The aim of this study was to clone Fra a 1 genes from F. × ananassa, according to the sequences provided by the F. vesca genome, to heterologously express the Fra a 1 genes in Escherichia coli and to functionally characterize the corresponding recombinant proteins and define their gene expression levels in various tissues. The recombinant proteins were tested for RNase activity and used in phosphorylation assays and basophil activation test. Moreover, the binding of the Fra a 1-Associated protein (FaAP) to Fra a 1.04-1.08 and the molecular interplay between in vitro strawberry plants and the Verticillium dahliae pathogen were also investigated.
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The aim of this study was to clone Fra a 1 genes from F. × ananassa, according to the sequences provided by the F. vesca genome, to heterologously express the Fra a 1 genes in Escherichia coli and to functionally characterize the corresponding recombinant proteins and define their gene expression levels in various tissues. The recombinant proteins were tested for RNase activity and used in phosphorylation assays and basophil activation test. Moreover, the binding of the Fra a 1-Associated protei...
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