The isolation and characterization of dammarenediol synthase gene from Panax quinquefolius and its heterologous co-expression with cytochrome P450 gene PqD12H in yeast

被引:39
作者
Wang, Le [1 ]
Zhao, Shou-Jing [1 ]
Cao, Hao-Jie [1 ]
Sun, Yao [2 ]
机构
[1] Jilin Univ, Sch Biol & Agr Engn, Changchun 130023, Peoples R China
[2] Changchun Univ Technol, Sch Biol & Agr Engn, Changchun, Peoples R China
基金
高等学校博士学科点专项科研基金; 美国国家科学基金会; 国家高技术研究发展计划(863计划);
关键词
Panax quinquefolius; Dammarenediol synthase; Overexpression; Heterologous co-expression; Protopanaxadiol; GINSENOSIDE BIOSYNTHESIS; TRITERPENE; EXPRESSION; SAPONINS; ROOT; ACCUMULATION; CATALYZES; ENZYME;
D O I
10.1007/s10142-014-0384-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Panax quinquefolius is one of perennial herbs and well known for its outstanding pharmacological activity. Ginsenosides are thought to be the main active ingredients in Panax quinquefolius and exist in many kinds of plant genus Panax (ginseng). Dammarenediol synthase, which is considered as a key enzyme in ginsenoside biosynthesis pathway can convert 2, 3-oxidosqualene into dammarenediol-II. However, the dammarenediol synthase gene in Panax quinquefolius has not been identified. Here, we cloned and identified a dammarenediol synthase gene from Panax quinquefolius (PqDS, GenBank accession No. KC316048) at the first time, and reverse transcription-PCR (RT-PCR) analysis also showed an obvious transcription increase of PqDS in the methyl jasmonate (MeJA)-induced hairy roots. Ectopic expression of PqDS in yeast resulted in the production of dammarenediol-II was confirmed by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry (LC/APCIMS). Moreover, overexpression of PqDS in transgenic hairy roots could increase the transcription of gene PqDS and another P450 gene PqD12H (encoding protopanaxadiol synthase in Panax quinquefolius), the accumulation of ginsenosides also increased at the same time. In addition, both PqDS and PqD12H gene co-expressed in recombinant yeast result in the production of protopanaxadiol was detected by LC/APCIMS; this result also provides a new strategy for the abundant production of protopanaxadiol in vitro.
引用
收藏
页码:545 / 557
页数:13
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