Cloning, Sequence Analysis and Prokaryotic Expression ofGGPS Gene fromLepidium apetalum
10.11842/wst.2015.03.012
- VernacularTitle:北葶苈子GGPS基因的克隆、序列分析与原核表达
- Author:
Ligang MA
;
Le ZHAO
;
Yingchao LI
;
Weisheng FENG
;
Haixue KUANG
;
Xiaoke ZHENG
- Publication Type:Journal Article
- Keywords:
Lepidium apetalum;
GGPS;
gene cloning;
sequence analysis;
prokaryotic expression
- From:
World Science and Technology-Modernization of Traditional Chinese Medicine
2015;17(3):485-491
- CountryChina
- Language:Chinese
-
Abstract:
This study was aimed to clone the GGPS (geranylgeranyl pyrophosphate synthase) gene from Lepidium apetalum, to analyze its sequence, and to express the protein in E.coli expression system. Specific PCR cloning primers were designed for GGPS gene from Lepidium apetalum according to the full-length sequence from a previous transcriptome sequencing project. PCR amplification was performed with this primer pair on a leaf cDNA template. TA cloning, sequencing and sequence analysis were performed.GGPS gene from Lepidium apetalum was expressed in the E.coli expression system. The results showed that the full-lengthGGPS cDNA from Lepidium apetalum was 1 146 bp coding a protein of 381 amino acids. The LaGGPS protein had an isoprenoid synthase domain. According to a phylogenetic tree constructed with multiple alignment of GGPS protein sequences from various plant species, GGPS protein from Lepidium apetalum was the closest to Arabidopsis thaliana and Sinapis alba. The prokaryotic expression vectorpET-32a-LaGGPS was also constructed successfully. The protein was expressed in E.coli BL21 strain. It was concluded that the cloning and prokaryotic expression of LaGGPS gene provided a foundation for a follow-up research of its function with protein purification and activity analysis.
