DNA旋转酶
细菌
生物
DNA
微生物学
致病菌
生物膜
酶
DNA损伤
丁香假单胞菌
生物化学
抗菌剂
最小抑制浓度
抗菌活性
致病性
化学
细菌性疾病
作者
Zhiyan Wang,Congting Gao,Rajamanikandan Sundarraj,Dongxiao Shi,Zhe Ni,Jun-An Ma,XiangJing WANG,Wensheng Xiang,Zhiguang Yuchi,Chongxi Liu
标识
DOI:10.1021/acs.jafc.5c13698
摘要
The growing resistance of phytopathogenic bacteria highlights the need for new bactericides. DNA gyrase, essential in bacteria but absent in plants and animals, is an underexploited target for agricultural bactericides. Here, we modeled the Ralstonia solanacearum GyrA-GyrB-DNA complex using AlphaFold3 and conducted structure-based virtual screening of 1.27 million compounds. Among 100 tested candidates, GI-A14 showed potent, broad-spectrum antibacterial activity against R. solanacearum, Pseudomonas syringae pv tomato, and Xanthomonas oryzae pv oryzae, with minimum inhibitory concentrations of 1-4 μg/mL. Enzymatic assays confirmed that GI-A14 stabilizes the gyrase-DNA cleavage complex, indicating a DNA-interfacial inhibition mechanism. Furthermore, GI-A14 significantly attenuated the pathogenicity and biofilm formation of R. solanacearum. In planta, GI-A14 provided strong protection against bacterial wilt, speck, and blight, outperforming the commercial agent zhongshengmycin. These results establish DNA gyrase as a viable molecular target for plant disease control and identify GI-A14 as a promising lead compound for next-generation green bactericides.
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