首页> 外文期刊>Functional & integrative genomics >The isolation and characterization of dammarenediol synthase gene from Panax quinquefolius and its heterologous co-expression with cytochrome P450 gene PqD12H in yeast
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The isolation and characterization of dammarenediol synthase gene from Panax quinquefolius and its heterologous co-expression with cytochrome P450 gene PqD12H in yeast

机译:西洋参中达玛烯二醇合成酶基因的分离,鉴定及其与细胞色素P450基因PqD12H的异源共表达

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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 chromatographyatmospheric 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.
机译:西洋参是多年生草本植物之一,以其出色的药理活性而闻名。人参皂苷被认为是西洋参的主要活性成分,并存在于许多人参植物中。丹参二醇合酶被认为是人参皂苷生物合成途径中的关键酶,可以将2,3-氧化角鲨烯转化为丹参二醇-II。但是,尚未发现西洋参中的达玛烯二醇合酶基因。在这里,我们首次从西洋参中克隆并鉴定了丹烯二醇合成酶基因(PqDS,GenBank登录号KC316048),逆转录PCR(RT-PCR)分析也显示茉莉酸甲酯中PqDS的转录明显增加。 (MeJA)引起的毛根。通过液相色谱-常压化学电离质谱法(LC / APCIMS)证实了酵母中PqDS的异位表达导致了达玛烯二醇-II的产生。此外,在转基因毛状根中过表达PqDS可以增加PqDS基因和另一个P450基因PqD12H(西洋参中编码原托人二醇合成酶)的转录,同时人参皂甙的积累也增加。另外,通过LC / APCIMS检测到重组酵母中共表达的PqDS和PqD12H基因均导致了原托沙糖醇的产生。该结果也为在体外大量生产原泊那沙二醇提供了新的策略。

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