INVESTIGADORES
ROSLI Hernan Guillermo
congresos y reuniones científicas
Título:
Differential expression of genes and enzymes involved in cell wall degradation during ripening of strawberry cultivars
Autor/es:
MARTÍNEZ, GUSTAVO ADOLFO; ROSLI, HERNÁN GUILLERMO; VILLARREAL, NATALIA M.; BUSTAMANTE, CLAUDIA ANABEL; DOTTO, MARCELA CLAUDIA; CIVELLO, PEDRO MARCOS
Lugar:
Talca, Chile
Reunión:
Workshop; Post Harvest Fruit, the path to success; 2004
Institución organizadora:
Universidad de Talca, Chile
Resumen:
Strawberry is a non-climeteric fleshy fruit, which softens quickly and has a short post-harvest life. Cell wall disassembly contributes to fruit softening through the combined action of cell wall enzymes and proteins like polygalacturonases (PG), pectin methyl esterases (PME), endoglucanases (Egase), beta-xylosidases (beta-Xyl), beta-galactosidases (beta-Gal) and expansins (Exp), among others. We have compared the activity the activity of these enzymes and the expression of PG (spG), Egase (FaCel1) and Exp (FaExp1, FaExp2, FaExp5 y FaExp6) genes during ripening of two strawberry varieties with different fruit softening rates (Camarosa and Toyonaka, being the first one the firmest). PG activity was detected earlier, at white stage, in Toyonaka than in Camarosa, and the PG profile was different along ripening. PME increased during ripening until white stage and then remained constant, without differences between varieties. Egase and beta-Gal activities increased during ripening in both cultivars. Two beta-Xyl activity peaks were found in Toyonaka along ripening, but only one in Camarosa. The activity of Egase, beta-Gal and beta-Xyl was higher in Toyonaka cultivar. Northern-blot analysis of spG, FaCel1 and FaXyl1 genes correlated with the corresponding enzyme activity data. In Toyonaka, spG and FaXyl1 expression was detected at high level from white stage to the end of ripening, while in Camarosa the expression of both genes began later. FaCel1 expression began in white stage and increased along ripening, and no difference between varieties was found. In the case of expansins, a clear correlation was found between expression of FaExp1, FaExp2 and FaExp5 genes and the difference in cultivar firmness, while no correlation in FaExp6 expression was evident. We conclude that the differences in firmness exhibited by these two strawberry cultivars correlate with differential expression along ripening of a set of genes and enzymes involved in cell wall disassembly, which includes at least three expansins, a polygalacturonase and a beta-xylosidase.