메뉴 건너뛰기




Volumn 23, Issue 3, 2006, Pages 291-296

Regioselective hydroxylation, reduction, and glycosylation of diphenyl compounds by cultured plant cells of Eucalyptus perriniana

Author keywords

Benzophenone; Biotransformation; Bisphenol A; Diphenyl compounds; Eucalyptus perriniana

Indexed keywords

EUCALYPTUS; EUCALYPTUS PERRINIANA;

EID: 33746065297     PISSN: 13424580     EISSN: 13476114     Source Type: Journal    
DOI: 10.5511/plantbiotechnology.23.291     Document Type: Article
Times cited : (17)

References (17)
  • 1
    • 0029005176 scopus 로고
    • In vitro conversion of environmental estrogenic chemical bisphenol A to DNA binding metabolite(s)
    • Atkinson A, Roy D (1995) In vitro conversion of environmental estrogenic chemical bisphenol A to DNA binding metabolite(s). Biochem Biophys Res Commum 210: 424-433
    • (1995) Biochem Biophys Res Commum , vol.210 , pp. 424-433
    • Atkinson, A.1    Roy, D.2
  • 2
    • 45949124341 scopus 로고
    • Triterpenoids from eucalyptus perriniana cultured cells
    • Furuya T, Orihara Y, Hayashi C (1987) Triterpenoids from eucalyptus perriniana cultured cells. Phytochem 26: 715-719
    • (1987) Phytochem , vol.26 , pp. 715-719
    • Furuya, T.1    Orihara, Y.2    Hayashi, C.3
  • 3
    • 0037182323 scopus 로고    scopus 로고
    • Phytoremediation of bisphenol A by cultured suspension cells of Eucalyptus perriniana-regioselective hydroxylation and glycosylation
    • Hamada H, Tomi R, Asada Y, Furuya T (2002) Phytoremediation of bisphenol A by cultured suspension cells of Eucalyptus perriniana-regioselective hydroxylation and glycosylation. Tetrahedron Lett 43: 4087-4089
    • (2002) Tetrahedron Lett , vol.43 , pp. 4087-4089
    • Hamada, H.1    Tomi, R.2    Asada, Y.3    Furuya, T.4
  • 4
    • 0025216788 scopus 로고
    • Gentisate 1,2-dioxygenase from pseudomonas. Purification, characterization, and comparison of the enzymes from Pseudomonas testosteroni and Pseudomonas acidovorans
    • Harpel MR, Lipscomb JD (1990) Gentisate 1,2-dioxygenase from pseudomonas. Purification, characterization, and comparison of the enzymes from Pseudomonas testosteroni and Pseudomonas acidovorans. J Biol Chem 265: 6301-6311
    • (1990) J Biol Chem , vol.265 , pp. 6301-6311
    • Harpel, M.R.1    Lipscomb, J.D.2
  • 5
    • 0034279979 scopus 로고    scopus 로고
    • Degradation of bisphenol A by the lignin-degrading enzyme, manganese peroxidase, produced by the white-rot basidiomycete, Pleurotus ostreatus
    • Hirano T, Honda Y, Watanabe T, Kuwahara M (2000) Degradation of bisphenol A by the lignin-degrading enzyme, manganese peroxidase, produced by the white-rot basidiomycete, Pleurotus ostreatus. Biosci Biotechnol Biochem 64: 1958-1962
    • (2000) Biosci Biotechnol Biochem , vol.64 , pp. 1958-1962
    • Hirano, T.1    Honda, Y.2    Watanabe, T.3    Kuwahara, M.4
  • 9
    • 0000443167 scopus 로고
    • Glucosylation of salicyl alcohol by Gardenia jasminoides cell cultures
    • Mizukami H, Terao T, Amano A, Ohashi H (1986) Glucosylation of salicyl alcohol by Gardenia jasminoides cell cultures. Plant Cell Physiol 27: 645
    • (1986) Plant Cell Physiol , vol.27 , pp. 645
    • Mizukami, H.1    Terao, T.2    Amano, A.3    Ohashi, H.4
  • 10
    • 0042756224 scopus 로고
    • Effect of substituent groups on the glucosyl conjugation of xenobiotic phenols by cultured cells of Gardenia jasminoides
    • Mizutani H, Hirano A, Ohashi H (1987) Effect of substituent groups on the glucosyl conjugation of xenobiotic phenols by cultured cells of Gardenia jasminoides. Plant Sci 48: 11-15
    • (1987) Plant Sci , vol.48 , pp. 11-15
    • Mizutani, H.1    Hirano, A.2    Ohashi, H.3
  • 11
    • 0032894856 scopus 로고    scopus 로고
    • New screening methods for chemicals with hormonal activities using interaction of nuclear hormone receptor with coactivator
    • Nishikawa J, Saito K, Goto J, Dakeyama F, Matsuo M, Nishihara T (1999) New screening methods for chemicals with hormonal activities using interaction of nuclear hormone receptor with coactivator. Toxicol Appl Pharmacol 154: 76-83
    • (1999) Toxicol Appl Pharmacol , vol.154 , pp. 76-83
    • Nishikawa, J.1    Saito, K.2    Goto, J.3    Dakeyama, F.4    Matsuo, M.5    Nishihara, T.6
  • 13
    • 0037127574 scopus 로고    scopus 로고
    • Biotransformation of phenolic compounds by the cultured cells of Catharanthus roseus
    • Shimoda K, Yamane S, Hirakawa H, Ohta S, Hirata T (2002) Biotransformation of phenolic compounds by the cultured cells of Catharanthus roseus. J Mol Catal B: Enz 16: 275-281
    • (2002) J Mol Catal B: Enz , vol.16 , pp. 275-281
    • Shimoda, K.1    Yamane, S.2    Hirakawa, H.3    Ohta, S.4    Hirata, T.5
  • 14
    • 44949269802 scopus 로고
    • Biotransformation of exogenous substrates by plant cell cultures
    • Suga T, Hirata T (1990) Biotransformation of exogenous substrates by plant cell cultures. Phytochem 29: 2393-2406
    • (1990) Phytochem , vol.29 , pp. 2393-2406
    • Suga, T.1    Hirata, T.2
  • 15
    • 0001074178 scopus 로고
    • Glucosylation of phenolic compounds by plant cell cultures
    • Tabata M, Unetani Y, Oya M, Tanaka S (1988) Glucosylation of phenolic compounds by plant cell cultures. Phytochem 27: 809-813
    • (1988) Phytochem , vol.27 , pp. 809-813
    • Tabata, M.1    Unetani, Y.2    Oya, M.3    Tanaka, S.4
  • 16
    • 0000496173 scopus 로고
    • Glucosylation of phenolic compounds by root culture of Panax ginseng
    • Ushiyama M, Furuya T (1989) Glucosylation of phenolic compounds by root culture of Panax ginseng. Phytochem 28: 3009-3013
    • (1989) Phytochem , vol.28 , pp. 3009-3013
    • Ushiyama, M.1    Furuya, T.2
  • 17
    • 0033152656 scopus 로고    scopus 로고
    • Glucuronidation of the environmental oestrogen bisphenol A by an isoform of UDP-glucuronosyltransferase, UGT2B1, in the rat liver
    • Yokota H, Iwano H, Endo M, Kobayashi T, Inoue H, Ikushiro S (1999) Glucuronidation of the environmental oestrogen bisphenol A by an isoform of UDP-glucuronosyltransferase, UGT2B1, in the rat liver. Biochem J 340: 405-409
    • (1999) Biochem J , vol.340 , pp. 405-409
    • Yokota, H.1    Iwano, H.2    Endo, M.3    Kobayashi, T.4    Inoue, H.5    Ikushiro, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.