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Volumn 7, Issue , 2008, Pages

Yeast cell factories for fine chemical and API production

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BUTANEDIOL; 2 AMINO 5 (1,3 DIOXOLAN 2 YL) PENTANOIC ACID; 2 HYDROXY CYCLOPENTANE CARBONITRILE; 3 HYDROXYACYL COENZYME A DEHYDROGENASE; 5 HYDROXYHEXANENITRILE; AMINOALCOHOL; ASTAXANTHIN; BETA CAROTENE; BETA HYDROXY ISOBUTYRIC ACID; BETA HYDROXY N BUTYRIC ACID; CHIRAL BETA HYDROXY ESTER; CORTODOXONE; EPHEDRINE; ETHYL 5 HYDROXYHEXANOATE; FUNGAL ENZYME; HEXAHOMOSERINE; HYDROCORTISONE; LYCOPENE; LYSINE; NATURAL PRODUCT; PHENETHYL ALCOHOL; PHENYLALANINE; PREGNENOLONE; PROGESTERONE; PSEUDOEPHEDRINE; STYRENE OXIDE; TALAMPANEL; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; ZEAXANTHIN;

EID: 59049091116     PISSN: None     EISSN: 14752859     Source Type: Journal    
DOI: 10.1186/1475-2859-7-25     Document Type: Review
Times cited : (99)

References (245)
  • 1
    • 0012827998 scopus 로고
    • Ancient Egyptian Cereal Processing: Beyond the Artistic Record
    • Delwen S Ancient Egyptian Cereal Processing: Beyond the Artistic Record Cambridge Archaeological Journal 1993, 276-283
    • (1993) Cambridge Archaeological Journal , pp. 276-283
    • Delwen, S.1
  • 2
    • 0029816864 scopus 로고    scopus 로고
    • Investigation of Ancient Egyptian Baking and Brewing Methods by Correlative Microscopy
    • 8662535
    • Delwen S Investigation of Ancient Egyptian Baking and Brewing Methods by Correlative Microscopy Science 1996, 273:488-490 8662535
    • (1996) Science , vol.273 , pp. 488-490
    • Delwen, S.1
  • 4
    • 0037348872 scopus 로고    scopus 로고
    • Beginnings of microbiology and biochemistry: The contribution of yeast research
    • Barnett JA Beginnings of microbiology and biochemistry: The contribution of yeast research Microbiology-Sgm 2003, 149:557-567
    • (2003) Microbiology-Sgm , vol.149 , pp. 557-567
    • Barnett, J.A.1
  • 5
    • 84980123367 scopus 로고
    • Verhalten der verschiedenen Zucker gegen reine Hefen
    • Fischer E Thierfelder H Verhalten der verschiedenen Zucker gegen reine Hefen Ber Dtsch Chem Ges 1894, 27:2031-2037
    • (1894) Ber Dtsch Chem Ges , vol.27 , pp. 2031-2037
    • Fischer, E.1    Thierfelder, H.2
  • 7
    • 0000870544 scopus 로고
    • Die Kinetik der Invertasewirkung
    • Michaelis L Menten ML Die Kinetik der Invertasewirkung Biochem Z 1913, 49:333-369
    • (1913) Biochem Z , vol.49 , pp. 333-369
    • Michaelis, L.1    Menten, M.L.2
  • 11
    • 0000230465 scopus 로고
    • The phenomenon of enzymatic adaptation and its bearing on problems of genetics and cellular differentiation
    • Monod J The phenomenon of enzymatic adaptation and its bearing on problems of genetics and cellular differentiation Growth 1947, 11:223-289
    • (1947) Growth , vol.11 , pp. 223-289
    • Monod, J.1
  • 12
    • 0025787953 scopus 로고
    • Cell-Cycle Regulation in the Yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe
    • Forsburg SL Nurse P Cell-Cycle Regulation in the Yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe Annual Review of Cell Biology 1991, 7:227-256 1809348
    • (1991) Annual Review of Cell Biology , vol.7 , pp. 227-256
    • Forsburg, S.L.1    Nurse, P.2
  • 13
    • 0026343121 scopus 로고
    • 25 Years of Cell-Cycle Genetics
    • 1204781 1783298
    • Hartwell LH 25 Years of Cell-Cycle Genetics Genetics 1991, 129:975-980 1204781 1783298
    • (1991) Genetics , vol.129 , pp. 975-980
    • Hartwell, L.H.1
  • 14
    • 0028675509 scopus 로고
    • Molecular Taxonomy of the Yeasts
    • 7747515
    • Kurtzman CP Molecular Taxonomy of the Yeasts Yeast 1994, 10:1727-1740 7747515
    • (1994) Yeast , vol.10 , pp. 1727-1740
    • Kurtzman, C.P.1
  • 15
    • 0345019244 scopus 로고    scopus 로고
    • Principles and methods used in yeast classification, and an overview of currently accepted yeast genera
    • Berlin, Heidelberg: Springer-Verlag Wolf K
    • Boekhout T Kurtzman CP Principles and methods used in yeast classification, and an overview of currently accepted yeast genera Nonconventional Yeasts in biotechnology. A Handbook Berlin, Heidelberg: Springer-Verlag Wolf K 1996, 1-99
    • (1996) Nonconventional Yeasts in Biotechnology. A Handbook , pp. 1-99
    • Boekhout, T.1    Kurtzman, C.P.2
  • 17
    • 9144272680 scopus 로고    scopus 로고
    • A history of research on yeasts 8: Taxonomy
    • 15515119
    • Barnett JA A history of research on yeasts 8: Taxonomy Yeast 2004, 21:1141-1193 15515119
    • (2004) Yeast , vol.21 , pp. 1141-1193
    • Barnett, J.A.1
  • 18
    • 31944449602 scopus 로고    scopus 로고
    • Introduction to Yeasts
    • Chichester: John Wiley & Sons Ltd
    • Walker GM Introduction to Yeasts Yeast Physiology and Biotechnology Chichester: John Wiley & Sons Ltd 1998, 1-9
    • (1998) Yeast Physiology and Biotechnology , pp. 1-9
    • Walker, G.M.1
  • 20
    • 36949031286 scopus 로고    scopus 로고
    • Yeast genome evolution - The origin of the species
    • 17621376
    • Scannell DR Butler G Wolfe KH Yeast genome evolution - the origin of the species Yeast 2007, 24:929-942 17621376
    • (2007) Yeast , vol.24 , pp. 929-942
    • Scannell, D.R.1    Butler, G.2    Wolfe, K.H.3
  • 21
    • 59049090907 scopus 로고
    • The three fermentation-forms of sugar, their coherences and balance
    • Neuberg C Hirsch J Reinfurth E The three fermentation-forms of sugar, their coherences and balance Biochemische Zeitschrift 1920, 105:307-336
    • (1920) Biochemische Zeitschrift , vol.105 , pp. 307-336
    • Neuberg, C.1    Hirsch, J.2    Reinfurth, E.3
  • 22
    • 0000921648 scopus 로고
    • The carbon chain of attached enzymes (carboligase)
    • Neuberg C Hirsch J The carbon chain of attached enzymes (carboligase) Biochemische Zeitschrift 1921, 115:282-310
    • (1921) Biochemische Zeitschrift , vol.115 , pp. 282-310
    • Neuberg, C.1    Hirsch, J.2
  • 25
    • 0023875288 scopus 로고
    • Microbial and Enzymatic Processes for the Production of Biologically and Chemically Useful Compounds
    • Yamada H Shimizu S Microbial and Enzymatic Processes for the Production of Biologically and Chemically Useful Compounds Angewandte Chemie-International Edition in English 1988 ,27:622-642
    • (1988) Angewandte Chemie-International Edition in English , vol.27 , pp. 622-642
    • Yamada, H.1    Shimizu, S.2
  • 26
    • 34247103699 scopus 로고    scopus 로고
    • Minimum genome factory: Innovation in bioprocesses through genome science
    • Fujio T Minimum genome factory: Innovation in bioprocesses through genome science Biotechnology and Applied Biochemistry 2007, 46:145-146
    • (2007) Biotechnology and Applied Biochemistry , vol.46 , pp. 145-146
    • Fujio, T.1
  • 30
    • 84920564546 scopus 로고
    • Baker's yeast as a reagent in organic synthesis
    • Servi S Baker's yeast as a reagent in organic synthesis Synthesis-Stuttgart 1990, 1-25
    • (1990) Synthesis-Stuttgart , pp. 1-25
    • Servi, S.1
  • 33
    • 0001931718 scopus 로고
    • Biochemical Reductions at the Expense of Sugars
    • Neuberg C Biochemical Reductions at the Expense of Sugars Advances in Carbohydrate Chemistry 1949, 4:75-117
    • (1949) Advances in Carbohydrate Chemistry , vol.4 , pp. 75-117
    • Neuberg, C.1
  • 34
    • 12044253833 scopus 로고
    • Bakers Yeast Mediated Transformations in Organic Chemistry
    • Csuk R Glanzer BI Bakers Yeast Mediated Transformations in Organic Chemistry Chemical Reviews 1991, 91:49-97
    • (1991) Chemical Reviews , vol.91 , pp. 49-97
    • Csuk, R.1    Glanzer, B.I.2
  • 36
    • 0347474982 scopus 로고    scopus 로고
    • Recent developments in asymmetric reduction of ketones with biocatalysts
    • Nakamura K Yamanaka R Matsuda T Harada T Recent developments in asymmetric reduction of ketones with biocatalysts Tetrahedron-Asymmetry 2003, 14:2659-2681
    • (2003) Tetrahedron-Asymmetry , vol.14 , pp. 2659-2681
    • Nakamura, K.1    Yamanaka, R.2    Matsuda, T.3    Harada, T.4
  • 37
    • 34547137887 scopus 로고    scopus 로고
    • Biocatalytic ketone reduction - A powerful tool for the production of chiral alcohols - Part II: Whole-cell reductions
    • Goldberg K Schroer K Lutz S Liese A Biocatalytic ketone reduction - a powerful tool for the production of chiral alcohols - part II: whole-cell reductions Applied Microbiology and Biotechnology 2007, 76:249-255
    • (2007) Applied Microbiology and Biotechnology , vol.76 , pp. 249-255
    • Goldberg, K.1    Schroer, K.2    Lutz, S.3    Liese, A.4
  • 38
    • 0035313656 scopus 로고    scopus 로고
    • Dehydrogenases and transaminases in asymmetric synthesis
    • 11282337
    • Stewart JD Dehydrogenases and transaminases in asymmetric synthesis Current Opinion in Chemical Biology 2001, 5:120-129 11282337
    • (2001) Current Opinion in Chemical Biology , vol.5 , pp. 120-129
    • Stewart, J.D.1
  • 40
    • 0001596563 scopus 로고    scopus 로고
    • Dehydrogenases in the synthesis of chiral compounds
    • New York: Marcel Dekker Patel RN
    • Kula M-R Kragl U Dehydrogenases in the synthesis of chiral compounds Stereoselective Biocatalysis New York: Marcel Dekker Patel RN 2000, 839-866
    • (2000) Stereoselective Biocatalysis , pp. 839-866
    • Kula, M.-R.1    Kragl, U.2
  • 41
    • 0036378340 scopus 로고    scopus 로고
    • Chiral synthesis of secondary alcohols using Geotrichum candidum
    • 12237828
    • Nakamura K Matsuda T Harada T Chiral synthesis of secondary alcohols using Geotrichum candidum Chirality 2002, 14:703-708 12237828
    • (2002) Chirality , vol.14 , pp. 703-708
    • Nakamura, K.1    Matsuda, T.2    Harada, T.3
  • 42
  • 43
    • 0035713259 scopus 로고    scopus 로고
    • Biocatalytic synthesis of intermediates for the synthesis of chiral drug substances
    • 11849941
    • Patel RN Biocatalytic synthesis of intermediates for the synthesis of chiral drug substances Current Opinion in Biotechnology 2001, 12:587-604 11849941
    • (2001) Current Opinion in Biotechnology , vol.12 , pp. 587-604
    • Patel, R.N.1
  • 44
    • 84913063444 scopus 로고
    • Specification of the stereospecificity of some oxidoreductases by diamond lattice sections
    • Prelog V Specification of the stereospecificity of some oxidoreductases by diamond lattice sections Pure and Applied Chemistry 1964, 9:119-130
    • (1964) Pure and Applied Chemistry , vol.9 , pp. 119-130
    • Prelog, V.1
  • 45
    • 0001716385 scopus 로고
    • Asymmetric Reductions 12. Stereoselective Ketone Reductions by Fermenting Yeast
    • 14211626
    • Macleod R Prosser H Fikentscher L Mosher HS Lanyi J Asymmetric Reductions 12. Stereoselective Ketone Reductions by Fermenting Yeast Biochemistry 1964, 3:838 14211626
    • (1964) Biochemistry , vol.3 , pp. 838
    • Macleod, R.1    Prosser, H.2    Fikentscher, L.3    Mosher, H.S.4    Lanyi, J.5
  • 46
    • 0003031978 scopus 로고
    • Stereochemical Control of Yeast Reductions. 2. Quantitative Treatment of the Kinetics of Competing Enzyme-Systems for A Single Substrate
    • Chen CS Zhou BN Girdaukas G Shieh WR Vanmiddlesworth F Gopalan AS Sih CJ Stereochemical Control of Yeast Reductions. 2. Quantitative Treatment of the Kinetics of Competing Enzyme-Systems for A Single Substrate Bioorganic Chemistry 1984, 12:98-117
    • (1984) Bioorganic Chemistry , vol.12 , pp. 98-117
    • Chen, C.S.1    Zhou, B.N.2    Girdaukas, G.3    Shieh, W.R.4    Vanmiddlesworth, F.5    Gopalan, A.S.6    Sih, C.J.7
  • 47
    • 0033592487 scopus 로고    scopus 로고
    • Improving the stereoselectivity of baker's yeast reductions by genetic engineering
    • 10825967
    • Rodriguez S Kayser M Stewart JD Improving the stereoselectivity of baker's yeast reductions by genetic engineering Organic Letters 1999, 1:1153-1155 10825967
    • (1999) Organic Letters , vol.1 , pp. 1153-1155
    • Rodriguez, S.1    Kayser, M.2    Stewart, J.D.3
  • 51
    • 0001166301 scopus 로고
    • Stereoselectivity of Yeast Reductions - An Improved Procedure for the Preparation of Ethyl (S)-3-Hydroxybutanoate and (S)-2-Hydroxymethylbutanoate
    • Ehrler J Giovannini F Lamatsch B Seebach D Stereoselectivity of Yeast Reductions - An Improved Procedure for the Preparation of Ethyl (S)-3-Hydroxybutanoate and (S)-2-Hydroxymethylbutanoate Chimia 1986, 40:172-173
    • (1986) Chimia , vol.40 , pp. 172-173
    • Ehrler, J.1    Giovannini, F.2    Lamatsch, B.3    Seebach, D.4
  • 52
    • 0025089938 scopus 로고
    • Stereochemical Control in Microbial Reduction 13. A Novel Method to Synthesize (L)-Beta-Hydroxyl Esters by the Reduction with Baker's Yeast
    • Nakamura K Kawai Y Ohno A Stereochemical Control in Microbial Reduction 13. A Novel Method to Synthesize (L)-Beta-Hydroxyl Esters by the Reduction with Baker's Yeast Tetrahedron Letters 1990, 31:267-270
    • (1990) Tetrahedron Letters , vol.31 , pp. 267-270
    • Nakamura, K.1    Kawai, Y.2    Ohno, A.3
  • 53
  • 54
    • 0343580463 scopus 로고    scopus 로고
    • The effect of absorbing resins on substrate concentration and enantiomeric excess in yeast reduction
    • DArrigo P Fantoni GP Servi S Strini A The effect of absorbing resins on substrate concentration and enantiomeric excess in yeast reduction Tetrahedron-Asymmetry 1997, 8:2375-2379
    • (1997) Tetrahedron-Asymmetry , vol.8 , pp. 2375-2379
    • DArrigo, P.1    Fantoni, G.P.2    Servi, S.3    Strini, A.4
  • 55
    • 33744536417 scopus 로고    scopus 로고
    • Water immiscible ionic liquids as solvents for whole cell biocatalysis
    • 16413078
    • Pfruender H Jones R Weuster-Botz D Water immiscible ionic liquids as solvents for whole cell biocatalysis Journal of Biotechnology 2006, 124:182-190 16413078
    • (2006) Journal of Biotechnology , vol.124 , pp. 182-190
    • Pfruender, H.1    Jones, R.2    Weuster-Botz, D.3
  • 57
    • 0037144679 scopus 로고    scopus 로고
    • Dynamic kinetic resolution of 2-oxocycloalkanecarbonitriles: Chemoenzymatic syntheses of optically active cyclic beta- and gamma-amino alcohols
    • 12227816
    • Dehli JR Gotor V Dynamic kinetic resolution of 2-oxocycloalkanecarbonitriles: Chemoenzymatic syntheses of optically active cyclic beta- and gamma-amino alcohols Journal of Organic Chemistry 2002, 67:6816-6819 12227816
    • (2002) Journal of Organic Chemistry , vol.67 , pp. 6816-6819
    • Dehli, J.R.1    Gotor, V.2
  • 58
    • 0037120192 scopus 로고    scopus 로고
    • Asymmetric total synthesis of (-)-callystatin A and (-)-20-epi-callystatin A employing chemical and biological methods
    • Enders D Vicario JL Job A Wolberg M Muller M Asymmetric total synthesis of (-)-callystatin A and (-)-20-epi-callystatin A employing chemical and biological methods Chemistry-A European Journal 2002, 8:4272-4284
    • (2002) Chemistry-A European Journal , vol.8 , pp. 4272-4284
    • Enders, D.1    Vicario, J.L.2    Job, A.3    Wolberg, M.4    Muller, M.5
  • 59
    • 0034354272 scopus 로고    scopus 로고
    • Enantioselective microbial reduction with baker's yeast on an industrial scale
    • Bertau M Burli M Enantioselective microbial reduction with baker's yeast on an industrial scale Chimia 2000, 54:503-507
    • (2000) Chimia , vol.54 , pp. 503-507
    • Bertau, M.1    Burli, M.2
  • 60
    • 0033405867 scopus 로고    scopus 로고
    • Chemo-enzymatic synthesis of (R)- and (S)-3,4-dichlorophenylbutanolide intermediate in the synthesis of sertraline
    • Barbieri C Caruso E D'Arrigo P Fantoni GP Servi S Chemo-enzymatic synthesis of (R)- and (S)-3,4-dichlorophenylbutanolide intermediate in the synthesis of sertraline Tetrahedron-Asymmetry 1999, 10:3931-3937
    • (1999) Tetrahedron-Asymmetry , vol.10 , pp. 3931-3937
    • Barbieri, C.1    Caruso, E.2    D'Arrigo, P.3    Fantoni, G.P.4    Servi, S.5
  • 62
    • 21344461509 scopus 로고    scopus 로고
    • Biotransformations for the production of the chiral drug (S)-Duloxetine catalyzed by a novel isolate of Candida tropicalis
    • Soni P Banerjee UC Biotransformations for the production of the chiral drug (S)-Duloxetine catalyzed by a novel isolate of Candida tropicalis Applied Microbiology and Biotechnology 2005, 67:771-777
    • (2005) Applied Microbiology and Biotechnology , vol.67 , pp. 771-777
    • Soni, P.1    Banerjee, U.C.2
  • 63
    • 33745963786 scopus 로고    scopus 로고
    • An aqueous-organic two-phase bioprocess for efficient production of the natural aroma chemicals 2-phenylethanol and 2-phenylethylacetate with yeast
    • Etschmann MMW Schrader J An aqueous-organic two-phase bioprocess for efficient production of the natural aroma chemicals 2-phenylethanol and 2-phenylethylacetate with yeast Applied Microbiology and Biotechnology 2006, 71:440-443
    • (2006) Applied Microbiology and Biotechnology , vol.71 , pp. 440-443
    • Etschmann, M.M.W.1    Schrader, J.2
  • 64
    • 0035988038 scopus 로고    scopus 로고
    • Extractive bioconversion of 2-phenylethanol from L-phenylalanine by Saccharomyces cerevisiae
    • 12052068
    • Stark D Munch T Sonnleitner B Marison IW von Stockar U Extractive bioconversion of 2-phenylethanol from L-phenylalanine by Saccharomyces cerevisiae Biotechnology Progress 2002, 18:514-523 12052068
    • (2002) Biotechnology Progress , vol.18 , pp. 514-523
    • Stark, D.1    Munch, T.2    Sonnleitner, B.3    Marison, I.W.4    von Stockar, U.5
  • 65
    • 1842583994 scopus 로고    scopus 로고
    • Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols
    • 15062771
    • Kroutil W Mang H Edegger K Faber K Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols Current Opinion in Chemical Biology 2004, 8:120-126 15062771
    • (2004) Current Opinion in Chemical Biology , vol.8 , pp. 120-126
    • Kroutil, W.1    Mang, H.2    Edegger, K.3    Faber, K.4
  • 66
  • 67
    • 0035024562 scopus 로고    scopus 로고
    • Synthesis of optically pure ethyl (S)-4-chloro-3-hydroxybutanoate by Escherichia coli transformant cells coexpressing the carbonyl reductase and glucose dehydrogenase genes
    • Kizaki N Yasohara Y Hasegawa J Wada M Kataoka M Shimizu S Synthesis of optically pure ethyl (S)-4-chloro-3-hydroxybutanoate by Escherichia coli transformant cells coexpressing the carbonyl reductase and glucose dehydrogenase genes Applied Microbiology and Biotechnology 2001, 55:590-595
    • (2001) Applied Microbiology and Biotechnology , vol.55 , pp. 590-595
    • Kizaki, N.1    Yasohara, Y.2    Hasegawa, J.3    Wada, M.4    Kataoka, M.5    Shimizu, S.6
  • 68
    • 0033890961 scopus 로고    scopus 로고
    • Organic transformations catalyzed by engineered yeast cells and related systems
    • 10975455
    • Stewart JD Organic transformations catalyzed by engineered yeast cells and related systems Current Opinion in Biotechnology 2000, 11:363-368 10975455
    • (2000) Current Opinion in Biotechnology , vol.11 , pp. 363-368
    • Stewart, J.D.1
  • 71
    • 34047189417 scopus 로고    scopus 로고
    • Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family
    • 17353140
    • Stuermer R Hauer B Hall M Faber K Asymmetric bioreduction of activated C= C bonds using enoate reductases from the old yellow enzyme family Current Opinion in Chemical Biology 2007, 11:203-213 17353140
    • (2007) Current Opinion in Chemical Biology , vol.11 , pp. 203-213
    • Stuermer, R.1    Hauer, B.2    Hall, M.3    Faber, K.4
  • 72
    • 0018485158 scopus 로고
    • Purification and some properties of a hitherto-unknown enzyme reducing the carbon-carbon double-bond of alpha,beta-unsaturated carboxylate anions
    • 477658
    • Tischer W Bader J Simon H Purification and some properties of a hitherto-unknown enzyme reducing the carbon-carbon double-bond of alpha,beta-unsaturated carboxylate anions European Journal of Biochemistry 1979, 97:103-112 477658
    • (1979) European Journal of Biochemistry , vol.97 , pp. 103-112
    • Tischer, W.1    Bader, J.2    Simon, H.3
  • 73
    • 84986409354 scopus 로고
    • Synthesis of Optically Active Natural Carotenoids and Structurally Related Compounds. 1. Synthesis of Chiral Key Compound (4R, 6R)-4-Hydroxy-2,2,6-Trimethylcyclohexanone
    • Leuenberger HGW Boguth W Widmer E Zell R Synthesis of Optically Active Natural Carotenoids and Structurally Related Compounds. 1. Synthesis of Chiral Key Compound (4R, 6R)-4-Hydroxy-2,2,6-Trimethylcyclohexanone Helvetica Chimica Acta 1976, 59:1832-1849
    • (1976) Helvetica Chimica Acta , vol.59 , pp. 1832-1849
    • Leuenberger, H.G.W.1    Boguth, W.2    Widmer, E.3    Zell, R.4
  • 75
    • 0035910865 scopus 로고    scopus 로고
    • Asymmetric reduction of nitroalkenes with baker's yeast
    • Kawai Y Inaba Y Tokitoh N Asymmetric reduction of nitroalkenes with baker's yeast Tetrahedron-Asymmetry 2001, 12:309-318
    • (2001) Tetrahedron-Asymmetry , vol.12 , pp. 309-318
    • Kawai, Y.1    Inaba, Y.2    Tokitoh, N.3
  • 76
    • 0001393485 scopus 로고
    • Asymmetric Reduction of Nitro Olefins by Fermenting Baker's Yeast
    • Ohta H Kobayashi N Ozaki K Asymmetric Reduction of Nitro Olefins by Fermenting Baker's Yeast Journal of Organic Chemistry 1989, 54:1802-1804
    • (1989) Journal of Organic Chemistry , vol.54 , pp. 1802-1804
    • Ohta, H.1    Kobayashi, N.2    Ozaki, K.3
  • 77
    • 0018347070 scopus 로고
    • Total Synthesis of Natural Alpha-Tocopherol 1. Preparation of Bifunctional Optically-Active Precursors for the Synthesis of the Side-Chain by Means of Microbiological Transformations
    • Leuenberger HGW Boguth W Barner R Schmid M Zell R Total Synthesis of Natural Alpha-Tocopherol 1. Preparation of Bifunctional Optically-Active Precursors for the Synthesis of the Side-Chain by Means of Microbiological Transformations Helvetica Chimica Acta 1979, 62:455-463
    • (1979) Helvetica Chimica Acta , vol.62 , pp. 455-463
    • Leuenberger, H.G.W.1    Boguth, W.2    Barner, R.3    Schmid, M.4    Zell, R.5
  • 78
    • 37049068182 scopus 로고
    • Biocatalytic Reduction of the Carbon-Carbon Double-Bond of 5-Benzylidenethiazolidine-2,4-Diones - Synthesis of (+/ -)-5-(4-(2-[Methyl(2-Pyridyl)Amino]Ethoxy)Benzyl)Thiazolidine-2,4-Dione (Brl-49653), Its (R)-(+)-Enantiomer and Analogs
    • Cantello BCC Eggleston DS Haigh D Haltiwanger RC Heath CM Hindley RM Jennings KR Sime JT Woroniecki SR Facile Biocatalytic Reduction of the Carbon-Carbon Double-Bond of 5-Benzylidenethiazolidine-2,4-Diones - Synthesis of (+/ -)-5-(4-(2-[Methyl(2-Pyridyl)Amino]Ethoxy)Benzyl)Thiazolidine-2,4-Dione (Brl-49653), Its (R)-(+)-Enantiomer and Analogs Journal of the Chemical Society-Perkin Transactions 1 1994, 3319-3324
    • (1994) Journal of the Chemical Society-Perkin Transactions , vol.1 , pp. 3319-3324
    • Cantello, B.C.C.1    Eggleston, D.S.2    Haigh, D.3    Haltiwanger, R.C.4    Heath, C.M.5    Hindley, R.M.6    Jennings, K.R.7    Sime, J.T.8    Woroniecki, S.R.9
  • 81
    • 33747764281 scopus 로고    scopus 로고
    • Stereoselective enone reductions by Saccharomyces carlsbergensis old yellow enzyme
    • Swiderska MA Stewart JD Stereoselective enone reductions by Saccharomyces carlsbergensis old yellow enzyme Journal of Molecular Catalysis B: Enzymatic 2006, 42:52-54
    • (2006) Journal of Molecular Catalysis B: Enzymatic , vol.42 , pp. 52-54
    • Swiderska, M.A.1    Stewart, J.D.2
  • 82
    • 4644333528 scopus 로고    scopus 로고
    • Cloning and overexpression of the old yellow enzyme gene of Candida macedoniensis, and its application to the production of a chiral compound
    • 15464593
    • Kataoka M Kotaka A Thiwthong R Wada M Nakamori S Shimizu S Cloning and overexpression of the old yellow enzyme gene of Candida macedoniensis, and its application to the production of a chiral compound Journal of Biotechnology 2004, 114:1-9 15464593
    • (2004) Journal of Biotechnology , vol.114 , pp. 1-9
    • Kataoka, M.1    Kotaka, A.2    Thiwthong, R.3    Wada, M.4    Nakamori, S.5    Shimizu, S.6
  • 83
    • 0003049911 scopus 로고
    • Microbial metabolism of methanol 1. Formation and crystallization of methanol-oxidizing enzyme in a methanol-utilizing yeast, Kloeckera sp. No 2201
    • Tani Y Ogata K Nishikaw H Miya T Microbial metabolism of methanol 1. Formation and crystallization of methanol-oxidizing enzyme in a methanol-utilizing yeast, Kloeckera sp. No 2201 Agricultural and Biological Chemistry 1972, 3:68
    • (1972) Agricultural and Biological Chemistry , vol.36 , pp. 68
    • Tani, Y.1    Ogata, K.2    Nishikaw, H.3    Miya, T.4
  • 84
    • 84996024994 scopus 로고
    • Microbial metabolism of methanol 2. Properties of crystalline alcohol oxidase from Kloeckera sp. No 2201
    • Tani Y Miya T Ogata K Microbial metabolism of methanol 2. Properties of crystalline alcohol oxidase from Kloeckera sp. No 2201 Agricultural and Biological Chemistry 1972, 36:76
    • (1972) Agricultural and Biological Chemistry , vol.36 , pp. 76
    • Tani, Y.1    Miya, T.2    Ogata, K.3
  • 85
    • 0005202151 scopus 로고
    • Oxidation of Methanol, Formaldehyde and Formate by a Candida Species
    • Fujii T Tonomura K Oxidation of Methanol, Formaldehyde and Formate by a Candida Species Agricultural and Biological Chemistry 1972, 36:2297-2306
    • (1972) Agricultural and Biological Chemistry , vol.36 , pp. 2297-2306
    • Fujii, T.1    Tonomura, K.2
  • 86
    • 34447520336 scopus 로고    scopus 로고
    • Biocatalytic racemization of synthetically important functionalized alpha-hydroxyketones using microbial cells
    • Nestl BM Bodlenner A Stuermer R Hauer B Kroutil W Faber K Biocatalytic racemization of synthetically important functionalized alpha-hydroxyketones using microbial cells Tetrahedron-Asymmetry 2007, 18:1465-1474
    • (2007) Tetrahedron-Asymmetry , vol.18 , pp. 1465-1474
    • Nestl, B.M.1    Bodlenner, A.2    Stuermer, R.3    Hauer, B.4    Kroutil, W.5    Faber, K.6
  • 87
    • 0026661770 scopus 로고
    • Asymmetric Carbon-Carbon Bond Formation Using Sulfoxide-Stabilized Carbanions
    • Walker AJ Asymmetric Carbon-Carbon Bond Formation Using Sulfoxide-Stabilized Carbanions Tetrahedron-Asymmetry 1992, 3:961-998
    • (1992) Tetrahedron-Asymmetry , vol.3 , pp. 961-998
    • Walker, A.J.1
  • 93
    • 41449115768 scopus 로고    scopus 로고
    • Preparation of optically pure alkyl 3-(hetero-2-yl)-3-hydroxypropanoates by Candida parapsilosis ATCC 7330 mediated deracemisation
    • Titu D Chadha A Preparation of optically pure alkyl 3-(hetero-2-yl)-3-hydroxypropanoates by Candida parapsilosis ATCC 7330 mediated deracemisation Journal of Molecular Catalysis B: Enzymatic 2008, 52-3:168-172
    • (2008) Journal of Molecular Catalysis B: Enzymatic , vol.52-53 , pp. 168-172
    • Titu, D.1    Chadha, A.2
  • 94
    • 84918053284 scopus 로고
    • The behaviour of estrogen hormones with the effect of fermenting yeast: Biochemistry transformation of oestrogen ester in alpha- estradiol
    • Mamoli L The behaviour of estrogen hormones with the effect of fermenting yeast: Biochemistry transformation of oestrogen ester in alpha- estradiol Berichte der Deutschen Chemischen Gesellschaft 1938, 71:2696-2698
    • (1938) Berichte Der Deutschen Chemischen Gesellschaft , vol.71 , pp. 2696-2698
    • Mamoli, L.1
  • 95
    • 0022277838 scopus 로고
    • Proteinases, proteolysis and biological control in the yeast Saccharomyces cerevisiae
    • 3916861
    • Achstetter T Wolf DH Proteinases, proteolysis and biological control in the yeast Saccharomyces cerevisiae Yeast 1985, 1:139-157 3916861
    • (1985) Yeast , vol.1 , pp. 139-157
    • Achstetter, T.1    Wolf, D.H.2
  • 98
    • 59049088217 scopus 로고
    • Microbial resolution of racemic 2,2-dimethylcyclopropanecarboxamide in the manufacture of the acid
    • (EP 502525 A1)
    • Robins K Gilligan T Microbial resolution of racemic 2,2-dimethylcyclopropanecarboxamide in the manufacture of the acid (EP 502525 A1) 1992
    • (1992)
    • Robins, K.1    Gilligan, T.2
  • 99
    • 0025759183 scopus 로고
    • Synthesis of Optically Active Compounds - A Large Scale Perspective
    • Crosby J Synthesis of Optically Active Compounds - A Large Scale Perspective Tetrahedron 1991, 47:4789-4846
    • (1991) Tetrahedron , vol.47 , pp. 4789-4846
    • Crosby, J.1
  • 101
    • 0036322165 scopus 로고    scopus 로고
    • Development of dynamic kinetic resolution processes for biocatalytic production of natural and nonnatural L-amino acids
    • May O Verseck S Bommarius A Drauz K Development of dynamic kinetic resolution processes for biocatalytic production of natural and nonnatural L-amino acids Organic Process Research & Development 2002, 6:452-457
    • (2002) Organic Process Research & Development , vol.6 , pp. 452-457
    • May, O.1    Verseck, S.2    Bommarius, A.3    Drauz, K.4
  • 102
    • 3142660254 scopus 로고    scopus 로고
    • Cloning and sequencing of an epoxide hydrolase gene from Rhodosporidium paludigenum
    • 15497443
    • Labuschagne M Botes AL Albertyn J Cloning and sequencing of an epoxide hydrolase gene from Rhodosporidium paludigenum Dna Sequence 2004, 15:202-205 15497443
    • (2004) Dna Sequence , vol.15 , pp. 202-205
    • Labuschagne, M.1    Botes, A.L.2    Albertyn, J.3
  • 104
    • 59049089610 scopus 로고    scopus 로고
    • Protein design on pyruvate decarboxylase (PDC) by site-directed mutagenesis
    • Berlin, Heidelberg, New York: Springer Scheper T
    • Pohl M Protein design on pyruvate decarboxylase (PDC) by site-directed mutagenesis New enzymes for organic synthesis Berlin, Heidelberg, New York: Springer Scheper T 1999, 15
    • (1999) New Enzymes for Organic Synthesis , pp. 15
    • Pohl, M.1
  • 105
    • 0010396235 scopus 로고
    • Transformations of non-conventional substrates by fermenting baker's yeast: Production of optically active methyl-diols from aldehydes
    • Fuganti C Grasselli P Transformations of non-conventional substrates by fermenting baker's yeast: Production of optically active methyl-diols from aldehydes Chemistry & Industry (London, UK) 1977, 983
    • (1977) Chemistry & Industry (London, UK) , pp. 983
    • Fuganti, C.1    Grasselli, P.2
  • 106
    • 0024863733 scopus 로고
    • Baker's yeast-mediated synthesis of natural products
    • Washington DC: ACS Symp Ser, Am Chem Soc Whitaker JR, Sonnet PE
    • Fuganti C Grasselli P Baker's yeast-mediated synthesis of natural products Biocatalysis in Agricultural Biotechnology Washington DC: ACS Symp Ser, Am Chem Soc Whitaker JR, Sonnet PE 1989, 359
    • (1989) Biocatalysis in Agricultural Biotechnology , pp. 359
    • Fuganti, C.1    Grasselli, P.2
  • 108
    • 0029011504 scopus 로고
    • L-Threonine aldolase in organic synthesis - Preparation of novel beta-hydroxy-alpha-amino acids
    • Vassilev VP Uchiyama T Kajimoto T Wong CH L-Threonine aldolase in organic synthesis - preparation of novel beta-hydroxy-alpha-amino acids Tetrahedron Letters 1995, 36:4081-4084
    • (1995) Tetrahedron Letters , vol.36 , pp. 4081-4084
    • Vassilev, V.P.1    Uchiyama, T.2    Kajimoto, T.3    Wong, C.H.4
  • 109
    • 0001379950 scopus 로고
    • Mechanism of Phenylacetylcarbinol Synthesis by Yeast
    • 169548 13069399
    • Smith PF Hendlin D Mechanism of Phenylacetylcarbinol Synthesis by Yeast Journal of Bacteriology 1953, 65:440-445 169548 13069399
    • (1953) Journal of Bacteriology , vol.65 , pp. 440-445
    • Smith, P.F.1    Hendlin, D.2
  • 110
    • 0002241256 scopus 로고
    • Case studies in applied biocatalysis - From ideas to products
    • Harwood, USA: Academic Publishers Cabral JMS, Best D, Boross L, Tramper J
    • Cheetham PSJ Case studies in applied biocatalysis - from ideas to products Applied Biocatalysis Harwood, USA: Academic Publishers Cabral JMS, Best D, Boross L, Tramper J 1994, 87-89
    • (1994) Applied Biocatalysis , pp. 87-89
    • Cheetham, P.S.J.1
  • 111
    • 0026354817 scopus 로고
    • Biotransformations of Industrial Use
    • Kieslich K Biotransformations of Industrial Use Acta Biotechnologica 1991, 11:559-570
    • (1991) Acta Biotechnologica , vol.11 , pp. 559-570
    • Kieslich, K.1
  • 116
    • 0030785388 scopus 로고    scopus 로고
    • Application of biocatalysis and biotransformations to the synthesis of pharmaceuticals
    • Zaks A Dodds DR Application of biocatalysis and biotransformations to the synthesis of pharmaceuticals Drug Discovery Today 1997, 2:513-531
    • (1997) Drug Discovery Today , vol.2 , pp. 513-531
    • Zaks, A.1    Dodds, D.R.2
  • 117
    • 0030935037 scopus 로고    scopus 로고
    • Stereoselective biotransformations in synthesis of some pharmaceutical intermediates
    • 9097413
    • Patel RN Stereoselective biotransformations in synthesis of some pharmaceutical intermediates Advances in Applied Microbiology 1997, 43:91-140 9097413
    • (1997) Advances in Applied Microbiology , vol.43 , pp. 91-140
    • Patel, R.N.1
  • 119
    • 0033198325 scopus 로고    scopus 로고
    • Asymmetric bioreduction of (2-(4-nitro-phenyl)-N-(2-oxo-2-pyridin-3-yl-ethyl)-acetamide) to its corresponding (R) alcohol [(R)-N-(2-hydroxy-2-pyridin-3-yl-ethyl)-2-(4-nitro-phenyl)-acetamide] by using Candida sorbophila MY 1833
    • Chartrain M Roberge C Chung J McNamara J Zhao DL Olewinski R Hunt G Salmon P Roush D Yamazaki S et al Asymmetric bioreduction of (2-(4-nitro-phenyl)-N-(2-oxo-2-pyridin-3-yl-ethyl)-acetamide) to its corresponding (R) alcohol [(R)-N-(2-hydroxy-2-pyridin-3-yl-ethyl)-2-(4-nitro-phenyl)-acetamide] by using Candida sorbophila MY 1833 Enzyme and Microbial Technology 1999, 25:489-496
    • (1999) Enzyme and Microbial Technology , vol.25 , pp. 489-496
    • Chartrain, M.1    Roberge, C.2    Chung, J.3    McNamara, J.4    Zhao, D.L.5    Olewinski, R.6    Hunt, G.7    Salmon, P.8    Roush, D.9    Yamazaki, S.10
  • 122
    • 0035025463 scopus 로고    scopus 로고
    • Enzymatic synthesis of chiral intermediates for Omapatrilat, an antihypertensive drug
    • 11337276
    • Patel RN Enzymatic synthesis of chiral intermediates for Omapatrilat, an antihypertensive drug Biomolecular Engineering 2001, 17:167-182 11337276
    • (2001) Biomolecular Engineering , vol.17 , pp. 167-182
    • Patel, R.N.1
  • 125
    • 2442726095 scopus 로고
    • Amino acids and peptides
    • Weinheim: Verlag Chemie Kieslich K
    • Schmidt-Kastner G Egerer P Amino acids and peptides Biotechnology Weinheim: Verlag Chemie Kieslich K 1984, 6a:387-419
    • (1984) Biotechnology , vol.6 a , pp. 387-419
    • Schmidt-Kastner, G.1    Egerer, P.2
  • 127
    • 4644232675 scopus 로고    scopus 로고
    • Recombinant Protein Production in Yeasts
    • Totowa, NJ, USA: Humana Press Balbás P, Lorence A 15269428
    • Porro D Mattanovich D Recombinant Protein Production in Yeasts Methods in Molecular Biology Totowa, NJ, USA: Humana Press Balbás P, Lorence A 2004, 241:258 15269428
    • (2004) Methods in Molecular Biology , pp. 241-258
    • Porro, D.1    Mattanovich, D.2
  • 128
    • 0034537455 scopus 로고    scopus 로고
    • Heterologous protein production in methylotrophic yeasts
    • Gellissen G Heterologous protein production in methylotrophic yeasts Applied Microbiology and Biotechnology 2000, 54:741-750
    • (2000) Applied Microbiology and Biotechnology , vol.54 , pp. 741-750
    • Gellissen, G.1
  • 129
    • 0030725815 scopus 로고    scopus 로고
    • Production of recombinant proteins by methylotrophic yeasts
    • 9353229
    • Hollenberg CP Gellissen G Production of recombinant proteins by methylotrophic yeasts Current Opinion in Biotechnology 1997, 8:554-560 9353229
    • (1997) Current Opinion in Biotechnology , vol.8 , pp. 554-560
    • Hollenberg, C.P.1    Gellissen, G.2
  • 130
    • 0031010051 scopus 로고    scopus 로고
    • Application of yeasts in gene expression studies: A comparison of Saccharomyces cerevisiae, Hansenula polymorpha and Kluyveromyces lactis - A review
    • 9185853
    • Gellissen G Hollenberg CP Application of yeasts in gene expression studies: A comparison of Saccharomyces cerevisiae, Hansenula polymorpha and Kluyveromyces lactis - a review Gene 1997, 190:87-97 9185853
    • (1997) Gene , vol.190 , pp. 87-97
    • Gellissen, G.1    Hollenberg, C.P.2
  • 132
    • 0033955337 scopus 로고    scopus 로고
    • Heterologous protein expression in the methylotrophic yeast Pichia pastoris
    • 10640598
    • Cereghino JL Cregg JM Heterologous protein expression in the methylotrophic yeast Pichia pastoris Fems Microbiology Reviews 2000, 24:45-66 10640598
    • (2000) Fems Microbiology Reviews , vol.24 , pp. 45-66
    • Cereghino, J.L.1    Cregg, J.M.2
  • 136
    • 1842530397 scopus 로고    scopus 로고
    • Heterologous protein expression and secretion in the non-conventional yeast Yarrowia lipolytica: A review
    • 15063615
    • Madzak C Gaillardin C Beckerich JM Heterologous protein expression and secretion in the non-conventional yeast Yarrowia lipolytica: A review Journal of Biotechnology 2004, 109:63-81 15063615
    • (2004) Journal of Biotechnology , vol.109 , pp. 63-81
    • Madzak, C.1    Gaillardin, C.2    Beckerich, J.M.3
  • 137
    • 0033375049 scopus 로고    scopus 로고
    • Expression system for foreign genes using the fission yeast Schizosaccharomyces pombe
    • Giga-Hama Y Kumagai H Expression system for foreign genes using the fission yeast Schizosaccharomyces pombe Biotechnology and Applied Biochemistry 1999, 30:235-244
    • (1999) Biotechnology and Applied Biochemistry , vol.30 , pp. 235-244
    • Giga-Hama, Y.1    Kumagai, H.2
  • 138
    • 0025895183 scopus 로고
    • Toward A Science of Metabolic Engineering
    • 2047876
    • Bailey JE Toward A Science of Metabolic Engineering Science 1991, 252:1668-1675 2047876
    • (1991) Science , vol.252 , pp. 1668-1675
    • Bailey, J.E.1
  • 140
    • 0032600888 scopus 로고    scopus 로고
    • Metabolic fluxes and metabolic engineering
    • 10935750
    • Stephanopoulos G Metabolic fluxes and metabolic engineering Metabolic Engineering 1999, 1:1-11 10935750
    • (1999) Metabolic Engineering , vol.1 , pp. 1-11
    • Stephanopoulos, G.1
  • 146
    • 0034922896 scopus 로고    scopus 로고
    • Fuel ethanol production from lignocellulose: A challenge for metabolic engineering and process integration
    • Zaldivar J Nielsen J Olsson L Fuel ethanol production from lignocellulose: A challenge for metabolic engineering and process integration Applied Microbiology and Biotechnology 2001, 56:17-34
    • (2001) Applied Microbiology and Biotechnology , vol.56 , pp. 17-34
    • Zaldivar, J.1    Nielsen, J.2    Olsson, L.3
  • 148
    • 34548789083 scopus 로고    scopus 로고
    • Metabolic engineering for pentose utilization in Saccharomyces cerevisiae
    • Berlin, Heidelberg: Springer
    • Hahn-Haegerdal B Karhumaa K Jeppsson M Gorwa-Grauslund MF Metabolic engineering for pentose utilization in Saccharomyces cerevisiae Biofuels Berlin, Heidelberg: Springer 2007, 147-177
    • (2007) Biofuels , pp. 147-177
    • Hahn-Haegerdal, B.1    Karhumaa, K.2    Jeppsson, M.3    Gorwa-Grauslund, M.F.4
  • 149
    • 0036842385 scopus 로고    scopus 로고
    • Comparison of xylitol production in recombinant Saccharomyces cerevisiae strains harboring XYL1 gene of Pichia stipitis and GRE3 gene of S. cerevisiae
    • Kim MD Jeun YS Kim SG Ryu YW Seo JH Comparison of xylitol production in recombinant Saccharomyces cerevisiae strains harboring XYL1 gene of Pichia stipitis and GRE3 gene of S. cerevisiae Enzyme and Microbial Technology 2002, 31:862-866
    • (2002) Enzyme and Microbial Technology , vol.31 , pp. 862-866
    • Kim, M.D.1    Jeun, Y.S.2    Kim, S.G.3    Ryu, Y.W.4    Seo, J.H.5
  • 151
    • 33845379674 scopus 로고
    • Stereochemical Control of Yeast Reductions 5. Characterization of the Oxidoreductases Involved in the Reduction of Beta-Keto-Esters
    • Shieh WR Gopalan AS Sih CJ Stereochemical Control of Yeast Reductions 5. Characterization of the Oxidoreductases Involved in the Reduction of Beta-Keto-Esters Journal of the American Chemical Society 1985, 107:2993-2994
    • (1985) Journal of the American Chemical Society , vol.107 , pp. 2993-2994
    • Shieh, W.R.1    Gopalan, A.S.2    Sih, C.J.3
  • 152
    • 0035961481 scopus 로고    scopus 로고
    • Highly stereoselective reagents for beta-keto ester reductions by genetic engineering of baker's yeast
    • 11456752
    • Rodriguez S Kayser MM Stewart JD Highly stereoselective reagents for beta-keto ester reductions by genetic engineering of baker's yeast Journal of the American Chemical Society 2001, 123:1547-1555 11456752
    • (2001) Journal of the American Chemical Society , vol.123 , pp. 1547-1555
    • Rodriguez, S.1    Kayser, M.M.2    Stewart, J.D.3
  • 153
    • 0142186831 scopus 로고    scopus 로고
    • Screening of two complementary collections of Saccharomyces cerevisiae to identify enzymes involved in stereo-selective reductions of specific carbonyl compounds: An alternative to protein purification
    • Katz M Hahn-Haegerdal B Gorwa-Grauslund MF Screening of two complementary collections of Saccharomyces cerevisiae to identify enzymes involved in stereo-selective reductions of specific carbonyl compounds: An alternative to protein purification Enzyme and Microbial Technology 2003, 33:163-172
    • (2003) Enzyme and Microbial Technology , vol.33 , pp. 163-172
    • Katz, M.1    Hahn-Haegerdal, B.2    Gorwa-Grauslund, M.F.3
  • 154
    • 15044350989 scopus 로고    scopus 로고
    • Strain engineering for stereoselective bioreduction of dicarbonyl compounds by yeast reductases
    • 15780652
    • Johanson T Katz M Gorwa-Grauslund MF Strain engineering for stereoselective bioreduction of dicarbonyl compounds by yeast reductases Fems Yeast Research 2005, 5:513-525 15780652
    • (2005) Fems Yeast Research , vol.5 , pp. 513-525
    • Johanson, T.1    Katz, M.2    Gorwa-Grauslund, M.F.3
  • 157
    • 84907036250 scopus 로고
    • Preparative bioorganic chemistry. Part 10. Asymmetric reductions of bicyclo[2.2.2]octane-2,6-diones with baker's yeast
    • Mori K Nagano E Preparative bioorganic chemistry. Part 10. Asymmetric reductions of bicyclo[2.2.2]octane-2,6-diones with baker's yeast Biocatalysis 1990, 3:25-36
    • (1990) Biocatalysis , vol.3 , pp. 25-36
    • Mori, K.1    Nagano, E.2
  • 158
    • 54549118611 scopus 로고    scopus 로고
    • Integration of enzyme, strain and reaction engineering to overcome limitations of baker's yeast in the asymmetric reduction of α-keto esters
    • 101002/bit.21980
    • Kratzer R Egger S Nidetzky B Integration of enzyme, strain and reaction engineering to overcome limitations of baker's yeast in the asymmetric reduction of α-keto esters Biotechnology and Bioengineering 2008 101002/bit.21980.
    • (2008) Biotechnology and Bioengineering
    • Kratzer, R.1    Egger, S.2    Nidetzky, B.3
  • 159
    • 33847301957 scopus 로고    scopus 로고
    • Identification of Candida tenuis xylose reductase as highly selective biocatalyst for the synthesis of aromatic alpha-hydroxy esters and improvement of its efficiency by protein engineering
    • 17325801
    • Kratzer R Nidetzky B Identification of Candida tenuis xylose reductase as highly selective biocatalyst for the synthesis of aromatic alpha-hydroxy esters and improvement of its efficiency by protein engineering Chemical Communications 2007, 1047-1049 17325801
    • (2007) Chemical Communications , pp. 1047-1049
    • Kratzer, R.1    Nidetzky, B.2
  • 160
    • 33644636816 scopus 로고    scopus 로고
    • Synthesis of the food flavoring methyl benzoate by genetically engineered Saccharomyces cerevisiae
    • 16442655
    • Farhi M Dudareva N Masci T Weiss D Vainstein A Abeliovich H Synthesis of the food flavoring methyl benzoate by genetically engineered Saccharomyces cerevisiae Journal of Biotechnology 2006, 122:307-315 16442655
    • (2006) Journal of Biotechnology , vol.122 , pp. 307-315
    • Farhi, M.1    Dudareva, N.2    Masci, T.3    Weiss, D.4    Vainstein, A.5    Abeliovich, H.6
  • 161
    • 0141538616 scopus 로고    scopus 로고
    • The use of transgenic yeasts expressing a gene encoding a glycosyl-hydrolase as a tool to increase resveratrol content in wine
    • 11020039
    • González-Candelas L Gil JV Lamuela-Raventós RM Ramón D The use of transgenic yeasts expressing a gene encoding a glycosyl-hydrolase as a tool to increase resveratrol content in wine International Journal of Food Microbiology 2000, 59:179-183 11020039
    • (2000) International Journal of Food Microbiology , vol.59 , pp. 179-183
    • González-Candelas, L.1    Gil, J.V.2    Lamuela-Raventós, R.M.3    Ramón, D.4
  • 164
    • 0042967495 scopus 로고    scopus 로고
    • Candida molischiana beta-glucosidase production by Saccharomyces cerevisiae and its application in winemaking
    • Genoves S Gil JV Manzanares P Aleixandre JL Valles S Candida molischiana beta-glucosidase production by Saccharomyces cerevisiae and its application in winemaking Journal of Food Science 2003, 68:2096-2100
    • (2003) Journal of Food Science , vol.68 , pp. 2096-2100
    • Genoves, S.1    Gil, J.V.2    Manzanares, P.3    Aleixandre, J.L.4    Valles, S.5
  • 166
    • 33846273110 scopus 로고    scopus 로고
    • Modulating aroma compounds during wine fermentation by manipulating carnitine acetyltransferases in Saccharomyces cerevisiae
    • 17156120
    • Cordente AG Swiegers JH Hegardt FG Pretorius IS Modulating aroma compounds during wine fermentation by manipulating carnitine acetyltransferases in Saccharomyces cerevisiae Fems Microbiology Letters 2007, 267:159-166 17156120
    • (2007) Fems Microbiology Letters , vol.267 , pp. 159-166
    • Cordente, A.G.1    Swiegers, J.H.2    Hegardt, F.G.3    Pretorius, I.S.4
  • 169
    • 0000779198 scopus 로고    scopus 로고
    • A "designer yeast" that catalyzes the kinetic resolutions of 2-alkyl-substituted cyclohexanones by enantioselective Baeyer-Villiger oxidations
    • 11667712
    • Stewart JD Reed KW Zhu J Chen G Kayser MM A "designer yeast" that catalyzes the kinetic resolutions of 2-alkyl-substituted cyclohexanones by enantioselective Baeyer-Villiger oxidations Journal of Organic Chemistry 1996, 61:7652-7653 11667712
    • (1996) Journal of Organic Chemistry , vol.61 , pp. 7652-7653
    • Stewart, J.D.1    Reed, K.W.2    Zhu, J.3    Chen, G.4    Kayser, M.M.5
  • 170
    • 0001644454 scopus 로고    scopus 로고
    • Enantio- and regioselective Baeyer-Villiger oxidations of 2- and 3-substituted cyclopentanones using engineered bakers' yeast
    • 11672341
    • Kayser MM Chen G Stewart JD Enantio- and regioselective Baeyer-Villiger oxidations of 2- and 3-substituted cyclopentanones using engineered bakers' yeast Journal of Organic Chemistry 1998, 63:7103-7106 11672341
    • (1998) Journal of Organic Chemistry , vol.63 , pp. 7103-7106
    • Kayser, M.M.1    Chen, G.2    Stewart, J.D.3
  • 171
    • 7544225227 scopus 로고    scopus 로고
    • Production of (S)-styrene oxide by recombinant Pichia pastoris containing epoxide hydrolase from Rhodotorula glutinis
    • Lee EY Yoo SS Kim HS Lee SJ Oh YK Park S Production of (S)-styrene oxide by recombinant Pichia pastoris containing epoxide hydrolase from Rhodotorula glutinis Enzyme and Microbial Technology 2004, 35:624-631
    • (2004) Enzyme and Microbial Technology , vol.35 , pp. 624-631
    • Lee, E.Y.1    Yoo, S.S.2    Kim, H.S.3    Lee, S.J.4    Oh, Y.K.5    Park, S.6
  • 172
    • 37349007629 scopus 로고    scopus 로고
    • Coexpression of redox partners increases the hydrocortisone (cortisol) production efficiency in CYP11B1 expressing fission yeast Schizosaccharomyces pombe
    • 17935813
    • Hakki T Zearo S Dragan CA Bureik M Bernhardt R Coexpression of redox partners increases the hydrocortisone (cortisol) production efficiency in CYP11B1 expressing fission yeast Schizosaccharomyces pombe Journal of Biotechnology 2008, 133:351-359 17935813
    • (2008) Journal of Biotechnology , vol.133 , pp. 351-359
    • Hakki, T.1    Zearo, S.2    Dragan, C.A.3    Bureik, M.4    Bernhardt, R.5
  • 173
    • 34250716024 scopus 로고    scopus 로고
    • Biotechnological synthesis of drug metabolites using human cytochrome P450 2D6 heterologously expressed in fission yeast exemplified for the designer drug metabolite 4 ′-hydroxymethyl-alpha-pyrrolidinobutyrophenone
    • 17572388
    • Peters FT Dragan CA Wilde DR Meyer MR Zapp J Bureik M Maurer HH Biotechnological synthesis of drug metabolites using human cytochrome P450 2D6 heterologously expressed in fission yeast exemplified for the designer drug metabolite 4 ′-hydroxymethyl-alpha-pyrrolidinobutyrophenone Biochemical Pharmacology 2007, 74:511-520 17572388
    • (2007) Biochemical Pharmacology , vol.74 , pp. 511-520
    • Peters, F.T.1    Dragan, C.A.2    Wilde, D.R.3    Meyer, M.R.4    Zapp, J.5    Bureik, M.6    Maurer, H.H.7
  • 174
    • 0035041719 scopus 로고    scopus 로고
    • Redox enzymes used in chiral syntheses coupled to coenzyme regeneration
    • 11172694
    • Leonida MD Redox enzymes used in chiral syntheses coupled to coenzyme regeneration Current Medicinal Chemistry 2001, 8:345-369 11172694
    • (2001) Current Medicinal Chemistry , vol.8 , pp. 345-369
    • Leonida, M.D.1
  • 175
    • 0042933788 scopus 로고    scopus 로고
    • Recent developments in pyridine nucleotide regeneration
    • 12943852
    • Donk van der WA Zhao HM Recent developments in pyridine nucleotide regeneration Current Opinion in Biotechnology 2003, 14;421-426 12943852
    • (2003) Current Opinion in Biotechnology , vol.14 , pp. 421-426
    • Donk, W.A.1    Zhao, H.M.2
  • 176
    • 0041404265 scopus 로고    scopus 로고
    • Microbial conversion with cofactor regeneration using genetically engineered bacteria
    • Endo T Koizumi S Microbial conversion with cofactor regeneration using genetically engineered bacteria Advanced Synthesis & Catalysis 2001, 343:521-526
    • (2001) Advanced Synthesis & Catalysis , vol.343 , pp. 521-526
    • Endo, T.1    Koizumi, S.2
  • 177
    • 0344687415 scopus 로고    scopus 로고
    • Regeneration of cofactors for use in biocatalysis
    • 14662386
    • Zhao HM Donk van der WA Regeneration of cofactors for use in biocatalysis Current Opinion in Biotechnology 2003, 14:583-589 14662386
    • (2003) Current Opinion in Biotechnology , vol.14 , pp. 583-589
    • Zhao, H.M.1    Donk, W.A.2
  • 178
    • 0035862739 scopus 로고    scopus 로고
    • Expression of a cytoplasmic transhydrogenase in Saccharomyces cerevisiae results in formation of 2-oxoglutarate due to depletion of the NADPH pool
    • 11124698
    • Nissen TL Anderlund M Nielsen J Villadsen J Kielland-Brandt MC Expression of a cytoplasmic transhydrogenase in Saccharomyces cerevisiae results in formation of 2-oxoglutarate due to depletion of the NADPH pool Yeast 2001, 18:19-32 11124698
    • (2001) Yeast , vol.18 , pp. 19-32
    • Nissen, T.L.1    Anderlund, M.2    Nielsen, J.3    Villadsen, J.4    Kielland-Brandt, M.C.5
  • 181
    • 0032976492 scopus 로고    scopus 로고
    • Expression of the Escherichia coli pntA and pntB genes, encoding nicotinamide nucleotide transhydrogenase, in Saccharomyces cerevisiae and its effect on product formation during anaerobic glucose fermentation
    • Anderlund M Nissen TL Nielsen J Villadsen J Rydstrom J Hahn-Hagerdal B Kielland-Brandt MC Expression of the Escherichia coli pntA and pntB genes, encoding nicotinamide nucleotide transhydrogenase, in Saccharomyces cerevisiae and its effect on product formation during anaerobic glucose fermentation Applied and Environmental Microbiology 1999, 65:2333-2340
    • (1999) Applied and Environmental Microbiology , vol.65 , pp. 2333-2340
    • Anderlund, M.1    Nissen, T.L.2    Nielsen, J.3    Villadsen, J.4    Rydstrom, J.5    Hahn-Hagerdal, B.6    Kielland-Brandt, M.C.7
  • 182
    • 1642316901 scopus 로고    scopus 로고
    • Aerobic physiology of redox-engineered Saccharomyces cerevisiae strains modified in the ammonium assimilation for increased NADPH availability
    • 14554197
    • dos Santos MM Thygesen G Kotter P Olsson L Nielsen J Aerobic physiology of redox-engineered Saccharomyces cerevisiae strains modified in the ammonium assimilation for increased NADPH availability Fems Yeast Research 2003, 4:59-68 14554197
    • (2003) Fems Yeast Research , vol.4 , pp. 59-68
    • dos Santos, M.M.1    Thygesen, G.2    Kotter, P.3    Olsson, L.4    Nielsen, J.5
  • 183
    • 0033929520 scopus 로고    scopus 로고
    • Optimization of ethanol production in Saccharomyces cerevisiae by metabolic engineering of the ammonium assimilation
    • 10935936
    • Nissen TL Kielland-Brandt MC Nielsen J Villadsen J Optimization of ethanol production in Saccharomyces cerevisiae by metabolic engineering of the ammonium assimilation Metabolic Engineering 2000, 2:69-77 10935936
    • (2000) Metabolic Engineering , vol.2 , pp. 69-77
    • Nissen, T.L.1    Kielland-Brandt, M.C.2    Nielsen, J.3    Villadsen, J.4
  • 184
    • 33746891860 scopus 로고    scopus 로고
    • Cofactor engineering in Saccharomyces cerevisiae: Expression of a H2O-forming NADH oxidase and impact on redox metabolism
    • 16473032
    • Heux S Cachon R Dequin S Cofactor engineering in Saccharomyces cerevisiae: Expression of a H2O-forming NADH oxidase and impact on redox metabolism Metabolic Engineering 2006, 8:303-314 16473032
    • (2006) Metabolic Engineering , vol.8 , pp. 303-314
    • Heux, S.1    Cachon, R.2    Dequin, S.3
  • 186
    • 33847273107 scopus 로고    scopus 로고
    • Permeability issues in whole-cell bioprocesses and cellular membrane engineering
    • Chen RRZ Permeability issues in whole-cell bioprocesses and cellular membrane engineering Applied Microbiology and Biotechnology 2007, 74:730-738
    • (2007) Applied Microbiology and Biotechnology , vol.74 , pp. 730-738
    • Chen, R.R.Z.1
  • 187
    • 0033526666 scopus 로고    scopus 로고
    • Production of S-lactoylglutathione by high activity whole cell biocatalysts prepared by permeabilization of recombinant Saccharomyces cerevisiae with alcohols
    • Liu Y Hama H Fujita Y Kondo A Inoue Y Kimura A Fukuda H Production of S-lactoylglutathione by high activity whole cell biocatalysts prepared by permeabilization of recombinant Saccharomyces cerevisiae with alcohols Biotechnology and Bioengineering 1999, 64:54-60
    • (1999) Biotechnology and Bioengineering , vol.64 , pp. 54-60
    • Liu, Y.1    Hama, H.2    Fujita, Y.3    Kondo, A.4    Inoue, Y.5    Kimura, A.6    Fukuda, H.7
  • 188
    • 3142697009 scopus 로고    scopus 로고
    • Lactulose production by beta-galactosidase in permeabilized cells of Kluyveromyces lactis
    • Lee YJ Kim CS Oh DK Lactulose production by beta-galactosidase in permeabilized cells of Kluyveromyces lactis Applied Microbiology and Biotechnology 2004, 64:787-793
    • (2004) Applied Microbiology and Biotechnology , vol.64 , pp. 787-793
    • Lee, Y.J.1    Kim, C.S.2    Oh, D.K.3
  • 189
    • 2342604387 scopus 로고    scopus 로고
    • Immobilization of catalase by entrapment of permeabilized yeast cells in hen egg white using glutaraldehyde
    • Kubal BS D'Souza SF Immobilization of catalase by entrapment of permeabilized yeast cells in hen egg white using glutaraldehyde Journal of Biochemical and Biophysical Methods 2004 59:61-64
    • (2004) Journal of Biochemical and Biophysical Methods , vol.59 , pp. 61-64
    • Kubal, B.S.1    D'Souza, S.F.2
  • 190
    • 0034690580 scopus 로고    scopus 로고
    • Stabilization of D-amino acid oxidase and catalase in permeabilized Rhodotorula gracilis cells and its application for the preparation of alpha-ketoacids
    • Upadhya R Nagajyothi Bhat SG Stabilization of D-amino acid oxidase and catalase in permeabilized Rhodotorula gracilis cells and its application for the preparation of alpha-ketoacids Biotechnology and Bioengineering 2000, 68:430-436
    • (2000) Biotechnology and Bioengineering , vol.68 , pp. 430-436
    • Upadhya, R.1    Nagajyothi2    Bhat, S.G.3
  • 192
    • 0034764034 scopus 로고    scopus 로고
    • Yeast whole-cell biocatalyst constructed by intracellular overproduction of Rhizopus oryzae lipase is applicable to biodiesel fuel production
    • Matsumoto T Takahashi S Kaieda M Ueda M Tanaka A Fukuda H Kondo A Yeast whole-cell biocatalyst constructed by intracellular overproduction of Rhizopus oryzae lipase is applicable to biodiesel fuel production Applied Microbiology and Biotechnology 2001, 57:515-520
    • (2001) Applied Microbiology and Biotechnology , vol.57 , pp. 515-520
    • Matsumoto, T.1    Takahashi, S.2    Kaieda, M.3    Ueda, M.4    Tanaka, A.5    Fukuda, H.6    Kondo, A.7
  • 193
    • 0037258562 scopus 로고    scopus 로고
    • Optimization of isonovalal production from alpha-pinene oxide using permeabilized cells of Pseudomonas rhodesiae CIP 107491
    • Fontanille P Larroche C Optimization of isonovalal production from alpha-pinene oxide using permeabilized cells of Pseudomonas rhodesiae CIP 107491 Applied Microbiology and Biotechnology 2003, 60:534-540
    • (2003) Applied Microbiology and Biotechnology , vol.60 , pp. 534-540
    • Fontanille, P.1    Larroche, C.2
  • 195
    • 0035125229 scopus 로고    scopus 로고
    • Cell surface display of organophosphorus hydrolase using ice nucleation protein
    • 11170483
    • Shimazu M Mulchandani A Chen W Cell surface display of organophosphorus hydrolase using ice nucleation protein Biotechnology Progress 2001, 17:76-80 11170483
    • (2001) Biotechnology Progress , vol.17 , pp. 76-80
    • Shimazu, M.1    Mulchandani, A.2    Chen, W.3
  • 197
    • 1642358668 scopus 로고    scopus 로고
    • Enantioselective transesterification using lipase-displaying yeast whole-cell biocatalyst
    • Matsumoto T Ito M Fukuda H Kondo A Enantioselective transesterification using lipase-displaying yeast whole-cell biocatalyst Applied Microbiology and Biotechnology 2004, 64:481-485
    • (2004) Applied Microbiology and Biotechnology , vol.64 , pp. 481-485
    • Matsumoto, T.1    Ito, M.2    Fukuda, H.3    Kondo, A.4
  • 198
    • 0036727246 scopus 로고    scopus 로고
    • Construction of yeast strains with high cell surface lipase activity by using novel display systems based on the Flo1p flocculation functional domain
    • Matsumoto T Fukuda H Ueda M Tanaka A Kondo A Construction of yeast strains with high cell surface lipase activity by using novel display systems based on the Flo1p flocculation functional domain Applied and Environmental Microbiology 2002, 68:4517-4522
    • (2002) Applied and Environmental Microbiology , vol.68 , pp. 4517-4522
    • Matsumoto, T.1    Fukuda, H.2    Ueda, M.3    Tanaka, A.4    Kondo, A.5
  • 199
    • 33747163601 scopus 로고    scopus 로고
    • Enhancement of activity of lipase-displaying yeast cells and their application to optical resolution of (R, S)-1-benzyloxy-3-chloro-2-propyl monosuccinate
    • 16889376
    • Nakamura Y Matsumoto T Nomoto F Ueda M Fukuda H Kondo A Enhancement of activity of lipase-displaying yeast cells and their application to optical resolution of (R, S)-1-benzyloxy-3-chloro-2-propyl monosuccinate Biotechnology Progress 2006, 22:998-1002 16889376
    • (2006) Biotechnology Progress , vol.22 , pp. 998-1002
    • Nakamura, Y.1    Matsumoto, T.2    Nomoto, F.3    Ueda, M.4    Fukuda, H.5    Kondo, A.6
  • 200
    • 2442508067 scopus 로고    scopus 로고
    • Molecular engineering of Rhizopus oryzae lipase using a combinatorial protein library constructed on the yeast cell surface
    • Shibamoto H Matsumoto T Fukuda H Kondo A Molecular engineering of Rhizopus oryzae lipase using a combinatorial protein library constructed on the yeast cell surface Journal of Molecular Catalysis B: Enzymatic 2004, 28:235-239
    • (2004) Journal of Molecular Catalysis B: Enzymatic , vol.28 , pp. 235-239
    • Shibamoto, H.1    Matsumoto, T.2    Fukuda, H.3    Kondo, A.4
  • 202
    • 34248359137 scopus 로고    scopus 로고
    • Characterization of cyclofructans from inulin by Saccharomyces cerevisiae strain displaying cell-surface cycloinulooligosaccharide fructanotransferase
    • Kim HJ Lee JH Kim HC Lee JW Kim YH Nam SW Characterization of cyclofructans from inulin by Saccharomyces cerevisiae strain displaying cell-surface cycloinulooligosaccharide fructanotransferase Journal of Microbiology and Biotechnology 2007, 17:695-700
    • (2007) Journal of Microbiology and Biotechnology , vol.17 , pp. 695-700
    • Kim, H.J.1    Lee, J.H.2    Kim, H.C.3    Lee, J.W.4    Kim, Y.H.5    Nam, S.W.6
  • 204
    • 34248672267 scopus 로고    scopus 로고
    • Preparation of a whole-cell biocatalyst of mutated Candida antarctica lipase B (mCALB) by a yeast molecular display system and its practical properties
    • Kato M Fuchimoto J Tanino T Kondo A Fukuda H Ueda M Preparation of a whole-cell biocatalyst of mutated Candida antarctica lipase B (mCALB) by a yeast molecular display system and its practical properties Applied Microbiology and Biotechnology 2007, 75:549-555
    • (2007) Applied Microbiology and Biotechnology , vol.75 , pp. 549-555
    • Kato, M.1    Fuchimoto, J.2    Tanino, T.3    Kondo, A.4    Fukuda, H.5    Ueda, M.6
  • 205
    • 0141817121 scopus 로고    scopus 로고
    • Improving tolerance of Candida antarctica lipase B towards irreversible thermal inactivation through directed evolution
    • 12968077
    • Zhang NY Suen WC Windsor W Xiao L Madison V Zaks A Improving tolerance of Candida antarctica lipase B towards irreversible thermal inactivation through directed evolution Protein Engineering 2003, 16:599-605 12968077
    • (2003) Protein Engineering , vol.16 , pp. 599-605
    • Zhang, N.Y.1    Suen, W.C.2    Windsor, W.3    Xiao, L.4    Madison, V.5    Zaks, A.6
  • 206
    • 0033803961 scopus 로고    scopus 로고
    • Cell surface engineering of yeast: Construction of arming yeast with biocatalyst
    • Ueda M Tanaka A Cell surface engineering of yeast: Construction of arming yeast with biocatalyst Journal of Bioscience and Bioengineering 2000, 90:125-136
    • (2000) Journal of Bioscience and Bioengineering , vol.90 , pp. 125-136
    • Ueda, M.1    Tanaka, A.2
  • 207
    • 41549136380 scopus 로고    scopus 로고
    • Versatile microbial surface-display for environmental remediation and biofuels production
    • 18321708
    • Wu CH Mulchandani A Chen W Versatile microbial surface-display for environmental remediation and biofuels production Trends in Microbiology 2008, 16:181-188 18321708
    • (2008) Trends in Microbiology , vol.16 , pp. 181-188
    • Wu, C.H.1    Mulchandani, A.2    Chen, W.3
  • 209
    • 2342638898 scopus 로고    scopus 로고
    • Synergistic saccharification, and direct fermentation to ethanol, of amorphous cellulose by use of an engineered yeast strain codisplaying three types of cellulolytic enzyme
    • Fujita Y Ito J Ueda M Fukuda H Kondo A Synergistic saccharification, and direct fermentation to ethanol, of amorphous cellulose by use of an engineered yeast strain codisplaying three types of cellulolytic enzyme Applied and Environmental Microbiology 2004, 70:1207-1212
    • (2004) Applied and Environmental Microbiology , vol.70 , pp. 1207-1212
    • Fujita, Y.1    Ito, J.2    Ueda, M.3    Fukuda, H.4    Kondo, A.5
  • 210
    • 0000708358 scopus 로고
    • Cell walls
    • London: Academic Press Rose AH, Harrison JS 2
    • Fleet GH Cell walls The Yeasts. Yeasts Organelles London: Academic Press Rose AH, Harrison JS 2 1991, 4:199-278
    • (1991) The Yeasts. Yeasts Organelles , vol.4 , pp. 199-278
    • Fleet, G.H.1
  • 211
    • 0027981822 scopus 로고
    • Cell-Wall Assembly in Yeast
    • 7985414
    • Klis FM Cell-Wall Assembly in Yeast Yeast 1994, 10:851-869 7985414
    • (1994) Yeast , vol.10 , pp. 851-869
    • Klis, F.M.1
  • 212
    • 40949088044 scopus 로고    scopus 로고
    • Efficient display of active lipase LipB52 with a Pichia pastoris cell surface display system and comparison with the LipB52 displayed on Saccharomyces cerevisiae cell surface
    • 18221563
    • Jiang ZB Gao B Ren R Tao XY Ma YS Wei DZ Efficient display of active lipase LipB52 with a Pichia pastoris cell surface display system and comparison with the LipB52 displayed on Saccharomyces cerevisiae cell surface Bmc Biotechnology 2008, 8:2267-459 18221563
    • (2008) Bmc Biotechnology , vol.8
    • Jiang, Z.B.1    Gao, B.2    Ren, R.3    Tao, X.Y.4    Ma, Y.S.5    Wei, D.Z.6
  • 215
    • 33645057433 scopus 로고    scopus 로고
    • Metabolic pathway engineering for complex polyketide biosynthesis in Saccharomyces cerevisiae
    • 16423069
    • Mutka SC Bondi SM Carney JR Da Silva NA Kealey JT Metabolic pathway engineering for complex polyketide biosynthesis in Saccharomyces cerevisiae Fems Yeast Research 2006, 6:40-47 16423069
    • (2006) Fems Yeast Research , vol.6 , pp. 40-47
    • Mutka, S.C.1    Bondi, S.M.2    Carney, J.R.3    Da Silva, N.A.4    Kealey, J.T.5
  • 216
    • 0025630190 scopus 로고
    • Elucidation of the Erwinia uredovora carotenoid biosynthetic pathway by functional analysis of gene products expressed in Escherichia coli
    • 210783 2254247
    • Misawa N Nakagawa M Kobayashi K Yamano S Izawa Y Nakamura K Harashima K Elucidation of the Erwinia uredovora carotenoid biosynthetic pathway by functional analysis of gene products expressed in Escherichia coli Journal of Bacteriology 1990, 172:6704-6712 210783 2254247
    • (1990) Journal of Bacteriology , vol.172 , pp. 6704-6712
    • Misawa, N.1    Nakagawa, M.2    Kobayashi, K.3    Yamano, S.4    Izawa, Y.5    Nakamura, K.6    Harashima, K.7
  • 217
    • 0028817748 scopus 로고
    • Structure and functional analysis of a marine bacterial carotenoid biosynthesis gene cluster and astaxanthin biosynthetic pathway proposed at the gene level
    • 177511 7592436
    • Misawa N Satomi Y Kondo K Yokoyama A Kajiwara S Saito T Ohtani T Miki W Structure and functional analysis of a marine bacterial carotenoid biosynthesis gene cluster and astaxanthin biosynthetic pathway proposed at the gene level Journal of Bacteriology 1995, 177:6575-6584 177511 7592436
    • (1995) Journal of Bacteriology , vol.177 , pp. 6575-6584
    • Misawa, N.1    Satomi, Y.2    Kondo, K.3    Yokoyama, A.4    Kajiwara, S.5    Saito, T.6    Ohtani, T.7    Miki, W.8
  • 218
    • 0031843028 scopus 로고    scopus 로고
    • Increased carotenoid production by the food yeast Candida utilis through metabolic engineering of the isoprenoid pathway
    • Shimada H Kondo K Fraser PD Miura Y Saito T Misawa N Increased carotenoid production by the food yeast Candida utilis through metabolic engineering of the isoprenoid pathway Applied and Environmental Microbiology 1998, 64:2676-2680
    • (1998) Applied and Environmental Microbiology , vol.64 , pp. 2676-2680
    • Shimada, H.1    Kondo, K.2    Fraser, P.D.3    Miura, Y.4    Saito, T.5    Misawa, N.6
  • 220
    • 0032477487 scopus 로고    scopus 로고
    • Metabolic engineering for the production of carotenoids in non-carotenogenic bacteria and yeasts
    • Misawa N Shimada H Metabolic engineering for the production of carotenoids in non-carotenogenic bacteria and yeasts Journal of Biotechnology 1998, 59:169-181
    • (1998) Journal of Biotechnology , vol.59 , pp. 169-181
    • Misawa, N.1    Shimada, H.2
  • 223
    • 0001221133 scopus 로고
    • Production of Carotenoids by Recombinant DNA Technology
    • Ausich RL Production of Carotenoids by Recombinant DNA Technology Pure and Applied Chemistry 1994, 66:1057-1062
    • (1994) Pure and Applied Chemistry , vol.66 , pp. 1057-1062
    • Ausich, R.L.1
  • 224
    • 0032412784 scopus 로고    scopus 로고
    • Biochemistry, cell biology and molecular biology of lipids of Saccharomyces cerevisiae
    • 9885152
    • Daum G Lees ND Bard M Dickson R Biochemistry, cell biology and molecular biology of lipids of Saccharomyces cerevisiae Yeast 1998, 14:1471-1510 9885152
    • (1998) Yeast , vol.14 , pp. 1471-1510
    • Daum, G.1    Lees, N.D.2    Bard, M.3    Dickson, R.4
  • 227
    • 33847378479 scopus 로고    scopus 로고
    • Engineering of the pyruvate dehydrogenase bypass in Saccharomyces cerevisiae for high-level production of isoprenoids
    • 17196416
    • Shiba Y Paradise EM Kirby J Ro D-K Keasling JD Engineering of the pyruvate dehydrogenase bypass in Saccharomyces cerevisiae for high-level production of isoprenoids Metabolic Engineering 2007, 9:160-168 17196416
    • (2007) Metabolic Engineering , vol.9 , pp. 160-168
    • Shiba, Y.1    Paradise, E.M.2    Kirby, J.3    Ro, D.-K.4    Keasling, J.D.5
  • 229
    • 0041728804 scopus 로고    scopus 로고
    • Metabolic engineering to produce sesquiterpenes in yeast
    • 12735738
    • Jackson BE Hart-Wells EA Matsuda SPT Metabolic engineering to produce sesquiterpenes in yeast Organic Letters 2003, 5:1629-1632 12735738
    • (2003) Organic Letters , vol.5 , pp. 1629-1632
    • Jackson, B.E.1    Hart-Wells, E.A.2    Matsuda, S.P.T.3
  • 233
    • 1642576078 scopus 로고    scopus 로고
    • Reconstitution of the entry point of plant phenylpropanoid metabolism in yeast (Saccharomyces cerevisiae) - Implications for control of metabolic flux into the phenylpropanoid pathway
    • 14607837
    • Ro DK Douglas CJ Reconstitution of the entry point of plant phenylpropanoid metabolism in yeast (Saccharomyces cerevisiae) - Implications for control of metabolic flux into the phenylpropanoid pathway Journal of Biological Chemistry 2004, 279:2600-2607 14607837
    • (2004) Journal of Biological Chemistry , vol.279 , pp. 2600-2607
    • Ro, D.K.1    Douglas, C.J.2
  • 234
    • 33847252518 scopus 로고    scopus 로고
    • Production of p-hydroxycinnamic acid from glucose in Saccharomyces cerevisiae and Escherichia coli by expression of heterologous genes from plants and fungi
    • 17204442
    • Vannelli T Qi WW Sweigard J Gatenby AA Sariaslani FS Production of p-hydroxycinnamic acid from glucose in Saccharomyces cerevisiae and Escherichia coli by expression of heterologous genes from plants and fungi Metabolic Engineering 2007, 9:142-151 17204442
    • (2007) Metabolic Engineering , vol.9 , pp. 142-151
    • Vannelli, T.1    Qi, W.W.2    Sweigard, J.3    Gatenby, A.A.4    Sariaslani, F.S.5
  • 235
    • 20444422841 scopus 로고    scopus 로고
    • Metabolic engineering of the phenylpropanoid pathway in Saccharomyces cerevisiae
    • Jiang HX Wood KV Morgan JA Metabolic engineering of the phenylpropanoid pathway in Saccharomyces cerevisiae Applied and Environmental Microbiology 2005, 71:2962-2969
    • (2005) Applied and Environmental Microbiology , vol.71 , pp. 2962-2969
    • Jiang, H.X.1    Wood, K.V.2    Morgan, J.A.3
  • 237
    • 84948780444 scopus 로고
    • Relations Between the Content of Aroma Compounds and the Sensory Evaluation of 10 Raspberry Varieties (Rubus Idaeus L)
    • Larsen M Poll L Callesen O Lewis M Relations Between the Content of Aroma Compounds and the Sensory Evaluation of 10 Raspberry Varieties (Rubus Idaeus L) Acta Agriculturae Scandinavica 1991, 41:447-454
    • (1991) Acta Agriculturae Scandinavica , vol.41 , pp. 447-454
    • Larsen, M.1    Poll, L.2    Callesen, O.3    Lewis, M.4
  • 241
    • 0031936276 scopus 로고    scopus 로고
    • Self-sufficient biosynthesis of pregnenolone and progesterone in engineered yeast
    • 9487528
    • Duport C Spagnoli R Degryse E Pompon D Self-sufficient biosynthesis of pregnenolone and progesterone in engineered yeast Nature Biotechnology 1998, 16:186-189 9487528
    • (1998) Nature Biotechnology , vol.16 , pp. 186-189
    • Duport, C.1    Spagnoli, R.2    Degryse, E.3    Pompon, D.4
  • 242
    • 0031856845 scopus 로고    scopus 로고
    • A mutation in a purported regulatory gene affects control of sterol uptake in Saccharomyces cerevisiae
    • 107415 9696767
    • Crowley JH Leak FW Shianna KV Tove S Parks LW A mutation in a purported regulatory gene affects control of sterol uptake in Saccharomyces cerevisiae Journal of Bacteriology 1998, 180:4177-4183 107415 9696767
    • (1998) Journal of Bacteriology , vol.180 , pp. 4177-4183
    • Crowley, J.H.1    Leak, F.W.2    Shianna, K.V.3    Tove, S.4    Parks, L.W.5
  • 243
    • 0033079834 scopus 로고    scopus 로고
    • Mechanism and specificity of the terminal thioesterase domain from the erythromycin polyketide synthase
    • 10021418
    • Gokhale RS Hunziker D Cane DE Khosla C Mechanism and specificity of the terminal thioesterase domain from the erythromycin polyketide synthase Chemistry & Biology 1999, 6;117-125 10021418
    • (1999) Chemistry & Biology , vol.6 , pp. 117-125
    • Gokhale, R.S.1    Hunziker, D.2    Cane, D.E.3    Khosla, C.4
  • 245
    • 0032004369 scopus 로고    scopus 로고
    • tRNA genes and retroelements in the yeast genome
    • 147333 9443958
    • Hani J Feldmann H tRNA genes and retroelements in the yeast genome Nucleic Acids Research 1998, 26;689-696 147333 9443958
    • (1998) Nucleic Acids Research , vol.26 , pp. 689-696
    • Hani, J.1    Feldmann, H.2


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