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Human gut microbial degradation of flavonoids : Structure-function relationships
Journal article   Peer reviewed

Human gut microbial degradation of flavonoids : Structure-function relationships

Andrean L SIMONS, Mathieu RENOUF, Suzanne HENDRICH and Patricia A MURPHY
Journal of agricultural and food chemistry, Vol.53(10), pp.4258-4263
2005
DOI: 10.1021/jf0500177
PMID: 15884869

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Abstract

The relationship between chemical structure and gut microbial degradation rates of 14 flavonoids, flavone, apigenin, chrysin, naringenin, kaempferol, genistein, daidzein, daidzin, puerarin, 7,4'-dihydroxyflavone, 6,4'-dihydroxyflavone, 5,4'-dihydroxyflavone, 5,3'-dihydroxyflavone, and 4'-hydroxyflavone, was investigated by anaerobically fermenting the flavonoids with human gut microflora (n = 11 subjects). Degradation rates for the 5,7,4'-trihydroxyl flavonoids, apigenin, genistein, naringenin, and kaempferol, were significantly faster than the other structural motifs. Puerarin was resistant to degradation by the gut microflora. Extensive degradation of flavonoids by gut microflora may result in lower overall bioavailability than those flavonoids that are slowly degraded because rapidly degrading flavonoids are less likely to be absorbed intact.
Fundamental and applied biological sciences. Psychology Food industries Biological and medical sciences

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