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甜樱桃体细胞胚胎发生及植株再生的研究
引用本文:吴雅琴,赵艳华,刘国俭,李春敏. 甜樱桃体细胞胚胎发生及植株再生的研究[J]. 华北农学报, 2006, 21(Z2): 125-128
作者姓名:吴雅琴  赵艳华  刘国俭  李春敏
作者单位:河北省农林科学院昌黎果树研究所,河北,昌黎,066600
基金项目:河北省农林科学院科研基金
摘    要:
以甜樱桃红灯为材料,幼果用0.1%HgCl2进行消毒,在无菌条件下取出未成熟胚子叶进行诱导,在胚成苗后进行继代和生根培养。培养结果表明,以MS为基本培养基,在2,4-D为2.0 mg/L时培养基上胚性愈伤组织诱导率较高,为53.7%;愈伤组织经过数次继代后转移至MS附加6-BA 1.0 mg/L和NAA 0.1 mg/L培养基上可诱导体细胞胚的形成,诱导率可达81.0%.体细胞胚在合适的培养基上可继续生长和增殖。

关 键 词:甜樱桃  愈伤组织  体细胞胚胎  植株再生
文章编号:1000-7091(2006)增刊-0125-04
修稿时间:2006-05-20

Somatic Embryogenesis of Sweet Cherry and Plantlet Regeneration
WU Ya-qin,ZHAO Yan-hua,LIU Guo-jian,LI Chun-min. Somatic Embryogenesis of Sweet Cherry and Plantlet Regeneration[J]. Acta Agriculturae Boreali-Sinica, 2006, 21(Z2): 125-128
Authors:WU Ya-qin  ZHAO Yan-hua  LIU Guo-jian  LI Chun-min
Abstract:
Cultivars sweet cherry Hongdeng was used as the materials.An immature pterodia was taken from young fruit disinfected with 0.1% HgCl-2.Shoot multiplication culture and rooting culture were conducted after emergence of seedlings.The result indicates that the embryogenic callus(EC) frequency was 53.1.% at 2 mg/L of 2,4-D added in MS medium,After subcultured for several times,somatic embryogenesis at high frequency(81.0%) was obtained on MS medium supplemented with 6-BA 1.0 mg/L NAA 0.1 mg/L.Somatic embryos can keep on growing and proliferating on appropriate medium.
Keywords:Sweet cherry  Callus  Somatic embryogenesis  Plantlet regeneration
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