Acknowledgement
This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF-2021R1A2C2007712).
References
- Han J (2019) Chemical aspects of gut metabolism of flavonoids. Metabolites 9: 136. doi: 10.3390/metabo9070136
- Pabich M, Materska M (2019) Biological effect of soy isoflavones in the prevention of civilization diseases. Nutrients 11: 1660. doi: 10.3390/nu11071660
- Kim M, Han J (2016) Isoflavone metabolism by human intestinal bacteria. Planta Med 82: S784. doi: 10.1055/s-0036-1596810
- Kim M, Lee J, Han J (2015) Deglycosylation of isoflavone C-glycosides by newly isolated human intestinal bacteria. J Sci Food Agric 95: 1925-1931. doi: 10.1002/jsfa.6900
- Sekikawa A, Wharton W, Butts B, Veliky CV, Garfein J, Li J, Goon S, Fort A, Li M, Hughes TM (2022) Potential protective mechanisms of S-equol, a metabolite of soy isoflavone by the gut microbiome, on cognitive decline and dementia. Int J Mol Sci 23:11921. doi: 10.3390/ijms231911921.
- Rostagno MA, Villares A, Guillamon E, Garcia-Lafuente A, Martinez JA (2009) Sample preparation for the analysis of isoflavones from soybeans and soy foods. J Chromatogr A 1216: 2-9. doi: 10.1016/j.chroma.2008.11.035
- Kim M, Marsh ENG, Kim SU, Han J (2010) Conversion of (3S,4R)-tetrahydrodaidzein to (3S)-equol by THD reductase: Proposed mechanism involving a radical intermediate. Biochemistry 49: 5582-5587. doi: 10.1021/bi100465y
- Wang XL, Hur HG, Lee JH, Kim KT, Kim SI (2005) Enantioselective synthesis of S-equol from dihydrodaidzein by a newly isolated anaerobic human intestinal bacterium. Appl Environ Microbiol 71:214-219. doi: 10.1128/AEM.71.1.214-219.2005
- Kim JS, Lee H, Nirmala FS, Jung CH, Kim MJ, Jang YJ, Ha TY, Ahn J (2019) Dihydrodaidzein and 6-hydroxydaidzein mediate the fermentation-induced increase of antiosteoporotic effect of soybeans in ovariectomized mice. FASEB J 33:3252-3263. doi: 10.1096/fj.201800953R
- Park HY, Kim M, Han J (2011) Stereospecific microbial production of isoflavanones from isoflavones and isoflavone glucosides. Appl Microbiol Biotechnol 91:1173-1181. doi: 10.1007/s00253-011-3310-7
- Won DH, Shin BK, Han J (2008) Synthesis and the absolute configurations of isoflavanone enantiomers. J Appl Biol Chem 51: 17-19. doi: 10.3839/jabc.2008.004
- Zhang Z, Schwartz S, Wagner L, Miller W (2000) A greedy algorithm for aligning DNA sequences. J Comput Biol 7: 203-214. doi: 10.1089/10665270050081478