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重组及诱导缬草毛状根中倍半萜代谢的调控

Regulation of sesquiterpenoid metabolism in recombinant and elicited Valeriana officinalis hairy roots.

作者信息

Ricigliano Vincent, Kumar Santosh, Kinison Scott, Brooks Christopher, Nybo S Eric, Chappell Joe, Howarth Dianella G

机构信息

Department of Biological Sciences, St. John's University, Jamaica, NY 11439, United States.

Department of Pharmaceutical Sciences, University of Kentucky, Lexington, KY 40546, United States.

出版信息

Phytochemistry. 2016 May;125:43-53. doi: 10.1016/j.phytochem.2016.02.011. Epub 2016 Feb 23.

DOI:10.1016/j.phytochem.2016.02.011
PMID:26920719
Abstract

The medicinal properties of Valerian (Valeriana officinalis) root preparations are attributed to the anxiolytic sesquiterpenoid valerenic acid and its biosynthetic precursors valerenal and valerenadiene, as well as the anti-inflammatory sesquiterpenoid β-caryophyllene. In order to study and engineer the biosynthesis of these pharmacologically active metabolites, a binary vector co-transformation system was developed for V. officinalis hairy roots. The relative expression levels and jasmonate-inducibility of a number of genes associated with sesquiterpenoid metabolism were profiled in roots: farnesyl pyrophosphate synthase (VoFPS), valerendiene synthase (VoVDS), germacrene C synthase (VoGCS), and a cytochrome P450 (CYP71D442) putatively associated with terpene metabolism based on sequence homology. Recombinant hairy root lines overexpressing VoFPS or VoVDS were generated and compared to control cultures. Overexpression of the VoFPS cDNA increased levels of the corresponding transcript 4- to 8-fold and sesquiterpene hydrocarbon accumulation by 1.5- to 4-fold. Overexpression of the VoVDS cDNA increased the corresponding transcript levels 5- to 9-fold and markedly increased yields of the oxygenated sesquiterpenoids valerenic acid and valerenal. Our findings suggest that the availability of cytoplasmic farnesyl diphosphate and valerenadiene are potential bottlenecks in Valeriana-specific sesquiterpenoid biosynthesis, which is also subject to regulation by methyl jasmonate elicitation.

摘要

缬草(缬草属药用植物)根制剂的药用特性归因于具有抗焦虑作用的倍半萜类化合物缬草酸及其生物合成前体缬草醛和缬草二烯,以及具有抗炎作用的倍半萜类化合物β-石竹烯。为了研究和设计这些药理活性代谢物的生物合成,开发了一种用于药用缬草毛状根的二元载体共转化系统。在根中分析了一些与倍半萜代谢相关基因的相对表达水平和茉莉酸诱导性:法尼基焦磷酸合酶(VoFPS)、缬草二烯合酶(VoVDS)、牻牛儿烯C合酶(VoGCS),以及基于序列同源性推测与萜类代谢相关的细胞色素P450(CYP71D442)。构建了过表达VoFPS或VoVDS的重组毛状根系,并与对照培养物进行比较。VoFPS cDNA的过表达使相应转录本水平提高了4至8倍,倍半萜烃积累量增加了1.5至4倍。VoVDS cDNA的过表达使相应转录本水平提高了5至9倍,并显著提高了氧化倍半萜类化合物缬草酸和缬草醛的产量。我们的研究结果表明,细胞质法尼基二磷酸和缬草二烯的可用性是缬草属特异性倍半萜生物合成中的潜在瓶颈,其也受到茉莉酸甲酯诱导的调控。

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