Zhang Miaohe, Feng Shuang, Song Junrong, Ruan Xianghui, Xue Wei
State Key Laboratory of Green Pesticide, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for R&D of Fine Chemicals, Guizhou University, Guiyang 550025, PR China; School of Chemical Engineering, Guizhou Institute of Technology, Guiyang 550025, PR China.
State Key Laboratory of Green Pesticide, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for R&D of Fine Chemicals, Guizhou University, Guiyang 550025, PR China; State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang 550014, PR China; Natural Products Research Center of Guizhou Province, Guiyang 550014, PR China.
J Adv Res. 2025 Jul;73:133-146. doi: 10.1016/j.jare.2024.08.039. Epub 2024 Sep 2.
Plant bacterial diseases take an incalculable toll on global food security. The indiscriminate use of chemical synthetic pesticide not only facilitates pathogen resistance of pathogenic bacteria, but also poses a major threat to human health and environmental protection. Therefore, it is of great economic value and scientific significance to develop a new antibacterial drug with environmental friendliness and unique mechanism of action.
To design and synthesize formononetin derivatives based on natural products, evaluate their in vitro and in vivo antibacterial activities and elucidate the mechanisms involved.
The synthesis was carried out by classical active group splicing method. The antibacterial activities were evaluated using turbidimetry and pot experiments. The antibacterial mechanism was further investigated using scanning electron microscopy (SEM), virulence factors, defense enzymes activities, proteomics and metabolomics.
40 formononetin derivatives containing benzyl piperidine were designed and synthesized. The antibacterial results demonstrated that H32 exhibited the most potent inhibitory effect against Xanthomonas oryzae pv. Oryzae (Xoo) with the EC of 0.07 μg/mL, while H6 displayed the highest inhibitory activity against Xanthomonas axonopodis pv. Citri (Xac) with the EC of 0.24 μg/mL. Furthermore, the control efficacy of H32 against rice bacterial leaf blight (BLB) and H6 against citrus canker (CC) was validated through pot experiments. SEM, virulence factors and host enzyme activities assay indicated that H32 could not only reduce the virulence of Xoo, but also activate the activities of defense enzymes and improve the disease resistance of host plants. The proteomics and metabolomics analysis demonstrated that H32 could inhibit the synthesis of branched-chain amino acids, make Xoo cells in a starvation state, inhibit its proliferation, weaken its virulence and reduce its colonization and infection of host cells.
Formononetin derivatives containing benzyl piperidine could be used as potentially effective inhibitors against Xanthomonas spp.
植物细菌病害对全球粮食安全造成了难以估量的损失。化学合成农药的滥用不仅会促使病原菌产生抗性,还对人类健康和环境保护构成重大威胁。因此,开发一种具有环境友好性和独特作用机制的新型抗菌药物具有重大的经济价值和科学意义。
基于天然产物设计并合成芒柄花素衍生物,评估其体外和体内抗菌活性,并阐明其作用机制。
采用经典的活性基团拼接法进行合成。通过比浊法和盆栽试验评估抗菌活性。利用扫描电子显微镜(SEM)、毒力因子、防御酶活性、蛋白质组学和代谢组学进一步研究抗菌机制。
设计并合成了40种含苄基哌啶的芒柄花素衍生物。抗菌结果表明,H32对水稻白叶枯病菌(Xoo)表现出最强的抑制作用,其EC50为0.07 μg/mL,而H6对柑橘溃疡病菌(Xac)表现出最高的抑制活性,其EC50为0.24 μg/mL。此外,通过盆栽试验验证了H32对水稻白叶枯病(BLB)和H6对柑橘溃疡病(CC)的防治效果。SEM、毒力因子和宿主酶活性测定表明,H32不仅能降低Xoo的毒力,还能激活防御酶的活性,提高宿主植物的抗病性。蛋白质组学和代谢组学分析表明,H32能抑制支链氨基酸的合成,使Xoo细胞处于饥饿状态,抑制其增殖,减弱其毒力,减少其在宿主细胞上的定殖和侵染。
含苄基哌啶的芒柄花素衍生物可作为潜在有效的抗黄单胞菌属抑制剂。