首页> 外文期刊>Plant and Cell Physiology >Cytochrome P450 CYP716A53v2 Catalyzes the Formation of Protopanaxatriol from Protopanaxadiol During Ginsenoside Biosynthesis in Panax Ginseng
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Cytochrome P450 CYP716A53v2 Catalyzes the Formation of Protopanaxatriol from Protopanaxadiol During Ginsenoside Biosynthesis in Panax Ginseng

机译:细胞色素P450 CYP716A53v2催化人参皂苷生物合成过程中由人参二醇产生的人参三醇中的人参三醇的形成。

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Ginseng (Panax ginseng C.A. Meyer) is one of the most popular medicinal herbs, and the root of this plant contains pharmacologically active components, called ginsenosides. Ginsenosides, a class of tetracyclic triterpene saponins, are synthesized from dammarenediol-II after hydroxylation by cytochrome P450 (CYP) and then glycosylation by a glycosyltransferase. Protopanaxadiol synthase, which is a CYP enzyme (CYP716A47) that catalyzes the hydroxylation of dammarenediol-II at the C-12 position to yield protopanaxadiol, was recently characterized. Here, we isolated two additional CYP716A subfamily genes (CYP716A52v2 and CYP716A53v2) and determined that the gene product of CYP716A53v2 is a protopanaxadiol 6-hydroxylase that catalyzes the formation of protopanaxatriol from protopanaxadiol during ginsenoside biosynthesis in P. ginseng. Both CYP716A47 and CYP716A53v2 mRNAs accumulated ubiquitously in all organs of ginseng plants. In contrast, CYP716A52v2 mRNA accumulated only in the rhizome. Methyl jasmonate (MeJA) treatment resulted in the obvious accumulation of CYP716A47 mRNA in adventitious roots. However, neither CYP716A52v2 nor CYP716A53v2 mRNA was affected by MeJA treatment during the entire culture period. The ectopic expression of CYP716A53v2 in recombinant WAT21 yeast resulted in protopanaxatriol production after protopanaxadiol was added to the culture medium. In vitro enzymatic activity assays revealed that CYP716A53v2 catalyzed the oxidation of protopanaxadiol to produce protopanaxatriol. The chemical structures of the protopanaxatriol products were confirmed using liquid chromatography–atmospheric pressure chemical ionization mass spectrometry (LC/APCIMS). Our results indicate that the gene product of CYP716A53v2 is a protopanaxadiol 6-hydroxylase that produces protopanaxatriol from protopanaxadiol, which is an important step in the formation of dammarane-type triterpene aglycones in ginseng saponin biosynthesis.
机译:人参(Panax ginseng C.A. Meyer)是最受欢迎的草药之一,这种植物的根部含有药理活性成分,称为人参皂甙。人参皂苷是一类四环三萜皂苷,是由丹马烯二醇-II通过细胞色素P450(CYP)进行羟基化后再通过糖基转移酶进行糖基化而合成的。最近表征了普托帕那二醇合酶,它是一种CYP酶(CYP716A47),它催化达玛烯二醇-II在C-12位置的羟基化,从而产生普托帕那二醇。在这里,我们分离了两个额外的CYP716A亚家族基因(CYP716A52v2和CYP716A53v2),并确定CYP716A53v2的基因产物是人参皂苷生物合成过程中催化原卟啉二醇形成原卟啉二醇6-羟化酶。 CYP716A47和CYP716A53v2 mRNA均在人参植物的所有器官中普遍积累。相反,CYP716A52v2 mRNA仅在根茎中积累。茉莉酸甲酯(MeJA)处理导致不定根中CYP716A47 mRNA的明显积累。但是,在整个培养期间,MeJA处理均不会影响CYP716A52v2和CYP716A53v2 mRNA。 CYP716A53v2在重组WAT21酵母中的异位表达导致在向培养基中添加原泊那沙二醇后产生了原泊那沙三醇。体外酶活性测定表明,CYP716A53v2催化原托那沙糖醇的氧化生成原托那沙三醇。使用液相色谱-大气压化学电离质谱法(LC / APCIMS)确认了原托那沙三醇产品的化学结构。我们的结果表明,CYP716A53v2的基因产物是一种原卟啉二醇6-羟化酶,该酶从原卟啉二醇产生原卟啉三醇,这是人参皂苷生物合成中丹玛烷型三萜糖苷配基形成的重要步骤。

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