Found 2 structures.
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1. Compound ID: 21696
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b-D-Glcp-(1-3)-+
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-6)-b-D-Glcp-(1-3)-a-D-Galp-(1-6)-{{{-b-D-Glcp-(1-6)-}}}/n=2/-b-D-Glcp-(1-3)-b-D-Glcp-(1- |
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Structure type: structural motif or average structure
; 15300
Compound class: glucogalactan
Contained glycoepitopes: IEDB_135614,IEDB_136906,IEDB_137472,IEDB_140529,IEDB_141794,IEDB_141806,IEDB_142488,IEDB_146664,IEDB_151528,IEDB_153543,IEDB_167069,IEDB_190606,IEDB_241101,IEDB_983931,SB_192,SB_7
The structure is contained in the following publication(s):
- Article ID: 8767
Siu KC, Xu L, Chen X, Wu JY "Molecular properties and antioxidant activities of polysaccharides isolated from alkaline extract of wild Armillaria ostoyae mushrooms" -
Carbohydrate Polymers 137 (2016) 739-746
This study aims to discover novel and bioactive polysaccharides (PS) from wild Armillaria ostoyae, a honey mushroom species. Two PS designated AkPS1V-1 (66.6 kDa) and AkPS1V-2 (15.3 kDa) were isolated and fractionated by anion ion exchange (IEC) and size exclusion chromatography (SEC) from the alkaline extract of A. ostoyae mushrooms. AkPS1V-1 was a glucan composed of solely glucose residues and AkPS1V-2 a heteropolysaccharide composed of glucose and galactose at 6:1 molar ratio. AkPS1V-2 exhibited higher antioxidant activities than AkPS1V-1 based on reducing power, radical scavenging and metal chelating assays. The structure of AkPS1V-2 was further analyzed and elucidated as a branched galactoglucan with a backbone composed of (1→6)-β-D-glucopyranosyl, (1→3)-β-D-glucopyranosyl, (1→3)-α-D-galactopyranosyl and (1→3,6)-β-D-glucopyranosyl residues at 3:1:1:1 ratio, and side chain of (1→3)-β-D-glucopyranosyl residue. This is the first report on a pure PS structure and its antioxidant activities from this mushroom species.
structure, polysaccharides, extraction, Antioxidant activity, Fractionation, Armillaria ostoyae
NCBI PubMed ID: 26686187Publication DOI: 10.1016/j.carbpol.2015.05.061Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: Wu JY
Institutions: Department of Applied Biology & Chemical Technology, State Key Laboratory of Chinese Medicine and Molecular Pharmacology in Shenzhen, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, College of Agricultural Resource and Environment, Heilongjiang University, Harbin, China
Methods: 13C NMR, 1H NMR, GC-MS, FTIR, HPLC, viscosity measurement, acetylation, statistical analysis, methylation analysis, SEC, reduction with NaBH4, antioxidant activities, HPGPC, HMBC, radical scavenging assay, TFA hydrolysis
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2. Compound ID: 23635
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b-D-Glcp-(1-2)-+
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-6)-b-D-Glcp-(1-6)-b-D-Glcp-(1-6)-b-D-Galp-(1- |
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Structure type: structural motif or average structure
Compound class: polysaccharide, galactoglucan
Contained glycoepitopes: IEDB_136044,IEDB_137472,IEDB_141794,IEDB_141806,IEDB_142488,IEDB_146664,IEDB_153218,IEDB_190606,IEDB_241101,IEDB_983931,SB_165,SB_166,SB_187,SB_192,SB_195,SB_7,SB_88
The structure is contained in the following publication(s):
- Article ID: 9709
Liu JJ, Hou YK, Wang X, Zhou XT, Yin JY, Nie SP "Recent advances in the biosynthesis of fungal glucan structural diversity" -
Carbohydrate Polymers 329 (2024) ID 121782
Glucans are the most abundant class of macromolecule polymers in fungi, which are commonly found in Ascomycota and Basidiomycota. Fungal glucans are not only essential for cell integrity and function but also crucial for the immense industrial interest in high value applications. They present a variety of structural characteristics at the nanoscale due to the high regulation of genes and the involvement of stochastic processes in synthesis. However, although recent findings have demonstrated the genes of glucans synthesis are relatively conserved across diverse fungi, the formation and organization of diverse glucan structures is still unclear in fungi. Here, we summarize the structural features of fungal glucans and the recent developments in the mechanisms of glucans biosynthesis. Furthermore, we propose the engineering strategies of targeted glucan synthesis and point out the remaining challenges in the synthetic process. Understanding the synthesis process of diverse glucans is necessary for tailoring high value glucan towards specific applications. This engineering strategy contributes to enable the sustainable and efficient production of glucan diversity
biosynthesis, gene, diversity, glucan, fungi, target glucan
NCBI PubMed ID: 38286552Publication DOI: 10.1016/j.carbpol.2024.121782Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: Yin JY
; Nie SP
Institutions: State Key Laboratory of Food Science and Resources, China-Canada Joint Lab of Food Science and Technology (Nanchang), Nanchang University, Nanchang, China, Food Laboratory of Zhongyuan, Henan, China
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