메뉴 건너뛰기




Volumn , Issue , 2007, Pages 71-76

Biotransformation of terpenes and steroids by fungi

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84892770928     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1142/9789812707444_0006     Document Type: Chapter
Times cited : (3)

References (30)
  • 2
    • 0015037881 scopus 로고
    • Isolation and characterization of cytotoxic principles from Hyptis verticillata Jacq
    • German VF. Isolation and characterization of cytotoxic principles from Hyptis verticillata Jacq. J Pharm Sei 1971; 60: 649-50
    • (1971) J Pharm Sei , vol.60 , pp. 649-650
    • German, V.F.1
  • 4
    • 0028065719 scopus 로고
    • Lignans and other compounds from the Mixe Indian medicinal plant Hyptis verticillata
    • Kuhnt M, Rimpler H, Heinrich M. Lignans and other compounds from the Mixe Indian medicinal plant Hyptis verticillata. Phytochemistry 1994; 36: 485489
    • (1994) Phytochemistry , vol.36 , pp. 485489
    • Kuhnt, M.1    Rimpler, H.2    Heinrich, M.3
  • 5
    • 37949015271 scopus 로고    scopus 로고
    • Characterisation of a flavonol and several lignans from Hyptis verticillata
    • Porter RBR, Reese PB. Characterisation of a flavonol and several lignans from Hyptis verticillata. Jamaican Journal of Science & Technology 1998; 9: 17-27
    • (1998) Jamaican Journal of Science & Technology , vol.9 , pp. 17-27
    • Porter, R.B.R.1    Reese, P.B.2
  • 9
    • 17544382027 scopus 로고    scopus 로고
    • New skeletal sesquiterpenoids, caprariolides A - D, from Capraria biflora and their insecticidal activity
    • Collins DO, Gallimore WA, Reynolds WF, Williams LAD, Reese PB. New skeletal sesquiterpenoids, caprariolides A - D, from Capraria biflora and their insecticidal activity. J Nat Prod 2000; 63: 1515-8
    • (2000) J Nat Prod , vol.63 , pp. 1515-1518
    • Collins, D.O.1    Gallimore, W.A.2    Reynolds, W.F.3    Williams, L.A.D.4    Reese, P.B.5
  • 10
    • 0000587448 scopus 로고
    • Structures of stemodin and stemodinone
    • Knoll WMJ, Huxtable RJ. Structures of stemodin and stemodinone. J Am Chem Soc 1973; 95: 2705-6
    • (1973) J Am Chem Soc , vol.95 , pp. 2705-2706
    • Knoll, W.M.J.1    Huxtable, R.J.2
  • 12
    • 0032709550 scopus 로고    scopus 로고
    • Cytotoxic terpenoids from the Formosan soft coral Nephthea brassica
    • Duh C, Wang S, Weng Y, Chiang MY, Dai C. Cytotoxic terpenoids from the Formosan soft coral Nephthea brassica. J Nat Prod 1999; 62: 1518-21
    • (1999) J Nat Prod , vol.62 , pp. 1518-1521
    • Duh, C.1    Wang, S.2    Weng, Y.3    Chiang, M.Y.4    Dai, C.5
  • 13
    • 0032538584 scopus 로고    scopus 로고
    • Structurally novel bioconversion products of the marine natural product sarcophine effectively inhibit JB6 cell transformation
    • El Sayed KA, Hamann MT, Waddling CA, Jensen C, Lee, SK, Andersson Dunstan C, Pezzuto, JM. Structurally novel bioconversion products of the marine natural product sarcophine effectively inhibit JB6 cell transformation. J Org Chem 1998; 63: 7449-55
    • (1998) J Org Chem , vol.63 , pp. 7449-7455
    • El Sayed, K.A.1    Hamann, M.T.2    Waddling, C.A.3    Jensen, C.4    Lee, S.K.5    Andersson Dunstan, C.6    Pezzuto, J.M.7
  • 14
    • 0029973020 scopus 로고    scopus 로고
    • Cytotoxic cembranoids from the soft corals Sinularia gibberosa and Sarcophyton trocheliophorum
    • Duh C, Hou R. Cytotoxic cembranoids from the soft corals Sinularia gibberosa and Sarcophyton trocheliophorum. J Nat Prod 1996; 59: 595-8
    • (1996) J Nat Prod , vol.59 , pp. 595-598
    • Duh, C.1    Hou, R.2
  • 16
    • 0034119752 scopus 로고    scopus 로고
    • Biotransformation of cadinane sesquiterpenes by Beauveria bassiana ATCC 7159
    • Buchanan GO, Williams LAD, Reese PB. Biotransformation of cadinane sesquiterpenes by Beauveria bassiana ATCC 7159. Phytochemistry 2000; 54: 3945
    • (2000) Phytochemistry , vol.54 , pp. 3945
    • Buchanan, G.O.1    Williams, L.A.D.2    Reese, P.B.3
  • 17
    • 0037017450 scopus 로고    scopus 로고
    • Microbial transformation of cadina-4,10(15)-dien-3-one, aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740
    • Collins DO, Ruddock PLD, Chiverton de Grasse J, Reynolds WF, Reese PB. Microbial transformation of cadina-4,10(15)-dien-3-one, aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740. Phytochemistry 2002; 59: 479-88
    • (2002) Phytochemistry , vol.59 , pp. 479-488
    • Collins, D.O.1    Ruddock, P.L.D.2    Chiverton de Grasse, J.3    Reynolds, W.F.4    Reese, P.B.5
  • 18
    • 0037017449 scopus 로고    scopus 로고
    • Biotransformation of cadina-4,10(15)-dien-3-one and 3?-hydroxycadina-4,10(15)-diene by Curvularia lunata ATCC 12017
    • Collins DO, Reese PB. Biotransformation of cadina-4,10(15)-dien-3-one and 3?-hydroxycadina-4,10(15)-diene by Curvularia lunata ATCC 12017. Phytochemistry 2002; 59: 489-92
    • (2002) Phytochemistry , vol.59 , pp. 489-492
    • Collins, D.O.1    Reese, P.B.2
  • 19
    • 0036629122 scopus 로고    scopus 로고
    • Aromadendrane transformations by Curvularia lunata ATCC 12017
    • Collins DO, Reynolds WF, Reese PB. Aromadendrane transformations by Curvularia lunata ATCC 12017. Phytochemistry. 2002; 60: 475-81
    • (2002) Phytochemistry , vol.60 , pp. 475-481
    • Collins, D.O.1    Reynolds, W.F.2    Reese, P.B.3
  • 20
    • 0035970122 scopus 로고    scopus 로고
    • Bio transformation of diterpenes and diterpene derivatives by Beauveria bassiana ATCC 7159
    • Buchanan GO, Reese PB. Bio transformation of diterpenes and diterpene derivatives by Beauveria bassiana ATCC 7159. Phytochemistry 2001; 56: 141-51
    • (2001) Phytochemistry , vol.56 , pp. 141-151
    • Buchanan, G.O.1    Reese, P.B.2
  • 21
    • 0037116414 scopus 로고    scopus 로고
    • Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
    • Chen ARM, Reese PB. Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142. Phytochemistry 2002; 59: 57-62
    • (2002) Phytochemistry , vol.59 , pp. 57-62
    • Chen, A.R.M.1    Reese, P.B.2
  • 22
    • 1542375403 scopus 로고    scopus 로고
    • Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
    • Martin GDA, Reynolds WF, Reese PB. Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145. Phytochemistry. 2004; 65: 701-10
    • (2004) Phytochemistry , vol.65 , pp. 701-710
    • Martin, G.D.A.1    Reynolds, W.F.2    Reese, P.B.3
  • 23
    • 4344714020 scopus 로고    scopus 로고
    • Investigation of the importance of the C-2 and C-13 oxygen functions in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
    • Martin GDA, Reynolds WF, Reese PB. Investigation of the importance of the C-2 and C-13 oxygen functions in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145. Phytochemistry 2004; 65: 2211-7
    • (2004) Phytochemistry , vol.65 , pp. 2211-2217
    • Martin, G.D.A.1    Reynolds, W.F.2    Reese, P.B.3
  • 24
    • 0032713322 scopus 로고    scopus 로고
    • Steroid transformations with Fusarium oxysporum f. sp. cubense and Colletotrichum musae
    • Wilson MR, Gallimore WA, Reese PB. Steroid transformations with Fusarium oxysporum f. sp. cubense and Colletotrichum musae. Steroids 1999; 64: 834-43
    • (1999) Steroids , vol.64 , pp. 834-843
    • Wilson, M.R.1    Gallimore, W.A.2    Reese, P.B.3
  • 25
    • 25944467420 scopus 로고
    • Microbial oxidation of ecdysones. A convenient preparation of rubrosterone
    • Tom W, Abul-Hajj YJ, Koreeda MJ. Microbial oxidation of ecdysones. A convenient preparation of rubrosterone. J Chem Soc Chem Commun 1975; 24-5
    • (1975) J Chem Soc Chem Commun , pp. 24-25
    • Tom, W.1    Abul-Hajj, Y.J.2    Koreeda, M.J.3
  • 26
    • 84967501006 scopus 로고
    • 15?-Hydroxy-4-androstene-3,17-dione
    • inventor, Schering AQ assignee. 15?-Hydroxy-4-androstene-3,17-dione. German Patent DE 3,403,862.1985 Aug 8
    • Petzoldt K., inventor, Schering AQ assignee. 15?-Hydroxy-4-androstene-3,17-dione. German Patent DE 3,403,862. 1985 Aug 8. Chem Abs 104:166905q
    • (1985) Chem Abs , vol.104 , pp. 166905
    • Petzoldt, K.1
  • 27
    • 0003188813 scopus 로고
    • Reactions with microorganisms. XII. Conversion of toad poison (bufadienolide) by microorganisms. 2. 12?-Hydroxyresibufogenin
    • Schuepback M, Tamm Ch. Reactions with microorganisms. XII. Conversion of toad poison (bufadienolide) by microorganisms. 2. 12?-Hydroxyresibufogenin. Helv Chim Acta 1964; 47: 2217-26
    • (1964) Helv Chim Acta , vol.47 , pp. 2217-2226
    • Schuepback, M.1    Ch, T.2
  • 28
    • 0017900229 scopus 로고
    • Microbial 7- and 15-hydroxylations of C-19 steroids
    • Defaye G, Luche MJ, Chambaz EM. Microbial 7- and 15-hydroxylations of C-19 steroids. J Steroid Biochem 1978; 9: 331-6
    • (1978) J Steroid Biochem , vol.9 , pp. 331-336
    • Defaye, G.1    Luche, M.J.2    Chambaz, E.M.3
  • 29
    • 0032843185 scopus 로고    scopus 로고
    • Steroid transformations with Exophiala jeanselmei var. lecaniicorni and Ceratocystis paradoxa
    • Porter RBR, Gallimore WA, Reese PB. Steroid transformations with Exophiala jeanselmei var. lecaniicorni and Ceratocystis paradoxa. Steroids 1999; 64: 770-9
    • (1999) Steroids , vol.64 , pp. 770-779
    • Porter, R.B.R.1    Gallimore, W.A.2    Reese, P.B.3
  • 30
    • 0029971779 scopus 로고    scopus 로고
    • Styrene metabolism in Exophiala jeanselmei and involvement of a cytochrome P-450-dependent styrene monooxygenase
    • Cox HHJ, Faber BW, van Heiningen WNM. Styrene metabolism in Exophiala jeanselmei and involvement of a cytochrome P-450-dependent styrene monooxygenase. Appl Environ Microbiol. 1996; 62: 1471-4
    • (1996) Appl Environ Microbiol , vol.62 , pp. 1471-1474
    • Cox, H.H.J.1    Faber, B.W.2    Van Heiningen, W.N.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.