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新型含各种含氮杂环侧链的噁二唑的设计、合成及抗菌性能。

Design, synthesis, and antimicrobial behavior of novel oxadiazoles containing various N-containing heterocyclic pendants.

机构信息

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for R&D of Fine Chemicals of Guizhou University, Guiyang, China.

College of Pharmacy, East China University of Science & Technology, Shanghai, China.

出版信息

Pest Manag Sci. 2020 Aug;76(8):2681-2692. doi: 10.1002/ps.5814. Epub 2020 Apr 4.

Abstract

BACKGROUND

The gradually elevated outbreak of plant bacterial diseases severely limits agricultural products and small amounts of pesticides can manage them. Our group has previously synthesized and screened the antimicrobial activity of diverse 1,3,4-oxadiazole thioether/sulfone compounds bridged by a sulfur atom at the 2-position of 1,3,4-oxadiazole. However, few studies have evaluated the effect of eliminating the sulfur atom on bioactivity. Herein, a novel type of N-containing heterocyclic pendants-tagged 1,3,4-oxadiazoles bridged by alkyl chains only was systematically synthesized and evaluated for their antimicrobial activities.

RESULTS

Bioassay results revealed that antibacterial efficacy increased by 551- and 314-fold against the corresponding phytopathogens Xanthomonas oryzae pv. oryzae and X. axonopodis pv. citri compared to commercial agents bismerthiazol and thiodiazole copper. In vivo trials showed that C exerted remarkable curative activity against rice bacterial blight with a control effectiveness of 52.9% at 200 μg mL . Antibacterial mechanism research found that C could reduce the hypersensitive response behavior and pathogenicity of Xoo through targeting the type III secretion system (T3SS) at a lower drug dose. This outcome was verified by observing the significantly down-regulated proteins and representative genes from the related quantitative proteomics and qRT-PCR assays.

CONCLUSION

This study can inspire the design of innovative molecular frameworks targeting the T3SS of phytopathogens for controlling bacterial infections. © 2020 Society of Chemical Industry.

摘要

背景

植物细菌性疾病的逐渐爆发严重限制了农产品的产量,而少量的农药就能对其进行治理。我们的团队之前已经合成并筛选了多种通过硫原子桥接在 1,3,4-恶二唑 2-位的 1,3,4-恶二唑硫醚/砜化合物的抗菌活性。然而,很少有研究评估消除硫原子对生物活性的影响。在此,我们系统地合成了一种新型含氮杂环取代的 1,3,4-恶二唑,仅通过烷基链桥接,用于评估其抗菌活性。

结果

生物测定结果表明,与商业药剂双脒噻唑和噻二唑铜相比,针对相应的植物病原菌稻白叶枯病菌和柑橘溃疡病菌,化合物 C 的抑菌活性分别提高了 551 倍和 314 倍。体内试验表明,C 在 200μg·mL 时对水稻细菌性条斑病表现出显著的治疗活性,防治效果为 52.9%。抗菌机制研究发现,C 可以通过靶向 III 型分泌系统(T3SS)在较低的药物剂量下降低 Xoo 的过敏反应行为和致病性。这一结果通过观察相关定量蛋白质组学和 qRT-PCR 分析中代表性基因和下调蛋白得到了验证。

结论

本研究可以为设计针对植物病原菌 T3SS 的创新分子框架以控制细菌感染提供启示。 © 2020 英国化学学会。

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