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Rapid screening and identification of α ‐glucosidase inhibitors from mulberry leaves using enzyme‐immobilized magnetic beads coupled with HPLC/MS and NMR
Author(s) -
Tao Yi,
Zhang Yufeng,
Cheng Yiyu,
Wang Yi
Publication year - 2013
Publication title -
biomedical chromatography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.4
H-Index - 65
eISSN - 1099-0801
pISSN - 0269-3879
DOI - 10.1002/bmc.2761
Subject(s) - chemistry , chromatography , enzyme , covalent bond , high performance liquid chromatography , glucosidases , biochemistry , organic chemistry
α ‐Glucosidase plays important roles in the digestion and absorption of carbohydrates in the small intestine. The inhibition of α ‐glucosidase is regarded as a potential way to treat diabetes. We established an approach to screening α ‐glucosidase inhibitors from medicinal plants using enzyme‐coated magnetic bead. Using 1‐(3‐dimethyl‐aminopropyl)‐3‐ethylcarbodiimide and N ‐hydroxysuccinimide as reaction reagents, α ‐glucosidase was immobilized on the magnetic beads by covalent linkage. The conjugation of α ‐glucosidase to the magnetic beads was characterized using scanning electron microscope and X‐ray diffractometer. The proposed approach was applied in fishing potential α ‐glucosidase inhibitors from extract of Morus alba , a Chinese medicinal plant. The structures of potential active compounds were identified via liquid chromatography–mass spectrometry and nuclear magnetic resonance. The results demonstrated that two flavonoids (isoquercitrin and astragalin) could bind to α ‐glucosidase, which was confirmed via conventional α ‐glucosidase inhibitory assay. Our findings suggested that enzyme‐coated magnetic beads may be suitable for discovering active compounds from medicinal plants. Copyright © 2012 John Wiley & Sons, Ltd.