多粘菌拟杆菌
肉汤微量稀释
金黄色葡萄球菌
微生物学
生物膜
细菌
抗生素耐药性
抗生素
美国foulbrood
次生代谢物
化学
生物
最小抑制浓度
生物化学
基因
孢子
遗传学
作者
Na Zhao,Mingjiao Huang,Yang Yang,Ruxia Cai,Jian Peng,Guo Guo
标识
DOI:10.3389/fmicb.2025.1617807
摘要
The results show that MEZ6 secondary metabolites can inhibit MRSA growth, prevent biofilm formation, reduce the expression of virulence genes (agrA, spa, and clf-1), disrupt cell structure, increase membrane permeability, and lead to the accumulation of ROS. Through systematic characterization, MEZ6 metabolites maybe tryptophan-associated fraction (TAF). This study establishes a systematic theoretical framework for the development and application of bacterial metabolites.
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