Promotion of artemisinin content in Artemisia annua by overexpression of multiple artemisinin biosynthetic pathway genes

被引:38
作者
Shi, Pu [1 ]
Fu, Xueqing [1 ]
Liu, Meng [1 ]
Shen, Qian [1 ]
Jiang, Weimin [1 ]
Li, Ling [1 ]
Sun, Xiaofen [1 ]
Tang, Kexuan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Agr & Biol, Fudan SJTU Nottingham Plant Biotechnol R&D Ctr, Key Lab Urban Agr South,Minist Agr,Plant Biotechn, Shanghai 200240, Peoples R China
关键词
Artemisinin yield; Artemisia annua; Agrobacterium tumefaciens; Metabolic engineering; IN-VIVO TRANSFORMATIONS; ANTIMALARIAL-DRUG; KEY ENZYME; AMORPHA-4,11-DIENE SYNTHASE; TRANSCRIPTION FACTOR; MOLECULAR-CLONING; CPR GENES; PLANTS; CYP71AV1; ACID;
D O I
10.1007/s11240-017-1173-z
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
Artemisinin, isolated from an annual herbaceous plant Artemisia annua L., is an effective antimalarial compound. However, artemisinin is accumulated in small amounts (0.01-0.1% leaf dry weight) in A. annua, resulting in constant high artemisinin price. Although metabolic engineering of partial artemisinin metabolic pathway in yeast achieved great success, artemisinin from A. annua is still the important business resource. Here, we report on the generation of transgenic plants with simultaneously overexpressing four artemisinin biosynthetic pathway genes, amorpha-4,11-diene synthase gene (ADS), amorpha-4,11-diene 12-monooxygenase gene (CYP71AV1), cytochrome P450 reductase gene (CPR), and aldehyde dehydrogenase 1 gene (ALDH1) via Agrobacterium-mediated transformation. The qRT-PCR analysis demonstrated that the introduced four genes of the transgenic lines were all highly expressed. Through high-performance liquid chromatography analysis, the artemisinin contents were increased markedly in transformants, with the highest being 3.4-fold higher compared with non-converter. These results indicate that overexpression of multiple artemisinin biosynthetic pathway genes is a promising approach to improve artemisinin yield in A. annua.
引用
收藏
页码:251 / 259
页数:9
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