IN-SITU IDENTIFICATION OF MAJOR METABOLITES IN THE RED ALGA GRACILARIOPSIS-LEMANEIFORMIS USING HIGH-RESOLUTION MAGIC-ANGLE-SPINNING NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY
A. Broberg et al., IN-SITU IDENTIFICATION OF MAJOR METABOLITES IN THE RED ALGA GRACILARIOPSIS-LEMANEIFORMIS USING HIGH-RESOLUTION MAGIC-ANGLE-SPINNING NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY, Planta, 206(2), 1998, pp. 300-307
The content of low-molecular-weight compounds in the red alga Gracilar
iopsis lemaneiformis [(Bory) Dawson, Acleto, et Foldvik] has been anal
ysed in-situ using high-resolution magic angle spinning (HR-MAS) nucle
ar magnetic resonance (NMR) spectroscopy. The major heteroside was sho
wn to be floridoside, but digeneaside and isofloridoside were also det
ected in the alga. Other major components were isethionic acid and the
amino acids taurine and citrulline. The results from the HR-MAS NMR a
nalysis were confirmed with high-resolution NMR spectroscopy, high-res
olution fast atom bombardment mass spectrometry (FABMS) and GC-MS, on
material isolated from the studied alga, but also on authentic samples
.