Development of the devices for synthetic biology of triterpene saponins at an early stage: cloning and expression profiling of squalene epoxidase genes in panax notoginseng.
- Author:
Yun-Yun NIU
1
;
Xiao-Xuan ZHU
;
Hong-Mei LUO
;
Chao SUN
;
Lin-Fang HUANG
;
Shi-Lin CHEN
Author Information
1. National Engineering Laboratory for Breeding of Endangered Medicinal Materials, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China.
- Publication Type:Journal Article
- MeSH:
Acetates;
pharmacology;
Amino Acid Sequence;
Cloning, Molecular;
Cyclopentanes;
pharmacology;
Flowers;
metabolism;
Gene Expression Regulation, Enzymologic;
Gene Expression Regulation, Plant;
Oxylipins;
pharmacology;
Panax notoginseng;
genetics;
metabolism;
Phylogeny;
Phytosterols;
biosynthesis;
Plant Growth Regulators;
pharmacology;
Plant Leaves;
metabolism;
Plant Roots;
metabolism;
Plant Stems;
metabolism;
Plants, Medicinal;
genetics;
metabolism;
Saponins;
biosynthesis;
Squalene Monooxygenase;
biosynthesis;
chemistry;
genetics;
Synthetic Biology;
Triterpenes;
metabolism
- From:
Acta Pharmaceutica Sinica
2013;48(2):211-218
- CountryChina
- Language:Chinese
-
Abstract:
Synthetic biology of traditional Chinese medicine (TCM) is a new and developing subject based on the research of secondary metabolite biosynthesis for nature products. The early development of synthetic biology focused on the screening and modification of parts or devices, and establishment of standardized device libraries. Panax notoginseng (Burk.) F.H.Chen is one of the most famous medicinal plants in Panax species. Triterpene saponins have important pharmacological activities in P. notoginseng. Squalene epoxidase (SE) has been considered as a key rate-limiting enzyme in biosynthetic pathways of triterpene saponins and phytosterols. SE acts as one of necessary devices for biosynthesis of triterpene saponins and phytosterols in vitro via synthetic biology approach. Here we cloned two genes encoding squalene epoxidase (PnSE1 and PnSE2) and analyzed the predict amino acid sequences by bioinformatic analysis. Further, we detected the gene expression profiling in different organs and the expression level of SEs in leaves elicited by methyl jasmonate (MeJA) treatment in 4-year-old P notoginseng using real-time quantitative PCR (real-time PCR). The study will provide a foundation for discovery and modification of devices in previous research by TCM synthetic biology. PnSE1 and PnSE2 encoded predicted proteins of 537 and 545 amino acids, respectively. Two amino acid sequences predicted from PnSEs shared strong similarity (79%), but were highly divergent in N-terminal regions (the first 70 amino acids). The genes expression profiling detected by real-time PCR, PnSE1 mRNA abundantly accumulated in all organs, especially in flower. PnSE2 was only weakly expressed and preferentially in flower. MeJA treatment enhanced the accumulation of PnSEI mRNA expression level in leaves, while there is no obvious enhancement of PnSE2 in same condition. Results indicated that the gene expressions of PnSE1 and PnSE2 were differently transcribed in four organs, and two PnSEs differently responded to MeJA stimuli. It was strongly suggested that PnSEs play different roles in secondary metabolite biosynthesis in P. notoginseng. PnSE1 might be involved in triterpenoid biosynthesis and PnSE2 might be involved in phytosterol biosynthesis.
