Brooker N, Windorski J, Bluml E
Pittsburg State University, College of Arts and Sciences, Department of Biology, Heckert-Wells Hall, 1701 South Broadway, Pittsburg, Kansas, USA.
Commun Agric Appl Biol Sci. 2008;73(2):81-9.
Development of new and improved antifungal compounds that are target-specific is backed by a strong Federal, public and commercial mandate. Many plant-derived chemicals have proven fungicidal properties, including the coumarins (1,2-Benzopyrone) found in a variety of plants such as clover, sweet woodruff and grasses. Preliminary research has shown the coumarins to be a highly active group of molecules with a wide range of antimicrobial activity against both fungi and bacteria. It is believed that these cyclic compounds behave as natural pesticidal defence molecules for plants and they represent a starting point for the exploration of new derivative compounds possessing a range of improved antifungal activity. Within this study, derivatives of coumarin that were modified with halogenated side groups were screened for their antifungal activity against a range of soil-borne plant pathogenic fungi. Fungi included in this in vitro screen included Macrophomina phaseolina (charcoal rot), Phytophthora spp. (damping off and seedling rot), Rhizoctonia spp. (damping off and root rot) and Pythium spp. (seedling blight), four phylogenetically diverse and economically important plant pathogens. Studies indicate that these halogenated coumarin derivatives work very effectively in vitro to inhibit fungal growth and some coumarin derivatives have higher antifungal activity and stability as compared to the original coumarin compound alone. The highly active coumarin derivatives are brominated, iodinated and chlorinated compounds and results suggest that besides being highly active, very small amounts can be used to achieve LD100 rates. In addition to the in vitro fungal inhibition assays, results of polymer seed coating compatibility and phytotoxicity testing using these compounds as seed treatments will also be reported. These results support additional research in this area of natural pesticide development.
开发新型且改良的、具有靶向特异性的抗真菌化合物,有着强大的联邦、公共及商业需求作为支撑。许多植物衍生的化学物质已被证明具有杀真菌特性,包括在三叶草、香车叶草和草类等多种植物中发现的香豆素(1,2-苯并吡喃)。初步研究表明,香豆素是一类高活性分子,对真菌和细菌都具有广泛的抗菌活性。据信,这些环状化合物是植物的天然杀虫防御分子,它们代表了探索具有一系列改良抗真菌活性的新衍生物的起点。在本研究中,对用卤代侧基修饰的香豆素衍生物进行了筛选,以检测其对一系列土壤传播的植物病原真菌的抗真菌活性。体外筛选中包括的真菌有菜豆壳球孢菌(炭腐病)、疫霉属(猝倒病和幼苗腐烂病)、丝核菌属(猝倒病和根腐病)和腐霉属(幼苗猝倒病),这四种在系统发育上不同且具有经济重要性的植物病原体。研究表明,这些卤代香豆素衍生物在体外能非常有效地抑制真菌生长,并且与单独的原始香豆素化合物相比,一些香豆素衍生物具有更高的抗真菌活性和稳定性。高活性香豆素衍生物是溴化、碘化和氯化化合物,结果表明,除了活性高之外,只需使用极少量就能达到100%致死剂量率。除了体外真菌抑制试验外,还将报告使用这些化合物作为种子处理剂的聚合物种子包衣兼容性和植物毒性测试结果。这些结果为天然农药开发这一领域的进一步研究提供了支持。