Sakae SuzukiKanyaratt SupaibulwatanaMasahiro MiiMasaru NakanoNiigata UniversityMahidol UniversityChiba University2018-09-072018-09-072001-07-05Plant Science. Vol.161, No.1 (2001), 89-97016894522-s2.0-0034967996https://repository.li.mahidol.ac.th/handle/20.500.14594/26391A system for producing transgenic plants was developed for the Liliaceous ornamental Agapanthus praecox ssp. orientalis (Leighton) Leighton via Agrobacterium-mediated genetic transformation. Leaf-derived embryogenic calli were inoculated with A. tumefaciens strain EHA101/pIG121Hm or LBA4404/pTOK233, both of which harbored the binary vector carrying the neomycin phosphotransferase II (NPTII), hygromycin phosphotransferase (HPT) and intron-containing β-glucuronidase (GUS-intron) genes in the T-DNA region. Following co-cultivation, the calli were transferred to a medium containing 1 mg 1-1picloram (PIC), 50 mg 1-1hygromycin and 500 mg 1-1cefotaxime, on which several hygromycin-resistant (Hygr) cell clusters were obtained 5-6 weeks after transfer. Agrobacterium strain, co-cultivation period and acetosyringone (AS) treatment during co-cultivation affected the number of Hygrcallus lines produced: the best result was obtained when embryogenic calli were co-cultivated with LBA4404/pTOK233 for 7 days in the presence of 20 mg 1-1AS. Hygrcalli were transferred to the same medium, but lacking PIC, for inducing somatic embryos. Somatic embryos thus obtained developed into complete plantlets following their transfer to a medium without PIC and antibiotics. All of them were verified to be stable transformants by GUS histochemical assay, PCR and Southern blot analyses. © 2001 Elsevier Science Ireland Ltd.Mahidol UniversityAgricultural and Biological SciencesBiochemistry, Genetics and Molecular BiologyArticleSCOPUS10.1016/S0168-9452(01)00393-4