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及其栽培子实体的生物学特性、驯化与抗氧化活性

Biological Characteristics and Domestication of and the Antioxidant Activity of Its Cultivated Fruiting Bodies.

作者信息

Wang Li-Bo, Qi Zheng-Xiang, Zhang Tao, Qian Ke-Qing, Lv Hai-Yan, Zhang Bo, Li Yu

机构信息

Engineering Research Center of Chinese Ministry of Education for Edible and Medicinal Fungi, Jilin Agricultural University, Changchun 130118, China.

College of Mycology, Jilin Agricultural University, Changchun 130118, China.

出版信息

J Fungi (Basel). 2025 Aug 15;11(8):594. doi: 10.3390/jof11080594.

DOI:10.3390/jof11080594
PMID:40863546
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12387684/
Abstract

Single-factor and orthogonal experiments were conducted to investigate the biological characteristics of strains isolated from wild fruiting bodies collected in Tekes County, Xinjiang Uygur Autonomous Region. Building upon the optimal mycelial culture conditions identified, domestication cultivation studies were performed, including experiments to induce fruiting body formation. Liquid strains were inoculated into substrates to monitor developmental stages from primordia formation to mature fruiting bodies, with macroscopic characteristics recorded throughout the cultivation process. Crude polysaccharides were extracted from the cultivated fruiting bodies using the water extraction and ethanol precipitation method. The scavenging rates of these polysaccharides against hydroxyl radicals (OH) and superoxide anion radicals (O) were measured to evaluate their in vitro antioxidant activity. Results demonstrated that the optimal growth conditions for were as follows: sucrose as the preferred carbon source, yeast extract powder as the optimal nitrogen source, a pH of 5.0, and a temperature of 30 °C. Among these factors, pH exerted the most significant influence on the mycelial growth rate, followed by nitrogen source, carbon source, and temperature. Mature fruiting bodies developed approximately 57 days after inoculation with liquid strains. The crude polysaccharide extraction yield from the cultivated fruiting bodies reached 7.07%, with a total polysaccharide content of 24.69% in the extract. The crude polysaccharides exhibited potent radical scavenging activity: at a concentration of 5.0 mg/mL, the hydroxyl radical scavenging rate was 56.74%, while the superoxide anion radical scavenging rate reached 78.3%. These findings indicate that possesses significant antioxidant potential.

摘要

开展单因素试验和正交试验,对从新疆维吾尔自治区特克斯县采集的野生子实体中分离得到的菌株的生物学特性进行研究。基于确定的最佳菌丝体培养条件,进行驯化栽培研究,包括诱导子实体形成的试验。将液体菌种接种到基质中,监测从原基形成到成熟子实体的发育阶段,并在整个栽培过程中记录宏观特征。采用水提取乙醇沉淀法从栽培的子实体中提取粗多糖。测定这些多糖对羟基自由基(OH)和超氧阴离子自由基(O)的清除率,以评估其体外抗氧化活性。结果表明,其最佳生长条件如下:蔗糖为首选碳源,酵母提取物粉为最佳氮源,pH值为5.0,温度为30℃。在这些因素中,pH值对菌丝体生长速率的影响最为显著,其次是氮源、碳源和温度。接种液体菌种后约57天发育出成熟子实体。栽培子实体的粗多糖提取率达到7.07%,提取物中总多糖含量为24.69%。粗多糖表现出较强的自由基清除活性:在浓度为5.0mg/mL时,羟基自由基清除率为56.74%,超氧阴离子自由基清除率达到78.3%。这些结果表明其具有显著的抗氧化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/4315fdff7c55/jof-11-00594-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/e078efd3cdfb/jof-11-00594-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/c8bdf9af9796/jof-11-00594-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/6e13c346064e/jof-11-00594-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/a75f33065ad0/jof-11-00594-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/b243be34ef62/jof-11-00594-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/4315fdff7c55/jof-11-00594-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/e078efd3cdfb/jof-11-00594-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/1b18a69a014a/jof-11-00594-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/636416e45d82/jof-11-00594-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/12e7a03606f2/jof-11-00594-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/c8bdf9af9796/jof-11-00594-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/6e13c346064e/jof-11-00594-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/a75f33065ad0/jof-11-00594-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8822/12387684/4315fdff7c55/jof-11-00594-g010.jpg

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