稻黄单胞菌
青枯菌
杨梅素
抗菌剂
苯并咪唑
EC50型
化学
生物测定
最小抑制浓度
微生物学
核化学
生物
生物化学
体外
病菌
类黄酮
有机化学
山奈酚
抗氧化剂
遗传学
作者
Mei Chen,Xuemei Tang,Tingting Liu,Feng Peng,Qing Zhou,Hui Luo,Ming He,Wei Xue
出处
期刊:Fitoterapia
[Elsevier]
日期:2020-12-11
卷期号:149: 104804-104804
被引量:16
标识
DOI:10.1016/j.fitote.2020.104804
摘要
A series of novel myricetin derivatives containing benzimidazole skeleton were constructed. The structure of compound 4g was further corroborated via X-ray single crystal diffractometer. The antimicrobial bioassays showed that all compounds exhibited potent inhibitory activities against Xanthomonas axonopodis pv. Citri (Xac), Ralstonia solanacearum (Rs) and Xanthomonas oryzae pv. Oryzae (Xoo) in vitro. Significantly, compound 4q showed the best inhibitory activities against Xoo, with the EC50 value of 8.2 μg/mL, which was better than thiodiazole copper (83.1 μg/mL) and bismerthiazol (60.1 μg/mL). In vivo experimental studies showed that compound 4q can treat rice bacterial leaf blight at 200 μg/mL, and the corresponding curative and protection efficiencies were 45.2 and 48.6%, respectively. Meanwhile, the antimicrobial mechanism of the compounds 4l and 4q were investigated through scanning electron microscopy (SEM). Studies showed that compounds 4l or 4q can cause deformation or rupture of Rs or Xoo cell membrane. These results indicated that novel benzimidazole-containing myricetin derivatives can be used as a potential antibacterial reagent.
科研通智能强力驱动
Strongly Powered by AbleSci AI