|
|
|
This article has been:browse 632times Download 424times |
Scan the code! |
|
灰树花菌丝体不同培养时期代谢组学分析 |
刘金容1,2, 张艳成2, 刘 演2, 张 强3, 吕虎强3,4, 牟光福2*
|
1. 广西师范大学 生命科学学院, 广西 桂林 541006;2. 广西喀斯特植物保育与恢复生态学重点实验室, 广西壮族自治区
中国科学院
广西植物研究所, 广西 桂林 541006;3. 桂林医学院 药学院 生药学教研室, 广西 桂林 541199;4. 中华全国供销合作总社西安生漆涂料研究所, 西安 710061
|
|
摘要: |
为了解不同生长时期灰树花(Grifola frondosa)菌丝体的代谢产物差异及其通路,该研究采用HPLC-MS/MS分析方法对培养10、20、30 d的灰树花菌丝体进行分析。结果表明:(1)共42类584种代谢物被鉴定出,其中159种、47种和165种代谢物在对照组(10 d vs 20 d、20 d vs 30 d、10 d vs 30 d)中表现出不同的积累模式,不同培养时间的代谢物成分差异显著。(2)培养10 d产生较多与促进菌丝体生长和氧化供能有关的物质,培养20 d产生或积累了多种对人体有益的次生代谢物,如橄榄苦甙、甘胆酸、N-甲基酪胺、Alprazolam,培养30 d菌丝体中含有多种与产生香气有关的物质。(3)KEGG代谢通路富集分析,10 d vs 20 d比较组、20 d vs 30 d比较组和10 d vs 30 d比较组分别富集到163条、81条、137条代谢通路,氨基酸代谢在菌丝体不同培养时间中的影响最大。该研究初步探索了灰树花菌丝体的差异代谢物及代谢通路,并发现不同培养时间灰树花菌丝体代谢产物具有明显的差异,以及菌丝体中部分成分含量与培养时间有关,对灰树花菌丝体的质量控制和机理研究具有一定的参考价值。 |
关键词: 灰树花菌丝体, 培养时间, 代谢产物, 代谢通路, HPLC-MS/MS |
DOI:10.11931/guihaia.gxzw202309037 |
分类号:Q946 |
文章编号:1000-3142(2024)07-1337-15 |
Fund project:国家自然科学基金(41661012); 广西植物研究所基本业务费(桂植业23009)。 |
|
Metabolomic analysis of Grifola frondosa mycelium in different culture periods |
LIU Jinrong1,2, ZHANG Yancheng2, LIU Yan2, ZHANG Qiang3,
LV Huqiang3,4, MOU Guangfu2*
|
1. College of Life Sciences, Guangxi Normal University, Guilin 541006, Guangxi, China;2. Guangxi Key Laboratory of Plant Conservation
and Restoration Ecology in Karst Terrain, Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy
of Sciences,Guilin 541006, Guangxi, China;3. Department of Pharmacognosy, Pharmacy School, Guilin Medical
University, Guilin 541199, Guangxi, China;4. Xi'an Research Institute of Chinese Lacquer Under All
China Federation of Supply and Marketing Cooperatives, Xi'an 710061, China
|
Abstract: |
To gain a comprehensive understanding of the metabolite differences and metabolic pathways involved in the mycelium of Grifola frondosa during various culture periods, this study employed HPLC-MS/MS analysis to thoroughly investigate the mycelium cultured for 10, 20, 30 d. The results were as follows:(1)We identified a total of 584 metabolites belonging to 42 different categories. Notably, among these metabolites, 159, 47, and 165 metabolites exhibited distinct accumulation patterns in the control comparison groups of 10 d vs 20 d, 20 d vs 30 d, and 10 d vs 30 d, respectively. This significant variation in metabolite composition across different culture periods suggested that the metabolic activities of the mycelium were dynamically changing as it grew.(2)During the early stage of culturing(10 d), the mycelium produced a higher concentration of metabolites related to promoting its growth and oxidative energy supply. As the culture progressed to 20 d, the mycelium began to produce or accumulate various secondary metabolites that were beneficial to humans. These included compounds like oleuropein, glycyrrhetic acid, N-methyltyramine, and alprazolam, which were known for their biological activities and potential in health benefits. As the culture progressed to 30 d, the mycelium contained multiple compounds were associated with aroma production.(3)To further understand the underlying metabolic processes, we conducted KEGG metabolic pathway enrichment analysis. This analysis revealed that the comparison groups of 10 d vs 20 d, 20 d vs 30 d, and 10 d vs 30 d were enriched in 163, 81, and 137 metabolic pathways, respectively. Among these, amino acid metabolism emerged as the most significantly influenced pathway in different culture periods, and this finding underscored the importance of amino acid metabolism in driving the metabolic activities of the mycelium during its growth cycle. In conclusion, this study initially explores the differential metabolites and metabolic pathways of the mycelium of G. frondosa, and finds that there are significant differences in the metabolites of the mycelium of G. frondosa in different culture periods, and that the contents of some components in the mycelium is related to the culture time, which has a certain reference value for the quality control and mechanism research of the mycelium of G. frondosa. |
Key words: mycelium of Grifola frondosa, culture time, metabolite, metabolic pathway, HPLC-MS/MS |
|
|
|
|
|