Shi Xiao-Shan, Yang Sui-Qun, Li Xiao-Ming, Li Yan-He, Wang Dun-Jia, Li Xin, Meng Ling-Hong, Zhou Xing-Wang, Wang Bin-Gui
CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, And Laboratory for Marine Biology and Biotechnology, Qingdao Marine Science and Technology Center, Nanhai Road 7, Qingdao, 266071, PR China; College of Chemistry and Chemical Engineering, Hubei Normal University, Cihu Road 11, Huangshi, 435002, PR China.
CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, And Laboratory for Marine Biology and Biotechnology, Qingdao Marine Science and Technology Center, Nanhai Road 7, Qingdao, 266071, PR China.
Phytochemistry. 2025 May;233:114379. doi: 10.1016/j.phytochem.2025.114379. Epub 2025 Jan 3.
Seven previously undescribed polyketide derivatives, fusariumtides A-G (1-7), together with three known analogues (8-10), were isolated from the culture extract of Fusarium asiaticum QA-6, an endophytic fungus obtained from the fresh stem tissue of the medicinal plant Artemisia argyi H. Lev. & Vaniot. Their structures were elucidated by detailed interpretation of 1D/2D NMR spectroscopic and mass spectrometric data, and the absolute configuration of compound 1 was established on the basis of X-ray crystallographic analysis and ECD and specific rotation (SR) calculations. The isolated compounds, which possessed a functionalized decalin moiety, were evaluated for antimicrobial activities. Compounds 1 and 10 exhibited broad-spectrum inhibitory activities against nine tested pathogenic bacteria with MIC values ranging from 1 to 64 μg/mL, while compound 8 showed potent inhibitory activities against aquatic pathogens Aeromonas hydrophilia, Pseudomonas aeruginosa, Vibrio harveyi, and V. vulnificus, which were comparable to/or stronger than those of the positive control chloramphenicol.
从药用植物艾蒿新鲜茎组织中分离得到的内生真菌亚洲镰孢菌QA-6的培养提取物中,分离出7种此前未描述的聚酮化合物衍生物,即镰孢菌素A-G(1-7),以及3种已知类似物(8-10)。通过对一维/二维核磁共振光谱和质谱数据的详细解析阐明了它们的结构,并基于X射线晶体学分析、电子圆二色谱(ECD)和比旋光度(SR)计算确定了化合物1的绝对构型。对具有官能团化十氢化萘部分的分离化合物进行了抗菌活性评估。化合物1和10对9种测试病原菌表现出广谱抑制活性,最低抑菌浓度(MIC)值范围为1至64μg/mL,而化合物8对嗜水气单胞菌、铜绿假单胞菌、哈维氏弧菌和创伤弧菌等水产病原菌表现出强效抑制活性,与阳性对照氯霉素相当或更强。