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Volume 20, Issue 12, Pages 940-947 (December 2009)


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The role of diet in the metabolism of daidzein by human faecal microbiota sampled from Italian volunteers

Claudio GardanaaCorresponding Author Informationemail address, Enrica Canzib, Paolo Simonettia

Received 30 June 2008; received in revised form 14 August 2008; accepted 15 August 2008. published online 15 December 2008.

Abstract 

The intestinal microbial transformation of daidzein into equol is subject to a wide inter-individual variability. The aim of this study was to investigate in vitro this transformation and to evaluate possible correlations between individual diet and equol production. The transformation of daidzein was investigated in anaerobic batch cultures inoculated with mixed fecal bacteria from 90 volunteers. The daidzein metabolism was monitored by liquid chromatography-mass spectrometry, and a chiral column was used to distinguish equol and dihydrodaidzein enantiomers. The obtained results show that daidzein was unchanged (≈27%) or degraded to equol (≈28%), O-desmethylangolensin (≈12%) or dihydrodaidzein (≈31%). Furthermore, some subjects (≈2%) are able to produce both equol and O-desmethylangolensin. Bacteria represent sub-dominant populations (105–109 cell/g wet faeces) in “slow” equol producers, while higher counts of equol-producing microorganisms (1010–1011 cell/g wet faeces) were found in “quick” equol producers. The in vitro test to evaluate equol-producing status is quick and not invasive, and the obtained results are comparable with those reported in vivo. Indeed, the only enantiomer present in the batch cultures containing equol was the S-form. No significant correlations between equol production, BMI, age and sex were found. It seems that the equol-producer group consumed less fibre, vegetables and cereals, and more lipids from animal sources.

a Division of Human Nutrition, Department of Food Science and Microbiology, University of Milan, 20133 Milan, Italy

b Division of Microbiology, University of Milan, 20133 Milan, Italy

Corresponding Author InformationCorresponding author. Tel.: +39 02 50316072; fax: +39 02 50316071.

PII: S0955-2863(08)00191-5

doi:10.1016/j.jnutbio.2008.08.006


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