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Cited by 729

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Deglycosylation of flavonoid and isoflavonoid glycosides by human small intestine and liver β‐glucosidase activity

Open access
Day, Andrea J, DuPont, M.Susan, Ridley, Saxon, Rhodes, Mike, Rhodes, Michael J.C, Morgan, Michael R.A, Williamson, Gary·1998·FEBS Letters

Abstract

Flavonoid and isoflavonoid glycosides are common dietary phenolics which may be absorbed from the small intestine of humans. The ability of cell‐free extracts from human small intestine and liver to deglycosylate various (iso)flavonoid glycosides was investigated. Quercetin 4′‐glucoside, naringenin 7‐glucoside, apigenin 7‐glucoside, genistein 7‐glucoside and daidzein 7‐glucoside were rapidly deglycosylated by both tissue extracts, whereas quercetin 3,4′‐diglucoside, quercetin 3‐glucoside, kaempferol 3‐glucoside, quercetin 3‐rhamnoglucoside and naringenin 7‐rhamnoglucoside remained unchanged. The K m for hydrolysis of quercetin 4′‐glucoside and genistein 7‐glucoside was ∼32±12 and ∼14±3 μM in both tissues respectively. The enzymatic activity of the cell‐free extracts exhibits similar properties to the cytosolic broad‐specificity β‐glucosidase previously described in mammals.

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Metadata

Authors
Day, A. J., DuPont, M. S., Ridley, S., Rhodes, M., Rhodes, M. J. C., Morgan, M. R. A., & Williamson, G.
Venue
FEBS Letters
Publisher
Wiley
Published
1998-09-25
Volume
436
Issue
1
Pages
71-75
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W2008905101
Cited by
729
References
1
FWCI
15.29
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Deglycosylation of flavonoid and isoflavonoid glycosides by human small intestine and liver β‐glucosidase activity. https://app.cochat.ai/papers/10.1016/s0014-5793(98)01101-6
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Day, A. J., DuPont, M. S., Ridley, S., Rhodes, M., Rhodes, M. J. C., Morgan, M. R. A., & Williamson, G. (1998). Deglycosylation of flavonoid and isoflavonoid glycosides by human small intestine and liver β‐glucosidase activity. FEBS Letters. https://doi.org/10.1016/s0014-5793(98)01101-6

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