Characterization of 5-enolpyruvylshikimate 3-phosphate synthase gene from Camptotheca acuminata

被引:14
作者
Gong, Y.
Liao, Z.
Chen, M.
Guo, B.
Jin, H.
Sun, X.
Tang, K. [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Agr & Biol, Plant Biotechnol Res Ctr, Shanghai Key Lab Biotechnol, Shanghai 200030, Peoples R China
[2] Fudan Univ, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[3] Ningbo Univ, Fac Life Sci & Biotechnol, Ningbo 315211, Peoples R China
关键词
RACE; shikimate pathway; tissue expression pattern;
D O I
10.1007/s10535-006-0086-1
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
5-enolpyruvylshikimate 3-phosphate synthase (EPSPS; 3-phosphoshikimate 1-carboxyvinyl-transferase; EC 2.5.1.19) is a critical enzyme in the shikimate pathway. The full-length EPSPS cDNA sequence (CaEPSPS, GenBank accession number: AY639815) was cloned and characterized for the first time from woody plant, Camptotheca acuminata, using rapid amplification of cDNA ends (RACE) technique. The full-length cDNA of CaEPSPS was 1778 bp containing a 1557 bp ORF (open reading frame) encoding a polypeptide of 519 amino acids with a calculated molecular mass of 55.6 kDa and an isoelectric point of 8.22. Comparative and bioinformatic analyses revealed that CaEPSPS showed extensive homology with EPSPSs from other plant species. CaEPSPS contained two highly conserved motifs owned by plant and most bacteria EPSPSs in its N-terminal region. Phylogenetic analysis revealed that CaEPSPS belonged to dicotyledonous plant EPSPS group. Tissue expression pattern analysis indicated that CaEPSPS was constitutively expressed in leaves, stems and roots, with the lower expression being found in roots. The coding sequence of CaEPSPS gene was successfully subcloned in a plasmid-Escherichia coli system (pET-32a), and the cells containing the plasmid carrying the CaEPSPS gene exhibited enhanced tolerance to herbicide glyphosate, compared to the control.
引用
收藏
页码:542 / 550
页数:9
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