Li Kunlong, Zhu Hongjie, Sun Changli, Tian Ge, Ma Xuan, Saravana Kumar Pachaiyappan, Weng Xiang, Yang Hu, Fang Runping, Liu Weilong, Shang Zhuo, Ma Junying, Ju Jianhua
Key Laboratory of Chemical Biology (Ministry of Education), Shandong Basic Science Research Center (Pharmacy), School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong 250012, China.
CAS 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, 164 West Xingang Road, Guangzhou, Guangdong 510301, China.
Org Lett. 2025 Jan 10;27(1):476-481. doi: 10.1021/acs.orglett.4c04491. Epub 2024 Dec 20.
Metabolic blockade-based genome mining of the marine sediment-derived SCSIO 07745 led to the discovery of 11 novel aminoquinolinone alkaloids, oxazoquinolinones A-J (-), characterized by an oxazolidone[3,2-α]quinoline-5,8-dione scaffold, and oxazoquinolinone K (), featuring an unprecedented fused 6/6/6/5 tetracyclic core ring system. Additionally, 5 new biosynthetic intermediates or shunt products (-) and a known metabolite sannanine () were identified. Their structures were elucidated by extensive spectroscopic analyses and a comparison of electronic circular dichroism and single-crystal X-ray diffraction. On the basis of the functional gene analyses and structures of the intermediates or shunt products, plausible biosynthetic pathways for compounds - were proposed. Additionally, oxazoquinolinone K () obviously inhibited cell invasion of human glioma cell line LN229 cells at 10 μM.
基于代谢阻断的海洋沉积物来源菌株SCSIO 07745的基因组挖掘,发现了11种新型氨基喹啉酮生物碱,即恶唑喹啉酮A - J(-),其特征为恶唑烷酮[3,2 - α]喹啉 - 5,8 - 二酮骨架,以及恶唑喹啉酮K(),具有前所未有的稠合6/6/6/5四环核心环系统。此外,还鉴定出5种新的生物合成中间体或分流产物(-)以及一种已知代谢产物山柑宁()。通过广泛的光谱分析以及电子圆二色性和单晶X射线衍射的比较阐明了它们的结构。基于功能基因分析以及中间体或分流产物的结构,提出了化合物 - 的合理生物合成途径。此外,恶唑喹啉酮K()在10 μM时明显抑制人胶质瘤细胞系LN229细胞的细胞侵袭。