摘要
用糜子蔗(sorghum×sugarcane)×miletsorghum茎尖愈伤组织为受体,通过基因枪轰击将Bar基因转入糜子蔗细胞;用除草剂Basta含量分别为1、25、5、10mg/L的8114诱导与分化培养基上选择抗性愈伤组织;在Basta含量为1与15mg/L筛选培养基上,选择出3个快速增殖并大量再生绿苗的体细胞无性系(Clone),如BarC1、BarC2、BarC3;BarC1、C2再生植株用Basta含量为1、25~5mg/L的溶液进行抗性检测,证明这些小植株具有极强的抗性。
The Bargenes were introduced into 〔(sorghum×sugarcane)×millet sorghum〕 callus cells using particle bombardment. The callus were cultured on the 8114 media with Basta, the Basta's concentration is 1, 25, and 5, 10mg/L.3 Clones with regenerated capacity were screened out on the media with Basta 1, 25mg/L, for example BarC1, BarC2, BarC3.The regenerated plant from BarC1、BarC2were cultured on the solution with Basta 15, 25, and 5mg/L, high resistance were obtained in these regenerated plants.
出处
《遗传》
CAS
CSCD
北大核心
1998年第3期23-26,共4页
Hereditas(Beijing)
关键词
糜子蔗
Bar基因转移
植株再生
(Sorghum×Sugarcane)×millet sorghum,Bargenes transformation,Plant regeneration