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Stereospecific microbial production of isoflavanones from isoflavones and isoflavone glucosides

  • Applied Microbial and Cell Physiology
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Abstract

A Gram-negative anaerobic microorganism, MRG-1, isolated from human intestine showed high activities of deglycosylation and reduction of daidzin, based on rapid TLC analysis. A rod-shaped strain MRG-1was identified as a new species showing 91.0% homology to Coprobacillus species, based on 16S rRNA sequence analysis. The strain MRG-1 showed β-glucosidase activity toward daidzin and genistin, and daidzein and genistein were produced, respectively. However, the strain MRG-1 did not react with flavone glycosides, flavanone glycosides, and isoflavone C-glucoside. Besides, MRG-1 showed stereoselective reductase activity to isoflavone, daidzein, genistein, 7-hydroxyisoflavone, and formononetin, resulting in the formation of corresponding R-isoflavanone enantiomers. The new isoflavanones of 7-hydroxyisoflavanone and dihydroformononetin were characterized by NMR, and the absolute configurations of the enantiomers were determined with CD spectroscopy. The kinetic study of the anaerobic biotransformation showed both activities were exceptionally fast compared to the reported conversion by other anaerobic bacteria.

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Acknowledgements

The authors thank Ms. Jae Eun Hwang for her excellent NMR measurements. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (No. 331-2008-1-F00014).

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Correspondence to Jaehong Han.

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Park, HY., Kim, M. & Han, J. Stereospecific microbial production of isoflavanones from isoflavones and isoflavone glucosides. Appl Microbiol Biotechnol 91, 1173–1181 (2011). https://doi.org/10.1007/s00253-011-3310-7

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  • DOI: https://doi.org/10.1007/s00253-011-3310-7

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