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首页> 外文期刊>Applied and Environmental Microbiology >PeBL1, a Novel Protein Elicitor from Brevibacillus laterosporus Strain A60, Activates Defense Responses and Systemic Resistance in Nicotiana benthamiana
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PeBL1, a Novel Protein Elicitor from Brevibacillus laterosporus Strain A60, Activates Defense Responses and Systemic Resistance in Nicotiana benthamiana

机译:PeBL1,一种新的来自短小芽孢杆菌A60菌株的蛋白激发子,激活了本氏烟草的防御反应和系统抗性

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We report the identification, characterization, and gene cloning of a novel protein elicitor (PeBL1) secreted from Brevibacillus laterosporus strain A60. Through a purification process consisting of ion-exchange chromatography and high-performance liquid chromatography (HPLC), we isolated a protein that was identified by electrospray ionization quadrupole time of flight tandem mass spectrometry (ESI–Q-TOF–MS-MS). The 351-bp PeBL1 gene produces a 12,833-Da protein with 116 amino acids that contains a 30-residue signal peptide. The PeBL1 protein was expressed in Escherichia coli. The recombinant protein can induce a typical hypersensitive response (HR) and systemic resistance in Nicotiana benthamiana, like the endogenous protein. PeBL1-treated N. benthamiana exhibited strong resistance to the infection of tobacco mosaic virus-green fluorescent protein (TMV-GFP) and Pseudomonas syringae pv. tabaci compared to control N. benthamiana. In addition, PeBL1 triggered a cascade of events that resulted in defense responses in plants, including reactive oxygen species (ROS) production, extracellular-medium alkalization, phenolic-compound deposition, and expression of several defense-related genes. Real-time quantitative-PCR analysis indicated that the known defense-related genes PR-1, PR-5, PDF1.2, NPR1, and PAL were upregulated to varying degrees by PeBL1. This research not only provides insights into the mechanism by which beneficial bacteria activate plant systemic resistance, but also sheds new light on a novel strategy for biocontrol using strain A60.
机译:我们报告鉴定,表征和基因克隆的一种新的蛋白引发剂(PeBL1),从枯草芽孢杆菌菌株A60分泌。通过由离子交换色谱和高效液相色谱(HPLC)组成的纯化过程,我们分离了通过电喷雾电离四极杆飞行时间串联质谱(ESI–Q-TOF–MS-MS)鉴定的蛋白质。 351 bp的PeBL1基因可产生12,833-Da的蛋白质,具有116个氨基酸,其中包含30个残基的信号肽。 PeBL1蛋白在大肠杆菌中表达。与内源蛋白一样,重组蛋白可以在本氏烟草中诱导典型的超敏反应(HR)和系统抗性。经PeBL1处理的本氏烟草对烟草花叶病毒绿色荧光蛋白(TMV-GFP)和丁香假单胞菌pv的感染表现出较强的抵抗力。烟粉虱与对照本氏烟草相比。此外,PeBL1触发了一系列事件,这些事件导致植物的防御反应,包括活性氧(ROS)的产生,细胞外中等碱化,酚类化合物的沉积以及几种防御相关基因的表达。实时定量PCR分析表明,已知的防御相关基因 PR-1 PR-5 PDF1.2 NPR1 PAL 。这项研究不仅为有益细菌激活植物系统抗性的机理提供了见解,而且为使用菌株A60进行生物防治的新策略提供了新的思路。

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