Plant Molecular Genetics Laboratory, AgResearch, Grasslands Research Centre, Private Bag 11008, Palmerston North, New Zealand.
Plant Cell Rep. 1994 Mar;13(6):303-8. doi: 10.1007/BF00232626.
A facile procedure has been developed to regenerate white clover (Trifolium repens L.) plants, rapidly and directly from cotyledon explants of 3 day old seedlings. Scanning electron microscopy and histological sectioning demonstrated that shoot meristems developed from individual epidermal cells on the adaxial surface of the cotyledonary stalk, proximal to the site of excision. Initial cell divisions occurred after 2 days of culture and regenerated plants were transferred to soil within 6-8 weeks. Regenerated plants were normal, flowered and set seed. The highest shoot regeneration frequency (an average of 20 shoots per cotyledon) was obtained using an MS based medium containing 1.0 mg 1(-1) 6-benzylaminopurine and 0.05 mg 1(-1) α-napthaleneacetic acid. A similar regeneration frequency was obtained from cotyledon explants taken from eight different white clover cultivars.
已经开发出一种简便的方法,可从 3 天大的幼苗子叶外植体快速、直接地再生白三叶草(Trifolium repens L.)植株。扫描电子显微镜和组织切片表明,茎尖分生组织从子叶柄的腹面单个表皮细胞发育而来,靠近切除部位。初始细胞分裂发生在培养 2 天后,再生植株在 6-8 周内转移到土壤中。再生植株正常开花结实。使用含有 1.0 mg l(-1)6-苄基氨基嘌呤和 0.05 mg l(-1)α-萘乙酸的基于 MS 的培养基,获得最高的芽再生频率(每个子叶平均 20 个芽)。从来自八个不同白三叶草品种的子叶外植体中获得了相似的再生频率。