Antony Ajitha, Veerappapillai Shanthi, Karuppasamy Ramanathan
Department of Biotechnology, School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, Tamil Nadu 632014 India.
3 Biotech. 2024 Jan;14(1):15. doi: 10.1007/s13205-023-03859-7. Epub 2023 Dec 18.
Rice blast disease, caused by , is the most devastating cereal killer worldwide. Note that melanin pigment is an essential factor of virulence, thus fungicides interfering with melanin biosynthesizing enzymes would reduce the pathogenicity. Scytalone dehydratase (SDH) is the key target for commercial fungicides, like carpropamid, due to its role in the dehydration reaction of the fungal melanin pathway. However, a single-point mutation (V75M) in SDH elicits resistance to carpropamid. A lack of effective fungicides against this resistant strain expedited the quest for novel bioactive inhibitors. Currently, bacterial endophytes like have been heralded for synthesizing bioactive metabolites to protect plants from phytopathogens. The literature search led to the identification of 21 spp. symbionts of paddy that can suppress growth. An antiSMASH server was used to explore spp. gene clusters and found 4463 putative metabolites. Besides, 745 unique metabolites were subjected to a series of virtual screening techniques. Ideally, this process identified five potential SDH inhibitors. The docking result highlights that the metabolite pseudopyronine A interacted hydrophobically with both Val75 of SDH and Met75 of SDH targets. Moreover, pseudopyronine A has a higher binding free energy with SDH (- 89.94 kcal/mol) and SDH (- 71.95 kcal/mol). Interestingly, the pyranones scaffold of pseudopyronine A was reported for antifungal activity against phytopathogens. Dynamic behavior confirms that pseudopyronine A has excellent conformational states with both SDH and SDH. Altogether, we hope that this study creates a new avenue for the discovery of novel phytopathogen inhibitors from endophytes.
The online version contains supplementary material available at 10.1007/s13205-023-03859-7.
由[病原体名称未给出]引起的稻瘟病是全球最具毁灭性的谷物杀手。请注意,黑色素色素是[病原体名称未给出]毒力的一个重要因素,因此干扰黑色素生物合成酶的杀菌剂会降低其致病性。由于其在真菌黑色素途径的脱水反应中的作用,细胞松弛素脱水酶(SDH)是商业杀菌剂如环丙酰胺的关键靶点。然而,SDH中的单点突变(V75M)会引发对环丙酰胺的抗性。缺乏针对这种抗性菌株的有效杀菌剂加速了对新型生物活性抑制剂的探索。目前,像[内生菌名称未给出]这样的细菌内生菌因能合成生物活性代谢物以保护植物免受植物病原体侵害而受到关注。文献检索导致鉴定出21种水稻共生菌,它们可以抑制[病原体名称未给出]的生长。使用antiSMASH服务器探索这些共生菌的基因簇,发现了4463种推定的代谢物。此外,对745种独特的代谢物进行了一系列虚拟筛选技术。理想情况下,这个过程鉴定出了五种潜在的SDH抑制剂。对接结果突出显示,代谢物假吡喃菌素A与SDH的Val75和SDH靶点的Met75都发生了疏水相互作用。此外,假吡喃菌素A与SDH(-89.94 kcal/mol)和SDH(-71.95 kcal/mol)具有更高的结合自由能。有趣的是,据报道假吡喃菌素A的吡喃酮支架对植物病原体具有抗真菌活性。动力学行为证实假吡喃菌素A与SDH和SDH都具有出色的构象状态。总之,我们希望这项研究为从内生菌中发现新型植物病原体抑制剂开辟一条新途径。
在线版本包含可在10.100