中华芽孢杆菌的化学成分及其化学分类意义

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiao-Xue Jiang , Lai-Wei Li , Xing-Ping Zhang , Ke-Pu Huang , Wen-Jie Ma , Li-Ping Tang , Kou Wang
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引用次数: 0

摘要

从中华Engleromyces sinensis子实体中分离得到23个化合物,包括3个麦角甾醇(1-3)、5个酚类衍生物(4-8)、5个生物碱(9-13)、1个内酯(14)和9个脂肪类衍生物(15-23)。所有化合物的结构都通过核磁共振波谱与先前报道的数据进行了比较。除化合物4、5、7、9外,其余化合物均为首次从木木科植物中分离得到。化合物1、9、10、16、18、19、20、22对α-葡萄糖苷酶均有体外抑制作用,其中化合物18对α-葡萄糖苷酶的抑制作用最显著(IC50 = 1.58±0.05 μM)。对18进行分子对接,分析潜在的结合位点。此外,还讨论了这些化合物的化学分类意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chemical constituents of Engleromyces sinensis and their chemotaxonomic significance

Chemical constituents of Engleromyces sinensis and their chemotaxonomic significance
Twenty-three compounds were isolated from the fruiting body of Engleromyces sinensis, including three ergosterols (13), five phenolic derivatives (48), five alkaloids (913), one lactone (14), and nine aliphatic derivatives (1523). The structures of all compounds were identified using NMR spectroscopy by comparison with previously reported data. Except for compounds 4, 5, 7, and 9, all other compounds were isolated from the family Xylariaceae for the first time. Compounds 1, 9, 10, 16, 18, 19, 20, and 22 exhibited inhibitory effects on α-glucosidase in vitro, with 18 showing the most significant inhibitory efficacy (IC50 = 1.58 ± 0.05 μM). Molecular docking was performed on 18 to analyze potential binding sites. Additionally, the chemotaxonomic significance of these compounds was discussed.
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来源期刊
Biochemical Systematics and Ecology
Biochemical Systematics and Ecology 生物-进化生物学
CiteScore
3.00
自引率
12.50%
发文量
147
审稿时长
43 days
期刊介绍: Biochemical Systematics and Ecology is devoted to the publication of original papers and reviews, both submitted and invited, in two subject areas: I) the application of biochemistry to problems relating to systematic biology of organisms (biochemical systematics); II) the role of biochemistry in interactions between organisms or between an organism and its environment (biochemical ecology). In the Biochemical Systematics subject area, comparative studies of the distribution of (secondary) metabolites within a wider taxon (e.g. genus or family) are welcome. Comparative studies, encompassing multiple accessions of each of the taxa within their distribution are particularly encouraged. Welcome are also studies combining classical chemosystematic studies (such as comparative HPLC-MS or GC-MS investigations) with (macro-) molecular phylogenetic studies. Studies that involve the comparative use of compounds to help differentiate among species such as adulterants or substitutes that illustrate the applied use of chemosystematics are welcome. In contrast, studies solely employing macromolecular phylogenetic techniques (gene sequences, RAPD studies etc.) will be considered out of scope. Discouraged are manuscripts that report known or new compounds from a single source taxon without addressing a systematic hypothesis. Also considered out of scope are studies using outdated and hard to reproduce macromolecular techniques such as RAPDs in combination with standard chemosystematic techniques such as GC-FID and GC-MS.
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