Biosynthesis of gallic acid in Rhus typhina: discrimination between alternative pathways from natural oxygen isotope abundance

• Published in: Phytochemistry (Oxford) Vol. 65; no. 20; pp. 2809 - 2813
• Main Authors: Werner, Roland A., Rossmann, Andreas, Schwarz, Christine, Bacher, Adelbert, Schmidt, Hanns-Ludwig, Eisenreich, Wolfgang
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Ltd 01.10.2004; Elsevier
• Subjects: Anacardiaceae; biochemical pathways; Biological and medical sciences; Biosynthesis; Carbon reduction; Fundamental and applied biological sciences. Psychology; Gallic acid; Gallic Acid - metabolism; Gallotannins; Isotope ratio mass spectrometry; isotopes; Mass Spectrometry; Metabolism; Metabolism. Physicochemical requirements; natural oxygen abundance; Natural oxygen isotope abundance; oxygen; Oxygen Isotopes - metabolism; Plant Leaves - metabolism; Plant physiology and development; Rhus - metabolism; Rhus typhina; spectral analysis; Gallic acid; Carbon reduction; Gallotannins; Biosynthesis; Isotope ratio mass spectrometry; Rhus typhina; Anacardiaceae; Natural oxygen isotope abundance; Plant leaf; Metabolic pathway; Dicotyledones; Angiospermae; Spermatophyta
• ISSN: 0031-9422; 1873-3700
• DOI: 10.1016/j.phytochem.2004.08.020

Studies on the 18O natural abundance of the phenolic oxygen atoms in gallic acid from Rhus typhina support its direct formation from dehydroshikimate. The biosynthetic pathway of gallic acid in leaves of Rhus typhina is studied by oxygen isotope ratio mass spectrometry at natural oxygen isotope abundance. The observed δ 18O-values of gallic acid indicate an 18O-enrichment of the phenolic oxygen atoms of more than 30‰ above that of the leaf water. This enrichment implies biogenetical equivalence with oxygen atoms of carbohydrates but not with oxygen atoms introduced by monooxygenase activation of molecular oxygen. It can be concluded that all phenolic oxygen atoms of gallic acid are retained from the carbohydrate-derived precursor 5-dehydroshikimate. This supports that gallic acid is synthesized entirely or predominantly by dehydrogenation of 5-dehydroshikimate.