甾体植物生长促进剂与植物病原体的酶促作用一种计算机方法

A. Carrasco-Carballo, Emiliano Marín-Merino, Penélope Merino-Montiel, Blanca Colín-Lozano, Sandra Luz Cabrera Hilerio, J. C. Hilario-Martínez, J. Sandoval-Ramírez
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引用次数: 0

摘要

甾体植物生长促进剂(SPGP)因其具有较高的促生活性和对多种逆境因子的抗性而受到广泛的研究。在我们的研究中,一个新的SPGP家族的22-氧胆甾醇化合物在油菜素内酯(BSs)的比较水平上脱颖而出。通过硅分子对接研究了新SPGP对植物病原菌的潜在活性,并与植物原几丁质酶B和1,3-β-葡聚糖酶的相关酶进行了检测。提出了9种几丁质酶B抑制剂和2种1,3-β-葡聚糖酶抑制剂。启动的研究分析了相互作用和空间水平,确定了与参考抑制剂相比,受体中关键氨基酸相互作用的存在。此外,还检测了AVR4和ECP6效应物。未发现阻断ECP6的化合物;可能是由于其高度亲水性环境的影响。在AVR4的情况下,两个SPGP的对接评分(DS)高于一个几丁质片段(内源性配体);这一事实证明了22-氧胆甾醇衍生物对植物病原体的潜在潜力,并通过增殖抑制进行特定调节。此外,该SPGP不影响对天然植物系统有益的共生真菌。
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Steroidal Plant Growth Promoters vs. Phytopathogens, via Enzymatic Regulation; An in Silico Approach
Steroidal plant growth promoters (SPGP) have been continuously studied due to their high activity increasing biomass and resistance to diverse stress fac-tors. In our hands, a new SPGP family of 22-oxocholestanic compounds stands out at a comparative level to brassinosteroids (BSs). The potential activity of new SPGP against phytopathogens was studied through in silico molecular docking, these assays were performed with relevant ensymes of phytopato-gens Chitinase B and 1,3-β-Glucanase. Nine Chitinase B inhibitors and two 1,3-β-Glucanase inhibitors were proposed. The launched study analyzed the interactional and spatial level, determining the presence of interactions with key amino acids in receptors in comparison to reference inhibitors. Even more, the AVR4 and ECP6 effectors were also examined. No compound that blocks ECP6 was found; due to, probably, the influence of its highly hydrophilic environment. In the case of AVR4, two SPGP showed a better docking score (DS) than a chitin fragment (endogenous ligand); this fact demonstrates the latent potential of the 22-oxocholestanic derivatives against phytopathogens, with a specific regulation via proliferation inhibition. Moreover, this SPGP does not affect the symbiotic fungi that are beneficial for the natural plant system.
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