首页 | 本学科首页   官方微博 | 高级检索  
检索        

不同理化因子对野葛悬浮培养细胞生长及异黄酮合成的影响
引用本文:方从兵,李贺勤,宛晓春,江昌俊.不同理化因子对野葛悬浮培养细胞生长及异黄酮合成的影响[J].中国中药杂志,2006,31(19):1580-1583.
作者姓名:方从兵  李贺勤  宛晓春  江昌俊
作者单位:安徽农业大学,农业部茶叶生物化学与生物技术重点实验室,安徽,合肥,230036
基金项目:国家自然科学基金;安徽省科技厅资助项目
摘    要:目的:探讨几种理化因子对野葛悬浮培养细胞的生长和异黄酮化合物生成的影响。方法:采用高效液相色谱法和植物细胞培养的方法。结果与结论:随着蔗糖质量浓度的提高,野葛培养细胞生长量和异黄酮的累积均逐步增高;野葛细胞培养体系中pH维持在5.4~5.8,对异黄酮的形成最为有利;随着活性炭处理用量的增加,野葛培养细胞的干重和异黄酮积累急剧下降;与此相反,XAD-4处理促进野葛细胞的干重增长和异黄酮的积累。

关 键 词:野葛  细胞培养  细胞生长  异黄酮  理化因子
文章编号:1001-5302(2006)19-1580-04
收稿时间:2005-11-04
修稿时间:2005-11-04

Effect of several physiochemical factors on cell growth and isoflavone accumulation of Pueraria lobata cell suspension culture
FANG Cong-bing;LI He-qin;WAN Xiao-chun;JIANG Chang-jun.Effect of several physiochemical factors on cell growth and isoflavone accumulation of Pueraria lobata cell suspension culture[J].China Journal of Chinese Materia Medica,2006,31(19):1580-1583.
Authors:FANG Cong-bing;LI He-qin;WAN Xiao-chun;JIANG Chang-jun
Institution:Key Laboratory of Tea Biochemistry and Biotechnology, Ministry of Agriculture, Anhui Agricultural University, Hefei 230036, China.
Abstract:Objective: To illustrate the effects of several physiochemical factors on cell growth and isoflavone accumulation of Pueraria lobata cell suspension cultures.Method: High performance liquid chromatography and plant tissue culture were applied.Result and Conclusion: Cell growth and isoflavone accumulation were significantly stimulated in P.lobata cell suspension cultures by the increase of the sucrose concentration.Maintaining the pH value at the range over 5.4 to 5.8 was most suitable for isoflavone accumulation in P.lobata cell suspension cultures.Cell dried weight and isoflavone accumulation decreased sharply with the increase of the treated concentration of active carbon,while XAD-4 significantly stimulated cell growth and isoflavone accumulation.
Keywords:Pueraria lobata  cell culture  cell growth  isoflavonoids  physiochemical factor
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号