Unknown

Dataset Information

0

Microbial Transformation of Flavonoids by Isaria fumosorosea ACCC 37814.


ABSTRACT: Glycosylation is an efficient strategy to modulate the solubility, stability, bioavailability and bioactivity of drug-like natural products. Biological methods, such as whole-cell biocatalyst, promise a simple but highly effective approach to glycosylate biologically active small molecules with remarkable regio- and stereo-selectivity. Herein, we use the entomopathogenic filamentous fungus Isaria fumosorosea ACCC 37814 to biotransform a panel of phenolic natural products, including flavonoids and anthraquinone, into their glycosides. Six new flavonoid (4-O-methyl)glucopyranosides are obtained and structurally characterized using high resolution mass and nuclear magnetic resonance spectroscopic techniques. These compounds further expand the structural diversity of flavonoid glycosides and may be used in biological study.

SUBMITTER: Dou F 

PROVIDER: S-EPMC6471136 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Microbial Transformation of Flavonoids by <i>Isaria fumosorosea</i> ACCC 37814.

Dou Fangmin F   Wang Zhi Z   Li Guiying G   Dun Baoqing B  

Molecules (Basel, Switzerland) 20190315 6


Glycosylation is an efficient strategy to modulate the solubility, stability, bioavailability and bioactivity of drug-like natural products. Biological methods, such as whole-cell biocatalyst, promise a simple but highly effective approach to glycosylate biologically active small molecules with remarkable regio- and stereo-selectivity. Herein, we use the entomopathogenic filamentous fungus <i>Isaria fumosorosea</i> ACCC 37814 to biotransform a panel of phenolic natural products, including flavon  ...[more]

Similar Datasets

| S-EPMC6222689 | biostudies-literature
| S-EPMC6149825 | biostudies-other
| S-EPMC6656742 | biostudies-literature
| S-EPMC5628805 | biostudies-literature
| S-EPMC4612611 | biostudies-literature
| S-EPMC6151793 | biostudies-literature
| S-EPMC5322360 | biostudies-literature
| S-EPMC7600585 | biostudies-literature
| S-EPMC5735356 | biostudies-literature
| S-EPMC5055314 | biostudies-literature