Abstract
A newly isolated rod-shaped, gram-negative anaerobic bacterium from human feces, named Julong 732, was found to be capable of metabolizing the isoflavone dihydrodaidzein to S-equol under anaerobic conditions. The metabolite, equol, was identified by using electron impact ionization mass spectrometry, (1)H and (13)C nuclear magnetic resonance spectroscopy, and UV spectral analyses. However, strain Julong 732 was not able to produce equol from daidzein, and tetrahydrodaidzein and dehydroequol, which are most likely intermediates in the anaerobic metabolism of dihydrodaidzein, were not detected in bacterial culture medium containing dihydrodaidzein. Chiral stationary-phase high-performance liquid chromatography eluted only one metabolite, S-equol, which was produced from a bacterial culture containing a racemic mixture of dihydrodaidzein. Strain Julong 732 did not show racemase activity to transform R-equol to S-equol and vice versa. Its full 16S rRNA gene sequence (1,429 bp) had 92.8% similarity to that of Eggerthella hongkongenis HKU10. This is the first report of a single bacterium capable of converting a racemic mixture of dihydrodaidzein to enantiomeric pure S-equol.
MeSH Terms
DNA, Ribosomal/analysis
Equol
Genes, rRNA
Gram-Negative Anaerobic Bacteria/isolation & purification,metabolism
Humans
Intestines/microbiology
Isoflavones/biosynthesis,chemistry,metabolism
Magnetic Resonance Spectroscopy
Molecular Sequence Data
RNA, Ribosomal, 16S/genetics
Sequence Analysis, DNA
Stereoisomerism
Chemicals
4',7-dihydroxy-3,4-dihydroisoflavone
DNA, Ribosomal
Isoflavones
RNA, Ribosomal, 16S
Equol
daidzein
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wang Xiu-Ling
School of Agricultural Biotechnology, Seoul National University, Seoul, Korea.
Hur Hor-Gil
Lee Je Hyeon
Kim Ki Tae
Kim Su-Il
References (26)
26 references, click to expand
-
Comparisons of percent equol producers between prostate cancer patients and controls: case-controlled studies of isoflavones in Japanese, Korean and American residents.
Jpn J Clin Oncol. 2004 Feb;34(2):86-9
PMID: 15067102
-
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
Mol Biol Evol. 1987 Jul;4(4):406-25
PMID: 3447015
-
Natural flavonoids and lignans are potent cytostatic agents against human leukemic HL-60 cells.
Life Sci. 1994;55(13):1061-9
PMID: 8084211
-
Isolation and identification of "diazepam-like" compounds from bovine urine.
J Nat Prod. 1983 Nov-Dec;46(6):852-61
PMID: 6330305
-
Antiproliferative effects of synthetic and naturally occurring flavonoids on tumor cells of the human breast carcinoma cell line, ZR-75-1.
Res Commun Chem Pathol Pharmacol. 1989 Apr;64(1):69-78
PMID: 2749004
-
Inhibition of in vitro microsomal lipid peroxidation by isoflavonoids.
Biochem Pharmacol. 1985 May 1;34(9):1367-9
PMID: 3994752
-
Dietary phyto-oestrogens and the menopause in Japan.
Lancet. 1992 May 16;339(8803):1233
PMID: 1349965
-
Differential effects of dietary phyto-oestrogens daidzein and equol on human breast cancer MCF-7 cells.
Eur J Cancer. 1997 Dec;33(14):2384-9
PMID: 9616286
-
Identification of lignans and phytoestrogens in urine of chimpanzees.
Clin Chim Acta. 1986 Jul 30;158(2):147-54
PMID: 3017606
-
Metabolism of daidzein and genistein by intestinal bacteria.
J Nat Prod. 1995 Dec;58(12):1892-6
PMID: 8691209
-
Anaerobic degradation of flavonoids by Clostridium orbiscindens.
Appl Environ Microbiol. 2003 Oct;69(10):5849-54
PMID: 14532034
-
Metabolites of dietary (soya) isoflavones in human urine.
Clin Chim Acta. 1993 Dec 31;223(1-2):9-22
PMID: 8143372
-
Degradation of quercetin and luteolin by Eubacterium ramulus.
Appl Environ Microbiol. 2001 Dec;67(12):5558-67
PMID: 11722907
-
Isolation of human intestinal bacteria metabolizing the natural isoflavone glycosides daidzin and genistin.
Arch Microbiol. 2000 Dec;174(6):422-8
PMID: 11195098
-
Nonsteroidal estrogens of dietary origin: possible roles in hormone-dependent disease.
Am J Clin Nutr. 1984 Sep;40(3):569-78
PMID: 6383008
-
Identification of equol in the urine of the domestic fowl.
Biochim Biophys Acta. 1961 Oct 28;53:403-4
PMID: 13880769
-
Equol, a natural estrogenic metabolite from soy isoflavones: convenient preparation and resolution of R- and S-equols and their differing binding and biological activity through estrogen receptors alpha and beta.
Bioorg Med Chem. 2004 Mar 15;12(6):1559-67
PMID: 15018930
-
Isolation of an anaerobic intestinal bacterium capable of cleaving the C-ring of the isoflavonoid daidzein.
Arch Microbiol. 2002 Jul;178(1):8-12
PMID: 12070764
-
Purification and chemical characterization of a potent inhibitor of the Na-K-Cl cotransport system in rat urine.
Biochem Biophys Res Commun. 1996 Apr 16;221(2):279-85
PMID: 8619846
-
The identification of the weak oestrogen equol [7-hydroxy-3-(4'-hydroxyphenyl)chroman] in human urine.
Biochem J. 1982 Feb 1;201(2):353-7
PMID: 7082293
-
Production and metabolism of lignans by the human faecal flora.
J Appl Bacteriol. 1985 Jan;58(1):37-43
PMID: 2984153
-
Antimutagens and anticarcinogens: a survey of putative interceptor molecules.
Environ Mol Mutagen. 1990;15(3):145-82
PMID: 2185012
-
Bioavailability of soybean isoflavones depends upon gut microflora in women.
J Nutr. 1995 Sep;125(9):2307-15
PMID: 7666247
-
Synthesis of novel mammalian metabolites of the isoflavonoid phytoestrogens daidzein and genistein.
Proc Soc Exp Biol Med. 1998 Mar;217(3):293-9
PMID: 9492338
-
Equol, a new inactive phenol isolated from the ketohydroxyoestrin fraction of mares' urine.
Biochem J. 1932;26(4):1227-32
PMID: 16744928
-
A urinary profile study of dietary phytoestrogens. The identification and mode of metabolism of new isoflavonoids.
J Steroid Biochem Mol Biol. 1995 Aug;54(3-4):167-84
PMID: 7662591