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首页> 外文期刊>BMC Molecular Biology >Expression of 3-hydroxy-3-methylglutaryl-CoA reductase , p-hydroxybenzoate-m-geranyltransferase and genes of phenylpropanoid pathway exhibits positive correlation with shikonins content in arnebia [ Arnebia euchroma (Royle) Johnston]
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Expression of 3-hydroxy-3-methylglutaryl-CoA reductase , p-hydroxybenzoate-m-geranyltransferase and genes of phenylpropanoid pathway exhibits positive correlation with shikonins content in arnebia [ Arnebia euchroma (Royle) Johnston]

机译:3-羟基-3-甲基戊二酰辅酶A还原酶的表达,对羟基苯甲酸酯-间-香叶基转移酶的表达和苯丙烷途径的基因与紫草中紫草素的含量呈正相关[紫草(Royle Johnston)]

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Geranyl pyrophosphate (GPP) and p-hydroxybenzoate (PHB) are the basic precursors involved in shikonins biosynthesis. GPP is derived from mevalonate (MVA) and/or 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway(s), depending upon the metabolite and the plant system under consideration. PHB, however, is synthesized by only phenylpropanoid (PP) pathway. GPP and PHB are central moieties to yield shikonins through the synthesis of m-geranyl-p-hydroxybenzoate (GHB). Enzyme p-hydroxybenzoate-m-geranyltransferase (PGT) catalyses the coupling of GPP and PHB to yield GHB. The present research was carried out in shikonins yielding plant arnebia [Arnebia euchroma (Royle) Johnston], wherein no molecular work has been reported so far. The objective of the work was to identify the preferred GPP synthesizing pathway for shikonins biosynthesis, and to determine the regulatory genes involved in the biosynthesis of GPP, PHB and GHB. A cell suspension culture-based, low and high shikonins production systems were developed to facilitate pathway identification and finding the regulatory gene. Studies with mevinolin and fosmidomycin, inhibitors of MVA and MEP pathway, respectively suggested MVA as a preferred route of GPP supply for shikonins biosynthesis in arnebia. Accordingly, genes of MVA pathway (eight genes), PP pathway (three genes), and GHB biosynthesis were cloned. Expression studies showed down-regulation of all the genes in response to mevinolin treatment, whereas gene expression was not influenced by fosmidomycin. Expression of all the twelve genes vis-à-vis shikonins content in low and high shikonins production system, over a period of twelve days at frequent intervals, identified critical genes of shikonins biosynthesis in arnebia. A positive correlation between shikonins content and expression of 3-hydroxy-3-methylglutaryl-CoA reductase (AeHMGR) and AePGT suggested critical role played by these genes in shikonins biosynthesis. Higher expression of genes of PP pathway was a general feature for higher shikonins biosynthesis.
机译:香叶基焦磷酸酯(GPP)和对羟基苯甲酸酯(PHB)是紫草素生物合成的基本前体。 GPP来源于甲羟戊酸(MVA)和/或2-C-甲基-D-赤藓糖醇4-磷酸(MEP)途径,这取决于所考虑的代谢物和植物系统。但是,PHB仅通过苯丙烷(PP)途径合成。 GPP和PHB是通过合成香叶基对羟基苯甲酸酯(GHB)产生紫草素的主要部分。酶对羟基苯甲酸酯-m-香叶基转移酶(PGT)催化GPP和PHB的偶联产生GHB。本研究是在紫草素生产的植物紫草[Arnebia euchroma(Royle)Johnston]中进行的,迄今为止尚未报道其分子作用。这项工作的目的是确定紫草素生物合成的优选GPP合成途径,并确定参与GPP,PHB和GHB生物合成的调控基因。开发了基于细胞悬浮培养物的低和高紫草素生产系统,以促进途径鉴定和寻找调节基因。分别用MVA和MEP途径抑制剂mevinolin和fosmidomycin进行的研究表明,MVA是GPP在紫草素生物合成中的首选GPP途径。因此,克隆了MVA途径(八个基因),PP途径(三个基因)和GHB生物合成的基因。表达研究表明,响应米维诺林处理,所有基因均下调,而基因表达不受磷霉素的影响。在低和高的紫草素生产系统中,十二个基因相对于紫草素含量的表达,在频繁间隔的十二天中,确定了紫草中紫草素生物合成的关键基因。紫草素含量与3-羟基-3-甲基戊二酰辅酶A还原酶(AeHMGR)和AePGT的表达呈正相关,表明这些基因在紫草素生物合成中起关键作用。 PP通路基因的高表达是紫草素生物合成的一个普遍特征。

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