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3-羟基-3-甲基戊二酰辅酶 A 还原酶、对羟基苯甲酸-m-香叶基转移酶和苯丙烷途径基因的表达与紫草(Arnebia euchroma(Royle)Johnston)中紫草素含量呈正相关。

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].

机构信息

Biotechnology Division, Institute of Himalayan Bioresource Technology (Council of Scientific and Industrial Research), Palampur (Himachal Pradesh)-176061, India.

出版信息

BMC Mol Biol. 2010 Nov 21;11:88. doi: 10.1186/1471-2199-11-88.

Abstract

BACKGROUND

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

香叶基焦磷酸(GPP)和对羟基苯甲酸(PHB)是紫草素生物合成中涉及的基本前体。GPP 来自于甲羟戊酸(MVA)和/或 2-C-甲基-D-赤藓醇 4-磷酸(MEP)途径(取决于代谢物和所考虑的植物系统)。然而,PHB 仅由苯丙氨酸途径合成。GPP 和 PHB 是通过合成 m-香叶基-p-羟基苯甲酸(GHB)产生紫草素的中心部分。对羟基苯甲酸-m-香叶基转移酶(PGT)催化 GPP 和 PHB 的偶联,生成 GHB。本研究在紫草素产生植物新疆紫草(Arnebia euchroma(Royle)Johnston)中进行,迄今为止尚未有分子方面的报道。该工作的目的是确定紫草素生物合成中 GPP 的首选合成途径,并确定参与 GPP、PHB 和 GHB 生物合成的调节基因。

结果

建立了基于细胞悬浮培养的低产和高产紫草素系统,以促进途径鉴定和寻找调节基因。使用 MVA 和 MEP 途径的抑制剂——mevinolin 和 fosmidomycin 的研究表明,MVA 是新疆紫草紫草素生物合成中 GPP 的首选供应途径。相应地,克隆了 MVA 途径(8 个基因)、PP 途径(3 个基因)和 GHB 生物合成基因。表达研究表明,所有基因在 mevinolin 处理下均下调,而基因表达不受 fosmidomycin 影响。在低产和高产紫草素生产系统中,每隔一段时间频繁取样 12 天,对 12 天内所有 12 个基因与紫草素含量的关系进行研究,鉴定了新疆紫草紫草素生物合成的关键基因。

结论

紫草素含量与 3-羟-3-甲基戊二酰辅酶 A 还原酶(AeHMGR)和 AePGT 表达之间的正相关表明这些基因在紫草素生物合成中起着关键作用。PP 途径基因的更高表达是高产紫草素的普遍特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b1/3002352/8c6c07ae3e69/1471-2199-11-88-1.jpg

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