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Phenolic profile of a Parma violet unveiled by chemical and fluorescence imaging.

AoB PLANTS · 6 Jul 2021 · 10.1093/aobpla/plab041

Abstract

The ability of phenolic compounds to autofluoresce upon illumination by UV or blue light was exploited to explore the nature and distribution of these metabolites within the flower petals, leaves and roots of the violet, Viola alba subsp. dehnhardtii . This was achieved through a dual complementary approach that combined fluorescence microscopy imaging of living intact tissues and chemical extraction of pulverized material. The blue to red fluorescence displayed by living tissues upon illumination was indicative of their richness in phenolic compounds. Phenolic acids were found in all tissues, while flavonoids characterized the aerial part of the plant, anthocyanidins being restricted to the petals. The chemical quantification of phenolics in plant extracts confirmed their tissue-specific distribution and abundance. A key finding was that the spectral signatures obtained through confocal microscopy of endogenous fluorophores in living tissues and their counterpart extracts share the same fluorescence patterns, pointing out the potential of fluorescence imaging of intact organs for a proper estimation of their phenolic content. In addition, this study highlighted a few distinct morphology cell types, in particular foliar-glandular-like structures, and jagged petal cell walls. Altogether, these data provide a comprehensive histochemical localization of phenolics in living tissues of a violet. Converting fluorescence imaging into a chemical imprint indicated that one can rely on fluorescence microscopy of intact living tissues as a rapid, non-destructive means to follow their phenolic imprint under various environmental conditions.

Plant phenotyping relevance

生体組織の蛍光画像からフェノール含量・分布を推定する非破壊的手法を、化学抽出による定量と比較検証しており、表現型取得法が中心です。

abstractpointing out the potential of fluorescence imaging of intact organs for a proper estimation of their phenolic content.
abstractfluorescence microscopy of intact living tissues as a rapid, non-destructive means to follow their phenolic imprint under various environmental conditions.

Code and data availability

The paper's phenotyping measurements (phenolic/flavonoid/anthocyanidin content data and fluorescence emission spectra of tissues and extracts) are stated to be available as Supporting Information (Tables S1–S3, Figure S1), but the supplied blocks contain no resolvable public URL for these files, and no author analysis,

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