Nair Vimal, Schuhmann Imelda, Anke Heidrun, Kelter Gerhard, Fiebig Heinz-Herbert, Helmke Elisabeth, Laatsch Hartmut
Institute of Organic and Biomolecular Chemistry, University of Göttingen, Göttingen, Germany.
Institute of Biotechnology and Drug Research, Kaiserslautern, Germany.
Planta Med. 2016 Jun;82(9-10):910-8. doi: 10.1055/s-0042-108204. Epub 2016 Jun 10.
From the gastrointestinal tract of a fish dredged near the South Orkney Islands in Antarctica, we isolated the psychrotolerant bacterial strain T262, which belongs to the species Vibrio splendidus. Investigation of this strain led to the isolation of a series of 15 bis- and trisindole derivatives. Among them, six new indole alkaloids, namely, turbomycin C [4'-n-butoxyphenyl-bis(1H-indol-3-yl)methane, 1a], turbomycin D [4'-n-propoxyphenyl-bis(1H-indol-3-yl)methane, 1b], turbomycin E [4'-ethoxyphenyl-bis(1H-indol-3-yl)methane, 1c], turbomycin F [4'-methoxy-3',5'-dinitrophenyl-bis(1H-indol-3-yl)methane, 2], trisindolal (3a), and 4-(1H-indol-3-yl-sulfanyl)phenol (4). Another new bisindole derivative elucidated as 2-(indol-3-ylmethyl)-indol-3-ylethanol (7a) was obtained together with six known compounds from the psychrotolerant Arthrobacter psychrochitiniphilus strain T406, isolated from the excrement of penguins. Some of the isolated compounds showed activity against both gram-positive and gram-negative bacteria at 10 µg/paper disk. Trisindolal (3a) was active against the peronosporomycetes Botrytis cinerea and Phytophthora infestans, and some of the indole derivatives indicated promising cytotoxicity towards human tumor cell lines. By exhibiting a mean IC50 of 0.45 µg/mL (1.17 µM), trisindolal (3a) showed pronounced potency and selectivity in a panel of 11 human tumor cell lines derived from 10 different tumor histotypes.
我们从在南极洲南奥克尼群岛附近捕捞的一条鱼的胃肠道中,分离出了耐冷细菌菌株T262,它属于灿烂弧菌物种。对该菌株的研究导致分离出了一系列15种双吲哚和三吲哚衍生物。其中有六种新的吲哚生物碱,即土霉素C [4'-正丁氧基苯基-双(1H-吲哚-3-基)甲烷,1a]、土霉素D [4'-正丙氧基苯基-双(1H-吲哚-3-基)甲烷,1b]、土霉素E [4'-乙氧基苯基-双(1H-吲哚-3-基)甲烷,1c]、土霉素F [4'-甲氧基-3',5'-二硝基苯基-双(1H-吲哚-3-基)甲烷,2]、三吲哚醛(3a)和4-(1H-吲哚-3-基硫烷基)苯酚(4)。从企鹅粪便中分离出的耐冷嗜冷几丁质节杆菌菌株T406中,还获得了另一种被鉴定为2-(吲哚-3-基甲基)-吲哚-3-基乙醇(7a)的新双吲哚衍生物以及六种已知化合物。一些分离出的化合物在10 μg/纸片时对革兰氏阳性菌和革兰氏阴性菌均有活性。三吲哚醛(3a)对卵菌灰葡萄孢和致病疫霉有活性,一些吲哚衍生物对人肿瘤细胞系显示出有前景的细胞毒性。三吲哚醛(3a)在一组来自10种不同肿瘤组织类型的11种人肿瘤细胞系中,表现出平均IC50为0.45 μg/mL(1.17 μM),显示出显著的效力和选择性。