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毛刺槐花药培养及再生植株的获得
引用本文:曹晓燕,王喆之,赵银萍.毛刺槐花药培养及再生植株的获得[J].西北植物学报,2003,23(3):456-459.
作者姓名:曹晓燕  王喆之  赵银萍
作者单位:1. 陕西师范大学生命科学学院,西安,710062
2. 西安联合大学化学与生物系,西安,710065
摘    要:以毛刺槐的花药为材料,开展其组织培养和植株再生系统的研究。结果显示:将毛刺槐的花药接种在MS附加2,4—D0.1mg/L和BA3.0mg/L的培养基上,20d时花药愈伤组织诱导率可达41.5%。花药愈伤组织在MS附加BA5.0mg/L的分化培养基上继代培养2个月后,可分化出许多绿色的芽点,待不定芽长至2—3cm高时将其切下,转入MS附加IBA1.0mg/L的生根培养基上,2周后即可得到完整的再生植株。同时,研究就4℃低温预处理和蔗糖浓度对毛刺槐花药培养的影响进行了研究和讨论。

关 键 词:毛刺槐  花药培养  再生植株  组织培养  愈伤组织  培养基
文章编号:1000-4025(2003)03-0456-04
修稿时间:2002年12月20

Anther culture and plant regeneration of Robinia hispida
CAO Kiao-yan,WANG Zhe-zhi,ZHAO Yin-ping.Anther culture and plant regeneration of Robinia hispida[J].Acta Botanica Boreali-Occidentalia Sinica,2003,23(3):456-459.
Authors:CAO Kiao-yan  WANG Zhe-zhi  ZHAO Yin-ping
Abstract:The anthers of Robinia hispida were cultured and the results showed that the highest induction rate of callus was 41. 5% when they were cultured on MS medium supplemented with 2,4-D 0. 1 mg/L and BA 3. 0 mg/L for 20 days. Green buds formed from the callus after 2 months subcultured on MS medium supplemented with BA 5. 0 mg/L. When the shoots grew to 2-3 cm long,they were detached and trans-ferred to MS medium supplemented with IBA 1. 0 mg/L for rooting. The shoots produced roots within 2 weeks of culture and formed complete plantlets. At the same time,the effects of pretreatment of low tem-perature at 4 C and the concentration of sucrose on anther culture were studied and discussed.
Keywords:Rohinia hispida  anther culture jregenerated plantlets  callus
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