Optimizing the micropropagation protocol for Rosa canina L. elite genotype propagation in the Belgrade area

Abstract

Rosa canina L. (dog rose) is an important ornamental, edible and medicinal plant. It has been used as a rootstock for ornamental roses, grown in plantations for fruit harvesting and it is suitable for revegetation of abandoned mine lands. The propagation of native genotypes that are well adapted to local conditions can provide planting material for both revegetation and plantation purpose. Micropropagation is the most suitable method for a rapid vegatative propagation of selected wild genotypes, but an increased presence of pathogens as well as higher contamination rate during culture establishment were expected. An occurrence of a specific Fe-chlorosis during in vitro propagation of roses is also possible. Therefore, the optimal period and disinfection protocol for establishing sterile in vitro culture of selected genotypes of dog rose was investigated, as well as an effect of increasing the FeEDTA concentration in the MS medium during multiplication phase. The obtained results showed that the optimal time for taking initial explants corresponds to optimal time for taking green cuttings in traditional vegetative propagation by softwood cuttings, and the best results were achieved using shoots collected in the first week of May, when the flowers were open. The iron chelate concentration in the medium affected the mean number of shoots, and doubling of its concentration resulted in a considerably higher number of shoots per explant.