메뉴 건너뛰기




Volumn 37, Issue 1, 2005, Pages 121-125

Reduction of ethyl benzoylformate mediated by Saccharomyces cerevisiae entrapped in alginate fibers with double gel layers in a continuously operated reactor

Author keywords

Calcium alginate; Continuously operated reactor; Ethyl (R) mandelate; Ethyl benzoylformate; Saccharomyces cerevisiae

Indexed keywords

AROMATIC COMPOUNDS; CELL CULTURE; CHEMICAL REACTORS; KETONES;

EID: 18144368945     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.enzmictec.2005.02.011     Document Type: Article
Times cited : (22)

References (23)
  • 1
    • 0036900263 scopus 로고    scopus 로고
    • The production of fine chemicals by biotransformations
    • A.J.J. Straathof, S. Panke, and A. Schmid The production of fine chemicals by biotransformations Curr Opin Biotechnol 13 2002 548 556
    • (2002) Curr Opin Biotechnol , vol.13 , pp. 548-556
    • Straathof, A.J.J.1    Panke, S.2    Schmid, A.3
  • 2
    • 0347474982 scopus 로고    scopus 로고
    • Recent developments in asymmetric reduction of ketones with biocatalysts
    • K. Nakamura, R. Yamanaka, T. Matsuda, and T. Harada Recent developments in asymmetric reduction of ketones with biocatalysts Tetrahedron Asymmetry 14 2003 2659 2681
    • (2003) Tetrahedron Asymmetry , vol.14 , pp. 2659-2681
    • Nakamura, K.1    Yamanaka, R.2    Matsuda, T.3    Harada, T.4
  • 4
    • 0037015413 scopus 로고    scopus 로고
    • Reduction of ethyl 3-oxobutanote using non-growing baker's yeast in a continuosly operated reactor with cell retention
    • I. Chin-Joe, J. Haberland, A.J.J. Straathof, J.A. Jongejan, A. Liese, and J.J. Heijnen Reduction of ethyl 3-oxobutanote using non-growing baker's yeast in a continuosly operated reactor with cell retention Enzyme Microb Technol 31 2002 665 672
    • (2002) Enzyme Microb Technol , vol.31 , pp. 665-672
    • Chin-Joe, I.1    Haberland, J.2    Straathof, A.J.J.3    Jongejan, J.A.4    Liese, A.5    Heijnen, J.J.6
  • 5
    • 0037007536 scopus 로고    scopus 로고
    • Membrane reactor development for the kinetic resolution of ethyl 2-hydroxy-4-phenylbutyrate
    • A. Liese, U. Kragl, H. Kierkels, and B. Schulze Membrane reactor development for the kinetic resolution of ethyl 2-hydroxy-4-phenylbutyrate Enzyme Microb Technol 30 2002 673 681
    • (2002) Enzyme Microb Technol , vol.30 , pp. 673-681
    • Liese, A.1    Kragl, U.2    Kierkels, H.3    Schulze, B.4
  • 6
    • 0037009164 scopus 로고    scopus 로고
    • Role of water activity and temperature on activity and stability of dried whole cells of Saccharomyces cerevisiae in a continuous solid-gas bioreactor
    • I. Goubet, T. Maugard, S. Lamare, and M.D. Legoy Role of water activity and temperature on activity and stability of dried whole cells of Saccharomyces cerevisiae in a continuous solid-gas bioreactor Enzyme Microb Technol 31 2002 425 430
    • (2002) Enzyme Microb Technol , vol.31 , pp. 425-430
    • Goubet, I.1    Maugard, T.2    Lamare, S.3    Legoy, M.D.4
  • 7
    • 0032530092 scopus 로고    scopus 로고
    • Continuous process for large-scale preparation of chiral alcohols with baker's yeast immobilized on chrysotile fibers
    • R. Wendhausen Jr., P.J.S. Moran, I. Joekes, and J.A.R. Rodrigues Continuous process for large-scale preparation of chiral alcohols with baker's yeast immobilized on chrysotile fibers J Mol Catal B Enzym 5 1998 69 73
    • (1998) J Mol Catal B Enzym , vol.5 , pp. 69-73
    • Wendhausen Jr., R.1    Moran, P.J.S.2    Joekes, I.3    Rodrigues, J.A.R.4
  • 8
    • 0030568515 scopus 로고    scopus 로고
    • Large-scale production of chiral alcohols with baker's yeast
    • T. Kometani, H. Yoshii, and R. Matsuno Large-scale production of chiral alcohols with baker's yeast J Mol Catal B Enzym 1 1996 45 52
    • (1996) J Mol Catal B Enzym , vol.1 , pp. 45-52
    • Kometani, T.1    Yoshii, H.2    Matsuno, R.3
  • 9
  • 10
    • 0034234048 scopus 로고    scopus 로고
    • Microencapsulation of microbial cells
    • J.K. Park, and H.N. Chang Microencapsulation of microbial cells Biotechnol Adv 18 2000 303 319
    • (2000) Biotechnol Adv , vol.18 , pp. 303-319
    • Park, J.K.1    Chang, H.N.2
  • 11
    • 0017473389 scopus 로고
    • The immobilization of microbial cells, subcellular organelles, and enzymes in calcium alginates gels
    • M. Kierstan, and C. Bucke The immobilization of microbial cells, subcellular organelles, and enzymes in calcium alginates gels Biotechnol Bioeng 19 1977 387 397
    • (1977) Biotechnol Bioeng , vol.19 , pp. 387-397
    • Kierstan, M.1    Bucke, C.2
  • 12
    • 0000360815 scopus 로고
    • A novel immobilization method for prevention of cell leakeage from the gel matrix
    • H. Tanaka, S. Irie, and H. Ochi A novel immobilization method for prevention of cell leakeage from the gel matrix J Ferment Bioeng 68 1989 216 219
    • (1989) J Ferment Bioeng , vol.68 , pp. 216-219
    • Tanaka, H.1    Irie, S.2    Ochi, H.3
  • 13
    • 0029922332 scopus 로고    scopus 로고
    • Efficient production of chitinase by immobilized Wasabia japonica cells in double-layered gel fibers
    • H. Tanaka, Y. Kaneko, H. Aoyagi, Y. Yamamoto, and Y. Funukaga Efficient production of chitinase by immobilized Wasabia japonica cells in double-layered gel fibers J Ferment Bioeng 81 1996 220 225
    • (1996) J Ferment Bioeng , vol.81 , pp. 220-225
    • Tanaka, H.1    Kaneko, Y.2    Aoyagi, H.3    Yamamoto, Y.4    Funukaga, Y.5
  • 14
    • 0029973674 scopus 로고    scopus 로고
    • Efficient production of chitinase by immobilized Wasabia japonica protoplasts in double-layered gel fibers
    • H. Tanaka, H. Aoyagi, Y. Yamamoto, and Y. Funukaga Efficient production of chitinase by immobilized Wasabia japonica protoplasts in double-layered gel fibers J Ferment Bioeng 81 1996 394 399
    • (1996) J Ferment Bioeng , vol.81 , pp. 394-399
    • Tanaka, H.1    Aoyagi, H.2    Yamamoto, Y.3    Funukaga, Y.4
  • 15
    • 0034684069 scopus 로고    scopus 로고
    • Stereocontrolled reduction of α-keto esters with thermophilic actinomycete, Satreptomyces thermocyaneoviolaceus IFO 14271
    • K. Ishihara, H. Yamaguchi, H. Hamada, N. Nakajima, and K. Nakamura Stereocontrolled reduction of α-keto esters with thermophilic actinomycete, Satreptomyces thermocyaneoviolaceus IFO 14271 J Mol Catal B Enzym 10 2000 429 434
    • (2000) J Mol Catal B Enzym , vol.10 , pp. 429-434
    • Ishihara, K.1    Yamaguchi, H.2    Hamada, H.3    Nakajima, N.4    Nakamura, K.5
  • 16
    • 0034725679 scopus 로고    scopus 로고
    • Stereoselective reductions with macrocyclic NADH models
    • U. Gran, O. Wennerström, and G. Westman Stereoselective reductions with macrocyclic NADH models Tetrahedron Asymmetry 11 2000 3027 3040
    • (2000) Tetrahedron Asymmetry , vol.11 , pp. 3027-3040
    • Gran, U.1    Wennerström, O.2    Westman, G.3
  • 17
    • 0034297982 scopus 로고    scopus 로고
    • Stereocontrolled reduction of α- And β-keto esters with micro green algae, Chlorella strains
    • K. Ishihara, H. Yamaguchi, N. Adachi, H. Hamada, and N. Nakajima Stereocontrolled reduction of α- and β-keto esters with micro green algae, Chlorella strains Biosci Biotechnol Biochem 64 2000 2099 2103
    • (2000) Biosci Biotechnol Biochem , vol.64 , pp. 2099-2103
    • Ishihara, K.1    Yamaguchi, H.2    Adachi, N.3    Hamada, H.4    Nakajima, N.5
  • 18
    • 37049082393 scopus 로고
    • Biocatalytic preparation of chiral alcohols by enantioselective reduction with immobilized cells of carrot
    • Y. Akakabe, M. Takahashi, M. Kamezawa, K. Kikuchi, H. Tachibana, and T. Ohtani Biocatalytic preparation of chiral alcohols by enantioselective reduction with immobilized cells of carrot J Chem Soc Perkin Trans 1 10 1 1995 1295 1298
    • (1995) J Chem Soc Perkin Trans 1 , vol.10 , Issue.1 , pp. 1295-1298
    • Akakabe, Y.1    Takahashi, M.2    Kamezawa, M.3    Kikuchi, K.4    Tachibana, H.5    Ohtani, T.6
  • 19
    • 0026351322 scopus 로고
    • Studies of the reductive biostransformation of seleted carbonyl compounds by whole cells and extracts of baker's yeast Saccharomyces cerevisiae
    • C.S. Young, and O.P. Ward Studies of the reductive biostransformation of seleted carbonyl compounds by whole cells and extracts of baker's yeast Saccharomyces cerevisiae Biotechnol Bioeng 38 1991 1280 1284
    • (1991) Biotechnol Bioeng , vol.38 , pp. 1280-1284
    • Young, C.S.1    Ward, O.P.2
  • 20
    • 2342556510 scopus 로고    scopus 로고
    • The regioisomeric triphenylaminoethanols - Comparison of their effiency in enantioselective catalysis
    • M. Braun, R. Fleischeir, B. Mai, M.A. Scheneider, and S. Lachenicht The regioisomeric triphenylaminoethanols - comparison of their effiency in enantioselective catalysis Adv Synth Catal 346 2004 474 482
    • (2004) Adv Synth Catal , vol.346 , pp. 474-482
    • Braun, M.1    Fleischeir, R.2    Mai, B.3    Scheneider, M.A.4    Lachenicht, S.5
  • 21
    • 1542336744 scopus 로고    scopus 로고
    • Chiral synthesis of (2S, 3S)-2-(2-morpholin-2-yl-2-phenylmethoxy)phenol
    • J. Prabhakaran, V.J. Majo, J.J. Mann, and J.S.D. Kumar Chiral synthesis of (2S, 3S)-2-(2-morpholin-2-yl-2-phenylmethoxy)phenol Chirality 16 2004 168 173
    • (2004) Chirality , vol.16 , pp. 168-173
    • Prabhakaran, J.1    Majo, V.J.2    Mann, J.J.3    Kumar, J.S.D.4
  • 22
    • 33845376028 scopus 로고
    • On the use of the O-methylmandelate ester for establishment of absolute configuration of secundary alcohols
    • B.M. Trost, J.L. Belletire, S. Godleski, P.G. Mcdougal, J.M. Balkovec, and J.J. Baldwin On the use of the O-methylmandelate ester for establishment of absolute configuration of secundary alcohols J Org Chem 51 1986 2370 2374
    • (1986) J Org Chem , vol.51 , pp. 2370-2374
    • Trost, B.M.1    Belletire, J.L.2    Godleski, S.3    McDougal, P.G.4    Balkovec, J.M.5    Baldwin, J.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.