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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Overexpression and purification of PWL2D, a mutant of the effector protein PWL2 from Magnaporthe grisea

Texto completo
Autor(es):
Schneider, D. R. S. [1] ; Saraiva, A. M. [1] ; Azzoni, A. R. [1] ; Miranda, H. R. C. A. N. [1] ; de Toledo, M. A. S. [1] ; Pelloso, A. C. [1] ; Souza, A. P. [2, 1]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas, CBMEG, BR-13083970 Campinas, SP - Brazil
[2] Univ Estadual Campinas, Dept Biol Vegetal, Inst Biol, BR-13083970 Campinas, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Protein Expression and Purification; v. 74, n. 1, p. 24-31, NOV 2010.
Citações Web of Science: 5
Resumo

The rice blast disease caused by the ascomycete Magnaporthe grisea continues to cause a tremendous impact in rice (Oryza sativa) cultures around the world. Elucidating the molecular basis of the fungus interactions with its host might help increase the general understanding of the pathogen-host relationship. At the moment of invasion, the fungus secretes effectors that modify host defenses and cellular processes as they successively invade living rice cells. PWL2, an effector protein, is a known AVR (avirulence) gene product. The PWL2 gene prevents the fungus from infecting weeping lovegrass (Eragrostis curvula). In this study, we identified a PWL2 allele gene (which we termed PWL2D) in a strain of M. grisea. The sequence of PWL2D has only two bases different from that of PWL2, producing alterations in residue 90 and residue 142. However, the alteration of residue 90 (from D(90) to N(90)) is critical to gene function. Here, we cloned the gene PWL2D in a pET System vector, expressed the gene product in Escherichia coli and evaluated by spectroscopic techniques some aspects of the PWL2D structure. While TRX-tagged PWL2D is prone to aggregation, the solubility of PWL2D is improved when it is overexpressed without its original signal peptide. Expression and purification procedures for these constructs are described. Finally, we found out that the protein seems to be an intrinsically disordered protein. Results from these studies will facilitate structural analysis of PWL2D and might contribute to understanding the gene's function and of fungal/plant interactions. (C) 2010 Elsevier Inc. All rights reserved. (AU)

Processo FAPESP: 03/08963-0 - Caracterização estrutural e funcional de proteínas relacionadas a patogenicidade de Magnaporthe grisea (teleomorfo de Pyricularia grisea)
Beneficiário:Anete Pereira de Souza
Linha de fomento: Auxílio à Pesquisa - Regular