Valeriana officinalis

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Hauptverfasser: Ricigliano, Vincent, Kumar, Santosh, Kinison, Scott, Brooks, Christopher, Nybo, S. Eric, Chappell, Joe, Howarth, Dianella G.
Format: Recurso digital
Veröffentlicht: Zenodo 2016
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author Ricigliano, Vincent
Kumar, Santosh
Kinison, Scott
Brooks, Christopher
Nybo, S. Eric
Chappell, Joe
Howarth, Dianella G.
author_facet Ricigliano, Vincent
Kumar, Santosh
Kinison, Scott
Brooks, Christopher
Nybo, S. Eric
Chappell, Joe
Howarth, Dianella G.
contents <p><b><i>2.1. Establishment and characterization of V. officinalis hairy roots</i></b></p><p><i>V. officinalis</i> hairy roots were generated using <i>Agrobacterium rhizogenes</i> -mediated transformation of <i>in vitro</i> grown leaf explants. This genetic manipulation relies on conjugative transfer and integration of <i>A. rhizogenes</i> root-inducing plasmid DNA into the host plant nuclear genome. <i>V. officinalis</i> seeds were aseptically germinated and hairy roots were initiated on <i>in vitro</i> leaf explants. Single root segments were removed from different explants to afford independent transgenic events, which were maintained on hormone-free solid medium. Isogenic lines were used to initiate shake flask cultures and generate clonal biomass for molecular and biochemical analyses (Fig. S1).</p><p>As a metabolic qualification of the hairy root cultures, chemical profiles of hairy roots transformed with <i>A. rhizogenes</i> harboring Ri plasmid pRi15834 were compared to those of roots from wild type, soil-grown <i>V. officinalis</i> plants. Root biomass was powdered in liquid nitrogen, the materials fully lysed by mixing with an equal volume of acetone, followed by the addition of an equal volume of water, then partitioned into hexane. Aliquots of the hexane extracts were analyzed directly by GC–MS, as well as dried under nitrogen prior to trimethylsilyl diazomethane derivatization for GC–MS (Fig. 2, Fig. S7). The chemical profile of extracts from roots of wild type plants exhibited qualitative and quantitative differences relative to the hairy root cultures. The pRi15834 lines tended to accumulate fewer constituents than the roots from soil grown plants, but the levels of β- caryophyllene (<b>5</b>) and valerenal (<b>7</b>) were elevated while valerenadiene (<b>6</b>) and valerenic acid (<b>8</b>) were comparable (Fig. 2).</p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_10530239
institution Zenodo
language
publishDate 2016
publisher Zenodo
record_format zenodo
spellingShingle Valeriana officinalis
Ricigliano, Vincent
Kumar, Santosh
Kinison, Scott
Brooks, Christopher
Nybo, S. Eric
Chappell, Joe
Howarth, Dianella G.
Biodiversity
Taxonomy
Plantae
Tracheophyta
Magnoliopsida
Dipsacales
Caprifoliaceae
Valeriana
Valeriana officinalis
<p><b><i>2.1. Establishment and characterization of V. officinalis hairy roots</i></b></p><p><i>V. officinalis</i> hairy roots were generated using <i>Agrobacterium rhizogenes</i> -mediated transformation of <i>in vitro</i> grown leaf explants. This genetic manipulation relies on conjugative transfer and integration of <i>A. rhizogenes</i> root-inducing plasmid DNA into the host plant nuclear genome. <i>V. officinalis</i> seeds were aseptically germinated and hairy roots were initiated on <i>in vitro</i> leaf explants. Single root segments were removed from different explants to afford independent transgenic events, which were maintained on hormone-free solid medium. Isogenic lines were used to initiate shake flask cultures and generate clonal biomass for molecular and biochemical analyses (Fig. S1).</p><p>As a metabolic qualification of the hairy root cultures, chemical profiles of hairy roots transformed with <i>A. rhizogenes</i> harboring Ri plasmid pRi15834 were compared to those of roots from wild type, soil-grown <i>V. officinalis</i> plants. Root biomass was powdered in liquid nitrogen, the materials fully lysed by mixing with an equal volume of acetone, followed by the addition of an equal volume of water, then partitioned into hexane. Aliquots of the hexane extracts were analyzed directly by GC–MS, as well as dried under nitrogen prior to trimethylsilyl diazomethane derivatization for GC–MS (Fig. 2, Fig. S7). The chemical profile of extracts from roots of wild type plants exhibited qualitative and quantitative differences relative to the hairy root cultures. The pRi15834 lines tended to accumulate fewer constituents than the roots from soil grown plants, but the levels of β- caryophyllene (<b>5</b>) and valerenal (<b>7</b>) were elevated while valerenadiene (<b>6</b>) and valerenic acid (<b>8</b>) were comparable (Fig. 2).</p>
title Valeriana officinalis
topic Biodiversity
Taxonomy
Plantae
Tracheophyta
Magnoliopsida
Dipsacales
Caprifoliaceae
Valeriana
Valeriana officinalis
url https://doi.org/10.5281/zenodo.10530239