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<dc:title>Isolation and Quantification of Mandelonitrile from Arabidopsis thaliana Using Gas Chromatography/Mass Spectrometry</dc:title>
<dc:creator>Arnáiz Alonso, Ana</dc:creator>
<dc:creator>Vallejo García, Jorge Lucas</dc:creator>
<dc:creator>Vallejos Calzada, Saúl</dc:creator>
<dc:creator>Diaz, Isabel</dc:creator>
<dc:subject>Benzaldehyde cyanohydrin</dc:subject>
<dc:subject>Mandelonitrile</dc:subject>
<dc:subject>Hydroxynitrile lyase</dc:subject>
<dc:subject>Arabidopsis thaliana</dc:subject>
<dc:subject>Spider mite</dc:subject>
<dc:subject>Cyanogenic glycosides</dc:subject>
<dc:subject>Cyanohydrin</dc:subject>
<dc:subject>Química orgánica</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:description>Protocolo</dc:description>
<dc:description>Mandelonitrile is a nitrogen-containing compound, considered an essential secondary metabolite. Chemically, it is&#xd;
a cyanohydrin derivative of benzaldehyde, with relevant functions in different physiological processes including&#xd;
defense against phytophagous arthropods. So far, procedures for detecting mandelonitrile have been effectively&#xd;
applied in cyanogenic plant species such as Prunus spp. Nevertheless, its presence in Arabidopsis thaliana,&#xd;
considered a non-cyanogenic species, has never been determined. Here, we report the development of an accurate&#xd;
protocol for mandelonitrile quantification in A. thaliana within the context of A. thaliana–spider mite interaction.&#xd;
First, mandelonitrile was isolated from Arabidopsis rosettes using methanol; then, it was derivatized by silylation&#xd;
to enhance detection and, finally, it was quantified using gas chromatography–mass spectrometry. The selectivity&#xd;
and sensitivity of this method make it possible to detect low levels of mandelonitrile (LOD 3 ppm) in a plant species&#xd;
considered non-cyanogenic that, therefore, will have little to no cyanogenic compounds, using a small quantity of&#xd;
starting material (≥ 100 mg).</dc:description>
<dc:description>This work was supported by funds of “La Caixa” Foundation (LCF/PR18/51130007) and Ministerio de Universidades-European Union in the frame of NextGenerationEU RD 289/2021 (Universidad Politécnica de Madrid).</dc:description>
<dc:date>2023-06-21T11:57:21Z</dc:date>
<dc:date>2023-06-21T11:57:21Z</dc:date>
<dc:date>2023-06</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
<dc:identifier>2331-8325</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/7714</dc:identifier>
<dc:identifier>10.21769/BioProtoc.4700</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Bio-protocol. 2023, V. 13, n. 12, e4700</dc:relation>
<dc:relation>https://doi.org/10.21769/BioProtoc.4700</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona//LCF%2FPR%2FPR18%2F51130007//Fluoración Directa de Nitrocompuestos y Sales de Heteroaril Fosfonio: Síntesis de Fluorocompuestos/FluNitroPhos/</dc:relation>
<dc:rights>Atribución 4.0 Internacional</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Bio-protocol LLC</dc:publisher>
<europeana:object>https://riubu.ubu.es/bitstream/10259/7714/4/Arnaiz-Bio-protocol_2023.pdf.jpg</europeana:object>
<europeana:provider>Hispana</europeana:provider>
<europeana:type>TEXT</europeana:type>
<europeana:rights>http://creativecommons.org/licenses/by/4.0/</europeana:rights>
<europeana:dataProvider>RIUBU. Repositorio Institucional de la Universidad de Burgos</europeana:dataProvider>
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