中文摘要 |
火鶴花Anthurium sp. T2營養系試管苗葉片,以半量之Murashige及Skoog配方(1/2 MS)為基本培養基,單獨添加生長素Picloram或2,4-D不易再生芽體,但有少量的癒合組織形成;添加0.5 mg/l TDZ於2,4-D(0~0.5 mg/l)培養基,不定芽形成率介於10~30%;不論在1/2 MS或MS培養基,添加TDZ均能誘導癒合組織形成。T18營養系試管苗葉片培養於以全量MS及0.5 mg/l TDZ為基本培養基,添加Picloram之處理,易形成癒合組織,而不定芽形成率均較含單獨TDZ者低;再生之植株其外觀正常。
A method of plant regeneration from in vitro lamina culture of Anthurium by supplementing thidiazuron with either 2,4-D or picloram is examined. Whole leaf blade of T2 lamina produced few callus on 1/2 MS medium supplemented with 2,4-D or picloram. A combination of 2,4-D (0.1~1mg/l) and TDZ (0.5mg/l) led to 10~30 % of the explants regenerating adventitious shoots. MS medium supplemented with 0.5 mg/l TDZ and picloram (0.1~1mg/l) induced 0~70% shoot formation in T18 lamina. Reducing salt strength to one half promoted callus formation. Normal and rooted plantlets were recovered and subcultured on the same medium |