-
1
-
-
0027529354
-
Lipase-catalyzed asymmetric hydrolysis of 3-phenylglycidic acid esters, the key intermediate in the synthjesis of diltiazem hydrochloride
-
Matsumae H., Furui M., Shibatani T. Lipase-catalyzed asymmetric hydrolysis of 3-phenylglycidic acid esters, the key intermediate in the synthjesis of diltiazem hydrochloride. J Ferment Bioeng. 75:1993;93-98.
-
(1993)
J Ferment Bioeng
, vol.75
, pp. 93-98
-
-
Matsumae, H.1
Furui, M.2
Shibatani, T.3
-
2
-
-
0032912844
-
Efficient alternative synthetic route to diltiazem via (2R,3S)-3-(4-methoxyphenyl) glycidamide
-
Yamada S., Tsujoka I., Shibatani T., Yoshioka R. Efficient alternative synthetic route to diltiazem via (2R,3S)-3-(4-methoxyphenyl) glycidamide. Chem Pharm Bull. 47:1999;146-150.
-
(1999)
Chem Pharm Bull
, vol.47
, pp. 146-150
-
-
Yamada, S.1
Tsujoka, I.2
Shibatani, T.3
Yoshioka, R.4
-
3
-
-
0002769886
-
Biotransformations with lipases
-
H.J. Rehm, & G. Reed. Weinheim: Wiley-VCH. [Kelly DR (Series Editor): Biotechnology, vol 8a, part 3.]. A broad overview on lipases, covering basic information on lipases (e.g. structure/function relationships, application of lipases under different conditions, and the range of industrial applications) but also giving a detailed insight into the scope and limitations in terms of substrate specificity and the application of lipases in specific syntheses.
-
Kazlauskas R., Bornscheuer U.T. Biotransformations with lipases. Rehm H.J., Reed G. Biotransformations I. 1998;37-191 Wiley-VCH, Weinheim. [Kelly DR (Series Editor): Biotechnology, vol 8a, part 3.]. A broad overview on lipases, covering basic information on lipases (e.g. structure/function relationships, application of lipases under different conditions, and the range of industrial applications) but also giving a detailed insight into the scope and limitations in terms of substrate specificity and the application of lipases in specific syntheses.
-
(1998)
Biotransformations I
, pp. 37-191
-
-
Kazlauskas, R.1
Bornscheuer, U.T.2
-
4
-
-
0030220432
-
Efficient procedures for the large-scale preparation of (1S,2S)-trans-2-methoxycyclohexanol, a key chiral intermediate in the synthesis of tricyclic β-lactam antibiotics
-
Stead P., Marley H., Mahmoudian M., Webb G., Noble D., Ip Y.T., Piga E., Rossi T., Roberts S., Dawson M.J. Efficient procedures for the large-scale preparation of (1S,2S)-trans-2-methoxycyclohexanol, a key chiral intermediate in the synthesis of tricyclic β-lactam antibiotics. Tetrahedron - Asymmetry. 7:1996;2247-2250.
-
(1996)
Tetrahedron - Asymmetry
, vol.7
, pp. 2247-2250
-
-
Stead, P.1
Marley, H.2
Mahmoudian, M.3
Webb, G.4
Noble, D.5
Ip, Y.T.6
Piga, E.7
Rossi, T.8
Roberts, S.9
Dawson, M.J.10
-
6
-
-
22644449223
-
Biocatalytic production of chiral intermediates
-
Ladner W.E., Ditrich K. Biocatalytic production of chiral intermediates. Chimica Oggi. 7/8:1999;51-54.
-
(1999)
Chimica Oggi
, vol.78
, pp. 51-54
-
-
Ladner, W.E.1
Ditrich, K.2
-
7
-
-
0031795317
-
One biocatalyst - many applications: The use of Candida antarctica B-lipase in organic synthesis
-
Anderson E.M., Karin M., Kirk O. One biocatalyst - many applications: the use of Candida antarctica B-lipase in organic synthesis. Biocatalysis Biotransform. 16:1998;181-204.
-
(1998)
Biocatalysis Biotransform
, vol.16
, pp. 181-204
-
-
Anderson, E.M.1
Karin, M.2
Kirk, O.3
-
8
-
-
0032167489
-
Microbial lipases form versatile tools for biotechnology
-
Review on lipase applications illustrating the wide applicability of lipases for (dynamic) kinetic resolutions.
-
Jaeger K.E., Reetz M.T. Microbial lipases form versatile tools for biotechnology. Trends Biotechnol. 16:1998;396-403. Review on lipase applications illustrating the wide applicability of lipases for (dynamic) kinetic resolutions.
-
(1998)
Trends Biotechnol
, vol.16
, pp. 396-403
-
-
Jaeger, K.E.1
Reetz, M.T.2
-
9
-
-
0032897271
-
The realm of microbial lipases in biotechnology
-
Pandey A., Benjamin S., Soccol C.R., Nigam P., Krieger N., Soccol V.T. The realm of microbial lipases in biotechnology. Biotechnol Appl Biochem. 29:1999;119-131.
-
(1999)
Biotechnol Appl Biochem
, vol.29
, pp. 119-131
-
-
Pandey, A.1
Benjamin, S.2
Soccol, C.R.3
Nigam, P.4
Krieger, N.5
Soccol, V.T.6
-
10
-
-
0030914481
-
Cross-linked crystals of subtilisin - versatile catalyst for organic synthesis
-
Wang Y.F., Yakovlevsky K., Zhang B.L., Margolin A.L. Cross-linked crystals of subtilisin - versatile catalyst for organic synthesis. J Org Chem. 62:1997;3488-3495.
-
(1997)
J Org Chem
, vol.62
, pp. 3488-3495
-
-
Wang, Y.F.1
Yakovlevsky, K.2
Zhang, B.L.3
Margolin, A.L.4
-
11
-
-
0032947378
-
Enzymatic synthesis of silicon-containing dipeptides with 3-trimethyl silylalanine
-
Ishikawa H., Yamanaka H., Kawamoto T., Tanaka A. Enzymatic synthesis of silicon-containing dipeptides with 3-trimethyl silylalanine. Appl Microbiol Biotechnol. 51:1999;470-473.
-
(1999)
Appl Microbiol Biotechnol
, vol.51
, pp. 470-473
-
-
Ishikawa, H.1
Yamanaka, H.2
Kawamoto, T.3
Tanaka, A.4
-
12
-
-
0344654051
-
Thermolysin
-
M.C. Flickinger, & S.W. Drew. New York: John Wiley and Sons
-
Hanzawa S., Kidokoro S.I. Thermolysin. Flickinger M.C., Drew S.W. Encyclopedia of Bioprocess Technology: Fermentation, Biocatalysis, and Bioseparation. 1999;2527-2535 John Wiley and Sons, New York.
-
(1999)
Encyclopedia of Bioprocess Technology: Fermentation, Biocatalysis, and Bioseparation
, pp. 2527-2535
-
-
Hanzawa, S.1
Kidokoro, S.I.2
-
13
-
-
84889798780
-
Aspartame
-
M.C. Flickinger, & S.W. Drew. New York: John Wiley and Sons. Comprehensive review on the production of aspartame by DSM/Tosoh and alternative processes. It includes the history of the discovery of the process and some process characteristics.
-
Hanzawa S. Aspartame. Flickinger M.C., Drew S.W. Encyclopedia of Bioprocess Technology: Fermentation, Biocatalysis, and Bioseparation. 1999;201-210 John Wiley and Sons, New York. Comprehensive review on the production of aspartame by DSM/Tosoh and alternative processes. It includes the history of the discovery of the process and some process characteristics.
-
(1999)
Encyclopedia of Bioprocess Technology: Fermentation, Biocatalysis, and Bioseparation
, pp. 201-210
-
-
Hanzawa, S.1
-
14
-
-
0002267204
-
Amino acid amidase catalyzed preparation and further transformations of enantiopure α-amino acids
-
J. Stubenrauch. New York: Marcel Decker Inc. The article describes the identification, characterisation, cloning and overexpression of amidases and their application for the production of enantiomerically pure compounds.
-
Sonke T., Kaptein B., Boesten W.H.J., Broxterman Q.B., Kamphuis J., Formaggio F., Toniolo C., Rutjes F.P.J.T., Schoemaker H.E. Amino acid amidase catalyzed preparation and further transformations of enantiopure α-amino acids. Stubenrauch J. Stereoselective Biocatalysis. 1999;23-58 Marcel Decker Inc, New York. The article describes the identification, characterisation, cloning and overexpression of amidases and their application for the production of enantiomerically pure compounds.
-
(1999)
Stereoselective Biocatalysis
, pp. 23-58
-
-
Sonke, T.1
Kaptein, B.2
Boesten, W.H.J.3
Broxterman, Q.B.4
Kamphuis, J.5
Formaggio, F.6
Toniolo, C.7
Rutjes, F.P.J.T.8
Schoemaker, H.E.9
-
15
-
-
0344654050
-
Industrial applications of immobilized biocatalysts and biomaterials
-
Chibata I. Industrial applications of immobilized biocatalysts and biomaterials. Adv Mol Cell Biol. 15A:1996;151-160.
-
(1996)
Adv Mol Cell Biol
, vol.15
, pp. 151-160
-
-
Chibata, I.1
-
16
-
-
0001495722
-
Biocatalysis in organic synthesis. Part 9. Highly enantioselective kinetic resolution of secondary alcohols catalyzed by acylase
-
Faraldos J., Arroyo E., Herradon B. Biocatalysis in organic synthesis. Part 9. Highly enantioselective kinetic resolution of secondary alcohols catalyzed by acylase. Synlett. 4:1997;367-370.
-
(1997)
Synlett
, vol.4
, pp. 367-370
-
-
Faraldos, J.1
Arroyo, E.2
Herradon, B.3
-
17
-
-
0001081201
-
Penicillin acylase in the industrial production of β-lactam antibiotics
-
Article on the use of acylases for the production of semi-synthetic antibiotics. Enzymatic coupling of β-lactam nuclei with sidechains catalysed by hydrolytic enzymes.
-
Bruggink A., Roos E.C., de Vroom E. Penicillin acylase in the industrial production of β-lactam antibiotics. Org Process Res Dev. 2:1998;128-133. Article on the use of acylases for the production of semi-synthetic antibiotics. Enzymatic coupling of β-lactam nuclei with sidechains catalysed by hydrolytic enzymes.
-
(1998)
Org Process Res Dev
, vol.2
, pp. 128-133
-
-
Bruggink, A.1
Roos, E.C.2
De Vroom, E.3
-
18
-
-
0344222647
-
(S)-2-chloropropanoic acid: Developments in its industrial manufacture
-
A.N. Collins, G.N. Sheldrake, & J. Crosby. Chichester : Wiley
-
Taylor S.C. (S)-2-chloropropanoic acid: developments in its industrial manufacture. Collins A.N., Sheldrake G.N., Crosby J. Chirality in Industry II. 1999;207-223 Wiley, Chichester.
-
(1999)
Chirality in Industry II
, pp. 207-223
-
-
Taylor, S.C.1
-
19
-
-
0030737815
-
Controlled racemisation of optically active organic compounds: Prospects for asymmetric transformation
-
Ebbers E.J., Ariaans G.J.A., Houbiers J.P.M., Bruggink A., Zwanenburg B. Controlled racemisation of optically active organic compounds: prospects for asymmetric transformation. Tetrahedron. 53:1997;9417-9476.
-
(1997)
Tetrahedron
, vol.53
, pp. 9417-9476
-
-
Ebbers, E.J.1
Ariaans, G.J.A.2
Houbiers, J.P.M.3
Bruggink, A.4
Zwanenburg, B.5
-
20
-
-
0033023975
-
Dynamic kinetic resolution
-
A comprehensive overview on new developments in dynamic kinetic resolution.
-
El Gihani M.R., Williams J.M.J. Dynamic kinetic resolution. Curr Opin Chem Biol. 3:1999;11-15. A comprehensive overview on new developments in dynamic kinetic resolution.
-
(1999)
Curr Opin Chem Biol
, vol.3
, pp. 11-15
-
-
El Gihani, M.R.1
Williams, J.M.J.2
-
21
-
-
0032540651
-
Dynamic enzymatic resolution of thioesters
-
Ulm P.-J., Drueckhammer D.G. Dynamic enzymatic resolution of thioesters. J Am Chem Soc. 120:1998;5605-5609.
-
(1998)
J Am Chem Soc
, vol.120
, pp. 5605-5609
-
-
Ulm, P.-J.1
Drueckhammer, D.G.2
-
22
-
-
0031049952
-
Biocatalytic deracemization techniques: Dynamic resolutions and stereoinversions
-
K. Faber. Stuttgart: Verlag
-
Stecher H., Faber K. Biocatalytic deracemization techniques: dynamic resolutions and stereoinversions. Faber K. Synthesis. 1997;1-17 Verlag, Stuttgart.
-
(1997)
Synthesis
, pp. 1-17
-
-
Stecher, H.1
Faber, K.2
-
23
-
-
0033593289
-
Selective racemisation of esters: Relevance to enzymatic hydrolysis reactions
-
Dinh P.M., Williams J.M.J. Selective racemisation of esters: relevance to enzymatic hydrolysis reactions. Tetrahedron Lett. 40:1999;749-752.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 749-752
-
-
Dinh, P.M.1
Williams, J.M.J.2
-
24
-
-
0033518869
-
Ruthenium- And enzyme-catalyzed dynamic kinetic resolution of secondary alcohols
-
The authors describe combination of lipase resolution and in situ racemization catalyzed by transition metals, which results in a process with theoretically a quatitative yield.
-
Persson B.A., Larsson A.L.E., Le Ray M., Bäckvall J.-E. Ruthenium- and enzyme-catalyzed dynamic kinetic resolution of secondary alcohols. J Am Chem Soc. 121:1999;1645-1650. The authors describe combination of lipase resolution and in situ racemization catalyzed by transition metals, which results in a process with theoretically a quatitative yield.
-
(1999)
J Am Chem Soc
, vol.121
, pp. 1645-1650
-
-
Persson, B.A.1
Larsson, A.L.E.2
Le Ray, M.3
Bäckvall, J.-E.4
-
25
-
-
0032491912
-
Identification of the open reading frame for the Pseudomonas putida D-hydantoinase gene and expression of the gene in Escherichia coli
-
Chien H.R., Jih Y.-L., Yang W.-Y., Hsu W.-H. Identification of the open reading frame for the Pseudomonas putida D-hydantoinase gene and expression of the gene in Escherichia coli. Biochim Biophys Acta. 1395:1998;68-77.
-
(1998)
Biochim Biophys Acta
, vol.1395
, pp. 68-77
-
-
Chien, H.R.1
Jih, Y.-L.2
Yang, W.-Y.3
Hsu, W.-H.4
-
26
-
-
0031977176
-
Efficient conversion of 5-substituted hydantoins to D-α amino acids using recombinant Escherichia coli strains
-
Grifantini R., Galli G., Carpani G., Pratesi C., Frascotti G., Grandi G. Efficient conversion of 5-substituted hydantoins to D-α amino acids using recombinant Escherichia coli strains. Microbiology. 144:1998;947-954.
-
(1998)
Microbiology
, vol.144
, pp. 947-954
-
-
Grifantini, R.1
Galli, G.2
Carpani, G.3
Pratesi, C.4
Frascotti, G.5
Grandi, G.6
-
27
-
-
0030474954
-
Cloning and overexpression of thermostable D-hydantoinase from thermophile in E. coli and its application to the synthesis of optictally active D-amino acids
-
Lee D.-C., Lee S.-G., Hong S.-P., Sung M.-H., Kim H.-S. Cloning and overexpression of thermostable D-hydantoinase from thermophile in E. coli and its application to the synthesis of optictally active D-amino acids. Ann New York Acad Sci. 864:1999;401-405.
-
(1999)
Ann New York Acad Sci
, vol.864
, pp. 401-405
-
-
Lee, D.-C.1
Lee, S.-G.2
Hong, S.-P.3
Sung, M.-H.4
Kim, H.-S.5
-
28
-
-
0032151863
-
Relationship between an increase in thermostability and amino acid substitutions in N-carbamyl-D-amino acid amidohydrolase
-
Ikenaka Y., Nanba H., Yajima K., Yamada Y., Takano M., Takahashi S. Relationship between an increase in thermostability and amino acid substitutions in N-carbamyl-D-amino acid amidohydrolase. Biosci Biotechnol Biochem. 62:1998;1672-1675.
-
(1998)
Biosci Biotechnol Biochem
, vol.62
, pp. 1672-1675
-
-
Ikenaka, Y.1
Nanba, H.2
Yajima, K.3
Yamada, Y.4
Takano, M.5
Takahashi, S.6
-
29
-
-
0024951234
-
Production of D- And L-amino acids from D,L-5-monosubstituted hydantoins
-
Syldatk C., Dombach G., Gross C., Müller R., Wagner F. Production of D- and L-amino acids from D,L-5-monosubstituted hydantoins. Ann New York Acad Sci. 864:1999;323-329.
-
(1999)
Ann New York Acad Sci
, vol.864
, pp. 323-329
-
-
Syldatk, C.1
Dombach, G.2
Gross, C.3
Müller, R.4
Wagner, F.5
-
30
-
-
0031817075
-
Molecular evolution of hydantoinases
-
May O., Habenicht A., Mattes R., Syldatk, Siemann M. Molecular evolution of hydantoinases. Biol Chem. 379:1998;743-747.
-
(1998)
Biol Chem
, vol.379
, pp. 743-747
-
-
May, O.1
Habenicht, A.2
Mattes, R.3
Syldatk4
Siemann, M.5
-
31
-
-
0032568190
-
Substrate-dependent enantioselectivity of a novel hydantoinase from Arthrobacter aurscens DSM375: Purification and characterization as a new member of the cyclic amidases
-
May O., Siemann M., Pietzsch M., Kiess M., Mattes R., Syldatk C. Substrate-dependent enantioselectivity of a novel hydantoinase from Arthrobacter aurscens DSM375: purification and characterization as a new member of the cyclic amidases. J Biotechnol. 61:1998;1-13.
-
(1998)
J Biotechnol
, vol.61
, pp. 1-13
-
-
May, O.1
Siemann, M.2
Pietzsch, M.3
Kiess, M.4
Mattes, R.5
Syldatk, C.6
-
33
-
-
0001194360
-
Enantiocomplementary epoxide hydrolyses as a preparative route to both enantiomers of styrene oxide
-
Pedragosa-Moreau S., Archelas A., Furstoss R. Enantiocomplementary epoxide hydrolyses as a preparative route to both enantiomers of styrene oxide. J Org Chem. 58:1993;5533-5536.
-
(1993)
J Org Chem
, vol.58
, pp. 5533-5536
-
-
Pedragosa-Moreau, S.1
Archelas, A.2
Furstoss, R.3
-
34
-
-
33748638617
-
Deracemization of (+/-)-2,3-disubstituted oxiranes via biocatalytic hydrolysis using bacterial epoxide hydrolastes: Kinetics of an enantioconvergent process
-
Kroutil W., Mischitz M., Faber K. Deracemization of (+/-)-2,3-disubstituted oxiranes via biocatalytic hydrolysis using bacterial epoxide hydrolastes: kinetics of an enantioconvergent process. J Chem Soc Perkin Trans. 24:1997;3629-3636.
-
(1997)
J Chem Soc Perkin Trans
, vol.24
, pp. 3629-3636
-
-
Kroutil, W.1
Mischitz, M.2
Faber, K.3
-
35
-
-
0032576854
-
Chemoenzymatic deracemization of (+/-)-2,2-disubstituted oxiranes
-
Orru R.V.A., Mayer S.F., Kroutil W., Faber K. Chemoenzymatic deracemization of (+/-)-2,2-disubstituted oxiranes. Tetrahedron. 54:1998;859-874.
-
(1998)
Tetrahedron
, vol.54
, pp. 859-874
-
-
Orru, R.V.A.1
Mayer, S.F.2
Kroutil, W.3
Faber, K.4
-
36
-
-
0030848933
-
Microbiological transformations 3. 7. An enantioconvergent synthesis of the β-blocker (R)-nifénalol using a combined chemoenzymatic approach
-
Pedragosa-Moreau S., Morisseau C., Baratti J., Zylber J., Archelas A., Furstoss R. Microbiological transformations 3. 7. An enantioconvergent synthesis of the β-blocker (R)-nifénalol using a combined chemoenzymatic approach. Tetrahedron. 53:1997;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
-
37
-
-
0030831509
-
Enzymatic desymmetrization of prochiral 2-substituted-1,3-propanediols: A practical chemoenzymatic synthesis of a key precursor of SCH51048, a broad-spectrum orally active antifungal agent
-
Morgan B., Dodds D.R., Zaks A., Andrews D.R., Klesse R. Enzymatic desymmetrization of prochiral 2-substituted-1,3-propanediols: a practical chemoenzymatic synthesis of a key precursor of SCH51048, a broad-spectrum orally active antifungal agent. J Org Chem. 62:1997;7736-7743.
-
(1997)
J Org Chem
, vol.62
, pp. 7736-7743
-
-
Morgan, B.1
Dodds, D.R.2
Zaks, A.3
Andrews, D.R.4
Klesse, R.5
-
38
-
-
0029872834
-
Enantioselective synthesis through enzymatic asymmetrization
-
Schoffers E., Golebiowski A., Johnson C.R. Enantioselective synthesis through enzymatic asymmetrization. Tetrahedron. 52:1996;3769-3826.
-
(1996)
Tetrahedron
, vol.52
, pp. 3769-3826
-
-
Schoffers, E.1
Golebiowski, A.2
Johnson, C.R.3
-
39
-
-
0000085691
-
Biotransformations in the synthesis of enantiopure bioactive molecules
-
Johnson C.R. Biotransformations in the synthesis of enantiopure bioactive molecules. Acc Chem Res. 31:1998;333-341.
-
(1998)
Acc Chem Res
, vol.31
, pp. 333-341
-
-
Johnson, C.R.1
-
40
-
-
0031577572
-
Enhancement of catalytic acitvity by gene truncation: Activation of L-aspartase from Escherichia coli
-
Jayasekara M.M.K., Saribas A.S., Viola R.E. Enhancement of catalytic acitvity by gene truncation: activation of L-aspartase from Escherichia coli. Biochem Biophys Res Commun. 238:1997;411-414.
-
(1997)
Biochem Biophys Res Commun
, vol.238
, pp. 411-414
-
-
Jayasekara, M.M.K.1
Saribas, A.S.2
Viola, R.E.3
-
41
-
-
0345084878
-
Preparation of N-substituted aspartic acids via enantiospecific conjugate addition of N-nucleophiles to fumaric acids using methylaspartase: Synthetic utility and mechanistic applications
-
Gulsa M.S., Akhtar M., Gani D. Preparation of N-substituted aspartic acids via enantiospecific conjugate addition of N-nucleophiles to fumaric acids using methylaspartase: synthetic utility and mechanistic applications. J Chem Soc Perkin Trans. 1:1997;649-655.
-
(1997)
J Chem Soc Perkin Trans
, vol.1
, pp. 649-655
-
-
Gulsa, M.S.1
Akhtar, M.2
Gani, D.3
-
42
-
-
0032569785
-
Enzyme catalysed formation of (S)-cyanohydrins derived from aldehydes and ketones in a biphasic solvent system
-
Griengl H., Klempier N., Pochlauer P., Schmidt M., Shi N.Y., Zabelinskaja-Mackova A.A. Enzyme catalysed formation of (S)-cyanohydrins derived from aldehydes and ketones in a biphasic solvent system. Tetrahedron. 54:1998;14477-14486.
-
(1998)
Tetrahedron
, vol.54
, pp. 14477-14486
-
-
Griengl, H.1
Klempier, N.2
Pochlauer, P.3
Schmidt, M.4
Shi, N.Y.5
Zabelinskaja-Mackova, A.A.6
-
43
-
-
0031259717
-
High-level intracellular epression of hydroxinitrile lyase from the tropical rubber tree Hevea brasiliensis in microbial hosts
-
Hasslacher M., Schall M., Hayn M., Bona R., Rumbold K., Lück I, Griengl H., Kohlwin S.D., Schwab H. High-level intracellular epression of hydroxinitrile lyase from the tropical rubber tree Hevea brasiliensis in microbial hosts. Protein Expr Purif. 11:1997;61-71.
-
(1997)
Protein Expr Purif
, vol.11
, pp. 61-71
-
-
Hasslacher, M.1
Schall, M.2
Hayn, M.3
Bona, R.4
Rumbold, K.5
Lück, I.6
Griengl, H.7
Kohlwin, S.D.8
Schwab, H.9
-
44
-
-
0009625961
-
Biotransformation for the production of L-carnitine: Strain selection, biochemical and genetic background, scale-up and process design
-
A.N. Collins, J. Crosby, & G.N. Sheldrake. Chichester: John Wiley and Sons
-
Zimmermann T.P., Robins K.T.J.W., Hoeks F.W.J.M.M. Biotransformation for the production of L-carnitine: strain selection, biochemical and genetic background, scale-up and process design. Collins A.N., Crosby J., Sheldrake G.N. Chirality in lndustry II. 1995;287-305 John Wiley and Sons, Chichester.
-
(1995)
Chirality in Lndustry II
, pp. 287-305
-
-
Zimmermann, T.P.1
Robins, K.T.J.W.2
Hoeks, F.W.J.M.M.3
-
46
-
-
0026480892
-
Enzymatic synthesis of acrylamide: A success story not yet over
-
Kobayashi M., Nagasawa T., Yamada H. Enzymatic synthesis of acrylamide: a success story not yet over. Trends Biotechnol. 10:1992;402-408.
-
(1992)
Trends Biotechnol
, vol.10
, pp. 402-408
-
-
Kobayashi, M.1
Nagasawa, T.2
Yamada, H.3
-
47
-
-
0031017622
-
A Pseudomonas putida capable of stereoselective hydrolysis of nitriles
-
Fallon R.D., Stieglitz B., Turner I. Jr. A Pseudomonas putida capable of stereoselective hydrolysis of nitriles. Appl Microbiol Biotechnol. 47:1997;156-161.
-
(1997)
Appl Microbiol Biotechnol
, vol.47
, pp. 156-161
-
-
Fallon, R.D.1
Stieglitz, B.2
Turner I., Jr.3
-
48
-
-
0031963112
-
Enantioslelective hydration of 2-arylpropionitriles by a nitrile hydratase from Agrobacterium tumefaciens strain D3
-
Bauer R., Knackmuss H.-J., Stolz A. Enantioslelective hydration of 2-arylpropionitriles by a nitrile hydratase from Agrobacterium tumefaciens strain D3. Appl Microbiol Biotechnol. 49:1998;89-95.
-
(1998)
Appl Microbiol Biotechnol
, vol.49
, pp. 89-95
-
-
Bauer, R.1
Knackmuss, H.-J.2
Stolz, A.3
-
49
-
-
33748831300
-
Regioselective biotransformations of dinitriles using Rhodococcus sp. AJ270
-
Meth-Cohn O., Wang M.-X. Regioselective biotransformations of dinitriles using Rhodococcus sp. AJ270. J Chem Soc Perkin Trans. 21:1997;3197-3204.
-
(1997)
J Chem Soc Perkin Trans
, vol.21
, pp. 3197-3204
-
-
Meth-Cohn, O.1
Wang, M.-X.2
-
50
-
-
0345084461
-
Chemo- And enantioselective hydrolysis of nitriles and acid amides, respectively, with resting cells of Rhodococcus sp. C3II and Rhodococcus erythropolis MP50
-
Effenberger F., Graef B.W. Chemo- and enantioselective hydrolysis of nitriles and acid amides, respectively, with resting cells of Rhodococcus sp. C3II and Rhodococcus erythropolis MP50. J Biotechnol. 60:1998;165-174.
-
(1998)
J Biotechnol
, vol.60
, pp. 165-174
-
-
Effenberger, F.1
Graef, B.W.2
-
51
-
-
0042228531
-
Chemoenzymatic production of lactams from aliphatic α,ω-dinitrils
-
Gavagan J.E., Fager S.K., Fallon R.D., Folsom P.W., Herkes F.E., Eisenberg A., Hann E.C., DiCosimo R. Chemoenzymatic production of lactams from aliphatic α,ω-dinitrils. J Org Chem. 63:1998;4792-4801.
-
(1998)
J Org Chem
, vol.63
, pp. 4792-4801
-
-
Gavagan, J.E.1
Fager, S.K.2
Fallon, R.D.3
Folsom, P.W.4
Herkes, F.E.5
Eisenberg, A.6
Hann, E.C.7
Dicosimo, R.8
-
52
-
-
0001093905
-
Biocatalysis in orgainc synthesis: The use of nitrile- And amide-hydrolysing microorganisms
-
Sugai T., Yamazaki T., Yokoyama M., Ohta H. Biocatalysis in orgainc synthesis: the use of nitrile- and amide-hydrolysing microorganisms. Biosci Biotechnol Biochem. 61:1997;1419-1427.
-
(1997)
Biosci Biotechnol Biochem
, vol.61
, pp. 1419-1427
-
-
Sugai, T.1
Yamazaki, T.2
Yokoyama, M.3
Ohta, H.4
-
53
-
-
0032481065
-
Extractive biocatalysis: A powerful tool in selectivity control in yeast biotransformations
-
This paper describes the continuous removal of product (in situ product removal, ISPR) and the benificial effects on the enantioselectivity of Baker's yeast reductions.
-
D'Arrigo P., Fuganti C., Fantoni G.P., Servi S. Extractive biocatalysis: a powerful tool in selectivity control in yeast biotransformations. Tetrahedron. 54:1998;15017-15026. This paper describes the continuous removal of product (in situ product removal, ISPR) and the benificial effects on the enantioselectivity of Baker's yeast reductions.
-
(1998)
Tetrahedron
, vol.54
, pp. 15017-15026
-
-
D'Arrigo, P.1
Fuganti, C.2
Fantoni, G.P.3
Servi, S.4
-
54
-
-
0031450596
-
Enzymatic production of ethyl (R)-4-chloro-3-hydroxybutanoate: Asymmetric reduction of ethyl 4-chloro-3-oxobutanoate by an Escherichia coli transformant expressing the aldehyde reductase gene from yeast
-
Kataoka M., Rohani L.P.S., Yamamoto K., Wada M., Kawabata H., Kita K., Yanase H., Shimizu S. Enzymatic production of ethyl (R)-4-chloro-3-hydroxybutanoate: asymmetric reduction of ethyl 4-chloro-3-oxobutanoate by an Escherichia coli transformant expressing the aldehyde reductase gene from yeast. Appl Microbiol Biotechnol. 48:1997;699-703.
-
(1997)
Appl Microbiol Biotechnol
, vol.48
, pp. 699-703
-
-
Kataoka, M.1
Rohani, L.P.S.2
Yamamoto, K.3
Wada, M.4
Kawabata, H.5
Kita, K.6
Yanase, H.7
Shimizu, S.8
-
55
-
-
0343196685
-
Enzymatic reduction of α-keto acids leading to L-amino acids, D- Or L-hydroxy acids
-
Krix G., Bommarius A.S., Drauz K., Kottenhahn M., Schwarm M., Kula M.-R. Enzymatic reduction of α-keto acids leading to L-amino acids, D- or L-hydroxy acids. J Biotechnol. 53:1997;29-39.
-
(1997)
J Biotechnol
, vol.53
, pp. 29-39
-
-
Krix, G.1
Bommarius, A.S.2
Drauz, K.3
Kottenhahn, M.4
Schwarm, M.5
Kula, M.-R.6
-
56
-
-
0031864423
-
Purification, characterization and immobilization of an NADPH-dependent enzyme involved in the chiral specific reduction of the keto ester M, an intermediate in the synthesis of the anti-astma drug, Montelukast, from Microbacterium campoquemadoensis (MB5614)
-
Shafiee A., Motamedi H., King A. Purification, characterization and immobilization of an NADPH-dependent enzyme involved in the chiral specific reduction of the keto ester M, an intermediate in the synthesis of the anti-astma drug, Montelukast, from Microbacterium campoquemadoensis (MB5614). Appl Microbiol Biotechnol. 49:1998;709-717.
-
(1998)
Appl Microbiol Biotechnol
, vol.49
, pp. 709-717
-
-
Shafiee, A.1
Motamedi, H.2
King, A.3
-
57
-
-
0033017776
-
A new biocatalyst for production of optically pure aryl epoxides by styrene monooxygenase from Pseudomonas fluorescens st
-
Di G.P., Colmegna A., Galli E., Sello G., Pelizzoni F., Bestetti G. A new biocatalyst for production of optically pure aryl epoxides by styrene monooxygenase from Pseudomonas fluorescens st. Appl Env Microbiol. 65:1999;2794-2797.
-
(1999)
Appl Env Microbiol
, vol.65
, pp. 2794-2797
-
-
Di, G.P.1
Colmegna, A.2
Galli, E.3
Sello, G.4
Pelizzoni, F.5
Bestetti, G.6
-
58
-
-
0031745849
-
Towards a biocatalyst for (S)-styrene oxide production: Characterization of the styrene degradation pathway of Pseudomonas sp. strain VLB120
-
Panke S., Witholt B., Schmid A., Wubbolts M.G. Towards a biocatalyst for (S)-styrene oxide production: characterization of the styrene degradation pathway of Pseudomonas sp. strain VLB120. Appl Env Microbiol. 64:1998;2032-2043.
-
(1998)
Appl Env Microbiol
, vol.64
, pp. 2032-2043
-
-
Panke, S.1
Witholt, B.2
Schmid, A.3
Wubbolts, M.G.4
-
59
-
-
0032079788
-
Alkene monooxygenase-catalyzed whole cell epoxidation in a two-liquid phase system
-
Prichanont S., Leak D.J., Stuckey D.C. Alkene monooxygenase-catalyzed whole cell epoxidation in a two-liquid phase system. Enzyme Microb Technol. 22:1998;471-479.
-
(1998)
Enzyme Microb Technol
, vol.22
, pp. 471-479
-
-
Prichanont, S.1
Leak, D.J.2
Stuckey, D.C.3
-
60
-
-
0000265909
-
Biological routes to optically active epoxides
-
A.N. Collins, G.N. Sheldrake, & J. Crosby. Chichester: Wiley
-
Furuhashi K. Biological routes to optically active epoxides. Collins A.N., Sheldrake G.N., Crosby J. Chirality in Industry. 1992;167-186 Wiley, Chichester.
-
(1992)
Chirality in Industry
, pp. 167-186
-
-
Furuhashi, K.1
-
61
-
-
0031731648
-
Novel biosynthetic approaches to the production of unnatural amino acids using transaminases
-
Taylor P.P., Pantaleone D.P., Senkpeil R.F., Fotheringham I.G. Novel biosynthetic approaches to the production of unnatural amino acids using transaminases. Trends Biotechnol. 16:1998;412-418.
-
(1998)
Trends Biotechnol
, vol.16
, pp. 412-418
-
-
Taylor, P.P.1
Pantaleone, D.P.2
Senkpeil, R.F.3
Fotheringham, I.G.4
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