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Barcelo, M.

Publications and source records attributed to Barcelo, M..

2 recordsLinked to original sources

Suppression of Pectinase Genes Confers Stable Enhancement of Fruit Firmness through Modulation of Pectin Structure in Strawberry

Fruit softening is primarily determined by modifications in the cell wall architecture, which are mediated by the coordinated activity of cell wall-degrading enzymes. In strawberry (Fragaria x ananassa Duch.), transgenic suppression of the genes encoding the pectinases polygalacturonase (PG), {beta}-galactosidase ({beta}Gal), and rhamnogalacturonan lyase (RGLyase), reduced fruit softening. In this study, we evaluated the fruit firmness phenotype of selected transgenic lines across several harvest years, from 3 to 9 years depending on the line, and analyzed the cell wall composition of ripe fruits using a carbohydrate microarray. Multiple linear regression analysis revealed that fruit firmness was significantly affected by both genotype and harvest year, while fruit size and soluble solids content showed no significant contribution. All pectinase-silenced lines exhibited increased firmness relative to the wild type, with those lines with PG down-regulated showing the most significant effects, followed by B-Gal and RGLyase fruits. The firmer phenotype was maintained stably in all the transgenic lines during the different years analyzed. Carbohydrate microarray analyses of sequentially extracted cell wall fractions demonstrated that transgenic ripe fruits retained higher levels of low methyl-esterified homogalacturonan (HG) and rhamnogalacturonan I (RG-I) epitopes compared to wild-type ripe fruits, resembling the composition of white-stage control fruits. Principal component analysis of microarray data revealed a clear separation between wild-type ripe fruits and transgenic lines, with the latter clustering near the earlier developmental stages of wild-type fruits. Correlation analysis further revealed positive associations between increased firmness and the abundance of high-methylated HG pectic epitopes in the water fraction, recognized with JIM7, and low-methylated HG abundance in the rest of the fractions (JIM5, LM18, and LM19). Overall, these results suggest that suppressing pectinase genes alters pectin remodeling during ripening, resulting in the retention of structurally intact pectin domains and increased fruit firmness. These genes are therefore excellent candidates for the improvement of this key quality trait in strawberry.

plant biology↗

FungalRoot: Global online database of plant mycorrhizal associations

O_LIThe urgent need to better understand profound impacts of mycorrhizas on functioning of terrestrial ecosystems, along with recent debates on resolving plant mycorrhizal associations, indicate that there is a great need for a comprehensive data of plant mycorrhizal associations able to support testing of ecological, biogeographic and phylogenetic hypotheses.\nC_LIO_LIHere present a database, FungalRoot, which summarizes publicly available data on plant mycorrhizal type and intensity of root colonization by mycorrhizal fungi, accompanied by rich meta-data. We collected and digitized data on plant mycorrhizal colonization intensity published until April 2019 in 9 globally most important languages. The data were assessed for quality and updated for plant taxonomy.\nC_LIO_LIThe FungalRoot database contains 36,303 species by site observations for 14,870 plant species, tripling the previously available amount in any compilation. The great majority of ectomycorrhizal and ericod mycorrhizal plants are trees and shrubs, 92% and 85% respectively. The majority of arbuscular mycorrhizal and of non-mycorrhizal plant species are herbaceous (50% and 70%).\nC_LIO_LIBesides acting as a compilation of referenced observations, our publicly available database provides a recommendation list of plant mycorrhizal status for ecological and evolutionary analyses to promote research on the links between above- and belowground biodiversity and functioning of terrestrial ecosystems.\nC_LI

ecology↗