Taxonomic group: fungi / Basidiomycota
(Phylum: Basidiomycota)
The structure was elucidated in this paperNCBI PubMed ID: 37769376Publication DOI: 10.1016/j.carres.2023.108960Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Z. Qiu <qiuz

hbtcm.edu.cn>; G. Zheng < zgh1227

sina.com>
Institutions: Institute of Biology and Medicine, College of Life Science and Health, Wuhan University of Science and Technology, Wuhan, 430081, China, School of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China
Most reported polysaccharides from Poria cocos (PCPs) in traditional Chinese medicine decoctions were water-soluble heteropolysaccharides while the water-insoluble PCPs were scarcely researched due to the poor water-solubility. In this study, a water-insoluble polysaccharide with high yield of 59%, and high purity with a glucan content of 98.8%, was isolated by diluted sodium hydroxide at low temperature and coded as PCPA. The chemical structure of PCPA was identified as a liner β-glucan with 1,3-linked glycosidic bond by the fourier infrared spectrum (FT-IR), ion chromatography (ICP), gas chromatography and mass spectrometry (GC-MS), and nuclear magnetic resonance (NMR) measurements. Importantly, PCPA was successfully used to construct hydrogels (PCPA-Gs) with good thermal stability, water retention ability and swelling property through simple physical cross-linking, due to the abundance of hydroxyl groups on glucan chains. Moreover, the rheology analysis of PCPA-Gs showed a rapid transition between gel and sol as well as the shear-thinning property. The hydrogel developed in this study holds promise for applications in the food, pharmaceutical, and cosmetic fields.
polysaccharide, polysaccharides, Rheology, Poria cocos, hydrogel
Structure type: homopolymer ; 171000-175000
Location inside paper: Fig. 2F, PCPA
Trivial name: a water-insoluble β-glucan (PCPA)
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, methylation, GC-MS, GC, FTIR, composition analysis, extraction, SEC-MALLS, rheological study, ion chromatography
Comments, role: the possible chemical structure of PCPA
NCBI Taxonomy refs (TaxIDs): 81056
Show glycosyltransferases
NMR conditions: in DMSO-d6 at 298 K
[as TSV]
13C NMR data:
Linkage Residue C1 C2 C3 C4 C5 C6
bDGlcp 103.51 73.34 86.65 68.88 76.80 61.35
1H NMR data:
Linkage Residue H1 H2 H3 H4 H5 H6
bDGlcp 4.52 3.27 3.47 3.22 3.25 3.36-3.41
1H/13C HSQC data:
Linkage Residue C1/H1 C2/H2 C3/H3 C4/H4 C5/H5 C6/H6
bDGlcp 103.51/4.52 73.34/3.27 86.65/3.47 68.88/3.22 76.80/3.25 61.35/3.36-3.41
1H NMR data:
| Linkage | Residue | H1 | H2 | H3 | H4 | H5 | H6 |
| | bDGlcp | 4.52 | 3.27 | 3.47 | 3.22 | 3.25 | 3.36 3.41 |
|
13C NMR data:
| Linkage | Residue | C1 | C2 | C3 | C4 | C5 | C6 |
| | bDGlcp | 103.51 | 73.34 | 86.65 | 68.88 | 76.80 | 61.35 |
|
There is only one chemically distinct structure: