机构地区:[1]湖南人文科技学院研究生教育教学部,湖南娄底417000 [2]中国热带农业科学院热带生物技术研究所,海南省海洋生物资源功能性成分研究与利用重点实验室,海南海口571101
出 处:《热带海洋学报》2025年第2期73-83,共11页Journal of Tropical Oceanography
基 金:国家自然科学基金项目(41776093);农业农村部财政专项(NFZX2021);湖南省研究生教学平台项目(湘教通[2019]370号)。
摘 要:文章对南海海绵共附生真菌Penicillium sp.G5A-11的化学成分及其细胞毒活性进行了研究。综合运用薄层色谱、硅胶柱色谱、凝胶柱色谱以及半制备型高效液相色谱等多种分离技术对海绵共附生真菌Penicillium sp.G5A-11的大米发酵产物进行分离纯化,依据波谱数据和理化常数分析并结合相关的文献数据比对,确定所分离化合物的结构,并用四唑盐比色(methylthiazolyldiphenyl-tetrazolium bromide,MTT)法对所鉴定的化合物进行了细胞毒活性测定。结果显示:从海绵共附生真菌Penicilliumsp.G5A-11中共分离鉴定了17个化合物,其结构分别鉴定为:N-乙酰酪胺(1)、 methyl2-(6-hydroxybenzothiazol-4-yl) acetate (2)、R-甲羟内酯(3)、烟酸(4)、altechromone A (5)、2,5-dimethy-7-hydroxychromone (6)、methyl7-hydroxy-2-methylchromone-5-carboxylate(7)、 stagonoculiepine[(2S,5R)-1-formyl-1,2,3,4-tetrahydro-5H-2,5-epiminobenzo[b]azepin-5-ylacetates](8)、(4R,5S)-5-(hydroxymethyl)-5-methyl-4-(3-oxobutyl)dihydrofuran-2(3H)-one(9)、9α-hydroxy-1,2,3,4,5,10,19-heptanorergosta-7,22-diene-6,9-lact (10)、3β,5α,9α-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one(11)、过氧化麦角甾醇(12)、(22E,24R)-24-methylcholesta-2,22-diene-3β,5α,6β-triol(13)、麦角甾醇(14)、豆甾醇/β-谷甾醇(15)、3β,5α-dihydroxy-(22E,24R)-ergosta-7,22-dien-6-one(16)和3β,5α-dihydroxy-6β-methoxyergosta-7,22-diene(17)。其中,化合物7和9为新天然产物。肿瘤细胞毒活性测试结果表明,化合物10对肿瘤细胞K562 (人慢性髓原白血病细胞)和SGC-7901 (人胃癌细胞)显示出细胞毒活性,其半数最大抑制浓度值分别为(12.07±0.12)μmol·L^(-1)和(13.17±0.02)μmol·L^(-1)。This paper investigated the chemical constituents of Penicillium sp.G5A-11,which was isolated from a sponge in the South China Sea,and their cytotoxicity.Various separation methods,including thin layer chromatography,silica gel column chromatography,gel column chromatography,and semi-preparative high-performance liquid chromatography,were used to isolate compounds from solid-rice culture of this marine derived fungus.Spectroscopic data,along with physical and chemical properties,were utilized to identify the structures of the isolated compounds,and compared with literature data.Their cytotoxic activities were tested by the MTT(methylthiazolyldiphenyl-tetrazolium bromide) method.Seventeen compounds were identified from the marine fungus Penicillium jiangxiense,including N-acetyltryptamine(1),methyl 2-(6-hydroxybenzothiazol-4-yl) acetate(2),Rmevalonolactone(3),nicotinic acid(4),altechromone A(5),2,5-dimethy-7-hydroxychromone(6),methyl 7-hydroxy-2-methylchromone-5-carboxylate(7),stagonoculiepine [(2S,5R)-1-formyl-1,2,3,4-tetrahydro-5H-2,5-epiminobenzo[b]azepin-5-yl acetates](8),(4R,5S)-5-(hydroxymethyl)-5-methyl-4-(3-oxobutyl) dihydrofuran-2(3H)-one(9),9α-hydroxy-1,2,3,4,5,10,19-heptanorergosta-7,22-diene-6,9-lact(10),3β,5α,9α-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one(11),ergosterol peroxide(5α,8α-epidioxy-24(R)-methylcholesta-6,22-dien-3β-ol)(12),(22E,24R)-24-methylcholesta-2,22-diene-3β,5α,6β-triol(13),ergosterol(14),stigmasterol/β-sitosterol(15),3β,5α-dihydroxy-(22E,24R)-ergosta-7,22-dien-6-one(16),and 3β,5α-dihydroxy-6β-methoxyergosta-7,22-diene(17).Among them,compounds 7 and 9 were new natural products.Cytotoxic activity tests showed that compound 10 was moderately cytotoxic to human chronic myeloid leukemia cells(K562) and human gastric cancer cells(SGC-7901) with IC_(50) values of(12.07 ± 0.12) μmol·L^(-1) and(13.17 ± 0.02) μmol·L^(-1),respectively.However,the results of the antiinflammatory activity test revealed that none of the compounds exhibited anti-inflammatory activity.
关 键 词:海洋真菌 Penicillium sp. 化学成分 细胞毒活性
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