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作 者:张海波[1,2,3] IMRAN Khan KUMAR Saurav 张丽萍 方壮杰[1,2] 张鑫雅 彭方 张长生 ZHANG Haibo;IMRAN Khan;KUMAR Saurav;ZHANG Liping;FANG Zhuangjie;ZHANG Xinya;PENG Fang;ZHANG Changsheng(Key Laboratory of Tropical Marine Bio-resources and Ecology,Guangdong Key Laboratory of Marine Materia Medica,RNAM Center for Marine Microbiology,South China Sea Institute of Oceanology,Chinese Academy of Sciences,Guangzhou 510301,China;University of Chinese Academy of Sciences,Beijing 100049,China;Southern Marine Science and Engineering Guangdong Laboratory(Guangzhou),Guangzhou 511458,China;Laboratory of Algal Biotechnology-Centre-Algatech,Institute of Microbiology of the Czech Academy of Sciences,Trebon 37981,Czech Republic;Wuhan University,China Center for Type Culture Collection,Wuhan 430072,China)
机构地区:[1]热带海洋生物资源与生态重点实验室,广东省海洋药物重点实验室,中国科学院南海海洋研究所海洋微生物研究中心,广东广州510301 [2]中国科学院大学,北京100049 [3]南方海洋科学与工程广东省实验室(广州),广东广州511458 [4]海藻生物技术实验室–海藻技术中心,捷克科学院微生物研究所,捷克共和国特热邦37981 [5]武汉大学,中国典型培养物保藏中心,湖北武汉430072
出 处:《热带海洋学报》2023年第2期132-140,共9页Journal of Tropical Oceanography
基 金:南方海洋科学与工程广东省实验室(广州)重大专项团队项目(GML2019ZD0406);国家自然科学基金项目(81872778,41911530078);国家重点研发计划项目(2018YFC1406705,2018YFC1406704)。
摘 要:从一块腐烂的鲸鱼骨头分离鉴定了一株真菌Penicillium sp. S2014503。利用大米固体发酵培养技术从该菌产物中获得10个化合物,通过核磁共振波谱数据比对分析结合质谱数据分析,手性化合物测定旋光值或者进行X-射线单晶衍射分析后将这10个化合物分别鉴定为emodin(1)、citreorosein(2)、tetrahydroaltersolanolB(3)、conioxanthoneA(4)、chrysogine(5)、pyramidamycin B (6)、germicidin O (7)、2-(6-hydroxy-5,7-dimethylbenzefuranone-4-yl) acetaldehyde (8)、astrophenone (9)和chenopodolans A (10)。经生物活性测试发现,化合物1和2对藤黄微球菌具有弱的抑制活性,化合物1、2和4对卤虫幼虫具有显著的致死毒性。此外,化合物1是中药大黄和虎杖的主要致泻成分。文章首次报道了来源于海洋动物样品鲸鱼骨的真菌Penicillium sp.能够生产大黄素类等活性天然产物。Penicillium sp.S2014503 was isolated from a rotten whale bone sample.Constituent analysis and bioactivity evaluation of S2014503 were carried out to find more bioactive compounds from this fungus.Chemical structures of the purified compounds produced by S2014503 were determined by comprehensive analysis of NMR(nuclear magnetic resonance),MS(Mass spectrum)data of each compound.Stereochemistry of chiral compounds were elucidated by comparison of specific rotation value with the reported ones or determined by X-ray diffraction analysis.Ten compounds emodin(1),citreorosein(2),tetrahydro altersolanol B(3),conioxanthone A(4),chrysogine(5),pyramidamycin B(6),germicidin O(7),2-(6-hydroxy-5,7-dimethylbenzefuranone-4-yl)acetaldehyde(8),astrophenone(9),and chenopodolans A(10)were found in the fermentation product of S2014503 which was cultured on a solid state rice medium.Bioactivities of all the isolated compounds were evaluated for the antibacterial activities and cytotoxicity against brine-shrimp larvae.Compounds 1 and 2 showed weak activity against Gram positive bacteria Micrococcus luteus.Compounds 1,2 and 4 were significantly cytotoxic against brine-shrimp larvae(Artemia salina)after 6 hours of incubation at room temperature.Interestingly,compound 1 was a well-known laxative ingredient of Traditional Chinese Medicine Rheum officinale and Polygonam cuspidatum.This work is the first report on the emodin analogs from a whale bone derived fungus Penicillium sp.
分 类 号:P735.4[天文地球—海洋生物学]
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