
Linkage Residue C1 C2 C3 C4 C5 C6
bDGlcp 103.3 73.4 76.4 70.0 75.5 68.6
1H NMR data:
Linkage Residue H1 H2 H3 H4 H5 H6
bDGlcp 4.26 3.02 3.19 3.14 3.31 3.59-3.99
1H/13C HSQC data:
Linkage Residue C1/H1 C2/H2 C3/H3 C4/H4 C5/H5 C6/H6
bDGlcp 103.3/4.26 73.4/3.02 76.4/3.19 70.0/3.14 75.5/3.31 68.6/3.59-3.99
1H NMR data:
| Linkage | Residue | H1 | H2 | H3 | H4 | H5 | H6 |
| | bDGlcp | 4.26 | 3.02 | 3.19 | 3.14 | 3.31 | 3.59 3.99 |
|
13C NMR data:
| Linkage | Residue | C1 | C2 | C3 | C4 | C5 | C6 |
| | bDGlcp | 103.3 | 73.4 | 76.4 | 70.0 | 75.5 | 68.6 |
|
There is only one chemically distinct structure: