Propagation of Drosera rotundifolia and Drosera capensis in an in vitro Culture System 1* 1 Ileana MICLEA , Marius ZĂHAN 1 *Department of Animal Reproduction,University of Agricultural Sciences and Veterinary Medicine, 3-5, Mănăştur Street, 400372, Cluj-Napoca, Romania. Corresponding author, e-mail:
[email protected] Bulletin UASVM Animal Science and Biotechnologies 74(2)/ 2017 Print ISSN 1843-5262; Electronic ISSN 1843-536X DOI:10.15835/buasvmcn-asb: 0018 ABSTRACT Drosera rotundifolia and Drosera capensis in vitro (Droseraceae) are carnivorous plants grown as ornamentals and sources for homeopathic medicine. The aim of this study was to optimize nutrient and growth regulator concentrations for the propagation of these species. Half strength MS medium (1/2MS) was supplemented with kinetin (0.5, 2, 5 mg/l) or 6-benzyladenine (3, 5 mg/l) and plantlets were transferred to 1/2MS with or without cytokinins. After 8 weeks rosette diameter, plant height, number of roots, root length were recorded and plants were cultured in fullD. strength rotundifolia MS, 1/2MS or 1/2MS with 0.5 mg/l α-naphthaleneacetic acid for the same period of time. Afterwards, plant characteristics (number of roots, root length, number of shoots, number of flower stalks) were assessed. For , shoot development and rosette diameter increased significantly in the medium with 0.5 mg/l kinetin and 3 mg/l 6-benzyladenine, whileD. capensis root development decreased. Plant growth regulator free medium was more suitable for root development than medium with α-naphthaleneacetic acid and thus supported the formation of significantly more flower stalks. For , kinetin was detrimental for shoot development, the optimumKeywords: medium auxins, for cytokinins, both shoot Drosera and root rotundifolia, formation Drosera being MS capensis, without in plant vitro growth regulators.