C-Ring Cleavage of Isoflavones Daidzein and Genistein by a Newly-Isolated Human Intestinal Bacterium Eubacterium ramulus Julong 601

  • Wang, Xiu-Ling (School of Agricultural Biotechnology, Seoul National University, College of Life Science, Agricultural University of Hebei) ;
  • Kim, Ki-Tae (Takara Korea Biomedical Unc.) ;
  • Lee, Je-Hyeon (Takara Korea Biomedical Unc.) ;
  • Hur, Hor-Gil (Department of Environmental Science and Engineering, Kwangju Institute of Science and Technology) ;
  • Kim, Su-Il (School of Agricultural Biotechnology, Seoul National University)
  • Published : 2004.08.01

Abstract

Julong 601, a Gram-positive anaerobic bacterium strain capable of cleaving the C-ring of isoflavones daidzein and genistein, was isolated from human feces. BLAST search revealed that its complete 16S rDNA gene sequence has 99% similarity to Eubacterium ramulus. Metabolites of daidzein and genistein were determined as O-desmethylangolensin (O-Dma) and 2-(4-hydroxyphenyl) propionic acid (2-HPPA), respectively, based on UV, EI-MS, and $^1H$ and ^{13}C$ NMR spectral analyses. Enantiomers of O-Dma and 2-HPPA were isolated by chiral stationary-phase HPLC (CSP HPLC). Cleavage of the C-ring of daidzein and genistein by strain Julong 601 was highly enantioselective. Specific rotation ([$\alpha]_D$) and circular dichroism (CD) spectra of the enantiomers are reported here for the first time. Biotransformation kinetics of daidzein and genistein indicated that the C-ring of genistein has a higher susceptibility to bacterial degradation than that of daidzein.

Keywords

References

  1. J. Steroid Biochem. Mol. Biol. v.41 Dietary phytoestrogens and cancer: in vitro and in vivo studies Adlercreutz ,H.;J. Mousavi;K. Clark;E. Hockerstedt;K. Hamalaimen;T. Wahala https://doi.org/10.1016/0960-0760(92)90359-Q
  2. Proc. Soc. Exp. Biol. Med. v.217 HPLC-mass spectrometry analysis of isoflavones Barnes, S.;L. Coward;M. Krik;J. Sfakianos
  3. Dictionary of National Products Buckkingham, J.
  4. J. Steroid Biochem. Mol. Biol. v.70 Biotransformation of genistein in the rat: Elucidation of metabolite structure by product ion mass fragmentology Coldham, N. G.;L. C. Howells;A. Santi;C. Montesissa;C. Langlauis;L. J. King;D. D. Macpherson;M. J. Sauer
  5. Biochem. J. v.128 Metabolism of apigenin and related compounds in the rat Griffiths, L. A.;G. E. Smith https://doi.org/10.1042/bj1280901
  6. Environ. Mol. Mutagen. v.15 Antimutagens and anticarcinogens: A survey of putative interceptor molecules Hartman, P. E.;D. M. Shankel https://doi.org/10.1002/em.2850150305
  7. Res. Commun. Chem. Pathol. Pharmacol. v.64 Antiproliferative effects of synthetic and naturally occurring flavonoids on tumor cells of the human breast carcinoma cell line, ZR-75-1 Hirano, T.;K. Oka;M. Akiba
  8. Life Sci. v.55 Natural flavonoids and lignans are potent cyto-static agents against human leukemic HL-60 cells Hirano, T.;M. Gotoh;K. Oka https://doi.org/10.1016/0024-3205(94)00641-5
  9. Arch. Microbiol. v.178 Isolation of an anaerobic intestinal bacterium capable of cleaving the C-ring of isoflavonoid daidzein Hur, H.G.;R. D. Beger;T. M. Heinze;J. J. O. Lay;J. P. Freeman;J. D. F. Rafii https://doi.org/10.1007/s00203-002-0414-6
  10. Biochem. Pharmacol. v.34 Inhibition of in vitro microsomal lipid peroxidation by isoflavonoids Jha, H. C.;G. V. Recklinghausen;F. Zilliken https://doi.org/10.1016/0006-2952(85)90672-0
  11. J. Steroid Biochem. Mol. Biol. v.54 A urinary profile study of dietary phytoestrogens. The identification and mode of metabolism of new isoflavonoids Joannou, G. E.;G. E. Kelly;A. Y. Keeder;M. Waring;C. C. Nelon https://doi.org/10.1016/0960-0760(95)00131-I
  12. Nucleic Acid Techniques inbacterial Systematics 16S/23S rRNA sequencing Lane. D. J.
  13. Arch. Microbiol. v.173 Anaerobic degradation of flavonoids by Eubacterium ramulus Sehneider, H.;M. Blaut https://doi.org/10.1007/s002030050010
  14. FEMS Microbiol. Lett. v.208 Anaerobic C-ring cleavage of genistein and daidzein by Eubacterium ramulus Schoefer, L.;R. Mohan;A. Braune;M. Birringer;M. Blaut https://doi.org/10.1111/j.1574-6968.2002.tb11081.x
  15. Am. J. Clin. Nutr. v.68 no.6SUP. Isoflavone content of infant formulas and the metabolic fate of these phytoestrogens in early life Setchell, K. D. R.;N. L. Zimmer;J. Cai;J. E. Heubi https://doi.org/10.1093/ajcn/68.6.1453S
  16. J. Endocrinol. v.52 Steroid and phytoestrogen binding to sheep uterine receptors in vitro Shutt, D. A.;R. I. Cox https://doi.org/10.1677/joe.0.0520299