1,4-Dimethoxyglucobrassicin in Barbarea and 4-Hydroxyglucobrassicin in Arabidopsis and Brassica

A novel indole glucosinolate, 1,4-dimethoxyglucobrassicin (1,4-dimethoxyindol-3-ylmethylglucosinolate), was isolated as the desulfo derivative from roots of the P-type of Barbarea vulgaris ssp. arcuata, and its structure was determined by spectroscopy including 2D NMR spectroscopy. 4-Hydroxyglucobra...

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Veröffentlicht in:Journal of agricultural and food chemistry 2001-03, Vol.49 (3), p.1502-1507
Hauptverfasser: Agerbirk, Niels, Petersen, Bent Larsen, Olsen, Carl Erik, Halkier, Barbara Ann, Nielsen, Jens Kvist
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Sprache:eng
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Zusammenfassung:A novel indole glucosinolate, 1,4-dimethoxyglucobrassicin (1,4-dimethoxyindol-3-ylmethylglucosinolate), was isolated as the desulfo derivative from roots of the P-type of Barbarea vulgaris ssp. arcuata, and its structure was determined by spectroscopy including 2D NMR spectroscopy. 4-Hydroxyglucobrassicin (4-hydroxyindol-3-ylmethylglucosinolate) was isolated as the desulfo derivative from green siliques (fruits) of Arabidopsis thaliana and identified by comparison of its 1H NMR spectrum with the spectrum of the known desulfoglucosinolate from Brassica napus. The delayed elution of desulfo indole glucosinolates from the DEAE Sephadex column used in sample preparation was examined, and the diode-array UV spectra of desulfo indole glucosinolates were measured, to ensure a reliable determination of 1,4-dimethoxyglucobrassicin and 4-hydroxyglucobrassicin with the existing analysis method based on the HPLC of desulfoglucosinolates. 1,4-Dimethoxyglucobrassicin was not detected in 10 other Arabidopsis, Brassica, and Barbarea species, indicating an evolutionarily recent mutation in the indole glucosinolate biosynthesis in B. vulgaris ssp. arcuata type P. Keywords: Brassicaceae; Barbarea; Arabidopsis; Brassica; 1,4-dimethoxyindol-3-ylmethylglucosinolate; 1,4-dimethoxyglucobrassicin; 4-hydroxyindol-3-ylmethylglucosinolate; 4-hydroxyglucobrassicin; desulfoglucosinolate; indole phytoalexin; NMR; MS; UV; HPLC
ISSN:0021-8561
1520-5118
DOI:10.1021/jf001256r