Taxonomic group: fungi / Basidiomycota
(Phylum: Basidiomycota)
NCBI PubMed ID: 38286552Publication DOI: 10.1016/j.carbpol.2024.121782Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: Yin JY <yinjy

ncu.edu.cn>; Nie SP <spnie

ncu.edu.cn>
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
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
Structure type: structural motif or average structure
Location inside paper: Fig. 1, mannogalactoglucan
Compound class: polysaccharide, mannogalactoglucan
Contained glycoepitopes: IEDB_136906,IEDB_137472,IEDB_137485,IEDB_141794,IEDB_141806,IEDB_142488,IEDB_144983,IEDB_144998,IEDB_146664,IEDB_151528,IEDB_152206,IEDB_190606,IEDB_983930,IEDB_983931,SB_192,SB_44,SB_7,SB_72
Comments, role: review; aDManp in the article changed to the bDManp due to the original structure in reference
Related record ID(s): 45710
NCBI Taxonomy refs (TaxIDs): 1562957
Show glycosyltransferases
There is only one chemically distinct structure:
Taxonomic group: fungi / Ascomycota
(Phylum: Ascomycota)
The structure was elucidated in this paperPublication DOI: 10.1016/j.carbpol.2006.06.003Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: lurong

isc.meiji.ac.jp
Institutions: Department of Industrial Chemistry, School of Science and Technology, Meiji University, Kawasaki-shi, Japan, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China, Applied Chemistry Department, Kitami Institute of Technology, Kitami, Japan
A water-soluble polysaccharide-part-2 separated from Paecilomyces tenuipes Samson was determined to be homogeneous by gel permeation chromatography (GPC). HPLC showed a monosaccharide containing d-glucose, d-galactose, and d-mannose at a ratio of about 2:1:1. The number-average molecular weight was estimated to be 10200. The specific rotation was determined to be [α]D2O = + 54 °. The GC-MS analysis of hydrolysates obtained from acid-catalyzed hydrolysis of both Paecilomyces tenuipes Samson-part-2 and its methylated product showed that it has a β-(1→6)-d-glucose main chain with β-(1→6)-d-mannose and β-(2→6)-d-galactose side chains. The results obtained from IR, 1H NMR, and 13C NMR analyses confirmed the proposed structure.
polysaccharide, HPLC, GC-MS, GPC, Paecilomyces tenuipes
Structure type: structural motif or average structure ; 10200
Location inside paper: p.346, paragraph 2, fig.6
Compound class: mannogalactoglucan
Contained glycoepitopes: IEDB_135614,IEDB_136044,IEDB_137472,IEDB_137485,IEDB_141794,IEDB_141806,IEDB_142488,IEDB_144983,IEDB_146664,IEDB_152206,IEDB_190606,IEDB_241101,IEDB_983930,IEDB_983931,SB_165,SB_166,SB_187,SB_192,SB_195,SB_44,SB_7,SB_72,SB_88
Methods: 13C NMR, 1H NMR, methylation, IR, GC-MS, acid hydrolysis, HPLC, GPC, optical rotation measurement, CC, evaporation
Comments, role: NMR signals of anomeric protons and carbons are published
NCBI Taxonomy refs (TaxIDs): 45847
Show glycosyltransferases
NMR conditions: in D2O / DSS at 313 K
1H NMR data: present in publication
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13C NMR data: present in publication
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There is only one chemically distinct structure: