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Study on the Secondary Metabolites from a Mangrove Rhizophora Stylosa Derived Fungus Diaporthe sp. and Their Antioxidant Activity
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Yuning QIN, Miaoping LIN, Xin QI, Humu LU, Yonghong LIU, Xiaowei LUO*
Chinese Pharmaceutical Journal | 2025, 60(7) : 704 - 709
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Chinese Pharmaceutical Journal | 2025, 60(7): 704-709
Study on the Secondary Metabolites from a Mangrove Rhizophora Stylosa Derived Fungus Diaporthe sp. and Their Antioxidant Activity
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Yuning QIN, Miaoping LIN, Xin QI, Humu LU, Yonghong LIU, Xiaowei LUO*
Affiliations
  • Guangxi Key Laboratory of Marine Drugs, Guangxi University Engineering Research Center of High-Efficient Utilization of Marine Traditional Chinese Medicine Resources, Institute of Marine Drugs, The First Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning 530200, China
Published: 2025-04-08 doi: 10.11669/cpj.2025.07.005
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OBJECTIVE To investigate the secondary metabolites and bioactivities of the mangrove Rhizophora stylosa derived fungus Diaporthe sp. SCSIO 41011. METHODS Various modern chromatographic methods were subjected to isolate and purify the fermentation products of the strain. The chemical structures of the obtained compounds were identified by nuclear magnetic resonance technology as well as literature data. The antibacterial activity, NF-κB luciferase inhibitory activity, and antioxidant activity of the compounds were determined. The antioxidant activity of the compounds was determined by 1,1-diphenyl-2-picrylhydrazy (DPPH) and ferric reducing ability of plasma (FRAP). RESULTS Seven compounds (1-7) were isolated from the fermentation products and were identified as nigrosporapyrone D (1), vermopyrone (2), tyrosol (3), 2-(2-hydroxyethyl)phenol (4), 3-phenylpropane-1,2-diol (5), 4-hydroxyphenethyl acetate (6), 2-hydroxyphenethyl acetate (7). The chemical structure of 2 was confirmed by X-ray single-crystal diffraction method for the first time herein. At the concentration of 1 mg·mL-1, the FRAP values of compounds 3, 6, and 7 were 208.75, 160.03, and 162.75 μmol·L-1, respectively. CONCLUSION Two pyranones (1 and 2) and five phenolic compounds (3-7) are characterized from the fungus, meanwhile compounds 1, 2, 4, 5, and 7 are isolated from the Diaporthe genus for the first time. And compounds 3, 6, and 7 show iron ion reduction/antioxidant capacity. This study would enrich the structural diversity of secondary metabolites of Diaporthe sp., and lays a foundation for further study on the natural products of mangrove endophytic fungi.

marine fungi  /  Diaporthe sp.  /  secondary metabolite  /  polyketide  /  antioxidant activity
Yuning QIN, Miaoping LIN, Xin QI, Humu LU, Yonghong LIU, Xiaowei LUO. Study on the Secondary Metabolites from a Mangrove Rhizophora Stylosa Derived Fungus Diaporthe sp. and Their Antioxidant Activity[J]. Chinese Pharmaceutical Journal, 2025 , 60 (7) : 704 -709 . DOI: 10.11669/cpj.2025.07.005
Year 2025 volume 60 Issue 7
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doi: 10.11669/cpj.2025.07.005
  • Receive Date:2024-08-27
  • Online Date:2025-11-11
  • Published:2025-04-08
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  • Received:2024-08-27
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    Guangxi Key Laboratory of Marine Drugs, Guangxi University Engineering Research Center of High-Efficient Utilization of Marine Traditional Chinese Medicine Resources, Institute of Marine Drugs, The First Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning 530200, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

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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