Molecular cloning and functional analysis of the gene encoding geranylgeranyl diphosphate synthase from Jatropha curcas

被引:0
作者
Lin, Juan [1 ]
Jin, YuanJie [1 ]
Zhou, Xin [1 ]
Wang, JingYa [1 ]
机构
[1] Fudan Univ, Inst Plant Biol, State Key Lab Genet Engn, Sch Life Sci, Shanghai 200433, Peoples R China
来源
AFRICAN JOURNAL OF BIOTECHNOLOGY | 2010年 / 9卷 / 23期
关键词
Jatropha curcas L; geranylgeranyl diphosphate synthase; rapid amplification of cDNA ends; genetic complementation; PYROPHOSPHATE SYNTHASE; CAROTENOID BIOSYNTHESIS; FARNESYL DIPHOSPHATE; ESCHERICHIA-COLI; EXPRESSION; IDENTIFICATION; CDNA; PURIFICATION; SYNTHETASE; ARABIDOPSIS;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Geranylgeranyl diphosphate (GGPP) synthase (GGPPS, EC: 2.5.1.29) catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic diphosphates to yield (all-E)-GGPP. GGPP is one of the key precursors in the biosynthesis of biologically significant isoprenoid compounds. Here we report for the first time the cloning of a full-length cDNA encoding GGPPS (Jc-GGPPS) from Jatropha curcas L. The full-length cDNA was 1414 base pair (bp), with an 1110-bp open reading frame (ORF) encoding a 370-amino-acids polypeptide. Bioinformatic analysis revealed that Jc-GGPPS is a member of the polyprenyltransferases with two highly conserved aspartate-rich motifs, and showed high homology to other plant GGPPSs. Phylogenetic tree analysis indicated that plant GGPPSs could be classified into two groups, angiosperm and gymnosperm, while Jc-GGPPS had closer relationship with angiosperm plant GGPPSs. Functional analysis of Jc-GGPPS in GGPPS-deficient mutant plasmid pAC-BETA (>= crtE) demonstrated that Jc-GGPPS mediated the biosynthesis of carotenoid and provided the general precursor for diterpenes biosynthesis.
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页码:3342 / 3351
页数:10
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