Cao Lu, Guo Jiaxuan, Tan Junfeng, Mu Yu, Jiang Yi, Huang Xueshi, Han Li
Institute of Microbial Pharmaceuticals, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China; Key Laboratory of Bioresource Research and Development of Liaoning Province, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China.
Yunnan Institute of Microbiology, Yunnan University, Kunming 650091, China.
Fitoterapia. 2025 Mar;181:106382. doi: 10.1016/j.fitote.2025.106382. Epub 2025 Jan 6.
Fifteen new aliphatic metabolites, 2-methylpyrimidin-4(3H)-ones (1,2), 2-methoxy-2-methyl-1,2-dihydro-3H-pyrrol-3-ones (4a/4b, 5a/5b), butyrolactones (6-9), and aliphatic metabolites (16-20) as well as known pyridin-2(1H)-one (3) and butyrolactone analogues (10-15) were obtained from the fermentation broth of Streptomyces antifungus isolated from the forest soil sample collected in Tengchong, China. Pyrimidin-4(3H)-one derivatives (1, 2) with an individual 2-methylpyrimidin-4(3H)-one skeleton is a kind of rarely reported compound and were firstly obtained from natural source. The structures of the new metabolites were elucidated by comprehensive spectroscopic analysis including data from experimental and calculated ECD spectra as well as Mosher's reagent derivative method. Compounds 1, 2, 18, and 19 exhibited optimal activity against Staphylococcus aureus with MIC values ranged from 12.5 to 50 μg/mL. Further investigation revealed that 1 effectively inhibited biofilm formation and destroyed the preformed biofilm of S. aureus through oxidative damage, thereby exerting antibacterial effect.
从中国腾冲采集的森林土壤样品中分离得到的抗真菌链霉菌发酵液中,获得了15种新的脂肪族代谢产物,即2-甲基嘧啶-4(3H)-酮(1,2)、2-甲氧基-2-甲基-1,2-二氢-3H-吡咯-3-酮(4a/4b,5a/5b)、丁内酯(6-9)和脂肪族代谢产物(16-20),以及已知的吡啶-2(1H)-酮(3)和丁内酯类似物(10-15)。具有单个2-甲基嘧啶-4(3H)-酮骨架的嘧啶-4(3H)-酮衍生物(1,2)是一种鲜有报道的化合物,首次从天然来源获得。通过包括实验和计算ECD光谱数据以及Mosher试剂衍生化方法在内的综合光谱分析,阐明了新代谢产物的结构。化合物1、2、18和19对金黄色葡萄球菌表现出最佳活性,MIC值范围为12.5至50μg/mL。进一步研究表明,1通过氧化损伤有效抑制金黄色葡萄球菌生物膜的形成并破坏其预先形成的生物膜,从而发挥抗菌作用。