扁蓿豆体细胞胚的诱导和植株再生

扁蓿豆实生苗的根、下胚轴、子叶、叶片和叶柄外植体，在含２，４—Ｄ２—０．２５ｍｇＬ－１与ＫＴ０．２５－２ｍｇＬ－１及２，４—Ｄ０．５ｍｇＬ－１与ＺＴ０．５ｍｇＬ－１或ＢＡＰ０．５ｍｇＬ－１与ＮＡＡ０．０５ｍｇＬ－１的ＭＳ琼脂培养基上均可产生愈伤组织．愈伤组织在含２，４—Ｄ０．５—０．１ｍｇＬ－１与ＫＴ０．５—０．１ｍｇＬ－１或ＢＡＰ０．２５＋ＮＡＡ０．０５ｍｇＬ－１的ＭＳ培养基上可诱导分化出体细胞胚．体细胞胚在无激素的培养基上发育成完整植株．用海藻酸钠包襄体细胞胚制成人工种子，其发芽率和植株转换率分别为９５％和５３％．

INDUCTION OF SOMATIC EMBRYOS AND PLANTREGENERATION OF MELISSITUS RUTHENICA L.

Explants of root,hypocotyl,cotyledon,leaf and petiole from seedlings of Melissitusruthenica L.could produce callus tissues when they were cultured on MS agar mediumcontaining 2,4-D 2-0.25mg L-l and KT 0.25-2mg L-1,or 2,4-D 0.5mg L-1 and ZT0.5mg L-1,or BAP 0.5mg L-1 and NAA 0.05mg L-1.Callus tissues Could be induced todifferentiate somatic embryos when they were transfered to MS medium containing 2,4-D0.5-0.1ing L-1 and KT 0.5-0.1mg L-1,or BAP 0.25mg L-1 and NAA 0.05mg L-1.Somatic embryos could develop into whole plants on hormone free MS medium.Somaticembryos were encapsulated by 1.5% alginate to prepare artificial seeds,of whichgermination rate and plant conversion rate were 95% and 53%, respectively.