摘要
在固体培养基中添加5ml·l-1原汁的蜂蜜,可加快细胞的生长速度,获得黄绿色、疏松、旺盛生长的愈伤组织,四种浓度的Na2S2O3·5H2O处理与对照的倍增时间呈非常显著差异。通过细胞悬浮培养比较,在S2中细胞倍增时间为2.46d,生长最快,细胞在S2、S4、S7、S8、S9、S10、S11、S12培养基中能连续正常继代生长,但生长速度有差异,在继代15次时,合并收集悬浮细胞,经气相色谱分析,银杏黄酮糖苷含量达到0.70%,接近叶片中的含量水平(0.75%)。
Experiment proved that when the additament of 5 ml. l -1 honey was added to the agarmedia, the population cell doubling time was clearly less than that of the control and the yellowish,loose and active callus was formed. There were very singnificant differences (P>0. 01) between the treatments of Sodium Thiosalfate and control in doubling time. The doubling time in theS2 medium was 2. 46 d, the suspension cells could be subcultured normally in S2.S4.S7.S8.S9.S10.S11 and S12 media, after 15 times, the suspension cells were harvested, the aglycones wereanalysed by gas chromatograph, the results showed that the content of the flavonol glycosides was0. 70 %, which approached the level of intact plant leaves (0. 75 %).
出处
《果树科学》
CSCD
北大核心
1999年第2期131-134,共4页
Journal of Fruit Science
基金
湖北省科委重点科技研究项目
关键词
银杏
悬浮细胞系
黄酮糖苷
Ginkgo biloba
Suspension cell line
Flavonol glycosides