Affiliation:
1. State Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Science, Beijing, China
Abstract
ABSTRACT
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.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
49 articles.
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