메뉴 건너뛰기




Volumn 44, Issue 5, 2009, Pages 572-577

A novel biotransformation process of 4′-demethylepipodophyllotoxin to 4′-demethylepipodophyllic acid by Bacillus fusiformis CICC 20463

Author keywords

4 Demethylepipodophyllic acid; 4 Demethylepipodophyllotoxin; Bacillus fusiformis; Biotransformation process development

Indexed keywords

BACILLUS FUSIFORMIS; BACILLUS SUBTILIS; BIOTRANSFORMATION PROCESS DEVELOPMENT; BIOTRANSFORMATION PRODUCTS; COMPARISON ANALYSIS; MACROPOROUS RESINS; P. AERUGINOSA; PSEUDOMONAS AERUGINOSA; SUBSTRATE CONVERSIONS; SUBTILIS;

EID: 64049097284     PISSN: 13595113     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.procbio.2009.01.010     Document Type: Article
Times cited : (8)

References (29)
  • 2
    • 0033744225 scopus 로고    scopus 로고
    • Production of podophyllotoxin from Podophyllum hexandrum: a potential natural product for clinically useful anticancer drugs
    • Giri A., and Narasu M.L. Production of podophyllotoxin from Podophyllum hexandrum: a potential natural product for clinically useful anticancer drugs. Cytotechnology 34 (2000) 17-26
    • (2000) Cytotechnology , vol.34 , pp. 17-26
    • Giri, A.1    Narasu, M.L.2
  • 3
    • 0032033637 scopus 로고    scopus 로고
    • Discovery of podophyllotoxins
    • Imbert T.F. Discovery of podophyllotoxins. Biochimie 80 (1998) 207-222
    • (1998) Biochimie , vol.80 , pp. 207-222
    • Imbert, T.F.1
  • 5
    • 64049088269 scopus 로고    scopus 로고
    • Catalytic modification of podophyllotoxin
    • (in Chinese)
    • Yang D.S., Wang X.L., and Wen P.H. Catalytic modification of podophyllotoxin. Ind Catal 9 1 (2001) 37-39 (in Chinese)
    • (2001) Ind Catal , vol.9 , Issue.1 , pp. 37-39
    • Yang, D.S.1    Wang, X.L.2    Wen, P.H.3
  • 6
    • 32344439156 scopus 로고    scopus 로고
    • A brief review on podophyllotoxin analogues
    • (in Chinese)
    • Gao R., Tian X., and Zhang X. A brief review on podophyllotoxin analogues. Chin Pest Sci 2 1 (2003) 1-6 (in Chinese)
    • (2003) Chin Pest Sci , vol.2 , Issue.1 , pp. 1-6
    • Gao, R.1    Tian, X.2    Zhang, X.3
  • 7
    • 0032168167 scopus 로고    scopus 로고
    • Etoposide: four decades of development of a topoisomerase II inhibitor
    • Hande K.R. Etoposide: four decades of development of a topoisomerase II inhibitor. Eur J Cancer 34 (1998) 1514-1521
    • (1998) Eur J Cancer , vol.34 , pp. 1514-1521
    • Hande, K.R.1
  • 8
    • 1542345035 scopus 로고    scopus 로고
    • Antitumor agents. Part 232: Synthesis of cyclosulfite podophyllotoxin analogues as novel prototype antitumor agents
    • Xiao Z.Y., Han S.Q., Bastow K.F., and Lee K.H. Antitumor agents. Part 232: Synthesis of cyclosulfite podophyllotoxin analogues as novel prototype antitumor agents. Bioor Med Chem Lett 14 (2004) 1581-1584
    • (2004) Bioor Med Chem Lett , vol.14 , pp. 1581-1584
    • Xiao, Z.Y.1    Han, S.Q.2    Bastow, K.F.3    Lee, K.H.4
  • 9
    • 33845401015 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new 4β-5-fu-substituted 4′-demethylepipodophyllotoxin derivatives
    • Zhang F.M., Yao X.J., Tian X., and Tu Y.Q. Synthesis and biological evaluation of new 4β-5-fu-substituted 4′-demethylepipodophyllotoxin derivatives. Molecules 11 (2006) 849-857
    • (2006) Molecules , vol.11 , pp. 849-857
    • Zhang, F.M.1    Yao, X.J.2    Tian, X.3    Tu, Y.Q.4
  • 10
    • 25844514216 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new 4β-anilino and 4β-imido-substituted podophyllotoxin congeners
    • Kamal A., Gayatri N.L., Reddy D.R., Reddy P.S.M.M., Arifuddin M., Dastida S.G., et al. Synthesis and biological evaluation of new 4β-anilino and 4β-imido-substituted podophyllotoxin congeners. Bioor Med Chem 13 (2005) 6218-6225
    • (2005) Bioor Med Chem , vol.13 , pp. 6218-6225
    • Kamal, A.1    Gayatri, N.L.2    Reddy, D.R.3    Reddy, P.S.M.M.4    Arifuddin, M.5    Dastida, S.G.6
  • 12
    • 0034916199 scopus 로고    scopus 로고
    • Biotransformations using plant cells, organ cultures and enzyme systems: current trends and future prospects
    • Giri A., Dhingra V., Giri C.C., Singhc A., Wardc O.P., and Narasua M.L. Biotransformations using plant cells, organ cultures and enzyme systems: current trends and future prospects. Biotechnol Adv 19 (2001) 175-199
    • (2001) Biotechnol Adv , vol.19 , pp. 175-199
    • Giri, A.1    Dhingra, V.2    Giri, C.C.3    Singhc, A.4    Wardc, O.P.5    Narasua, M.L.6
  • 13
    • 0036534231 scopus 로고    scopus 로고
    • Biocatalysis and biotransformation
    • Dordick J.S., and Clark D.S. Biocatalysis and biotransformation. Curr Opin Chem Biol 6 (2002) 123-124
    • (2002) Curr Opin Chem Biol , vol.6 , pp. 123-124
    • Dordick, J.S.1    Clark, D.S.2
  • 14
    • 0035174820 scopus 로고    scopus 로고
    • Biotransformation of lignans and neolignans
    • Miyazawa M. Biotransformation of lignans and neolignans. Curr Org Chem 5 (2001) 975-986
    • (2001) Curr Org Chem , vol.5 , pp. 975-986
    • Miyazawa, M.1
  • 16
    • 33846143466 scopus 로고    scopus 로고
    • Transformation of steroids by actinobacteria: a review
    • Donova M.V. Transformation of steroids by actinobacteria: a review. Appl Biochem Biotechnol 43 1 (2007) 1-14
    • (2007) Appl Biochem Biotechnol , vol.43 , Issue.1 , pp. 1-14
    • Donova, M.V.1
  • 18
    • 0035313630 scopus 로고    scopus 로고
    • Biocatalytic modification of natural products
    • Riva S. Biocatalytic modification of natural products. Curr Opin Chem Biol 5 (2001) 106-111
    • (2001) Curr Opin Chem Biol , vol.5 , pp. 106-111
    • Riva, S.1
  • 19
    • 0031576895 scopus 로고    scopus 로고
    • A novel enzymatic dehydrogenation of podophyllotoxin congeners by yeast cells
    • Kamal A., and Damayanthi Y. A novel enzymatic dehydrogenation of podophyllotoxin congeners by yeast cells. Bioorg Med Chem Lett 7 (1997) 657-662
    • (1997) Bioorg Med Chem Lett , vol.7 , pp. 657-662
    • Kamal, A.1    Damayanthi, Y.2
  • 20
    • 0000003081 scopus 로고
    • Biotransformation of podophyllum lignans in cell suspension cultures of Forsythia intermedia
    • Broomhead A.J., and Dewick P.M. Biotransformation of podophyllum lignans in cell suspension cultures of Forsythia intermedia. Phytochemistry 30 (1991) 1511-1517
    • (1991) Phytochemistry , vol.30 , pp. 1511-1517
    • Broomhead, A.J.1    Dewick, P.M.2
  • 21
    • 0032230133 scopus 로고    scopus 로고
    • Biotransformation of podophyllotoxin to picropodophyllin by microbes
    • Guo H.Z., Guo D.A., Fei X.Y., Cui Y.J., and Zheng J.H. Biotransformation of podophyllotoxin to picropodophyllin by microbes. J Asian Nat Prod Res 1 (1998) 99-102
    • (1998) J Asian Nat Prod Res , vol.1 , pp. 99-102
    • Guo, H.Z.1    Guo, D.A.2    Fei, X.Y.3    Cui, Y.J.4    Zheng, J.H.5
  • 22
    • 33947633482 scopus 로고    scopus 로고
    • Biotransformation of podophyllotoxin by Hordeum vulgare cell suspension cultures
    • Teng R.W., McManus D., Mau S.L., and Bacic A. Biotransformation of podophyllotoxin by Hordeum vulgare cell suspension cultures. Biocatal Biotransform 25 (2007) 1-8
    • (2007) Biocatal Biotransform , vol.25 , pp. 1-8
    • Teng, R.W.1    McManus, D.2    Mau, S.L.3    Bacic, A.4
  • 24
    • 1342281637 scopus 로고    scopus 로고
    • Synthesis of podophyllotoxin analogues: D-lactone-containing picropodophyllin, podophyllotoxin and 4′-demethylepipodophyllotoxin derivatives
    • Meresse P., Monneret C., and Bertounesque E. Synthesis of podophyllotoxin analogues: D-lactone-containing picropodophyllin, podophyllotoxin and 4′-demethylepipodophyllotoxin derivatives. Tetrahedron 60 (2004) 2657-2671
    • (2004) Tetrahedron , vol.60 , pp. 2657-2671
    • Meresse, P.1    Monneret, C.2    Bertounesque, E.3
  • 25
    • 37049089772 scopus 로고
    • Lignans and related phenols. Part XII. Application of nuclear magnetic double resonance to the arytetrahydronaphthalene class
    • Ayres D.C., Harris J.A., Jenkins P.N., and Phillips L. Lignans and related phenols. Part XII. Application of nuclear magnetic double resonance to the arytetrahydronaphthalene class. J Chem Soc Perkin Trans 9 (1988) 2573-2578
    • (1988) J Chem Soc Perkin Trans , vol.9 , pp. 2573-2578
    • Ayres, D.C.1    Harris, J.A.2    Jenkins, P.N.3    Phillips, L.4
  • 26
    • 64049084880 scopus 로고    scopus 로고
    • 2D NMR studies on 4β-5-fu-substituted derivatives of 4′-demethylepipodophyllotoxin
    • Jin X.L., Zhang F.M., Tian X., and Yang L. 2D NMR studies on 4β-5-fu-substituted derivatives of 4′-demethylepipodophyllotoxin. Chin J Magn Reson 19 3 (2002) 259-264
    • (2002) Chin J Magn Reson , vol.19 , Issue.3 , pp. 259-264
    • Jin, X.L.1    Zhang, F.M.2    Tian, X.3    Yang, L.4
  • 27
    • 33846173011 scopus 로고    scopus 로고
    • Bacillus subtilis epoxide hydrolase-catalyzed preparation of enantiopure 2-methylpropane-1,2,3-triol monobenzyl ether and its application to expeditious synthesis of (R)-bicalutamide
    • Fujino A., Asano M., Yamaguchi H., Shirasaka N., Sakoda A., Ikunaka M., et al. Bacillus subtilis epoxide hydrolase-catalyzed preparation of enantiopure 2-methylpropane-1,2,3-triol monobenzyl ether and its application to expeditious synthesis of (R)-bicalutamide. Tetrahedron Lett 48 (2007) 979-983
    • (2007) Tetrahedron Lett , vol.48 , pp. 979-983
    • Fujino, A.1    Asano, M.2    Yamaguchi, H.3    Shirasaka, N.4    Sakoda, A.5    Ikunaka, M.6
  • 28
    • 34347248751 scopus 로고    scopus 로고
    • Purification and characterization of trans-3-(4-methoxyphenyl) glycidic acid methyl ester hydrolyzing lipase from Pseudomonas aeruginosa
    • Singh S., and Banerjee U.C. Purification and characterization of trans-3-(4-methoxyphenyl) glycidic acid methyl ester hydrolyzing lipase from Pseudomonas aeruginosa. Process Biochem 42 (2007) 1063-1068
    • (2007) Process Biochem , vol.42 , pp. 1063-1068
    • Singh, S.1    Banerjee, U.C.2
  • 29
    • 0028518694 scopus 로고
    • Substrate specificity of the alkane hydroxylase system of Pseudomonas oleovorans GPo1
    • Beilen J.B., Kingma J., and Witholt B. Substrate specificity of the alkane hydroxylase system of Pseudomonas oleovorans GPo1. Enzyme Microb Technol 10 (1994) 904-911
    • (1994) Enzyme Microb Technol , vol.10 , pp. 904-911
    • Beilen, J.B.1    Kingma, J.2    Witholt, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.