Tissue Culture Laboratory, Department of Botany, National University of Singapore, Lower Kent Ridge Road, 119 260, Singapore.
Plant Cell Rep. 1996 Dec;16(3-4):204-9. doi: 10.1007/BF01890868.
High frequency, direct regeneration of shoots was induced in leaf cultures ofPaulownia tomentosa, P. fortunei x P. tomentosa andP. kawakamii. The optimum culture medium for the leaf explants derived from shoot cultures was Murashige-Skoog (MS) medium supplemented with 10 μM indole-3-acetic acid and 50 μM benzyladenine. Up to 40 shoots were obtained over a 4 month culture period from each leaf explant. Rooting occurred spontaneously in the shoots that were about 1 cm tall when subcultured on phytohormone-free MS medium. The plantlets could be transplanted successfully. Some of the transplantedP. tomentosa plantlets flowered in the greenhouse one year after transplanting. The protocol is suitable not only for rapid multiplication of the various species ofPaulownia, but also for analytical studies associated with adventitious shoot regeneration.
高频,直接再生芽在泡桐、泡桐杂交种和川崎泡桐的叶片培养中被诱导。对于由芽培养获得的叶片外植体来说,最适的培养基是添加了 10 μM 吲哚乙酸和 50 μM 苄基腺嘌呤的 Murashige-Skoog(MS)培养基。从每个叶片外植体可在 4 个月的培养期内获得多达 40 个芽。当将芽转移到不含植物激素的 MS 培养基上时,芽长约 1 厘米时会自发生根。可以成功地移栽植物。移栽一年后,一些泡桐植物在温室中开花。该方案不仅适用于泡桐各种物种的快速繁殖,也适用于与不定芽再生相关的分析研究。