TY - JOUR
T1 - Flavonoid diversification in different leaf compartments of Primula auricula (Primulaceae)
AU - Holzbach, Birgit
AU - Reuter, Viktor
AU - Bacher, Markus
AU - Schinnerl, Johann
AU - Brecker, Lothar
AU - Rosenau, Thomas
AU - Valant-Vetschera, Karin
N1 - Funding Information:
Thanks are due to Susanne Felsinger (NMR Center, Faculty of Chemistry, Universityof Vienna) for measuring NMR spectra, and to Peter Unteregger (MS Center, Faculty of Chemistry, University of Vienna) for recording mass spectra. We also thank Johannes Nikodemus Staudinger for technical assistance. Mag. Ch. Gilli (Department of Botany and Biodiversity Research, University of Vienna) kindly assisted with botanical taxonomy. Support of the Austrian Biorefinery Center Tulln (ABCT) is gratefully acknowledged. Part of this project was funded by “ Hochschuljubiläumsfonds der Stadt Wien ” (Project H-294808/2018 ).
Funding Information:
Thanks are due to Susanne Felsinger (NMR Center, Faculty of Chemistry, Universityof Vienna) for measuring NMR spectra, and to Peter Unteregger (MS Center, Faculty of Chemistry, University of Vienna) for recording mass spectra. We also thank Johannes Nikodemus Staudinger for technical assistance. Mag. Ch. Gilli (Department of Botany and Biodiversity Research, University of Vienna) kindly assisted with botanical taxonomy. Support of the Austrian Biorefinery Center Tulln (ABCT) is gratefully acknowledged. Part of this project was funded by ?Hochschuljubil?umsfonds der Stadt Wien? (Project H-294808/2018).
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/10
Y1 - 2021/10
N2 - Populations of Primula auricula L. subsp. auricula from Austrian Alps were studied for flavonoid composition of both farinose exudates and tissue of leaves. The leaf exudate yielded Primula-type flavones, such as unsubstituted flavone and its derivatives, while tissue flavonoids largely consisted of flavonol 3-O-glycosides, based upon kaempferol (3, 4) and isorhamnetin (5–7). Kaempferol 3-O-(2″-O-β-xylopyranosyl-[6″-O-β-xylopyranosyl]-β-glucopyranoside) (3) and isorhamnetin 3-O-(2″-O-β-xylopyranosyl-[6″-O-β-xylopyranosyl]-β-glucopyranoside) (6) are newly reported as natural compounds. Remarkably, two Primula type flavones were also detected in tissues, namely 3′-hydroxyflavone 3′-O-β-glucoside (1) and 3′,4′-dihydroxyflavone 4′-O-β-glucoside (2), of which (1) is reported here for the first time as natural product. All structures were unambiguously identified by NMR and MS data. Earlier reports on the occurrence of 7,2′-dihydroxyflavone 7-O-glucoside (macrophylloside) in this species could not be confirmed. This structure was now shown to correspond to 3′,4′-dihydroxyflavone 4′-O-glucoside (2) by comparison of NMR data. Observed exudate variations might be specific for geographically separated populations. The structural diversification between tissue and exudate flavonoids is assumed to be indicative for different ecological roles in planta.
AB - Populations of Primula auricula L. subsp. auricula from Austrian Alps were studied for flavonoid composition of both farinose exudates and tissue of leaves. The leaf exudate yielded Primula-type flavones, such as unsubstituted flavone and its derivatives, while tissue flavonoids largely consisted of flavonol 3-O-glycosides, based upon kaempferol (3, 4) and isorhamnetin (5–7). Kaempferol 3-O-(2″-O-β-xylopyranosyl-[6″-O-β-xylopyranosyl]-β-glucopyranoside) (3) and isorhamnetin 3-O-(2″-O-β-xylopyranosyl-[6″-O-β-xylopyranosyl]-β-glucopyranoside) (6) are newly reported as natural compounds. Remarkably, two Primula type flavones were also detected in tissues, namely 3′-hydroxyflavone 3′-O-β-glucoside (1) and 3′,4′-dihydroxyflavone 4′-O-β-glucoside (2), of which (1) is reported here for the first time as natural product. All structures were unambiguously identified by NMR and MS data. Earlier reports on the occurrence of 7,2′-dihydroxyflavone 7-O-glucoside (macrophylloside) in this species could not be confirmed. This structure was now shown to correspond to 3′,4′-dihydroxyflavone 4′-O-glucoside (2) by comparison of NMR data. Observed exudate variations might be specific for geographically separated populations. The structural diversification between tissue and exudate flavonoids is assumed to be indicative for different ecological roles in planta.
KW - Exudate flavonoids
KW - Flavonoid glycosides
KW - Organ specific diversification
KW - Primula auricula
UR - http://www.scopus.com/inward/record.url?scp=85110596462&partnerID=8YFLogxK
U2 - 10.1016/j.bse.2021.104310
DO - 10.1016/j.bse.2021.104310
M3 - Article
AN - SCOPUS:85110596462
SN - 0305-1978
VL - 98
JO - Biochemical Systematics and Ecology
JF - Biochemical Systematics and Ecology
M1 - 104310
ER -