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Biosynthesis of a Flavonol from a Flavanone by Establishing a One-pot Bienzymatic Cascade
Published on: August 14, 2019
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Sulfated flavanones and dihydroflavonols from willow
Clarice Noleto-Dias1, Claudia Harflett1, Michael H Beale1
1Department of Computational and Analytical Sciences, Rothamsted Research, West Common, Harpenden, Hertfordshire, AL5 2JQ, UK.
Phytochemistry Letters
|February 7, 2020
Summary
Four novel sulfated flavonoids were identified in willow hybrid species Salix × alberti. These compounds, including sulfated flavanones and dihydroflavonols, exhibit antioxidant activity, though reduced by sulfation.
Area of Science:
- Phytochemistry
- Plant biochemistry
- Natural products chemistry
Background:
- Sulfated flavonoids are rare in plants, with limited prior characterization.
- Mammalian metabolism of dietary flavonoids involves sulfation, suggesting potential biological roles.
Purpose of the Study:
- To isolate and characterize novel sulfated flavonoids from Salix × alberti.
- To investigate the in vitro antioxidant properties of these compounds.
Main Methods:
- Phytochemical profiling using NMR spectroscopy and high-resolution mass spectrometry.
- Isolation of four sulfated flavonoids: taxifolin-7-sulfate, dihydrokaempferol-7-sulfate, eridictyol-7-sulfate, and naringenin-7-sulfate.
- DPPH radical scavenging assay to evaluate antioxidant activity.
Main Results:
- Four sulfated flavonoids, previously unobserved in plants, were identified and structurally elucidated.
- Sulfation of taxifolin and eriodictyol attenuated their antioxidant activity but did not eliminate it.
Conclusions:
- Salix × alberti is a source of unique sulfated flavonoids.
- 7-sulfation impacts the antioxidant capacity of flavonoids, offering insights into their biological functions and metabolism.
Keywords:
AntioxidantS. × alberti L. (S. integra Thunb. × S. suchowensis) hybridSalicaceaeSulfated dihydroflavonolsSulfated flavanonesWillowMore Related Videos
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