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Purification and expression of a protein elicitor from Alternaria tenuissima and elicitor‐mediated defence responses in tobacco
Author(s) -
Mao J.,
Liu Q.,
Yang X.,
Long C.,
Zhao M.,
Zeng H.,
Liu H.,
Yuan J.,
Qiu D.
Publication year - 2010
Publication title -
annals of applied biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 80
eISSN - 1744-7348
pISSN - 0003-4746
DOI - 10.1111/j.1744-7348.2010.00398.x
Subject(s) - elicitor , biology , tobacco mosaic virus , complementary dna , open reading frame , expression vector , gene , hypersensitive response , peptide sequence , biochemistry , recombinant dna , plant disease resistance , genetics , virus
A new protein elicitor, PeaT1, was purified from the mycelium of Alternaria tenuissima by column chromatography. PeaT1 was identified as a heat‐stable and acidic protein. It induced systemic acquired resistance to tobacco mosaic virus (TMV) in tobacco plants but did not cause hypersensitive response. The elicitor‐encoding gene was cloned by rapid amplification of cDNA ends method. Sequence analysis revealed that the cDNA is 624 bp in length and the open reading frame encodes for a polypeptide of 207 amino acids with a nascent polypeptide‐associated complex domain. The peaT1 gene was cloned into the expression vector pET‐28a and transformed into Escherichia coli BL21 (DE3). The recombinant elicitor also triggered defence responses in intact tobacco plants. The availability of the pure protein offers the possibility to isolate the corresponding receptor and links it to the downstream signalling pathway.