1. Nucleoside 2′,3′-Cyclic Monophosphates in Aphanizomenon flos-aquae Detected through Nuclear Magnetic Resonance and Mass Spectrometry
- Author
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Alfonso Zambon, Valeria Righi, Adele Mucci, Maria Cecilia Rossi, Francesca Parenti, Emanuela Libertini, Zambon A., Righi V., Parenti F., Libertini E., Rossi M.C., and Mucci A.
- Subjects
Magnetic Resonance Spectroscopy ,Aphanizomenon flos-Aquae ,Aphanizomenon flos-aquae (dietary supplement) ,ESI-QO mass spectrometry ,Klamath algae ,nuclear magnetic resonance spectroscopy ,nucleoside 2′,3′-cyclic monophosphates ,Mass spectrometry ,Aphanizomenon ,Mass Spectrometry ,Oregon ,Nuclear magnetic resonance ,parasitic diseases ,Metabolome ,Molecule ,Nucleoside ,Spectroscopy ,Molecular Structure ,biology ,Chemistry ,General Chemistry ,Nuclear magnetic resonance spectroscopy ,biology.organism_classification ,nucleoside 2′ ,nucleoside 2′,3′-cyclic monophosphate ,General Agricultural and Biological Sciences ,3′-cyclic monophosphates - Abstract
Aphanizomenon flos-Aquae (AFA) cyanobacteria from Klamath Lake (Oregon) are considered a "superfood" due to their broad nutritional profile that has proved to have health-enhancing properties. The AFA metabolome is quite complex. Here, we present a study that, combining multinuclear 1H, 31P, and 13C Nuclear Magnetic Resonance (NMR) spectroscopy and high-resolution mass spectrometry, led to the detection of uncommon phosphorylated metabolites in AFA. We focused our attention on 31P NMR signals at 20 ppm, a chemical shift that usually points to the presence of phosphonates. The molecules contributing to 20 ppm 31P NMR signals revealed, instead, to be nucleoside 2′,3′-cyclic monophosphates. These metabolites were fully characterized by multinuclear 1H, 31P, and 13C NMR spectroscopy and high-resolution mass spectrometry.
- Published
- 2019
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