Tissue Localization of u.v.-B-Screening Pigments and of Chalcone Synthase mRNA in Needles of Scots Pine Seedlings

Epidermal tissue was isolated from Scots pine (Pinus sylvestris L.) needles by enzymatic digestion in order to study tissue distribution of u.v.-B-screening pigments. Up to 90% of the needle content of a group of diacylated flavonol glycosides that were structurally closely related was found in the...

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Published inThe New phytologist Vol. 132; no. 2; pp. 247 - 258
Main Authors Schnitzler, Jorg-Peter, Jungblut, Tim P., Heller, Werner, Kofferlein, Matthias, Hutzler, Peter, Heinzmann, Ulrich, Schmelzer, Elmon, Ernst, Dieter, Langebartels, Christian, Sandermann, Heinrich
Format Journal Article
LanguageEnglish
Published Oxford, UK Cambridge University Press 01.02.1996
Blackwell Publishing Ltd
Blackwell
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Summary:Epidermal tissue was isolated from Scots pine (Pinus sylvestris L.) needles by enzymatic digestion in order to study tissue distribution of u.v.-B-screening pigments. Up to 90% of the needle content of a group of diacylated flavonol glycosides that were structurally closely related was found in the epidermal layer. Among these metabolites, 3'',6''-di-para-coumaroyl-isoquercitrin and 3'',6''-di-para-coumaroyl-astragalin were the main u.v.-B-induced compounds in cotyledons and primary needles, respectively. However, catechin and astragalin (kaempferol 3-glucoside), two non-acylated flavonoid metabolites, were only observed in total needle extracts, and at levels independent of u.v.-B treatment. According to this metabolite distribution, the mRNA of chalcone synthase, the key enzyme to flavonoids, was found in epidermal and mesophyll as well as vascular tissues. The major alkaliextractable wall-bound phenolic metabolites, astragalin, 4-coumaric acid, and ferulic acid, a minor component of the cell wall, were also found exclusively in the epidermal layer. These compounds were not stimulated by u.v.-B irradiation within the experimental period. Staining of needle cross sections and epidermal layer preparations with Naturstoffreagenz A confirmed the specific localization of wall-bound astragalin in the outer wall of the epidermal layer. Model calculations of u.v.-B absorptions at 300 nm of soluble and cell-wall-bound metabolites of the epidermal layer revealed an almost complete shielding of the mesophyll tissue from u.v.-B radiation.
Bibliography:Fraunofer‐Institut für tmosphäRISCHE Umweltforschung, Kreuzeeckbanhnstraße 19, D‐82467 Garmisch Partenkirchen, Germany
ISSN:0028-646X
1469-8137
DOI:10.1111/j.1469-8137.1996.tb01844.x