Molecular cloning and functional expression analysis of a new gene encoding geranylgeranyl diphosphate synthase from hazel (Corylus avellana L. Gasaway)

被引:20
|
作者
Wang, Yechun [1 ]
Miao, Zhiqi [1 ]
Tang, Kexuan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Plant Biotechnol Res Ctr, Fudan SJTU Nottingham Plant Biotechnol R&D Ctr, Sch Agr & Biol, Shanghai 200240, Peoples R China
关键词
Geranylgeranyl diphosphate synthase (GGPP); Hazel; Taxol synthesis; RACE; PYROPHOSPHATE SYNTHASE; TAXOL; IDENTIFICATION; AGENT;
D O I
10.1007/s11033-009-9935-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Geranylgeranyl diphosphate synthase (GGPPS) [EC 2.5.1.29] catalyzes the biosynthesis of geranylgeranyl diphosphate (GGPP), which is a key precursor for diterpenes such as taxol. Herein, a full-length cDNA encoding GGPPS (designated as CgGGPPS) was cloned and characterized from hazel (Corylus avellana L. Gasaway), a taxol-producing angiosperms. The full-length cDNA of CgGGPPS was 1515 bp with a 1122 bp open reading frame (ORF) encoding a 373 amino acid polypeptide. The CgGGPPS genomic DNA sequence was also obtained, revealing CgGGPPS gene was not interrupted by an intron. Southern blot analysis indicated that CgGGPPS belonged to a small gene family. Tissue expression pattern analysis indicated that CgGGPPS expressed the highest in leaves. RT-PCR analysis indicated that CgGGPPS expression could be induced by exogenous methyl jasmonate acid. Furthermore, carotenoid accumulation was observed in Escherichia coli carrying pACCAR25 Delta crtE plasmid carrying CgGGPPS. The result revealed that cDNA encoded a functional GGPP synthase.
引用
收藏
页码:3439 / 3444
页数:6
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