Using molecular fine structure to identify optimal methods of extracting fungal glycogen

被引:0
|
作者
Ding, Zhen [1 ,2 ]
Li, Changfeng [3 ]
Neoh, Galex K. S. [4 ]
Li, Enpeng [1 ,2 ]
Gilbert, Robert G. [1 ,2 ,5 ]
机构
[1] Yangzhou Univ, Coll Agr, Jiangsu Key Lab Crop Genom & Mol Breeding, Key Lab Plant Funct Genom,Minist Educ, Yangzhou 225009, Peoples R China
[2] Yangzhou Univ, Coinnovat Ctr Modern Prod Technol Grain Crops, Yangzhou 225009, Peoples R China
[3] Yangzhou Univ, Dept Food Sci & Engn, Yangzhou 225009, Peoples R China
[4] Shanghai Univ, Sch Med, Shanghai 200444, Peoples R China
[5] Univ Queensland, Ctr Nutr & Food Sci, Queensland Alliance Agr & Food Innovat, Brisbane, Qld 4072, Australia
基金
中国国家自然科学基金;
关键词
Glycogen; Extraction; SEC; CHEMICAL-COMPOSITION; NUTRITIONAL-VALUE; DIURNAL CHANGES; POLYSACCHARIDES; ETHANOL; MUSHROOMS; STARCH;
D O I
10.1016/j.ijbiomac.2024.132445
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glycogen is a highly branched glucose polymer that is an energy storage material in fungi and animals. Extraction of glycogen from its source in a way that minimizes its molecular degradation is essential to investigate its native structure. In this study, the following extraction methods were compared: sucrose gradient density ultracentrifugation, thermal alkali, hot alcohol and hot water extractions. Molecular-size and chainlength distributions of glycogen were measured by size-exclusion chromatography and fluorophore-assisted carbohydrate electrophoresis, respectively. These two fine-structure features are the most likely structural characteristics to be degraded during extraction. The results show that the thermal alkali, hot alcohol and hot water extractions degrade glycogen molecular size and/or chain-length distributions, and that sucrose gradient density ultracentrifugation with neither high temperature nor alkaline treatment is the most suitable method for fungal glycogen extraction.
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页数:8
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