메뉴 건너뛰기




Volumn 50, Issue 10, 2015, Pages 1614-1617

Identification of 3′-hydroxygenistein as a potent melanogenesis inhibitor from biotransformation of genistein by recombinant Pichia pastoris

Author keywords

3 Hydroxygenistein; Genistein; Inhibition; Melanogenesis; Pichia pastoris; Tyrosinase

Indexed keywords

BIOCONVERSION; ENZYME INHIBITION; FLAVONOIDS;

EID: 84940721634     PISSN: 13595113     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.procbio.2015.06.007     Document Type: Article
Times cited : (22)

References (22)
  • 2
    • 84953320320 scopus 로고    scopus 로고
    • Natural, semisynthetic and synthetic tyrosinase inhibitors
    • S.Y. Lee, N. Baek, and T.G. Nam Natural, semisynthetic and synthetic tyrosinase inhibitors J. Enzyme Inhib. Med. Chem. 16 2015 1 13
    • (2015) J. Enzyme Inhib. Med. Chem. , vol.16 , pp. 1-13
    • Lee, S.Y.1    Baek, N.2    Nam, T.G.3
  • 3
    • 84870050261 scopus 로고    scopus 로고
    • Natural melanogenesis inhibitors acting through the down-regulation of tyrosinase activity
    • T.S. Chang Natural melanogenesis inhibitors acting through the down-regulation of tyrosinase activity Materials 5 2012 1661 1685
    • (2012) Materials , vol.5 , pp. 1661-1685
    • Chang, T.S.1
  • 4
    • 67649668609 scopus 로고    scopus 로고
    • An updated review of tyrosinase inhibitors
    • T.S. Chang An updated review of tyrosinase inhibitors Int. J. Mol. Sci. 10 2009 2440 2475
    • (2009) Int. J. Mol. Sci. , vol.10 , pp. 2440-2475
    • Chang, T.S.1
  • 5
    • 84940725785 scopus 로고    scopus 로고
    • Inhibition of melanogenesis by yeast extracts from cultivations of recombinant Pichia pastoris catalyzing ortho-hydroxylation of flavonoids
    • in press
    • T.S. Chang, and Y.H. Tsai Inhibition of melanogenesis by yeast extracts from cultivations of recombinant Pichia pastoris catalyzing ortho-hydroxylation of flavonoids Curr. Pharma. Biotechnol. 2015 (in press)
    • (2015) Curr. Pharma. Biotechnol.
    • Chang, T.S.1    Tsai, Y.H.2
  • 6
    • 33947600591 scopus 로고    scopus 로고
    • Two potent suicide substrates of mushroom tyrosinase: 7,8,4′-trihydroxyisoflavone and 5,7,8,4′-tetrahydroxyisoflavone
    • T.S. Chang Two potent suicide substrates of mushroom tyrosinase: 7,8,4′-trihydroxyisoflavone and 5,7,8,4′-tetrahydroxyisoflavone J. Agric. Food Chem. 55 2007 2010 2015
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 2010-2015
    • Chang, T.S.1
  • 7
    • 84896751799 scopus 로고    scopus 로고
    • Production of bioactive hydroxyflavones by using monooxygenase from Saccharothrix espanaensis
    • B.G. Kim, and J.H. Ahn Production of bioactive hydroxyflavones by using monooxygenase from Saccharothrix espanaensis J. Biotechnol. 176 2014 11 17
    • (2014) J. Biotechnol. , vol.176 , pp. 11-17
    • Kim, B.G.1    Ahn, J.H.2
  • 8
    • 79955593960 scopus 로고    scopus 로고
    • Construction and application of a functional library of cytochrome P450 monooxygenases from the filamentous fungus Aspergillus oryzae
    • N.H. Nazir, H. Ichinose, and H. Wariishi Construction and application of a functional library of cytochrome P450 monooxygenases from the filamentous fungus Aspergillus oryzae Appl. Environ. Microbiol. 77 2011 3147 3150
    • (2011) Appl. Environ. Microbiol. , vol.77 , pp. 3147-3150
    • Nazir, N.H.1    Ichinose, H.2    Wariishi, H.3
  • 10
    • 22144450357 scopus 로고    scopus 로고
    • Novel tempeh (fermented soyabean) isoflavones inhibit in vivo angiogenesis in the chicken chorioallantoic membrane assay
    • S. Kiriakidis, O. Högemeier, S. Starcke, F. Dombrowski, J.C. Hahne, M. Pepper, H.C. Jha, and N. Wernert Novel tempeh (fermented soyabean) isoflavones inhibit in vivo angiogenesis in the chicken chorioallantoic membrane assay Br. J. Nutr. 93 2005 317 323
    • (2005) Br. J. Nutr. , vol.93 , pp. 317-323
    • Kiriakidis, S.1    Högemeier, O.2    Starcke, S.3    Dombrowski, F.4    Hahne, J.C.5    Pepper, M.6    Jha, H.C.7    Wernert, N.8
  • 11
    • 58149472888 scopus 로고    scopus 로고
    • Assembly of non-natural electron transfer conduits in the cytochrome P450 system: A critical assessment and update of artificial redox constructs amenable to exploitation in biotechnological areas
    • P. Hlavica Assembly of non-natural electron transfer conduits in the cytochrome P450 system: a critical assessment and update of artificial redox constructs amenable to exploitation in biotechnological areas Biotechnol. Adv. 27 2009 103 121
    • (2009) Biotechnol. Adv. , vol.27 , pp. 103-121
    • Hlavica, P.1
  • 12
    • 33751426673 scopus 로고    scopus 로고
    • From miso, saké and shoyu to cosmetics: A century of science for kojic acid
    • R. Bentley From miso, saké and shoyu to cosmetics: a century of science for kojic acid Nat. Prod. Rep. 23 2006 1046 1062
    • (2006) Nat. Prod. Rep. , vol.23 , pp. 1046-1062
    • Bentley, R.1
  • 13
    • 78751508597 scopus 로고    scopus 로고
    • Inhibitory effect of danazol on melanogenesis in mouse B16 melanoma cells
    • T.S. Chang, and J.J. Lin Inhibitory effect of danazol on melanogenesis in mouse B16 melanoma cells Arch. Pharm. Res. 33 2010 1959 1965
    • (2010) Arch. Pharm. Res. , vol.33 , pp. 1959-1965
    • Chang, T.S.1    Lin, J.J.2
  • 14
    • 33749247249 scopus 로고    scopus 로고
    • The intracellular genistein metabolite 5,7,3′,4′-tetrahydroxyisoflavone mediates G2-M cell cycle arrest in cancer cells via modulation of the p38 signaling pathway
    • D.T. Nguyen, E. Hernandez-Montes, D. Vauzour, A.H. Schonthal, C. Rice-Evans, E. Cadenas, and J.P.E. Spencer The intracellular genistein metabolite 5,7,3′,4′-tetrahydroxyisoflavone mediates G2-M cell cycle arrest in cancer cells via modulation of the p38 signaling pathway Free Radic. Biol. Med. 41 2006 1225 1239
    • (2006) Free Radic. Biol. Med. , vol.41 , pp. 1225-1239
    • Nguyen, D.T.1    Hernandez-Montes, E.2    Vauzour, D.3    Schonthal, A.H.4    Rice-Evans, C.5    Cadenas, E.6    Spencer, J.P.E.7
  • 15
    • 36148974705 scopus 로고    scopus 로고
    • Inhibition of cellular proliferation by the genistein metabolite 5,7,3′,4′-tetrahydroxyisoflavone is mediated by DNA damage and activation of the ATR signalling pathway
    • D. Vauzour, K. Vafeiadou, C. Rice-Evans, E. Cadenas, and J.P.E. Spencer Inhibition of cellular proliferation by the genistein metabolite 5,7,3′,4′-tetrahydroxyisoflavone is mediated by DNA damage and activation of the ATR signalling pathway Arch. Biochem. Biophys. 468 2007 159 166
    • (2007) Arch. Biochem. Biophys. , vol.468 , pp. 159-166
    • Vauzour, D.1    Vafeiadou, K.2    Rice-Evans, C.3    Cadenas, E.4    Spencer, J.P.E.5
  • 16
    • 36549025883 scopus 로고    scopus 로고
    • HIV-1 protease and HIV-1 integrase inhibitory substances from Eclipta prostrata
    • S. Tewtrakul, S. Subhadhirasakul, S. Cheenpracha, and C. Karalai HIV-1 protease and HIV-1 integrase inhibitory substances from Eclipta prostrata Phytother. Res. 21 2007 1092 1095
    • (2007) Phytother. Res. , vol.21 , pp. 1092-1095
    • Tewtrakul, S.1    Subhadhirasakul, S.2    Cheenpracha, S.3    Karalai, C.4
  • 18
    • 11944274965 scopus 로고    scopus 로고
    • New isoflavones and pterocarpane with hepatoprotective activity from the stems of Erycibe expansa
    • H. Matsuda, T. Morikawa, F. Xu, K. Ninomiya, and M. Yoshikawa New isoflavones and pterocarpane with hepatoprotective activity from the stems of Erycibe expansa Planta Med. 70 2004 1201 1209
    • (2004) Planta Med. , vol.70 , pp. 1201-1209
    • Matsuda, H.1    Morikawa, T.2    Xu, F.3    Ninomiya, K.4    Yoshikawa, M.5
  • 19
    • 27644444019 scopus 로고    scopus 로고
    • Identifying 6,7,4′-trihydroxyisoflavone as a potent tyrosinase inhibitor
    • T.S. Chang, H.Y. Ding, and H.C. Lin Identifying 6,7,4′-trihydroxyisoflavone as a potent tyrosinase inhibitor Biosci. Biotechnol. Biochem. 69 2005 1999 2001
    • (2005) Biosci. Biotechnol. Biochem. , vol.69 , pp. 1999-2001
    • Chang, T.S.1    Ding, H.Y.2    Lin, H.C.3
  • 20
    • 34447633916 scopus 로고    scopus 로고
    • Tyrosinase inhibitors isolated from soygerm koji fermented with Aspergillus oryzae BCRC 32288
    • T.S. Chang, H.Y. Ding, S.S.K. Tai, and C.Y. Wu Tyrosinase inhibitors isolated from soygerm koji fermented with Aspergillus oryzae BCRC 32288 Food Chem. 105 2007 1430 1438
    • (2007) Food Chem. , vol.105 , pp. 1430-1438
    • Chang, T.S.1    Ding, H.Y.2    Tai, S.S.K.3    Wu, C.Y.4
  • 21
    • 74049104179 scopus 로고    scopus 로고
    • Natural ortho-dihydroxyisoflavone derivatives from aged Korean fermented soybean paste as potent tyrosinase and melanin formation inhibitors
    • J.S. Park, D.H. Kim, J.K. Lee, J.Y. Lee, D.H. Kim, H.K. Kim, H.J. Lee, and H.C. Kim Natural ortho-dihydroxyisoflavone derivatives from aged Korean fermented soybean paste as potent tyrosinase and melanin formation inhibitors Bioorg. Med. Chem. Lett. 20 2010 1162 1164
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 1162-1164
    • Park, J.S.1    Kim, D.H.2    Lee, J.K.3    Lee, J.Y.4    Kim, D.H.5    Kim, H.K.6    Lee, H.J.7    Kim, H.C.8
  • 22
    • 84864288059 scopus 로고    scopus 로고
    • Effects of ortho-dihydroxyisoflavone derivatives from Korean fermented soybean paste on melanogenesis in B16 melanoma cells and human skin equivalents
    • M.J. Goh, J.S. Park, J.H. Bae, D.H. Kim, H.K. Kim, and Y.J. Na Effects of ortho-dihydroxyisoflavone derivatives from Korean fermented soybean paste on melanogenesis in B16 melanoma cells and human skin equivalents Phytother. Res. 26 2012 1107 1112
    • (2012) Phytother. Res. , vol.26 , pp. 1107-1112
    • Goh, M.J.1    Park, J.S.2    Bae, J.H.3    Kim, D.H.4    Kim, H.K.5    Na, Y.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.