Gene cloning and expression level of bAS and their correlation with content of saponins in Eleutherococcus senticosus
10.7501/j.issn.0253-2670.2015.09.018
- Author:
Yue-Hong LONG
1
Author Information
1. College of Life Science, North China University of Science and Technology
- Publication Type:Journal Article
- Keywords:
Cloning;
Eleutherococcus senticosus (Rupr. et Maxim.) Maxim.;
Expression;
Triterpenoid saponins;
β-amyrin synthase gene
- From:
Chinese Traditional and Herbal Drugs
2015;46(9):1354-1359
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To clone β-amyrin synthase (bAS) gene from Eleutherococcus senticosus and analyze the effect of its expression on saponin contents. Methods: The sequence of cDNA of E. senticosus bAS was cloned by homologous cloning strategy. Quantitative real time PCR was developed to analyze the expression pattern of E. senticosus bAS gene. And E. senticosus saponin contents were measured by spectrophotometry method. Results: Length 1 223 and 1 226 bp of E. senticosus bAS1 and bAS2 genes were cloned. The results showed that bAS1 and bAS2 were expressed in the each growth period and every organ of E. senticosus, and the expression differed significantly (P < 0.05). bAS1 showed the highest expression when the plants were grown in germination stage, then rapidly depressed, and changed slightly in the end. The expression of bAS2 showed the characteristic of low-high-low. The expression of bAS1 in different organs of E. senticosus was constant, but the highest content of the expression of bAS2 was in the leaves. With the treatment of methyl jasmonate (MeJA), bAS2 expression has been significantly improved and bAS1 without a significant changing. There exists significantly positive correlation (P < 0.01) between the content of E. senticosus saponins and the expression levels of bAS2, and bAS1 without a significant difference. Conclusion: bAS2 may be a key enzyme gene in the biosynthesis of triterpenoid saponins.
