Selective hydrolysis of flavonoid glycosides by Curvularia lunata.
10.1016/S1875-5364(13)60080-1
- Author:
Jing-Yuan LIU
1
,
2
;
He-Shui YU
1
,
2
;
Bing FENG
3
;
Li-Ping KANG
1
,
2
;
Xu PANG
3
;
Cheng-Qi XIONG
3
;
Yang ZHAO
3
;
Chun-Mei LI
4
;
Yi ZHANG
4
;
Bai-Ping MA
5
Author Information
1. Beijing Institute of Radiation Medicine, Beijing 100850, China
2. Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
3. Beijing Institute of Radiation Medicine, Beijing 100850, China.
4. Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
5. Beijing Institute of Radiation Medicine, Beijing 100850, China. Electronic address: mabaiping@sina.com.
- Publication Type:Journal Article
- Keywords:
Biotransformation;
Curvularia lunata;
Flavonoid glycosides;
Glucosyl;
Rhamnosyl;
Selective Hydrolysis
- MeSH:
Ascomycota;
chemistry;
Flavonoids;
chemistry;
Glucosides;
chemistry;
Hydrolysis;
Mass Spectrometry;
Molecular Structure
- From:
Chinese Journal of Natural Medicines (English Ed.)
2013;11(6):684-689
- CountryChina
- Language:English
-
Abstract:
Twelve flavonoid glycosides were involved in the biotransformation of the glycosyl moieties by Curvularia lunata 3.4381, and the products were analyzed by UPLC/PDA-Q-TOF-MS(E). Curvularia lunata displayed hydrolyzing activities on the terminal Rha or Glc units of some flavonoid glycosides. Terminal Rha with a 1 → 2 linkage of isorhamnetin-3-O-neohesperidoside and typhaneoside could be hydrolyzed by Curvularia lunata, but terminal Rha with a 1 → 6 linkage of rutin, typhaneoside, and quercetin-3-O-apiosyl-(1 → 2)-[rhamnosyl-(1 → 6)]-glucoside could not be hydrolyzed. Curvularia lunata could also hydrolyze the Glc of icariin, floramanoside B, and naringin. This is the first report of the hydrolysis of glycosyl units of flavonoid glycosides by Curvularia lunata. A new way to convert naringin to naringenin was found in this research.
