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Production of Bioactive 3’-Hydroxystilbene Compounds Using the Flavin-Dependent Monooxygenase Sam5

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초록

The flavin-dependent monooxygenase Sam5 was previously reported to be a bifunctional hydroxylase with coumarate 3-hydroxylase and resveratrol 3’-hydroxylase activities. In this article, we showed the Sam5 enzyme has 3’-hydroxylation activities for methylated resveratrols (pinostilbene and pterostilbene), hydroxylated resveratrol (oxyresveratrol), and glycosylated resveratrol (piceid) as substrates. However, piceid, a glycone-type stilbene used as a substrate for bioconversion experiments with the Sam5 enzyme expressed in Escherichia coli, did not convert to the hydroxylated compound astringin, but it was converted by in vitro enzyme reactions. Finally, we report a novel catalytic activity of Sam5 monooxygenase for the synthesis of piceatannol derivatives, 3’-hydroxylated stilbene compounds. Development of this bioproduction method for the hydroxylation of stilbenes is challenging because of the difficulty in expressing P450-type hydroxylase in E. coli and regiospecific chemical synthesis.

Abstract

The flavin-dependent monooxygenase Sam5 was previously reported to be a bifunctional hydroxylase with coumarate 3-hydroxylase and resveratrol 3’-hydroxylase activities. In this article, we showed the Sam5 enzyme has 3’-hydroxylation activities for methylated resveratrols (pinostilbene and pterostilbene), hydroxylated resveratrol (oxyresveratrol), and glycosylated resveratrol (piceid) as substrates. However, piceid, a glycone-type stilbene used as a substrate for bioconversion experiments with the Sam5 enzyme expressed in Escherichia coli, did not convert to the hydroxylated compound astringin, but it was converted by in vitro enzyme reactions. Finally, we report a novel catalytic activity of Sam5 monooxygenase for the synthesis of piceatannol derivatives, 3’-hydroxylated stilbene compounds. Development of this bioproduction method for the hydroxylation of stilbenes is challenging because of the difficulty in expressing P450-type hydroxylase in E. coli and regiospecific chemical synthesis.

참고문헌 (26)

  1. Pandey BP, "Screening of bacterial cytochrome P450s responsible for regiospecific hydroxylation of (iso)flavonoids", Enzyme Microb. Technol., 48, pp.386~392 (2011)[DOI]
  2. Kim DH, "Generation of the human metabolite piceatannol from the anticancer-preventive agent resveratrol by bacterial cytochrome P450 BM3", Drug Metab. Dispos., 37, pp.932~936 (2009)[DOI]
  3. Furuya T, "Regioselective synthesis of piceatannol from resveratrol: catalysis by two-component flavin-dependent monooxygenase HpaBC in whole cells", Tetrahedron Lett., 55, pp.2853~2855 (2014)[DOI]
  4. Lin Y, "Biotechnological production of plantspecific hydroxylated phenylpropanoids", Biotechnol. Bioeng., 111, pp.1895~1899 (2014)[DOI]
  5. Furuya T, "Biocatalytic synthesis of 3,4,5,3',5'-pentahydroxy-trans-stilbene from piceatannol by two-component flavin-dependent monooxygenase HpaBC", Biosci. Biotechnol. Biochem., 80, pp.193~198 (2016)[DOI]
  6. Lin Y, "Biosynthesis of caffeic acid in Escherichia coli using its endogenous hydroxylase complex", Microb. Cell Fact., 11, pp.42~ (2012)[DOI]
  7. Prieto MA, "Characterization of an Escherichia coli aromatic hydroxylase with a broad substrate range", J. Bacteriol., 175, pp.2162~2167 (1993)[DOI]
  8. Heo KT, "Sam5, a coumarate 3-hydroxylase from Saccharothrix espanaensis: new insight into the piceatannol production as a resveratrol 3'- hydroxylase", ChemistrySelect, 2, pp.8785~8789 (2017)[DOI]
  9. Surh YJ, "Cancer chemoprevention with dietary phytochemicals", Nat. Rev. Cancer, 3, pp.768~780 (2003)[DOI]
  10. Potter GA, "The cancer preventative agent resveratrol is converted to the anticancer agent piceatannol by the cytochrome P450 enzyme CYP1B1", Br. J. Cancer, 86, pp.774~778 (2002)[DOI]
  11. Piotrowska H, "Biological activity of piceatannol: leaving the shadow of resveratrol", Mutat. Res., 750, pp.60~82 (2012)[DOI]
  12. Kwon JY, "Piceatannol, natural polyphenolic stilbene, inhibits adipogenesis via modulation of mitotic clonal expansion and insulin receptor-dependent insulin signaling in early phase of differentiation", J. Biol. Chem., 287, pp.11566~11578 (2012)[DOI]
  13. Ullrich R, "Enzymatic hydroxylation of aromatic compounds", Cell. Mol. Life Sci., 64, pp.271~293 (2007)[DOI]
  14. Cheng TC, "Potent anti-cancer effect of 3'-hydroxypterostilbene in human colon xenograft tumors", PLoS One, 9, pp.e111814~ (2014)[DOI]
  15. Kim YM, "Oxyresveratrol and hydroxystilbene compounds. Inhibitory effect on tyrosinase and mechanism of action", J. Biol. Chem., 277, pp.16340~16344 (2002)[DOI]
  16. Dziggel C, "Tools of pathway reconstruction and production of economically relevant plant secondary metabolites in recombinant microorganisms", Biotechnol. J., 12, pp.1600145~ (2017)[DOI]
  17. Kang SY, "Production of phenylacetyl-homoserine lactone analogs by artificial biosynthetic pathway in Escherichia coli", Microb. Cell Fact., 14, pp.191~ (2015)[DOI]
  18. Diaz E, "Biodegradation of aromatic compounds by Escherichia coli", Microbiol. Mol. Biol. Rev., 65, pp.523~569 (2001)[DOI]
  19. Spyrou G, "Characterization of the flavin reductase gene (fre) of Escherichia coli and construction of a plasmid for overproduction of the enzyme", J. Bacteriol., 173, pp.3673~3679 (1991)[DOI]
  20. 최옥식, "Construction of Artificial Biosynthetic Pathways for Resveratrol Glucoside Derivatives", Journal of Microbiology and Biotechnology, 24(5), pp.614~618 (2014), 한국미생물·생명공학회[DOI]
  21. Henry C, "Cellular uptake and efflux of trans-piceid and its aglycone trans-resveratrol on the apical membrane of human intestinal Caco-2 cells", J. Agric. Food Chem., 53, pp.798~803 (2005)[DOI]
  22. Day AJ, "Deglycosylation of flavonoid and isoflavonoid glycosides by human small intestine and liver beta-glucosidase activity", FEBS Lett., 436, pp.71~75 (1998)[DOI]
  23. Mikstacka R, "Inhibition of human recombinant cytochromes P450 CYP1A1 and CYP1B1 by trans-resveratrol methyl ethers", Mol. Nutr. Food Res., 51, pp.517~524 (2007)[DOI]
  24. Wilson MA, "Methoxylation enhances stilbene bioactivity in Caenorhabditis elegans", BMC Pharmacol., 8, pp.15~ (2008)[DOI]
  25. Nutakul W, "Inhibitory effects of resveratrol and pterostilbene on human colon cancer cells: a side-byside comparison", J. Agric. Food Chem., 59, pp.10964~10970 (2011)[DOI]
  26. Rimando AM, "Cancer chemopreventive and antioxidant activities of pterostilbene, a naturally occurring analogue of resveratrol", J. Agric. Food Chem., 50, pp.3453~3457 (2002)[DOI]

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