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Identification of biomarkers for resistance to fusarium oxysporum f. sp. cubense infection and in silico studies in musa paradisiaca cultivar puttabale through proteomic approach

机译:鉴定抗尖孢镰刀菌的生物标记f。 sp。蛋白质组学方法研究杂草芭蕉中的立方体感染和计算机病学研究

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摘要

Panama wilt caused by Fusarium oxysporum f. sp. cubense (Foc) is one of the major disease constraints of banana production. Previously, we reported the disease resistance Musa paradisiaca cv. puttabale clones developed from Ethylmethanesulfonate and Foc culture filtrate against Focudinoculation. Here, the same resistant clones and susceptible clones were used for the study of protein accumulation against Foc inoculation by two-dimensional gel electrophoresis (2-DE), their expression pattern and an in silico approach. The present investigation revealed mass-spectrometry identified 16 proteins that were over accumulated and 5 proteins that were under accumulatedudas compared to the control. The polyphosphoinositide binding protein ssh2p (PBPssh2p) and Indoleacetic acid-induced-like (IAA) protein showed significant up-regulation and down-regulation. The docking of the pathogenesis-related protein (PR) with the fungal protein endopolygalacturonaseud(PG) exemplify the three ionic interactions and seven hydrophobic residues that tends to good interaction at the active site of PG with free energy of assembly dissociation (1.5 kcal/mol). The protein-ligand docking of the Peptide methionine sulfoxide reductase chloroplastic-like proteinud(PMSRc) with the ligand �-1,3 glucan showed minimum binding energy (�6.48 kcal/mol) and docking energy (�8.2 kcal/mol) with an interaction of nine amino-acid residues. These explorations accelerate the research in designing the host pathogen interaction studies for the better managementudof diseases.
机译:尖孢镰刀菌引起的巴拿马枯萎f。 sp。立方体(Foc)是香蕉生产的主要疾病限制之一。先前,我们报道了抗病性天堂草(Musa paradisiaca)cv。从甲磺酸乙酯和Foc培养滤液中分离出的反对Foc udinoculation的腐殖菌无性系。在这里,相同的抗性克隆和易感克隆用于通过二维凝胶电泳(2-DE),表达模式和计算机方法研究针对Foc接种的蛋白质积累。本研究表明,与对照相比,质谱分析鉴定出了16种蛋白质的累积过量和5种蛋白质的累积不足。聚磷酸肌醇结合蛋白ssh2p(PBPssh2p)和吲哚乙酸诱导样(IAA)蛋白显示出明显的上调和下调。病程相关蛋白(PR)与真菌蛋白内聚半乳糖醛酸酶 ud(PG)的对接体现了三个离子相互作用和七个疏水残基,这些残基倾向于在PG的活性位点具有良好的组装解离自由能(1.5 kcal) / mol)。肽蛋氨酸亚砜还原酶叶绿体样蛋白 ud(PMSRc)与配体-1,3葡聚糖的蛋白质-配体对接显示了最小的结合能(6.48 kcal / mol)和对接能(8.2 kcal / mol)。与九个氨基酸残基的相互作用。这些探索加速了设计宿主病原体相互作用研究以更好地控制疾病的研究。

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