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Volumn 53, Issue 1, 1999, Pages 7-11

Resolution of 1,2-epoxyhexane by Rhodotorula glutinis using a two-phase membrane bioreactor

Author keywords

[No Author keywords available]

Indexed keywords

EPOXIDE;

EID: 0033492573     PISSN: 01757598     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002530051606     Document Type: Article
Times cited : (26)

References (14)
  • 1
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    • Archelas, A.1    Furstoss, R.2
  • 2
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    • Epoxide hydrolases as asymmetric catalysts
    • Archer IVJ (1997) Epoxide hydrolases as asymmetric catalysts. Tetrahedron 53: 15617-15662
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    • Archer, I.V.J.1
  • 3
    • 0027934450 scopus 로고
    • Chemical and biological synthesis of chiral epoxides
    • Besse P, Veschambre H (1994) Chemical and biological synthesis of chiral epoxides. Tetrahedron 50: 8885-8927
    • (1994) Tetrahedron , vol.50 , pp. 8885-8927
    • Besse, P.1    Veschambre, H.2
  • 4
    • 0031946536 scopus 로고    scopus 로고
    • Kinetic resolution for optically active epoxides by microbial enantioselective hydrolysis
    • Choi WJ, Huh EC, Park HJ, Lee EY, Choi CY (1998) Kinetic resolution for optically active epoxides by microbial enantioselective hydrolysis. Biotechnol Tech 12: 225-228
    • (1998) Biotechnol Tech , vol.12 , pp. 225-228
    • Choi, W.J.1    Huh, E.C.2    Park, H.J.3    Lee, E.Y.4    Choi, C.Y.5
  • 5
    • 0027158360 scopus 로고
    • Biotransformation of optically pure epoxides
    • De Bont JAM (1993) Biotransformation of optically pure epoxides. Tetrahedron Asymmetry 4: 1331-1340
    • (1993) Tetrahedron Asymmetry , vol.4 , pp. 1331-1340
    • De Bont, J.A.M.1
  • 6
    • 0024512944 scopus 로고
    • A Pseudomonas thrives in high concentrations of toluene
    • Inoue A, Horikoshi K (1989) A Pseudomonas thrives in high concentrations of toluene. Nature 338: 264-266
    • (1989) Nature , vol.338 , pp. 264-266
    • Inoue, A.1    Horikoshi, K.2
  • 7
    • 0031104802 scopus 로고    scopus 로고
    • Why are enzymes less active in organic solvents than in water?
    • Klibanov AM (1997) Why are enzymes less active in organic solvents than in water? Trends Biotechnol 15: 97-101
    • (1997) Trends Biotechnol , vol.15 , pp. 97-101
    • Klibanov, A.M.1
  • 8
    • 0033055661 scopus 로고    scopus 로고
    • Stereoselectivities of microbial epoxide hydrolases
    • Orru RVA, Faber K (1999) Stereoselectivities of microbial epoxide hydrolases. Curr Opin Chem Biol 3: 16-21
    • (1999) Curr Opin Chem Biol , vol.3 , pp. 16-21
    • Orru, R.V.A.1    Faber, K.2
  • 10
    • 0030848933 scopus 로고    scopus 로고
    • Microbiological transformations 37. An enantioconvergent synthesis of the β-blocker (R)-Nifknalol® using a combined chemoenzymatic approach
    • Pedragosa-Moreau S, Morisseau C, Baratti J, Zylber J, Archelas A, Furstoss R (1997) Microbiological transformations 37. An enantioconvergent synthesis of the β-blocker (R)-Nifknalol® using a combined chemoenzymatic approach. Tetrahedron 53: 9707-9714
    • (1997) Tetrahedron , vol.53 , pp. 9707-9714
    • Pedragosa-Moreau, S.1    Morisseau, C.2    Baratti, J.3    Zylber, J.4    Archelas, A.5    Furstoss, R.6
  • 11
    • 0027909869 scopus 로고
    • Toxicity of homologous series of organic solvents for the gram positive bacteria Arthrobacter and Nocardia sp. and the gram negative bacteria Acinetobacter and Pseudomonas sp
    • Vermue M, Sikkema J, Verheul A, Bakker R, Tramper J (1993) Toxicity of homologous series of organic solvents for the gram positive bacteria Arthrobacter and Nocardia sp. and the gram negative bacteria Acinetobacter and Pseudomonas sp. Biotechnol Bioeng 42: 747-758
    • (1993) Biotechnol Bioeng , vol.42 , pp. 747-758
    • Vermue, M.1    Sikkema, J.2    Verheul, A.3    Bakker, R.4    Tramper, J.5
  • 12
    • 0033545515 scopus 로고    scopus 로고
    • Epoxide hydrolases from yeasts and other sources: Versatile tools in biocatalysis
    • Weijers CAGM, de Bont JAM (1999) Epoxide hydrolases from yeasts and other sources: versatile tools in biocatalysis. J Mol Catal B: Enzymatic 6: 199-214
    • J Mol Catal B: Enzymatic , vol.6 , pp. 199-214
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  • 13
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    • (1998) Tetrahedron Asymmetry , vol.9 , pp. 467-473
    • Weijers, C.A.G.M.1    Botes, A.L.2    Van Dyk, M.S.3    De Bont, J.A.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.