Development of an RP-HPLC method for determination of salicylic acid and its metabolic intermediates from plant biosynthesis pathways

Warning

This publication doesn't include Faculty of Arts. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

KOŽUSZNIKOVÁ Eliška BITTOVÁ Miroslava KUBÁŇ Petr

Year of publication 2016
Type Article in Proceedings
Conference Advances in chromatography and electrophoresis & Chiranal 2016
MU Faculty or unit

Faculty of Science

Citation
Field Analytic chemistry
Keywords RP-HPLC; method validation; salicylic acid; gentisic acid; salicylaldehyde; saligenin
Description Salicylic acid (2-hydroxybenzoic acid, SA) belongs to a group of plant growth regulators that have an aromatic ring bearing a hydroxyl group or its functional derivative in the structure. SA functions as an important plant signaling compound that is synthesized in plants as a response to various pathogenic attacks or environmental stress (caused by microbes, insects, herbivores etc.). Two pathways of SA biosynthesis were described in the literature, but the production of SA is still not fully clarified. To better understand the various transformation pathways of SA, analytical methods capable of separating not only SA, but also other relevant compounds from the biotransformation cycles need to be developed. In this study, a reverse-phase high performance liquid chromatography (RP-HPLC) method for determination of SA and metabolic intermediates derived from its biosynthetic pathways (salicin (2-(hydroxymethyl)phenyl-beta-D-glucopyranoside), helicin (salicylaldehyde beta-D-glucoside), gentisic acid (2,5-dihydroxybenzoic acid), saligenin (2-hydroxybenzyl alcohol) and salicylaldehyde (2-hydroxybenzaldehyde) was developed. The method was then applied for analysis of samples from white willow (Salix alba), as willow cortex is well-known as a natural source of salicin and salicylic acid.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.