摘要
通过对岷山红三叶下胚轴和子叶再生体系建立的研究,获得愈伤组织诱导的最佳培养基为:Ms+2mg/L 2,4D+0.5mg/L 6-BA+2%蔗糖+0.6%琼脂,胚性愈伤组织诱导培养基为:MS+0.1mg/L IAA+0.5mg/L 6-BA+2%蔗糖+0.6%琼脂,芽诱导培养基为:B5+0.06mg/L NAA+2%蔗糖+0.6%琼脂,每瓶可以长出2~10条茎,将茎转入生根培养基后愈伤继代可持续出芽。最佳的生根培养基为:1/2MS+0.05mg/L NAA+1.5%蔗糖+0.8%琼脂。建立再生植株约需160d。
Tissue culture technique is the basis for plant breeding and genetic biodiversity research. Through the study in plant regeneration of hypocotyl and cotyledon of Trifolium pratense L. cv. Minshan, we found that the optimal callus induction medium was MS+2 mg/L 2,4 D+0. 5 mg/L 6-BA+2% sucrose+0.6% agar; the best medium for embryogenic callus induction was MS+0.1 mg/L IAA+0.5 rag/ L 6-BA+2% sucrose +0. 6% agar; bud induction medium was BS+0. 06 mg/L NAA+2% sucrose+ 0.6%. agar. In each bottle, 2 to 10 stems were obtained and then transferred into root induction medium, buds could continually grow. The optimal root induction medium was 1/2 MS+0.05 mg/L NAA+1.5% sucrose +0.8% agar. 160 d was needed for the establishment of plantlet.
出处
《草地学报》
CAS
CSCD
2008年第4期359-363,共5页
Acta Agrestia Sinica
基金
草业生态系统教育部省部共建重点实验室项目(CY-GG-2006-17)
中国博士后科学基金项目
关键词
岷山红三叶
愈伤组织
植株再生
Trifolium pratense L. cv. Minshan
Callus
Plant regeneration