메뉴 건너뛰기




Volumn 19, Issue 4, 1996, Pages 250-255

Asymmetric bioreduction of a ketosulfone to the corresponding trans-hydroxysulfone by the yeast Rhodotorula rubra MY 2169

Author keywords

Biocatalysis; Bioprocess; Bioreduction; Biotransformation; Carbonic anhydrase inhibitor; Fermentation

Indexed keywords

BIOCONVERSION; CELLS; DISEASES; DRUG PRODUCTS; ENZYME INHIBITION; PH EFFECTS; PHYSIOLOGY; REDUCTION; SOLVENTS; THERMAL EFFECTS; YEAST;

EID: 0030249070     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/0141-0229(95)00242-1     Document Type: Article
Times cited : (16)

References (27)
  • 1
    • 0011801455 scopus 로고
    • Nonchiral, homochiral, and composite chiral drugs
    • 1. Ariens E. Nonchiral, homochiral, and composite chiral drugs. TIBS 1993, 14, 168-76
    • (1993) TIBS , vol.14 , pp. 168-176
    • Ariens, E.1
  • 2
    • 33749942544 scopus 로고
    • Chiral drugs
    • Sept
    • 2. Stinson, S. Chiral drugs. Chem. Eng. News, 1994, Sept, 38-72
    • (1994) Chem. Eng. News , pp. 38-72
    • Stinson, S.1
  • 3
    • 0000714772 scopus 로고
    • Enzymes in organic synthesis
    • 3. Jones, B. Enzymes in organic synthesis. Tetrahedron 1986, 42, 3351-3403
    • (1986) Tetrahedron , vol.42 , pp. 3351-3403
    • Jones, B.1
  • 4
    • 0026354817 scopus 로고
    • Biotransformations of industrial use
    • 4. Kieslich, K. Biotransformations of industrial use. Acta Biotechnol. 1991, 11, 559-570
    • (1991) Acta Biotechnol. , vol.11 , pp. 559-570
    • Kieslich, K.1
  • 5
    • 0001137949 scopus 로고
    • Advances in biotransformation processes
    • 5. Lilly, M. Advances in biotransformation processes. Chem. Eng. Sci. 1994, 49, 151-159
    • (1994) Chem. Eng. Sci. , vol.49 , pp. 151-159
    • Lilly, M.1
  • 6
    • 0027588112 scopus 로고
    • Enzymes in the synthesis of chiral drugs
    • 6. Margolin, A. Enzymes in the synthesis of chiral drugs. Enzyme Microb. Technol. 1993, 15, 266-280
    • (1993) Enzyme Microb. Technol. , vol.15 , pp. 266-280
    • Margolin, A.1
  • 7
    • 12044253833 scopus 로고
    • Baker's yeast mediated transformations in organic chemistry
    • 7. Csuk, R. and Glanzer, B. Baker's yeast mediated transformations in organic chemistry. Chem. Rev. 1991, 91, 49-97
    • (1991) Chem. Rev. , vol.91 , pp. 49-97
    • Csuk, R.1    Glanzer, B.2
  • 9
    • 84920564546 scopus 로고
    • Baker's yeast as a reagent in organic synthesis
    • 9. Servi, S. Baker's yeast as a reagent in organic synthesis. Synthesis 1990, 1, 1-25
    • (1990) Synthesis , vol.1 , pp. 1-25
    • Servi, S.1
  • 10
    • 0025455982 scopus 로고
    • Reductive biotransformations of organic compounds by cells or enzymes of yeast
    • 10. Ward, O. and Young, C. Reductive biotransformations of organic compounds by cells or enzymes of yeast. Enzyme Microb. Technol. 1990, 12, 482-492
    • (1990) Enzyme Microb. Technol. , vol.12 , pp. 482-492
    • Ward, O.1    Young, C.2
  • 11
    • 37049067341 scopus 로고
    • Biotransformations using Clostridia: Stereospecific reductions of a β-ketoester
    • 11. Christen, M., Crout, D., Holt, R., Morris, J., and Simon, H. Biotransformations using Clostridia: Stereospecific reductions of a β-ketoester. J. Chem. Perkin Trans. 1992, 1, 491-493
    • (1992) J. Chem. Perkin Trans. , vol.1 , pp. 491-493
    • Christen, M.1    Crout, D.2    Holt, R.3    Morris, J.4    Simon, H.5
  • 12
    • 0027897733 scopus 로고
    • Enantioselective microbial reduction of 3,5-dioxo-6-(benzylozy) hexanoic acid, ethyl ester
    • 12. Patel, R., Banerjee, A., McNamee, C., Brzozowski, D., Hanson, R., and Szarka, L. Enantioselective microbial reduction of 3,5-dioxo-6-(benzylozy) hexanoic acid, ethyl ester. Enzyme Microb. Technol. 1993, 15, 1014-1021
    • (1993) Enzyme Microb. Technol. , vol.15 , pp. 1014-1021
    • Patel, R.1    Banerjee, A.2    McNamee, C.3    Brzozowski, D.4    Hanson, R.5    Szarka, L.6
  • 15
    • 0026471036 scopus 로고
    • Studies on the distribution and regulation of microbial keto ester reductases
    • 15. Peters, J., Zelinski, T., and Kulla, M. Studies on the distribution and regulation of microbial keto ester reductases. Appl. Microbiol. Biotechnol. 1992, 28, 334-340
    • (1992) Appl. Microbiol. Biotechnol. , vol.28 , pp. 334-340
    • Peters, J.1    Zelinski, T.2    Kulla, M.3
  • 16
    • 0023324366 scopus 로고
    • Screening for novel biocatalysts
    • 16. Cheetham, P. Screening for novel biocatalysts. Enzyme Microb. Technol. 1987, 9, 194-213
    • (1987) Enzyme Microb. Technol. , vol.9 , pp. 194-213
    • Cheetham, P.1
  • 17
    • 0021775497 scopus 로고
    • Double asymmetric synthesis and a new strategy for stereochemical control in organic synthesis
    • 17. Masamune, S., Choy, W., Petersen, J., and Sita, L. Double asymmetric synthesis and a new strategy for stereochemical control in organic synthesis. Angew. Chem. Int. Ed. Engl. 1985, 24, 1-76
    • (1985) Angew. Chem. Int. Ed. Engl. , vol.24 , pp. 1-76
    • Masamune, S.1    Choy, W.2    Petersen, J.3    Sita, L.4
  • 18
    • 0028981929 scopus 로고
    • Asymmetric bioreduction of a b-ketoester to (R)-hydroxyester by the fungus Mortierella alpina MF 5534
    • in press
    • 18. Chartrain, M., Armstrong, J., Katz, L., Keller, J., and Greasham, R. Asymmetric bioreduction of a b-ketoester to (R)-hydroxyester by the fungus Mortierella alpina MF 5534. J. Ferm. Bioeng. 1995, in press
    • (1995) J. Ferm. Bioeng.
    • Chartrain, M.1    Armstrong, J.2    Katz, L.3    Keller, J.4    Greasham, R.5
  • 20
    • 0001166301 scopus 로고
    • Stereoselectivity of yeast reductions - An improved procedure for the preparation of ethyl. (S)-3-hydroxybutanoate and (S)-2-hydroxymethylbutanoate
    • 20. Ehrler, J., Giovannini, F., Lamatsch, B., and Seebach, D. Stereoselectivity of yeast reductions - an improved procedure for the preparation of ethyl. (S)-3-hydroxybutanoate and (S)-2-hydroxymethylbutanoate. Forschung Chimia 1986, 40, 172-173
    • (1986) Forschung Chimia , vol.40 , pp. 172-173
    • Ehrler, J.1    Giovannini, F.2    Lamatsch, B.3    Seebach, D.4
  • 21
    • 0000342925 scopus 로고
    • Stereochemical control in microbial reduction. 4. Effect of cultivation conditions on the reduction of b-keto esters by methylotrophic yeasts
    • 21. Ushio, K., Inouye, K., Nakamura, K., Oka, S., and Ohno, A. Stereochemical control in microbial reduction. 4. Effect of cultivation conditions on the reduction of b-keto esters by methylotrophic yeasts. Tetrahedron Lett 1986, 27, 2657-2660
    • (1986) Tetrahedron Lett , vol.27 , pp. 2657-2660
    • Ushio, K.1    Inouye, K.2    Nakamura, K.3    Oka, S.4    Ohno, A.5
  • 22
    • 0000953988 scopus 로고
    • Stereochemical control in microbial reductions. XXI. Effect of organic solvents on reduction of a-keto esters mediated by Bakers' yeast
    • 22. Nakamura, K., Kondo, S., Kawai, Y., and Ohno, A. Stereochemical control in microbial reductions. XXI. Effect of organic solvents on reduction of a-keto esters mediated by Bakers' yeast. Bull. Chem. Soc. Jpn. 1993, 66, 2738-2743.
    • (1993) Bull. Chem. Soc. Jpn. , vol.66 , pp. 2738-2743
    • Nakamura, K.1    Kondo, S.2    Kawai, Y.3    Ohno, A.4
  • 23
    • 0028830034 scopus 로고
    • Improvement of enantioselectivity of microbial reduction by using organic solvent redox coupler system
    • 23. Nakamura, K., Inoue, Y., and Ohno, A. Improvement of enantioselectivity of microbial reduction by using organic solvent redox coupler system. Tetrahedron Lett 1995, 36, 265-266
    • (1995) Tetrahedron Lett , vol.36 , pp. 265-266
    • Nakamura, K.1    Inoue, Y.2    Ohno, A.3
  • 24
    • 0026245015 scopus 로고
    • Selective inhibition of R-enzymes by simple organic acids in yeast-catalysed reduction of ethyl 3-oxobutonate
    • 24. Ushio, K., Ebara, K., and Yamashita, T. Selective inhibition of R-enzymes by simple organic acids in yeast-catalysed reduction of ethyl 3-oxobutonate. Enzyme Microb. Technol. 1991, 13, 834-839
    • (1991) Enzyme Microb. Technol. , vol.13 , pp. 834-839
    • Ushio, K.1    Ebara, K.2    Yamashita, T.3
  • 25
    • 0024287174 scopus 로고
    • Purification and characterization of two oxidoreductases involved in the enantioselective reduction of 3-oxo, 4-oxo, and 5-oxo esters in Bakers' yeast
    • 25. Heidlas, J., Engel, K., and Tressl, R. Purification and characterization of two oxidoreductases involved in the enantioselective reduction of 3-oxo, 4-oxo, and 5-oxo esters in Bakers' yeast. Eur. J. Biochem. 1988, 172, 633-639
    • (1988) Eur. J. Biochem. , vol.172 , pp. 633-639
    • Heidlas, J.1    Engel, K.2    Tressl, R.3
  • 26
    • 0026245027 scopus 로고
    • Enantioselectivities of enzymes involved in the reduction of methylketones by Bakers' yeast
    • 26. Heidlas, J., Engel, K., and Tressl, R. Enantioselectivities of enzymes involved in the reduction of methylketones by Bakers' yeast. Enzyme Microb. Technol. 1991, 13, 817-821
    • (1991) Enzyme Microb. Technol. , vol.13 , pp. 817-821
    • Heidlas, J.1    Engel, K.2    Tressl, R.3
  • 27
    • 84985154137 scopus 로고
    • Production of (+)-(s)-ethyl 3-hydroxybutyrate and (-)-(R)-ethyl 3-hydroxybutyrate by microbial reduction of ethyl acetoacetate
    • 27. Wipf, B., Kupfer, E., Bertazzi, R., and Leuenberger, H. Production of (+)-(s)-ethyl 3-hydroxybutyrate and (-)-(R)-ethyl 3-hydroxybutyrate by microbial reduction of ethyl acetoacetate. Helvetica Chimica Acta 1983, 66, 485-488
    • (1983) Helvetica Chimica Acta , vol.66 , pp. 485-488
    • Wipf, B.1    Kupfer, E.2    Bertazzi, R.3    Leuenberger, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.