王航航, 李刚, 彭晓娉, 娄红祥. 狭叶十大功劳内生真菌Colletotrichum fioriniae F18的次级代谢产物研究J. 药学学报, 2018,53(11): 1862-1867. doi: 10.16438/j.0513-4870.2018-0838
引用本文: 王航航, 李刚, 彭晓娉, 娄红祥. 狭叶十大功劳内生真菌Colletotrichum fioriniae F18的次级代谢产物研究J. 药学学报, 2018,53(11): 1862-1867. doi: 10.16438/j.0513-4870.2018-0838
WANG Hang-hang, LI Gang, PENG Xiao-ping, LOU Hong-xiang. Secondary metabolites from Colletotrichum fioriniae F18, an endophytic fungus isolated from the medicinal plant Mahonia fortuneiJ. Acta Pharmaceutica Sinica, 2018,53(11): 1862-1867. doi: 10.16438/j.0513-4870.2018-0838
Citation: WANG Hang-hang, LI Gang, PENG Xiao-ping, LOU Hong-xiang. Secondary metabolites from Colletotrichum fioriniae F18, an endophytic fungus isolated from the medicinal plant Mahonia fortuneiJ. Acta Pharmaceutica Sinica, 2018,53(11): 1862-1867. doi: 10.16438/j.0513-4870.2018-0838

狭叶十大功劳内生真菌Colletotrichum fioriniae F18的次级代谢产物研究

Secondary metabolites from Colletotrichum fioriniae F18, an endophytic fungus isolated from the medicinal plant Mahonia fortunei

  • 摘要: 对分离自狭叶十大功劳茎中的一株内生真菌Colletotrichum fioriniae F18进行化学成分研究,从其大米发酵产物中分离得到1个新吲哚生物碱makomotindoline B(1)和2个已知吲哚衍生物:3-indoleacetic acidmethyl ester(2)和N-acetyltryptamine(3),以及6个芳香化合物:对羟基苯乙酸(4)、对羟基苯乙醇(5)、对甲氧基苯乙酸(6)、4-hydroxyphenethyl 2-(4-hydroxyphenyl) acetate(7)、regiolone(8)和N-苯乙基乙酰胺(9)。通过质谱和核磁共振等技术确定了上述化合物的结构,并通过圆二色谱ECD量子化学计算确定了化合物1的绝对构型。抗菌活性测试结果表明,化合物1~9Bacillus subtilisStaphylococcus aureusEscherichia coliPseudomonas aeruginosa无明显抑制作用,对基因缺陷型紫色杆菌Chromobacterium violaceum也无群体感应抑制活性。

     

    Abstract: Chemical investigation on the rice culture of an endophytic fungus Colletotrichum fioriniae F18, inhabiting in the stems of the medicinal plant Mahonia fortunei, led to the isolation of nine compounds. They included a new indole alkaloid, makomotindoline B (1), and two known indole derivatives, 3-indoleacetic acid methyl ester (2) and N-acetyltryptamine (3), together with six known aromatic compounds, 2-(4-hydroxyphenyl) acetic acid (4), 4-(2-hydroxyethyl)phenol (5), 2-(4-methoxyphenyl)acetic acid (6), 4-hydroxyphenethyl 2-(4-hydroxyphenyl)acetate (7), regiolone (8) and N-phenethylacetamide (9). The structures of these compounds were elucidated based on the analysis of spectroscopic data including MS and NMR. The absolute configuretion of compound 1 was determined by electronic circular dichroism (ECD) calculation. Antibacterial activity assay indicated that compounds 1-9 had no antibacterial activities against Bacillus subtilis, Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa, as well as no quorum sensing inhibitory (QSI) activity for Chromobacterium violaceum.

     

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