新的香豆素-肉桂酸混合物:有效的FtsZ抑制剂作为控制细菌感染的杀菌剂的替代品

IF 3.8 1区 农林科学 Q1 AGRONOMY
Si‐Yue Ma, Lin‐Li Yang, Jing‐Sha Yang, Ya Xiao, Guo‐Qing Wang, Hong‐Wu Liu, Yue Ding, Xiang Zhou, Li‐Wei Liu, Zhi‐Bing Wu, Song Yang
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However, although its application in pesticides remains limited, initiation of a FtsZ‐targeted antibacterial discovery strategy could help to prevent bacterial infection and drug/pesticide resistance.RESULTSTo discover a new FtsZ inhibitor, the attractive molecular hybridization strategy of introducing isopropanolamine linker was used in which representative active scaffolds for FtsZ inhibitors including coumarin and cinnamic acids were selected to devise new coumarin–cinnamic acid hybrids. 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引用次数: 0

摘要

ftsz,即丝化温度敏感突变蛋白Z,在原核生物的分裂过程中普遍存在且高度保守,因此近年来被认为是开发创新抗菌药物的关键靶点。然而,尽管其在农药中的应用仍然有限,但启动以FtsZ为目标的抗菌发现策略可能有助于预防细菌感染和药物/农药耐药性。结果采用引入异丙醇胺连接体的吸引分子杂交策略,选择香豆素和肉桂酸等具有代表性的FtsZ抑制剂活性支架,构建新的香豆素-肉桂酸杂交体,发现新的FtsZ抑制剂。有趣的是,化合物4d对米黄单胞菌具有良好的体外抑菌活性。oryzae [Xoo,中位有效浓度(EC50) = 1.45 mg L−1],优于参比试剂双巯唑(EC50 = 33.08 mg L−1),并表现出良好的体内抗Xoo活性(200 mg L−1的保护活性为50.46%)。此外,通过荧光成像、鸟苷三磷酸酶(GTPase)活性测定、荧光滴定、傅立叶变换红外光谱和计算模拟等机制分析表明,化合物4d可能选择性作用于鸟苷5′-三磷酸(GTP)结合位点,进一步抑制GTP酶活性[化合物4d的中位抑制浓度(IC50)值为170.55 μm],从而抑制细菌繁殖。毒性研究强调了化合物4d良好的药理特征和较低的植物毒性。结论本研究为推广以FtsZ为靶点的新型杀菌剂有效控制细菌感染提供了新的范例。这项工作为解决细菌耐药性和克服新农药开发中的瓶颈提供了新的见解。©2025化学工业协会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New coumarin–cinnamic acid hybrids: potent FtsZ inhibitors as alternatives to bactericides for controlling bacterial infection
BACKGROUNDFtsZ, namely filamenting temperature‐sensitive mutant protein Z, is pervasive and highly conserved in the division process of prokaryotic organisms, and thus recently has come to be regarded as a key target for the development of innovative antibacterial agents. However, although its application in pesticides remains limited, initiation of a FtsZ‐targeted antibacterial discovery strategy could help to prevent bacterial infection and drug/pesticide resistance.RESULTSTo discover a new FtsZ inhibitor, the attractive molecular hybridization strategy of introducing isopropanolamine linker was used in which representative active scaffolds for FtsZ inhibitors including coumarin and cinnamic acids were selected to devise new coumarin–cinnamic acid hybrids. Interestingly, compound 4d exhibited excellent in vitro antibacterial activity toward Xanthomonas oryzae pv. oryzae [Xoo, median effective concentration (EC50) = 1.45 mg L−1], which was better than that of the reference reagent bismerthiazol (EC50 = 33.08 mg L−1), and demonstrated commendable in vivo anti‐Xoo activity (protective activity: 50.46% for 200 mg L−1). Furthermore, mechanistic assays including fluorescence imaging, guanosine triphosphatase (GTPase) activity assay, fluorometric titration assays, Fourier transform infrared spectroscopy and computational simulations co‐elucidated that compound 4d may selectively act on the guanosine 5′‐triphosphate (GTP) binding site, further suppress the GTPase activity [median inhibitory concentration(IC50)value of compound 4d of 170.55 μm), thereby inhibiting bacterial reproduction. Toxicity studies accentuated the favorable pharmacological profile and low plant toxicity of compound 4d.CONCLUSIONThis study provides a new paradigm for extending new bactericides to efficiently control bacterial infections by targeting FtsZ. The work provides new insights for addressing bacterial drug resistance and overcoming bottlenecks in the development of novel pesticides. © 2025 Society of Chemical Industry.
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来源期刊
Pest Management Science
Pest Management Science 农林科学-昆虫学
CiteScore
7.90
自引率
9.80%
发文量
553
审稿时长
4.8 months
期刊介绍: Pest Management Science is the international journal of research and development in crop protection and pest control. Since its launch in 1970, the journal has become the premier forum for papers on the discovery, application, and impact on the environment of products and strategies designed for pest management. Published for SCI by John Wiley & Sons Ltd.
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