Our paper presents the results of the application of a micropropagation protocol developed at theFruit Research Station Cluj, in Rubus fruticosus cultivars ‘AŒaAanska bestrna’, ‘Chester Thornless’, ‘LochNess’ and ‘Navaho’. For the in vitro multiplication stage, Murashige & Skoog (MS) media supplementedwith 0.3 and 0.5 mg/l BAP and gelled with starch were used. Direct ex vitro rooting was carried out.The shoots regenerated in vitro in the multiplication stage were rooted ex vitro in two experimentaltreatments: float hydroculture and floating perlite beds. In cultivars ‘Loch Ness’ and ‘Chester’ 0.5 mg/lBAP yielded good results regarding in vitro proliferation and multiplication rates and the regeneratedshoots were vigorous, suitable for ex vitro rooting and acclimatization. In cultivars ‘Navaho’ and ‘AŒaAanskaBestrna’ the optimal BAP concentration was 0.3 mg/l, which ensured normal plantlet development. Theexperimental treatments with 3 and 4 microcuttings / vessel gave good results, whereas the ones with 1and 2 microcuttings / vessel did not yield satisfactory results regarding growth and proliferation. Wheatstarch was successfully used as a gelling agent in all the cultivars. In cultivar ‘AŒaAanska bestrna’ potatostarch gave very good results regarding in vitro proliferation. In the direct ex vitro rooting experimentsfloating perlite gave good results in all the cultivars. In cultivar ‘AŒaAanska bestrna’ ex vitro rooting in floathydroculture gave relatively poor results, with rooting percentages around 60 %.
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Fira et al. (2014) studied this question.
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