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| Authors: | F.H.M. Derks, A.J. van Dijk, C.H. Hänisch ten Cate, D.E.A. Florack, L.A.M. Dubois, D.P. de Vries |
Abstract:
A reproducible regeneration method via somatic embryogenesis was developed for various rose cultivars. In vitro induced roots were cultured on medium with high concentrations of auxins followed by culture on hormone-less medium.
Embryogenic callus with somatic embryos was obtained, which resulted into normal plants.
Transformation of embryogenic callus of 3 cultivars was performed with Agrobacterium tumefaciens, harbouring a binary vector containing a kanamycin resistance gene, a -glucuronidase (GUS) gene with an intron and a gene coding for the antibacterial cecropin B. Transgenic callus was obtained for all binary vectors used.
Transgenic somatic embryos were induced on transgenic callus of cultivar ‘Sonia’.
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