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Sensitization of Plant Pathogenic Fungi to the Tebuconazole-Based Commercial Fungicide Using Some Analogues of Natural Amino Acids

机译:一种使用氨基酸类似物的植物病原真菌对基于Tebuconazole的商业杀菌剂的敏化

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Commercial fungicides provide an efficient control of fungal diseases of crops. At the same time, plant pathogenic fungi can develop resistance to fungicides that results in epiphytoties and significant yield losses. The most common response of potato growers is more extensive use of fungicides associated with environmental pollution and a range of various health risks. Therefore, the search for approach preventing the development of pest resistance to fungicides is of great practical interest. A potentially new strategy to overcome or minimize this problem is an enhancement of pathogen sensitivity to fungicides using various chemical compounds. In this study, we examined several putative sensitizers chosen among structural analogues of some natural amino acids known for their inhibiting effect on the polyketide biosynthetic pathway, since polyketide mycotoxins play an important role in a pathogenicity of fungi. A possible synergism between the action of these compounds and a commercial fungicide Folicur on the growth of Phoma glomerata and Fusarium culmorum colonies was evaluated using the Limpel's criterion. For all four compounds tested, a significant chemosensitizing effect was revealed for both non-fungicidal and sub-fungicidal concentrations that confirmed the initial hypothesis. The further screening of other amino acid analogues for their chemosensitizing activity is planned, as well as the study of the mechanism of their sensitizing action. Revealing of a compound providing significant chemosensitizing effect and characterized by a relatively low cost of synthesis would provide a low-cost solution for reduction of fungicidal treatments, while still providing sufficient protection even against fungicide-resistant strains of plant pathogens.
机译:商业杀菌剂提供了对农作物的真菌疾病的有效控制。同时,植物致病性真菌可以产生对杀菌剂的抵抗力,导致骨骺和显着的产量损失。马铃薯种植者最常见的反应更广泛地使用与环境污染相关的杀菌剂和一系列各种健康风险。因此,寻求方法防止对杀菌剂的抗虫病的发展具有很大的实际兴趣。克服或最小化该问题的潜在新策略是利用各种化学化合物提高对杀菌剂的病原体敏感性。在这项研究中,我们检查了几种诱发的敏化剂,该推定致病剂选择了一些用于它们对聚酮化合物生物合成途径的抑制作用的一些天然氨基酸的结构类似物,因为聚酮霉毒素在真菌的致病性中发挥着重要作用。使用Limpel的标准评估这些化合物和商业杀菌剂的作用与商业杀菌剂的作用之间的可能协同作用,并使用Limpel的标准评估了对毛细血管和镰刀菌菌落的生长。对于测试的所有四种化合物,对于确认初步假设的非杀真菌和亚杀菌浓度,显示出显着的化学溶解效果。计划进一步筛选其他氨基酸类似物的化学溶解活性,以及​​对其致敏作用的机制的研究。揭示提供显着的化学融化效应的化合物并以相对低的合成成本为特征将提供低成本的解决方案,用于降低杀真菌处理,同时仍然仍提供足够的保护,即使对耐杀菌剂的植物病原菌菌株也是如此。

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