02785nam a2200253 a 450000100080000000500110000800800410001910000200006024501360008026001570021650000140037352018990038765000220228665300230230865300190233165300380235065300190238870000200240770000190242770000200244670000230246670000220248970000200251118870162011-04-29       2011    bl uuuu     u00u1 u    #d1 aSILVA, F. A. C.  aAction of the pathogenesis-related protein PR10 from Theobroma cacao in triggering response mechanisms of Moniliophtora perniciosa.  aIn: SIMPÓSIO BRASILEIRO DE GENÉTICA MOLECULAR DE PLANTAS, 3, 2011, Ilhéus. Resumos. [S. l.]: Sociedade Brasileira de Genética, 2011. 1 CD-ROM.c2011  apdf 35180  aCacao (Theobroma cacao L.) is an important commodity worldwide, but its production is limited by destructive diseases such witches? broom, due to the fungus Moniliophthora perniciosa. The high recombination rate and genetic variability of this fungus promoted resistance breakdown of cacao and annihilated the efforts made by the Brazilian government to reduce the disease impact on plantations. According to the literature, pathogenesis related-proteins (PRs) plays an important role in defense/resistance mechanisms of the plant submitted to various biotic and abiotic stresses. A cDNA clone encoding a PR10 (named TcPR10) was obtained from a cacao-M. perniciosa EST library. The corresponding recombinant protein (expressed in Escherichia coli BL21(DE3)) present a strong antifungal activity against M. perniciosa, as previously demonstrated. In this work, we developed a proteomic analysis of the fungus cultivated in the presence of TcPR10, using 2DE-MS/MS. M. perniciosa was grown in CPD 2% agar medium; after 15 days, the fungal hyphae were broken and were grown in presence of 3 µg/mL of TcPR10 for 1h.Then, the total proteins were extracted using the ADP method, followed by a simple cleaning using the method of SDS-dense and phenol. The quantification was made using a 2-D quantification kit. The proteins were extracted in triplicate and separated using a 12% bi-dimensional SDS-PAGE gel. The 2D map analysis showed approximately 300 ?spots? per gel (control and one hour treatment) with differential protein expression pattern. The analysis using a mass spectrometry (naniESI-Q-TOF) was made for the identification of the spots. We identified several proteins involved in fungal metabolism, carbohydrates/proteins metabolism, related proteins to growth and phytotoxics proteins. More spots have been identified to better understand the mechanism of fungi response to protein PR10.  amass spectrometry  aBi-dimensional gel  aFungal disease  aPathogenesis related-protein PR10  aTcPR10 protein1 aPIROVANI, C. P.1 aMENEZES, S. P.1 aSANTIAGO, A. S.1 aCASCARDO, J. M. C.1 aMICHELI, F. F. L.1 aGESTEIRA, A. S.