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Studies on the secondary metabolites of a marine-derived fungus Verticillium sp. SN-1
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Yan-liang QU1, Yong-zheng LIU1, Mei-fang PAN2, Le ZHOU2, *, Jian HUANG1, *
Acta Pharmaceutica Sinica | 2026, 61(7) : 2603 - 2610
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Acta Pharmaceutica Sinica | 2026, 61(7): 2603-2610
• Original Articles •
Studies on the secondary metabolites of a marine-derived fungus Verticillium sp. SN-1
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Yan-liang QU1, Yong-zheng LIU1, Mei-fang PAN2, Le ZHOU2, *, Jian HUANG1, *
Affiliations
  • 1School of Pharmacy, Harbin Medical University, Harbin 150081, China
  • 2School of Pharmacy, Shenzhen Technology University, Shenzhen 518118, China
Published: 2026-07-12 doi: 10.16438/j.0513-4870.2026-0160
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Verticillium-derived secondary metabolites have demonstrated promising biological activities, including antibacterial, antitumor, and antimalarial effects. To further explore the chemical diversity and bioactive potential of secondary metabolites from the genus Verticillium, the present study aimed to isolate and characterize secondary metabolites from the fermentation broth of the fungal strain Verticillium sp. SN-1 isolated from Daya Bay, Guangdong Province, China and to evaluate their antibacterial activities. Thirteen compounds were isolated from the crude extract of Verticillium sp. SN-1 using a combination of chromatographic techniques, including normal-phase silica gel column chromatography, reversed-phase ODS column chromatography, and semi-preparative high-performance liquid chromatography (HPLC). Their chemical structures were elucidated by comprehensive spectroscopic analyses, such as nuclear magnetic resonance (NMR) spectroscopy, ultraviolet (UV) spectroscopy, and mass spectrometry (MS). Based on spectral data interpretation, the compounds were identified as cytosporone G (1), verticillpyrone A (2), methyl 1, 5-dihydroxy-3-methylxanthone-6-carboxylate (3), acremonidin E (4), acremonoxide (5), alternethanoxin A (6), janthinone (7), 3-deoxy-methylsulochrin (8), astrophenone (9), acremoxanthone F (10), acremoxanthone C (11), acremoxanthone B (12), and acremonidin G (13). Among these isolates, compounds 1 and 2 were characterized as new compounds, while compounds 3-13 were known secondary metabolites. The antibacterial activities of all isolated compounds were evaluated using the broth microdilution method according to established protocols. The results showed that compounds 4 and 10-13 exhibited significant inhibitory effects against methicillin-resistant Staphylococcus aureus (MRSA), with minimum inhibitory concentrations (MIC) of 32, 16, 32, 8, and 8 μg·mL-1, respectively. Additionally, compounds 11-13 displayed inhibitory activities against Enterococcus faecalis, with corresponding MIC values of 32, 32, and 8 μg·mL-1.

marine fungus  /  Verticillium  /  secondary metabolite  /  antibacterial activity
曲晏良, 刘永铮, 潘美芳, 周乐, 黄健. 一株海洋来源真菌Verticillium sp. SN-1的次级代谢产物研究. 药学学报, 2026 , 61 (7) : 2603 -2610 . DOI: 10.16438/j.0513-4870.2026-0160
Yan-liang QU, Yong-zheng LIU, Mei-fang PAN, Le ZHOU, Jian HUANG. Studies on the secondary metabolites of a marine-derived fungus Verticillium sp. SN-1[J]. Acta Pharmaceutica Sinica, 2026 , 61 (7) : 2603 -2610 . DOI: 10.16438/j.0513-4870.2026-0160
Year 2026 volume 61 Issue 7
210
102
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doi: 10.16438/j.0513-4870.2026-0160
  • Receive Date:2026-02-04
  • Online Date:2026-09-21
  • Published:2026-07-12
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  • Received:2026-02-04
  • Revised:2026-05-20
Affiliations
    1School of Pharmacy, Harbin Medical University, Harbin 150081, China
    2School of Pharmacy, Shenzhen Technology University, Shenzhen 518118, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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