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西洋参冠瘿组织培养及其人参皂苷Re和人参皂苷Rg1的产生
引用本文:于荣敏 宋永波 张辉 叶文才 张荫麟 姚新生. 西洋参冠瘿组织培养及其人参皂苷Re和人参皂苷Rg1的产生[J]. 生物工程学报, 2003, 19(3): 372-375
作者姓名:于荣敏 宋永波 张辉 叶文才 张荫麟 姚新生
作者单位:1. 暨南大学药学院,广州,510632
2. 沈阳药科大学制药工程学院,沈阳,110016
3. 中国医学科学院药用植物研究所,北京,310031
4. 暨南大学药学院,广州,510632;沈阳药科大学制药工程学院,沈阳,110016
摘    要:考察了培养基组成、培养时间、接种量、pH值、肌醇浓度等对冠瘿组织生长及其人参皂苷含量的影响 ;用HPLC检测了冠瘿组织中人参皂苷Re和人参皂苷Rg1 的含量。高压纸层析电泳证实 ,根癌农杆菌Ti质粒上的T DNA片段已整合进入植物细胞核基因组中。在考察的 6种培养基中 ,White培养基最适合人参皂苷Rg1 的累积(0 0 95 % ) ,MS培养基最适合人参皂苷Re的累积 (0 194 % )。以MS为基本培养基培养 36d、32d时人参皂苷Re和人参皂苷Rg1 累积含量最高 (分别为 0 14 7%和 0 0 6 1% ) ;接种量为 4g、2g (FW flask) ,有利于人参皂苷Re和人参皂苷Rg1的累积 ;培养基pH 5 8时人参皂苷Re含量最高 (0 184 % ) ,培养基pH 5 6时人参皂苷Rg1 累积量最高 (0 0 5 4 % ) ;肌醇浓度为 0 0 5g L时 ,能促进人参皂苷Re合成 (0 182 % ) ,浓度为 0 30g L时 ,有利于人参皂苷Rg1 累积 (0 0 5 5 % )。

关 键 词:西洋参  冠瘿组织培养  人参皂苷Re  人参皂苷Rg1  高压液相色谱
文章编号:1000-3061(2003)03-0372-04
修稿时间:2002-11-13

Study on the Culture of Crown Gall from Panax quinquefolium and the Prouction of Its Secondary Metabolites--Ginsenosides Re and Rg1
YU Rong Min SONG Yong Bo ZHANG Hui YE Wen Cai ZHANG Yin Lin YAO Xin Sheng . Study on the Culture of Crown Gall from Panax quinquefolium and the Prouction of Its Secondary Metabolites--Ginsenosides Re and Rg1[J]. Chinese journal of biotechnology, 2003, 19(3): 372-375
Authors:YU Rong Min SONG Yong Bo ZHANG Hui YE Wen Cai ZHANG Yin Lin YAO Xin Sheng
Affiliation:College of Pharmacy, Jinan University, Guangzhou 510632, China. rongminyu99@hotmail.com
Abstract:It was clearly demonstrated that T-DNA of Agrobacterium tumefeciens Ti plasmid was integrated into the cells of crown gall in our experiment. This paper reported the influences of some kinds of physical-chemistry factors on the growth of crown gall of Panax quinquefolium and the production of its main active compounds--ginsenoside Re and ginsensoside Rg1. The results showed that White medium was the best one for ginsensoside Rg1 accumulation (0.095%) among the six media, but ginsensoside Re accumulation (0.194%) was the highest on the MS medium; The highest contents of ginsensoside Re (0.147%) and ginsensoside Rg1 (0.061%) were on the culture 36d and 32d after innoculum respectively; The optimum pH was 5.6 for ginsensoside Rg1 synthesis(0.054%), and 5.8 for ginsensoside Re synthesis(0. 184% ); The contents of ginsensoside Re and ginsensoside Rg1 was the highest in the inoculum of 4 g and 2 g/flask (FW) respectively. The result also indicated that the concentration of inositol in 0.05 g/L could obviously promote ginsensoside Re synthesis (0.182%), and in 0.30 g/L for ginsensoside Rg1 (0.055%).
Keywords:Panax quinquefolium    crown gall culture   ginsenoside Re  ginsenoside Rg 1   HPLC
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