-
1
-
-
0000321692
-
Enzyme-catalyzed processes in organic solvents
-
Zaks, A. and Klibanov, A.M., Enzyme-catalyzed processes in organic solvents, Proc. Natl. Acad. Sci. USA., 82, 3192-3196, 1985.
-
(1985)
Proc. Natl. Acad. Sci. USA.
, vol.82
, pp. 3192-3196
-
-
Zaks, A.1
Klibanov, A.M.2
-
2
-
-
0022724718
-
Enzymes that work in organic solvents
-
Kilbanov, A.M., Enzymes that work in organic solvents, Chemtech, 16, 354-359, 1986.
-
(1986)
Chemtech
, vol.16
, pp. 354-359
-
-
Kilbanov, A.M.1
-
3
-
-
0031104802
-
Why are enzymes less active in organic solvents than in water?
-
Klibanov, A.M., Why are enzymes less active in organic solvents than in water? Trends Biotechnol., 15, 97-101, 1997.
-
(1997)
Trends Biotechnol.
, vol.15
, pp. 97-101
-
-
Klibanov, A.M.1
-
4
-
-
0021170291
-
Biocatalysis in water-organic solvent 2-phase systems
-
Carrea, G., Biocatalysis in water-organic solvent 2-phase systems, Trends Biotechnol., 2, 102-106, 1984.
-
(1984)
Trends Biotechnol.
, vol.2
, pp. 102-106
-
-
Carrea, G.1
-
5
-
-
0023229878
-
Biocatalysis in multiphase reaction mixtures containing organic liquids
-
Halling, P.J., Biocatalysis in multiphase reaction mixtures containing organic liquids, Biotechnol. Adv., 5, 47-84, 1987.
-
(1987)
Biotechnol. Adv.
, vol.5
, pp. 47-84
-
-
Halling, P.J.1
-
6
-
-
0025697029
-
Stereospecific reduction of 3-keto acid-esters by a novel aldehyde reductase of Sporobolomyces salmonicolor in a water organic solvent 2-phasic system
-
Shimizu, S. and Yamada, H., Stereospecific reduction of 3-keto acid-esters by a novel aldehyde reductase of Sporobolomyces salmonicolor in a water organic solvent 2-phasic system, Ann. NY Acad. Sci., 613, 628-632, 1990.
-
(1990)
Ann. NY Acad. Sci.
, vol.613
, pp. 628-632
-
-
Shimizu, S.1
Yamada, H.2
-
7
-
-
0028396938
-
Thermodynamic predictions for biocatalysis in nonconventional media-theory, tests, and recommendations for experimental design and analysis
-
Halling, P.J., Thermodynamic predictions for biocatalysis in nonconventional media-theory, tests, and recommendations for experimental design and analysis, Enzyme Microb. Technol., 16, 178-206, 1994.
-
(1994)
Enzyme Microb. Technol.
, vol.16
, pp. 178-206
-
-
Halling, P.J.1
-
8
-
-
0141990714
-
Experimental and theoretical analysis of phase equilibria in a two-phase system used for biocatalytic esterifications
-
Heinemann, M. et al., Experimental and theoretical analysis of phase equilibria in a two-phase system used for biocatalytic esterifications, Biocatal. Biotrans., 21, 115-121, 2003.
-
(2003)
Biocatal. Biotrans.
, vol.21
, pp. 115-121
-
-
Heinemann, M.1
-
9
-
-
0346597977
-
Preparative enzymatic synthesis in biphasic aqueous-organic system
-
Martinek, K. et al., Preparative enzymatic synthesis in biphasic aqueous-organic system, Bioorganicheskaya Khimiya, 3, 696-702, 1977.
-
(1977)
Bioorganicheskaya Khimiya
, vol.3
, pp. 696-702
-
-
Martinek, K.1
-
10
-
-
0004284780
-
-
Elsevier, Amsterdam
-
Laane, C., Tramper, J., and Lilly, M.D., Biocatalysis in Organic Media, Elsevier, Amsterdam, 1987.
-
(1987)
Biocatalysis in Organic Media
-
-
Laane, C.1
Tramper, J.2
Lilly, M.D.3
-
11
-
-
0030903947
-
Chloroperoxidase-catalyzed oxidations in t-butyl alcohol/water mixtures
-
van Deurzen, M.P.J. et al., Chloroperoxidase-catalyzed oxidations in t-butyl alcohol/water mixtures, J. Mol. Catal. A Chemical, 117, 329-337, 1997.
-
(1997)
J. Mol. Catal. A Chemical
, vol.117
, pp. 329-337
-
-
van Deurzen, M.P.J.1
-
13
-
-
0034691792
-
Room-temperature ionic liquids as replacements for organic solvents in multiphase bioprocess operations
-
Cull, S.G. et al., Room-temperature ionic liquids as replacements for organic solvents in multiphase bioprocess operations, Biotechnol. Bioeng., 69, 227-233, 2000.
-
(2000)
Biotechnol. Bioeng.
, vol.69
, pp. 227-233
-
-
Cull, S.G.1
-
14
-
-
0034524760
-
Enzymatic catalysis of formation of Z-aspartame in ionic liquid-an alternative to enzymatic catalysis in organic solvents
-
Erbeldinger, M., Mesiano, A.J., and Russell, A.J., Enzymatic catalysis of formation of Z-aspartame in ionic liquid-an alternative to enzymatic catalysis in organic solvents, Biotechnol. Prog., 16, 1129-1131, 2000.
-
(2000)
Biotechnol. Prog.
, vol.16
, pp. 1129-1131
-
-
Erbeldinger, M.1
Mesiano, A.J.2
Russell, A.J.3
-
15
-
-
0036899228
-
Enzyme catalysis in ionic liquids
-
Kragl, U., Eckstein, M., and Kaftzik, N., Enzyme catalysis in ionic liquids, Curr. Opin. Biotechnol., 13, 565-571, 2002.
-
(2002)
Curr. Opin. Biotechnol.
, vol.13
, pp. 565-571
-
-
Kragl, U.1
Eckstein, M.2
Kaftzik, N.3
-
16
-
-
0037333337
-
Biocatalytic transformations in ionic liquids
-
van Rantwijk, F., Lau, R.M., and Sheldon, R.A., Biocatalytic transformations in ionic liquids, Trends Biotechnol., 21, 131-138, 2003.
-
(2003)
Trends Biotechnol.
, vol.21
, pp. 131-138
-
-
van Rantwijk, F.1
Lau, R.M.2
Sheldon, R.A.3
-
17
-
-
0003458662
-
-
Pergamon Press, Oxford
-
Wong, C.-H. and Whitesides, G.M., Enzymes in Synthetic Organic Chemistry, Pergamon Press, Oxford, 1994, pp. 12, 370.
-
(1994)
Enzymes in Synthetic Organic Chemistry
-
-
Wong, C.-H.1
Whitesides, G.M.2
-
18
-
-
0025115797
-
Reduction of acetophenone to R(+)-phenylethanol by a new alcohol dehydrogenase from Lactobacillus kefir
-
Hummel, W., Reduction of acetophenone to R(+)-phenylethanol by a new alcohol dehydrogenase from Lactobacillus kefir, Appl. Microbiol. Biotechnol., 34, 15-19, 1990.
-
(1990)
Appl. Microbiol. Biotechnol.
, vol.34
, pp. 15-19
-
-
Hummel, W.1
-
19
-
-
0035888133
-
Immobilized baker’s yeast reduction of ketones in an ionic liquid, [bmim]PF6 and water mix
-
Howarth, J., James, P., and Dai, J.F., Immobilized baker’s yeast reduction of ketones in an ionic liquid, [bmim]PF6 and water mix, Tetrahedron Lett., 42, 7517-7519, 2001.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 7517-7519
-
-
Howarth, J.1
James, P.2
Dai, J.F.3
-
20
-
-
0036899228
-
Enzyme catalysis in ionic liquids
-
Kragl, U., Eckstein, M., and Kaftzik, N., Enzyme catalysis in ionic liquids, Curr. Opin. Biotechnol., 13, 565-571, 2002.
-
(2002)
Curr. Opin. Biotechnol.
, vol.13
, pp. 565-571
-
-
Kragl, U.1
Eckstein, M.2
Kaftzik, N.3
-
21
-
-
0347474982
-
Recent developments in asymmetric reduction of ketones with biocatalysts
-
Nakamura, K. et al., Recent developments in asymmetric reduction of ketones with biocatalysts, Tetrahedron Asymmetry, 14, 2659-2681, 2003.
-
(2003)
Tetrahedron Asymmetry
, vol.14
, pp. 2659-2681
-
-
Nakamura, K.1
-
22
-
-
0033996124
-
Influence of water activity and aqueous solvent ordering on enzyme kinetics of alcohol dehydrogenase, lysozyme, and beta-galactosidase
-
Matsue, S. and Miyawaki, O., Influence of water activity and aqueous solvent ordering on enzyme kinetics of alcohol dehydrogenase, lysozyme, and beta-galactosidase, Enzyme Microb. Technol., 26, 342-347, 2000.
-
(2000)
Enzyme Microb. Technol.
, vol.26
, pp. 342-347
-
-
Matsue, S.1
Miyawaki, O.2
-
23
-
-
0037072990
-
Characteristics of magnetic nanoparticles-bound YADH in water/AOT/isooctane microemulsions
-
Liao, M.H. and Chen, D.H., Characteristics of magnetic nanoparticles-bound YADH in water/AOT/isooctane microemulsions, J. Mol. Catal. B Enzym., 18, 81-87, 2002.
-
(2002)
J. Mol. Catal. B Enzym.
, vol.18
, pp. 81-87
-
-
Liao, M.H.1
Chen, D.H.2
-
24
-
-
0041864254
-
Regioselective reduction of a steroid in a reversed micellar system with enzymatic NADH-regeneration
-
Hirakawa, H. et al., Regioselective reduction of a steroid in a reversed micellar system with enzymatic NADH-regeneration, Biochem. Eng. J., 16, 35-40, 2003.
-
(2003)
Biochem. Eng. J.
, vol.16
, pp. 35-40
-
-
Hirakawa, H.1
-
25
-
-
0037072991
-
Effects of mixed reverse micellar structure on stability and activity of yeast alcohol dehydrogenase
-
Chen, D.H. and Liao, M.H., Effects of mixed reverse micellar structure on stability and activity of yeast alcohol dehydrogenase, J. Mol. Catal. B Enzym., 18, 155-162, 2002.
-
(2002)
J. Mol. Catal. B Enzym.
, vol.18
, pp. 155-162
-
-
Chen, D.H.1
Liao, M.H.2
-
27
-
-
4544219870
-
Is the log P a convenient criterion to guide the choice of solvents for biphasic enzymatic reactions?
-
Villela Filho, M. et al., Is the log P a convenient criterion to guide the choice of solvents for biphasic enzymatic reactions? Angew. Chem. 115, 3101-3104, 2003.
-
(2003)
Angew. Chem.
, vol.115
, pp. 3101-3104
-
-
Villela Filho, M.1
-
28
-
-
85055578702
-
Enzymatische Gasphasenkatalyse zur Produktion chiraler Substanzen
-
Ferloni, C. et al., Enzymatische Gasphasenkatalyse zur Produktion chiraler Substanzen, Biokatalyse (Transkript Sonsderheft), 105-108, 2003.
-
(2003)
Biokatalyse (Transkript Sonsderheft)
, pp. 105-108
-
-
Ferloni, C.1
-
29
-
-
3042585916
-
Recent development in NAD(P)H regeneration for enzymatic reductions in one-and two-phase systems
-
Eckstein, M., Daußmann, T., and Kragl, U., Recent development in NAD(P)H regeneration for enzymatic reductions in one-and two-phase systems, Biocatal. Biotrans., 22, 89-96, 2004.
-
(2004)
Biocatal. Biotrans.
, vol.22
, pp. 89-96
-
-
Eckstein, M.1
Daußmann, T.2
Kragl, U.3
-
30
-
-
39049190841
-
Influence of water-miscible organic solvents on kinetics and enantioselectivity of the (R)-specific alcohol dehydrogenase from Lactobacillus brevis
-
Schumacher, J., Eckstein, M., and Kragl, U., Influence of water-miscible organic solvents on kinetics and enantioselectivity of the (R)-specific alcohol dehydrogenase from Lactobacillus brevis, Biotechnol. J., 1, 574-581, 2006.
-
(2006)
Biotechnol. J.
, vol.1
, pp. 574-581
-
-
Schumacher, J.1
Eckstein, M.2
Kragl, U.3
-
31
-
-
2442646281
-
Use of an ionic liquid in a two-phase system to improve an alcohol dehydrogenase catalysed reduction
-
Eckstein, M. et al., Use of an ionic liquid in a two-phase system to improve an alcohol dehydrogenase catalysed reduction, Chem. Comm., 1084-1085, 2004.
-
(2004)
Chem. Comm.
, pp. 1084-1085
-
-
Eckstein, M.1
-
32
-
-
1842583994
-
Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols
-
Kroutil, W. et al., Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols, Curr. Opin. Chem. Biol., 8, 120-126, 2004.
-
(2004)
Curr. Opin. Chem. Biol.
, vol.8
, pp. 120-126
-
-
Kroutil, W.1
-
33
-
-
85055537579
-
Maximise your equilibrium conversion in biphasic catalysed reactions: How to obtain reliable data for equilibrium constants?
-
press
-
Eckstein, M. et al., Maximise your equilibrium conversion in biphasic catalysed reactions: How to obtain reliable data for equilibrium constants? Adv. Syn. Catal., in press.
-
Adv. Syn. Catal.
-
-
Eckstein, M.1
-
34
-
-
0027300246
-
Repetitive batch as an efficient method for preparative scale enzymic synthesis of 5-azido-neuroaminic acid and 15N-L-glutamic acid
-
Kragl, U. et al., Repetitive batch as an efficient method for preparative scale enzymic synthesis of 5-azido-neuroaminic acid and 15N-L-glutamic acid, Tetrahedron Asymmetry, 4, 1193-1202, 1993.
-
(1993)
Tetrahedron Asymmetry
, vol.4
, pp. 1193-1202
-
-
Kragl, U.1
-
35
-
-
0030312717
-
Cofactor regeneration in biocatalysis in organic media
-
Adlercreutz, P., Cofactor regeneration in biocatalysis in organic media, Biocatal. Biotrans., 14, 1-30, 1996.
-
(1996)
Biocatal. Biotrans.
, vol.14
, pp. 1-30
-
-
Adlercreutz, P.1
-
36
-
-
9944242273
-
Entrapment of the alcohol dehydrogenase from Lactobacillus kefir in polyvinyl alcohol for the synthesis of chiral hydrophobic alcohols in organic solvents
-
De Temino, D.M., Hartmeier, W., and Ansorge-Schumacher, M.B., Entrapment of the alcohol dehydrogenase from Lactobacillus kefir in polyvinyl alcohol for the synthesis of chiral hydrophobic alcohols in organic solvents, Enzyme Microb. Technol., 36, 3-9, 2005.
-
(2005)
Enzyme Microb. Technol.
, vol.36
, pp. 3-9
-
-
De Temino, D.M.1
Hartmeier, W.2
Ansorge-Schumacher, M.B.3
-
37
-
-
2342420355
-
A new, mild cross-linking methodology to prepare cross-linked enzyme aggregates
-
Mateo, C. et al., A new, mild cross-linking methodology to prepare cross-linked enzyme aggregates, Biotechnol. Bioeng., 86, 273-276, 2004.
-
(2004)
Biotechnol. Bioeng.
, vol.86
, pp. 273-276
-
-
Mateo, C.1
-
38
-
-
0025882622
-
Denaturation capacity-a new quantitative criterion for selection of organic-solvents as reaction media in biocatalysis
-
Khmelnitsky, Y.L. et al., Denaturation capacity-a new quantitative criterion for selection of organic-solvents as reaction media in biocatalysis, Eur. J. Biochem. 198, 31-41, 1991.
-
(1991)
Eur. J. Biochem.
, vol.198
, pp. 31-41
-
-
Khmelnitsky, Y.L.1
-
39
-
-
0344983793
-
Enzymatic oxidative polymerization of 4-chloroguaiacol by laccase
-
Tanaka, T. et al., Enzymatic oxidative polymerization of 4-chloroguaiacol by laccase, J. Chem. Eng. Jap., 36, 1101-1106, 2003.
-
(2003)
J. Chem. Eng. Jap.
, vol.36
, pp. 1101-1106
-
-
Tanaka, T.1
-
40
-
-
0346035864
-
Laccase-catalysed synthesis of coupling products of phenolic substrates in different reactors
-
Pilz, R. et al., Laccase-catalysed synthesis of coupling products of phenolic substrates in different reactors, Appl. Microbiol. Biotechnol., 60, 708-712, 2003.
-
(2003)
Appl. Microbiol. Biotechnol.
, vol.60
, pp. 708-712
-
-
Pilz, R.1
-
41
-
-
4644241355
-
Laccase-mediated oxidation of the steroid hormone 17 beta-estradiol in organic solvents
-
Nicotra, S. et al., Laccase-mediated oxidation of the steroid hormone 17 beta-estradiol in organic solvents, Tetrahedron Asymmetry, 15, 2927-2931, 2004.
-
(2004)
Tetrahedron Asymmetry
, vol.15
, pp. 2927-2931
-
-
Nicotra, S.1
-
42
-
-
0015792215
-
The oxidation of steroid hormones by fungal laccase in emulsion of water and organic solvents
-
Lugaro, G., Carrea, G., and Cremonesi, P., The oxidation of steroid hormones by fungal laccase in emulsion of water and organic solvents, Arch. Biochem. Biophys., 159, 1-6, 1973.
-
(1973)
Arch. Biochem. Biophys.
, vol.159
, pp. 1-6
-
-
Lugaro, G.1
Carrea, G.2
Cremonesi, P.3
-
43
-
-
0000499563
-
Integrated biocatalytic synthesis on gramm scale: The highly enantioselective preparation of chiral oxiranes with styrene monooxygenase
-
Schmid, A. et al., Integrated biocatalytic synthesis on gramm scale: the highly enantioselective preparation of chiral oxiranes with styrene monooxygenase, Adv. Synth. Catal., 343, 732-737, 2001.
-
(2001)
Adv. Synth. Catal.
, vol.343
, pp. 732-737
-
-
Schmid, A.1
-
44
-
-
4544324488
-
Coupling of biocatalytic asymmetric epoxidation with NADH regeneration in organic-aqueous emulsions
-
Hofstetter, K. et al., Coupling of biocatalytic asymmetric epoxidation with NADH regeneration in organic-aqueous emulsions, Angew. Chem. Int. Ed., 43, 2163-2166, 2004.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 2163-2166
-
-
Hofstetter, K.1
-
45
-
-
0037023928
-
Use of isolated cyclohexanone monooxygenase from recombinant Escherichia coli as a biocatalyst for Baeyer-Villiger and sulfide oxidations
-
Zambianchi, F. et al., Use of isolated cyclohexanone monooxygenase from recombinant Escherichia coli as a biocatalyst for Baeyer-Villiger and sulfide oxidations, Biotechnol. Bioeng., 78, 489-496, 2002.
-
(2002)
Biotechnol. Bioeng.
, vol.78
, pp. 489-496
-
-
Zambianchi, F.1
-
46
-
-
3042839971
-
Microbiological transformations. 57. Facile and efficient resin-based in situ SFPR preparative-scale synthesis of an enantiopure “unexpected” lactone regioisomer via a Baeyer-Villiger oxidation process
-
Hilker, I. et al., Microbiological transformations. 57. Facile and efficient resin-based in situ SFPR preparative-scale synthesis of an enantiopure “unexpected” lactone regioisomer via a Baeyer-Villiger oxidation process, Org. Lett., 6, 1955-1958, 2004.
-
(2004)
Org. Lett.
, vol.6
, pp. 1955-1958
-
-
Hilker, I.1
-
47
-
-
0029588274
-
Application of a practical biocatalytic reduction to an enantioselective synthesis of the 5H-2,3-benzodiazepine Ly300164
-
Anderson, B.A. et al., Application of a practical biocatalytic reduction to an enantioselective synthesis of the 5H-2,3-benzodiazepine Ly300164, J. Am. Chem. Soc., 117, 12358-12359, 1995.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 12358-12359
-
-
Anderson, B.A.1
-
48
-
-
0031149187
-
Large-scale stereoselective enzymatic ketone reduction with in situ product removal via polymeric adsorbent resins
-
Vicenzi, J.T. et al., Large-scale stereoselective enzymatic ketone reduction with in situ product removal via polymeric adsorbent resins, Enzyme Microb. Technol., 20, 494-499, 1997.
-
(1997)
Enzyme Microb. Technol.
, vol.20
, pp. 494-499
-
-
Vicenzi, J.T.1
-
49
-
-
14644404972
-
Functionalization of the cytochrome P450cam monooxygenase system in the cell-like aqueous compartments of water-in-oil emulsions
-
Michizoe, J. et al., Functionalization of the cytochrome P450cam monooxygenase system in the cell-like aqueous compartments of water-in-oil emulsions, J. Biosci. Bioeng., 99, 12-17, 2005.
-
(2005)
J. Biosci. Bioeng.
, vol.99
, pp. 12-17
-
-
Michizoe, J.1
-
50
-
-
85055515213
-
-
http://www.brenda.uni-koeln.de/.
-
-
-
-
52
-
-
0014962438
-
Effects of salts and organic solvents on activity of citrate synthase
-
Wu, J.Y. and Yang, J.T., Effects of salts and organic solvents on activity of citrate synthase, J. Biol. Chem., 245, 3561, 1970.
-
(1970)
J. Biol. Chem.
, vol.245
, pp. 3561
-
-
Wu, J.Y.1
Yang, J.T.2
-
53
-
-
0018718811
-
Stimulation of glycogen-phosphorylase kinase from rabbit skeletalmuscle by organic-solvents
-
Singh, T.J. and Wang, J.H., Stimulation of glycogen-phosphorylase kinase from rabbit skeletalmuscle by organic-solvents, J. Biol. Chem., 254, 8466-8472, 1979.
-
(1979)
J. Biol. Chem.
, vol.254
, pp. 8466-8472
-
-
Singh, T.J.1
Wang, J.H.2
-
54
-
-
0028953366
-
Myristoyl CoA-Protein N-myristoyltransferase-subcellularlocalization, activation and kinetic-behavior in the presence of organic-solvents
-
Rajala, R.V.S. and Sharma, R.K., Myristoyl CoA-Protein N-myristoyltransferase-subcellularlocalization, activation and kinetic-behavior in the presence of organic-solvents, Biochem. Biophys. Res. Commun., 208, 617-623, 1995.
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.208
, pp. 617-623
-
-
Rajala, R.V.S.1
Sharma, R.K.2
-
55
-
-
77956714255
-
The properties of proteins in nonaqueous solvents
-
Singer, S.J., The properties of proteins in nonaqueous solvents, Adv. Prot. Chem., 17, 1-68, 1962.
-
(1962)
Adv. Prot. Chem.
, vol.17
, pp. 1-68
-
-
Singer, S.J.1
-
56
-
-
0343907783
-
Kinetic resolution of alpha-methylbenzylamine with omegatransaminase screened from soil microorganisms: Application of a biphasic system to overcome product inhibition
-
Shin, J.S. and Kim, B.G., Kinetic resolution of alpha-methylbenzylamine with omegatransaminase screened from soil microorganisms: application of a biphasic system to overcome product inhibition, Biotechnol. Bioeng., 55, 348-358, 1997.
-
(1997)
Biotechnol. Bioeng.
, vol.55
, pp. 348-358
-
-
Shin, J.S.1
Kim, B.G.2
-
57
-
-
0003610122
-
-
Wiley-VCH, Weinheim, Germany
-
Bornscheuer, U.T. and Kazlauskas, R.J., Hydrolases in Organic Synthesis. Regio-and Stereoselective Biotransformations, Wiley-VCH, Weinheim, Germany, 1999.
-
(1999)
Hydrolases in Organic Synthesis. Regio-and Stereoselective Biotransformations
-
-
Bornscheuer, U.T.1
Kazlauskas, R.J.2
-
58
-
-
0031023666
-
‘Interfacial activation’ of lipases: Facts and artifacts
-
Verger, R., ‘Interfacial activation’ of lipases: facts and artifacts, Trends Biotechnol., 15, 32-38, 1997.
-
(1997)
Trends Biotechnol.
, vol.15
, pp. 32-38
-
-
Verger, R.1
-
59
-
-
0032479388
-
Lipases: Interfacial enzymes with attractive applications
-
Schmid, R.D. and Verger, R., Lipases: interfacial enzymes with attractive applications, Angew. Chem. Int. Ed., 37, 1609-1633, 1998.
-
(1998)
Angew. Chem. Int. Ed.
, vol.37
, pp. 1609-1633
-
-
Schmid, R.D.1
Verger, R.2
-
60
-
-
0004717729
-
Enzymatic enantioselective hydrolysis of 2,2-dimethyl-1,3-dioxolane-4-carboxylic esters
-
Pottie, M., Vandereycken, J., and Vandewalle, M., Enzymatic enantioselective hydrolysis of 2,2-dimethyl-1,3-dioxolane-4-carboxylic esters, Tetrahedron Lett., 30, 5319-5322, 1989.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 5319-5322
-
-
Pottie, M.1
Vandereycken, J.2
Vandewalle, M.3
-
61
-
-
0007673575
-
The synthesis of chiral isopropylidene derivatives of 1,2,3-cyclohexanetriols by enzymatic differentiation
-
Dumortier, L., Vandereycken, J., and Vandewalle, M., The synthesis of chiral isopropylidene derivatives of 1,2,3-cyclohexanetriols by enzymatic differentiation, Tetrahedron Lett., 30, 3201-3204, 1989.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 3201-3204
-
-
Dumortier, L.1
Vandereycken, J.2
Vandewalle, M.3
-
62
-
-
37049074383
-
An insight into the enantioselective hydrolyses of cyclic acetates catalyzed by Pseudomonas fluorescens lipase
-
Xie, Z.F. et al., An insight into the enantioselective hydrolyses of cyclic acetates catalyzed by Pseudomonas fluorescens lipase, J. Chem. Soc. Chem. Commun., 966-977, 1988.
-
(1988)
J. Chem. Soc. Chem. Commun.
, pp. 966-977
-
-
Xie, Z.F.1
-
63
-
-
37049072250
-
Enzymatic preparation of tetrahydrofuran derivatives of high optical purity
-
Seemayer, R. and Schneider, M.P., Enzymatic preparation of tetrahydrofuran derivatives of high optical purity, J. Chem. Soc. Perkin 1, 2359-2360, 1990.
-
(1990)
J. Chem. Soc. Perkin
, vol.1
, pp. 2359-2360
-
-
Seemayer, R.1
Schneider, M.P.2
-
64
-
-
0006292058
-
A highly selective ester hydrolase from Pseudomonas sp. for the enzymatic preparation of enantiomerically pure secondary alcohols-chiral auxiliaries in organicsynthesis
-
Laumen, K. and Schneider, M.P., A highly selective ester hydrolase from Pseudomonas sp. for the enzymatic preparation of enantiomerically pure secondary alcohols-chiral auxiliaries in organicsynthesis, J. Chem. Soc. Chem. Commun., 598-600, 1988.
-
(1988)
J. Chem. Soc. Chem. Commun.
, pp. 598-600
-
-
Laumen, K.1
Schneider, M.P.2
-
65
-
-
0025317378
-
Kinetic resolution of 2-substituted esters catalyzed by a lipase ex Pseudomonas fluorescens
-
Kalaritis, P. et al., Kinetic resolution of 2-substituted esters catalyzed by a lipase ex Pseudomonas fluorescens, J. Org. Chem., 55, 812-815, 1990.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 812-815
-
-
Kalaritis, P.1
-
66
-
-
0000595704
-
Lipase-catalyzed asymmetric hydrolysis of esters having remote chiral prochiral centers
-
Hughes, D.L. et al., Lipase-catalyzed asymmetric hydrolysis of esters having remote chiral prochiral centers, J. Org. Chem., 55, 6252-6259, 1990.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 6252-6259
-
-
Hughes, D.L.1
-
67
-
-
0032768087
-
Why did biocatalysis in organic media not take off in the 1930s?
-
Halling, P. and Kvittingen, L., Why did biocatalysis in organic media not take off in the 1930s? Trends Biotechnol., 17, 343-344, 1999.
-
(1999)
Trends Biotechnol.
, vol.17
, pp. 343-344
-
-
Halling, P.1
Kvittingen, L.2
-
68
-
-
0010394430
-
Action of esterase in the presence of organic solvents
-
Sym, E.A., Action of esterase in the presence of organic solvents, Biochem. J., 30, 609-617, 1936.
-
(1936)
Biochem. J.
, vol.30
, pp. 609-617
-
-
Sym, E.A.1
-
69
-
-
0043252897
-
A study of cholesterol esterase in liver and brain
-
Sperry, W.M. and Brand, F.C., A study of cholesterol esterase in liver and brain, J. Biol. Chem., 137, 377-387, 1941.
-
(1941)
J. Biol. Chem.
, vol.137
, pp. 377-387
-
-
Sperry, W.M.1
Brand, F.C.2
-
70
-
-
0021699816
-
Unusual catalytic properties of usual enzymes
-
Cambou, B. and Klibanov, A.M., Unusual catalytic properties of usual enzymes, Ann. NY Acad Sci., 434, 219-223, 1984.
-
(1984)
Ann. NY Acad Sci.
, vol.434
, pp. 219-223
-
-
Cambou, B.1
Klibanov, A.M.2
-
71
-
-
0001627220
-
Pheromone synthesis. 101. Synthesis and bioactivity of optically active forms of 1-methyl-2-cyclohexen-1-ol, an aggregation pheromone Dendroctonus-pseudotsugae
-
Mori, K. et al., Pheromone synthesis. 101. Synthesis and bioactivity of optically active forms of 1-methyl-2-cyclohexen-1-ol, an aggregation pheromone Dendroctonus-pseudotsugae, Tetrahedron, 43, 2249-2254, 1987.
-
(1987)
Tetrahedron
, vol.43
, pp. 2249-2254
-
-
Mori, K.1
-
72
-
-
0025731655
-
A convenient synthesis of both enantiomers of seudenol and their conversion to 1-methyl-2-cyclohexen-1-ol (Mcol)
-
Johnston, B.D. et al., A convenient synthesis of both enantiomers of seudenol and their conversion to 1-methyl-2-cyclohexen-1-ol (Mcol), Tetrahedron Asymmetry, 2, 377-380, 1991.
-
(1991)
Tetrahedron Asymmetry
, vol.2
, pp. 377-380
-
-
Johnston, B.D.1
-
74
-
-
85055567161
-
Mehods for linking enzymes to insoluble carriers
-
Brandenberg, H., Mehods for linking enzymes to insoluble carriers, Angew. Chem. Int. Ed., 67, 244-246, 1955.
-
(1955)
Angew. Chem. Int. Ed.
, vol.67
, pp. 244-246
-
-
Brandenberg, H.1
-
75
-
-
0030378699
-
Characterization of hydrophobic sol-gel materials containing entrapped lipases
-
Reetz, M.T. et al., Characterization of hydrophobic sol-gel materials containing entrapped lipases, J. Sol-Gel Sci. Technol., 7, 35-43, 1996.
-
(1996)
J. Sol-Gel Sci. Technol.
, vol.7
, pp. 35-43
-
-
Reetz, M.T.1
-
76
-
-
27644480388
-
Generation of lipase-containing static emulsions in silicone spheres for synthesis in organic media
-
Buthe, A. et al., Generation of lipase-containing static emulsions in silicone spheres for synthesis in organic media, J. Mol. Catal. B Enzym., 35, 93-99, 2005.
-
(2005)
J. Mol. Catal. B Enzym.
, vol.35
, pp. 93-99
-
-
Buthe, A.1
-
77
-
-
17444396305
-
Immobilization of surfactant-lipase complexes and their high heat resistance in organic media
-
Goto, M., Hatanaka, C., and Goto, M., Immobilization of surfactant-lipase complexes and their high heat resistance in organic media, Biochem. Eng. J., 24, 91-94, 2005.
-
(2005)
Biochem. Eng. J.
, vol.24
, pp. 91-94
-
-
Goto, M.1
Hatanaka, C.2
Goto, M.3
-
78
-
-
0036843441
-
Modulation of the enantioselectivity of lipases via controlled immobilization and medium engineering: Hydrolytic resolution of mandelic acid esters
-
Palomo, J.M. et al., Modulation of the enantioselectivity of lipases via controlled immobilization and medium engineering: hydrolytic resolution of mandelic acid esters, Enzyme Microb. Technol., 31, 775-783, 2002.
-
(2002)
Enzyme Microb. Technol.
, vol.31
, pp. 775-783
-
-
Palomo, J.M.1
-
79
-
-
2942517661
-
Immobilization of cross-linked lipase aggregates within microporous polymeric membranes
-
Hilal, N., Nigmatullin, R., and Alpatova, A., Immobilization of cross-linked lipase aggregates within microporous polymeric membranes, J. Membrane Sci., 238, 131-141, 2004.
-
(2004)
J. Membrane Sci.
, vol.238
, pp. 131-141
-
-
Hilal, N.1
Nigmatullin, R.2
Alpatova, A.3
-
80
-
-
0000034575
-
Ionic liquids: New “solutions” for transition metal catalysis
-
Wasserscheid, P. and Keim, W., Ionic liquids: new “solutions” for transition metal catalysis, Angew. Chem. Int. Ed., 39, 3773-3789, 2000.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 3773-3789
-
-
Wasserscheid, P.1
Keim, W.2
-
81
-
-
0347417134
-
Room-temperature ionic liquids: Solvents for synthesis and catalysis
-
Welton, T., Room-temperature ionic liquids: solvents for synthesis and catalysis, Chem. Rev., 99, 2071-2083, 1999.
-
(1999)
Chem. Rev.
, vol.99
, pp. 2071-2083
-
-
Welton, T.1
-
82
-
-
0031127122
-
Ionic liquids for clean technology
-
Seddon, K.R., Ionic liquids for clean technology, J. Chem. Technol. Biotechnol., 68, 351-356, 1997.
-
(1997)
J. Chem. Technol. Biotechnol.
, vol.68
, pp. 351-356
-
-
Seddon, K.R.1
-
83
-
-
0034727946
-
Lipase-catalyzed reactions in ionic liquids
-
Lau, R.M. et al., Lipase-catalyzed reactions in ionic liquids, Org. Lett., 2, 4189-4191, 2000.
-
(2000)
Org. Lett.
, vol.2
, pp. 4189-4191
-
-
Lau, R.M.1
-
84
-
-
0035819970
-
Enzyme catalysis in ionic liquids: Lipase catalysed kinetic resolution of 1-phenylethanol with improved enantioselectivity
-
Schofer, S.H. et al., Enzyme catalysis in ionic liquids: lipase catalysed kinetic resolution of 1-phenylethanol with improved enantioselectivity, Chem. Commun., 425-426, 2001.
-
(2001)
Chem. Commun.
, pp. 425-426
-
-
Schofer, S.H.1
-
85
-
-
0036003112
-
Efficient lipase-catalyzed enantioselective acylation under reduced pressure conditions in an ionic liquid solvent system
-
Itoh, T., Akasaki, E., and Nishimura, Y., Efficient lipase-catalyzed enantioselective acylation under reduced pressure conditions in an ionic liquid solvent system, Chem. Lett., 154-155, 2002.
-
(2002)
Chem. Lett.
, pp. 154-155
-
-
Itoh, T.1
Akasaki, E.2
Nishimura, Y.3
-
86
-
-
0035861716
-
Improved preparation and use of room-temperature ionic liquids in lipase-catalyzed enantio-and regioselective acylations
-
Park, S. and Kazlauskas, R.J., Improved preparation and use of room-temperature ionic liquids in lipase-catalyzed enantio-and regioselective acylations, J. Org. Chem., 66, 8395-8401, 2001.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 8395-8401
-
-
Park, S.1
Kazlauskas, R.J.2
-
87
-
-
0026710269
-
Surfactant interference on lipase-catalyzed reactions in microemulsions
-
Skagerlind, P., Jansson, M., and Hult, K., Surfactant interference on lipase-catalyzed reactions in microemulsions, J. Chem. Technol. Biotechnol., 54, 277-282, 1992.
-
(1992)
J. Chem. Technol. Biotechnol.
, vol.54
, pp. 277-282
-
-
Skagerlind, P.1
Jansson, M.2
Hult, K.3
-
88
-
-
0023655595
-
Interesterification and synthesis by Candida cylindracea lipase in microemulsions
-
Bello, M., Thomas, D., and Legoy, M.D., Interesterification and synthesis by Candida cylindracea lipase in microemulsions, Biochem. Biophys. Res. Commun., 146, 361-367, 1987.
-
(1987)
Biochem. Biophys. Res. Commun.
, vol.146
, pp. 361-367
-
-
Bello, M.1
Thomas, D.2
Legoy, M.D.3
-
89
-
-
0027201601
-
Enantioselective synthesis of ibuprofen esters in AOT isooctane microemulsions by Candida cylindracea lipase
-
Hedstrom, G., Backlund, M., and Slotte, J.P., Enantioselective synthesis of ibuprofen esters in AOT isooctane microemulsions by Candida cylindracea lipase, Biotechnol. Bioeng., 42, 618-624, 1993.
-
(1993)
Biotechnol. Bioeng.
, vol.42
, pp. 618-624
-
-
Hedstrom, G.1
Backlund, M.2
Slotte, J.P.3
-
90
-
-
11044231158
-
Non-aqueous biocatalysis in heterogeneous solvent systems
-
Krieger, N. et al., Non-aqueous biocatalysis in heterogeneous solvent systems, Food Technol. Biotechnol., 42, 279-286, 2004.
-
(2004)
Food Technol. Biotechnol.
, vol.42
, pp. 279-286
-
-
Krieger, N.1
-
91
-
-
84953470833
-
Lipase activity and stability in supercritical carbon-dioxide
-
Nakamura, K. et al., Lipase activity and stability in supercritical carbon-dioxide, Chem. Eng. Commun., 45, 207-212, 1986.
-
(1986)
Chem. Eng. Commun.
, vol.45
, pp. 207-212
-
-
Nakamura, K.1
-
92
-
-
0346333493
-
Continuous flow enzymatic kinetic resolution and enantiomer separation using ionic liquid/supercritical carbon dioxide media
-
Reetz, M.T. et al., Continuous flow enzymatic kinetic resolution and enantiomer separation using ionic liquid/supercritical carbon dioxide media, Adv. Synth. Catal., 345, 1221-1228, 2003.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 1221-1228
-
-
Reetz, M.T.1
-
93
-
-
0037035334
-
Continuous green biocatalytic processes using ionic liquids and supercritical carbon dioxide
-
Lozano, P. et al., Continuous green biocatalytic processes using ionic liquids and supercritical carbon dioxide, Chem. Commun., 692-693, 2002.
-
(2002)
Chem. Commun.
, pp. 692-693
-
-
Lozano, P.1
-
94
-
-
0037035632
-
Biocatalysis in ionic liquids: Batchwise and continuous flow processes using supercritical carbon dioxide as the mobile phase
-
Reetz, M.T. et al., Biocatalysis in ionic liquids: batchwise and continuous flow processes using supercritical carbon dioxide as the mobile phase, Chem. Commun., 992-993, 2002.
-
(2002)
Chem. Commun.
, pp. 992-993
-
-
Reetz, M.T.1
-
95
-
-
0002203126
-
Chiral synthons by ester hydrolysis catalysed by pig liver esterase
-
Ohno, M. and Otsuka, M., Chiral synthons by ester hydrolysis catalysed by pig liver esterase, Org. React., 37, 1-55, 1990.
-
(1990)
Org. React.
, vol.37
, pp. 1-55
-
-
Ohno, M.1
Otsuka, M.2
-
96
-
-
0027138526
-
Selectivity-enhancement of hydrolase reactions
-
Faber, K., Ottolina, G., and Riva, S., Selectivity-enhancement of hydrolase reactions, Biocatalysis, 8, 91-132, 1993.
-
(1993)
Biocatalysis
, vol.8
, pp. 91-132
-
-
Faber, K.1
Ottolina, G.2
Riva, S.3
-
97
-
-
0031566715
-
Activity enhancement of pig liver esterase in organic solvents by colyophilization with methoxypolyethylene glycol: Kinetic resolution of alcohols
-
Ruppert, S. and Gais, H.J., Activity enhancement of pig liver esterase in organic solvents by colyophilization with methoxypolyethylene glycol: kinetic resolution of alcohols, Tetrahedron Asymmetry, 8, 3657-3664, 1997.
-
(1997)
Tetrahedron Asymmetry
, vol.8
, pp. 3657-3664
-
-
Ruppert, S.1
Gais, H.J.2
-
98
-
-
84918123834
-
A study of stereoselective hydrolysis of symmetrical diesters with pig-liver esterase
-
Mohr, P. et al., A study of stereoselective hydrolysis of symmetrical diesters with pig-liver esterase, Helv. Chim. Acta, 66, 2501-2511, 1983.
-
(1983)
Helv. Chim. Acta
, vol.66
, pp. 2501-2511
-
-
Mohr, P.1
-
99
-
-
84985544969
-
Hydrolytic enzymes in organic-synthesis. 3. Enzymatic syntheses of chiral building-blocks from prochiral meso-substrates preparation of methyl(hydrogen)-1,2-cycloalkanedicarboxylates
-
Schneider, M. et al., Hydrolytic enzymes in organic-synthesis. 3. Enzymatic syntheses of chiral building-blocks from prochiral meso-substrates preparation of methyl(hydrogen)-1,2-cycloalkanedicarboxylates, Angew. Chem. Int. Ed. Engl., 23, 67-68, 1984.
-
(1984)
Angew. Chem. Int. Ed. Engl.
, vol.23
, pp. 67-68
-
-
Schneider, M.1
-
100
-
-
0032104242
-
Alkaline proteases: A review
-
Anwar, A. and Saleemuddin, M., Alkaline proteases: a review, Bioresour. Technol., 64, 175-183, 1998.
-
(1998)
Bioresour. Technol.
, vol.64
, pp. 175-183
-
-
Anwar, A.1
Saleemuddin, M.2
-
101
-
-
0036323668
-
Bacterial alkaline proteases: Molecular approaches and industrial applications
-
Gupta, R., Beg, Q.K., and Lorenz, P., Bacterial alkaline proteases: molecular approaches and industrial applications, Appl. Microbiol. Biotechnol., 59, 15-32, 2002.
-
(2002)
Appl. Microbiol. Biotechnol.
, vol.59
, pp. 15-32
-
-
Gupta, R.1
Beg, Q.K.2
Lorenz, P.3
-
102
-
-
49249152719
-
Thermolysin-catalyzed condensation-reactions of N-substituted aspartic and glutamic acids with phenylalanine alkyl esters
-
Isowa, Y. et al., Thermolysin-catalyzed condensation-reactions of N-substituted aspartic and glutamic acids with phenylalanine alkyl esters, Tetrahedron Lett., 28, 2611-2612, 1979.
-
(1979)
Tetrahedron Lett.
, vol.28
, pp. 2611-2612
-
-
Isowa, Y.1
-
103
-
-
0002071155
-
Industrial Production of Aspartame
-
Wiley, Chichester
-
Oyama, K., Industrial Production of Aspartame, in: Chirality in Industry, Wiley, Chichester, 1992, pp. 237-247.
-
(1992)
Chirality in Industry
, pp. 237-247
-
-
Oyama, K.1
-
104
-
-
0034403231
-
Industrial biocatalysis: Past, present, and future
-
Wandrey, C., Liese, A., and Kihumbu, D., Industrial biocatalysis: past, present, and future, Org. Proc. Res. Dev., 4, 286-290, 2000.
-
(2000)
Org. Proc. Res. Dev.
, vol.4
, pp. 286-290
-
-
Wandrey, C.1
Liese, A.2
Kihumbu, D.3
-
105
-
-
0142183584
-
Comprehensive step-by-step engineering of an (R)-hydroxynitrile lyase for largescale asymmetric synthesis
-
Glieder, A. et al., Comprehensive step-by-step engineering of an (R)-hydroxynitrile lyase for largescale asymmetric synthesis, Angew. Chem. Int. Ed., 42, 4815-4818, 2003.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 4815-4818
-
-
Glieder, A.1
-
106
-
-
0027378489
-
The superiority of the 3rd-generation catalyst, Rhodococcus rhodochrous J1 nitrile hydratase, for industrial-production of acrylamide
-
Nagasawa, T., Shimizu, H., and Yamada, H., The superiority of the 3rd-generation catalyst, Rhodococcus rhodochrous J1 nitrile hydratase, for industrial-production of acrylamide, Appl. Microbiol. Biotechnol., 40, 189-195, 1993.
-
(1993)
Appl. Microbiol. Biotechnol.
, vol.40
, pp. 189-195
-
-
Nagasawa, T.1
Shimizu, H.2
Yamada, H.3
-
107
-
-
85007863317
-
Screening, isolation and taxonomical properties of microorganisms having acrylonitrile-hydrating activity
-
Watanabe, I., Satoh, Y., and Enomoto, K., Screening, isolation and taxonomical properties of microorganisms having acrylonitrile-hydrating activity, Agric. Biol. Chem., 51, 3193-3199, 1987.
-
(1987)
Agric. Biol. Chem.
, vol.51
, pp. 3193-3199
-
-
Watanabe, I.1
Satoh, Y.2
Enomoto, K.3
-
108
-
-
85007862588
-
Optimal conditions for cultivation of Rhodocossus sp. N-774 and for conversion of acrylonitrile to acrylamide by resting cells
-
Watanabe, I. et al., Optimal conditions for cultivation of Rhodocossus sp. N-774 and for conversion of acrylonitrile to acrylamide by resting cells, Agric. Biol. Chem., 51, 3201-3206, 1987.
-
(1987)
Agric. Biol. Chem.
, vol.51
, pp. 3201-3206
-
-
Watanabe, I.1
-
109
-
-
0041692758
-
Synthetic applications of nitrile-converting enzymes
-
Martinkova, L. and Mylerova, V., Synthetic applications of nitrile-converting enzymes, Curr. Org. Chem., 7, 1279-1295, 2003.
-
(2003)
Curr. Org. Chem.
, vol.7
, pp. 1279-1295
-
-
Martinkova, L.1
Mylerova, V.2
-
110
-
-
0031942411
-
Enzymatic nitrile hydrolysis in low water systems
-
Layh, N. and Willetts, A., Enzymatic nitrile hydrolysis in low water systems, Biotechnol. Lett., 20, 329-331, 1998.
-
(1998)
Biotechnol. Lett.
, vol.20
, pp. 329-331
-
-
Layh, N.1
Willetts, A.2
-
111
-
-
0033524351
-
Kinetic studies on the enzyme (S)-hydroxynitrile lyase from Hevea brasiliensis using initial rate methods and progress curve analysis
-
Bauer, M., Griengl, H., and Steiner, W., Kinetic studies on the enzyme (S)-hydroxynitrile lyase from Hevea brasiliensis using initial rate methods and progress curve analysis, Biotechnol. Bioeng., 62, 20-29, 1999.
-
(1999)
Biotechnol. Bioeng.
, vol.62
, pp. 20-29
-
-
Bauer, M.1
Griengl, H.2
Steiner, W.3
-
112
-
-
12444254611
-
Enzymatic hydrolysis of cyanohydrins with recombinant nitrile hydratase and amidase from Rhodococcus erythropolis
-
Reisinger, C. et al., Enzymatic hydrolysis of cyanohydrins with recombinant nitrile hydratase and amidase from Rhodococcus erythropolis, Biotechnol. Lett., 26, 1675-1680, 2004.
-
(2004)
Biotechnol. Lett.
, vol.26
, pp. 1675-1680
-
-
Reisinger, C.1
-
113
-
-
19744366251
-
Green solvents for sustainable organic synthesis: State of the art
-
Sheldon, R.A., Green solvents for sustainable organic synthesis: state of the art, Green Chem., 7, 267-278, 2005.
-
(2005)
Green Chem.
, vol.7
, pp. 267-278
-
-
Sheldon, R.A.1
-
114
-
-
11044237901
-
Hydroxynitrile lyases: Biological sources and application as biocatalysts
-
Fechter, M.H. and Griengl, H., Hydroxynitrile lyases: biological sources and application as biocatalysts, Food Technol. Biotechnol., 42, 287-294, 2004.
-
(2004)
Food Technol. Biotechnol.
, vol.42
, pp. 287-294
-
-
Fechter, M.H.1
Griengl, H.2
-
116
-
-
0030441331
-
Hydroxynitrile lyases: Functions and properties
-
Hickel, A., Hasslacher, M., and Griengl, H., Hydroxynitrile lyases: functions and properties, Physiol. Plant., 98, 891-898, 1996.
-
(1996)
Physiol. Plant.
, vol.98
, pp. 891-898
-
-
Hickel, A.1
Hasslacher, M.2
Griengl, H.3
-
117
-
-
0342656559
-
A convenient synthesis of optically active 5,5-disubstituted 4-amino-and 4-hydroxy-2(5H)-furanones from (S)-ketone cyanohydrins
-
Buhler, H., Bayer, A., and Effenberger, F., A convenient synthesis of optically active 5,5-disubstituted 4-amino-and 4-hydroxy-2(5H)-furanones from (S)-ketone cyanohydrins, Chem. Eur. J., 6, 2564-2571, 2000.
-
(2000)
Chem. Eur. J.
, vol.6
, pp. 2564-2571
-
-
Buhler, H.1
Bayer, A.2
Effenberger, F.3
-
118
-
-
0037416489
-
Substrate specificity of mutants of the hydroxynitrile lyase from Manihot esculenta
-
Buhler, H. et al., Substrate specificity of mutants of the hydroxynitrile lyase from Manihot esculenta, ChemBioChem, 4, 211-216, 2003.
-
(2003)
ChemBioChem
, vol.4
, pp. 211-216
-
-
Buhler, H.1
-
119
-
-
21044452029
-
Inversion of stereoselectivity by applying mutants of the hydroxynitrile lyase from Manihot esculenta
-
Buhler, H., Miehlich, B., and Effenberger, F., Inversion of stereoselectivity by applying mutants of the hydroxynitrile lyase from Manihot esculenta, ChemBioChem, 6, 711-717, 2005.
-
(2005)
ChemBioChem
, vol.6
, pp. 711-717
-
-
Buhler, H.1
Miehlich, B.2
Effenberger, F.3
-
121
-
-
0032569785
-
Enzyme catalysed formation of (S)-cyanohydrins derived from aldehydes and ketones in a biphasic solvent system
-
Griengl, H. et al., Enzyme catalysed formation of (S)-cyanohydrins derived from aldehydes and ketones in a biphasic solvent system, Tetrahedron, 54, 14477-14486, 1998.
-
(1998)
Tetrahedron
, vol.54
, pp. 14477-14486
-
-
Griengl, H.1
-
122
-
-
29144442307
-
Hydroxynitrile lyase catalysis in ionic liquid-containing systems
-
Lou, W.Y., Xu, R., and Zong, M.H., Hydroxynitrile lyase catalysis in ionic liquid-containing systems, Biotechnol. Lett., 27, 1387-1390, 2005.
-
(2005)
Biotechnol. Lett.
, vol.27
, pp. 1387-1390
-
-
Lou, W.Y.1
Xu, R.2
Zong, M.H.3
-
123
-
-
0033589825
-
Hydroxynitrile lyase at the diisopropyl ether/water interface: Evidence for interfacial enzyme activity
-
Hickel, A., Radke, C.J., and Blanch, H.W., Hydroxynitrile lyase at the diisopropyl ether/water interface: evidence for interfacial enzyme activity, Biotechnol. Bioeng., 65, 425-436, 1999.
-
(1999)
Biotechnol. Bioeng.
, vol.65
, pp. 425-436
-
-
Hickel, A.1
Radke, C.J.2
Blanch, H.W.3
-
124
-
-
0031051520
-
Molecular cloning of acetone cyanohydrin lyase from flax (Linum usitatissimum): Definition of a novel class of hydroxynitrile lyases
-
Trummler, K. and Wajant, H., Molecular cloning of acetone cyanohydrin lyase from flax (Linum usitatissimum): definition of a novel class of hydroxynitrile lyases, J. Biol. Chem., 272, 4770-4774, 1997.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 4770-4774
-
-
Trummler, K.1
Wajant, H.2
-
125
-
-
0042862842
-
A single residual replacement improves the folding and stability of recombinant cassava hydroxynitrile lyase in E. coli
-
Yan, G.H. et al., A single residual replacement improves the folding and stability of recombinant cassava hydroxynitrile lyase in E. coli, Biotechnol. Lett., 25, 1041-1047, 2003.
-
(2003)
Biotechnol. Lett.
, vol.25
, pp. 1041-1047
-
-
Yan, G.H.1
-
126
-
-
18044366809
-
A thermostable variant of fructose bisphosphate aldolase constructed by directed evolution also shows increased stability in organic solvents
-
Hao, J.J. and Berry, A., A thermostable variant of fructose bisphosphate aldolase constructed by directed evolution also shows increased stability in organic solvents, Prot. Eng. Des. Sel., 17, 689-697, 2004.
-
(2004)
Prot. Eng. Des. Sel.
, vol.17
, pp. 689-697
-
-
Hao, J.J.1
Berry, A.2
-
127
-
-
3042867053
-
Overproduction, purification, and characterization of heat-stable aldolase from Methanococcus jannaschii, a hyperthermophic archaea
-
Choi, I.G. et al., Overproduction, purification, and characterization of heat-stable aldolase from Methanococcus jannaschii, a hyperthermophic archaea, J. Biochem. Mol. Biol., 31, 130-134, 1998.
-
(1998)
J. Biochem. Mol. Biol.
, vol.31
, pp. 130-134
-
-
Choi, I.G.1
-
128
-
-
0032472314
-
Industrial biotransformations for the production of D-amino acids
-
Yagasaki, M. and Ozaki, A., Industrial biotransformations for the production of D-amino acids, J. Mol. Catal. B Enzym., 4, 1-11, 1998.
-
(1998)
J. Mol. Catal. B Enzym.
, vol.4
, pp. 1-11
-
-
Yagasaki, M.1
Ozaki, A.2
-
129
-
-
0027263160
-
Purification, cloning, and cofactor independence of glutamate racemase from Lactobacillus
-
Gallo, K.A. and Knowles, J.R., Purification, cloning, and cofactor independence of glutamate racemase from Lactobacillus, Biochemistry, 32, 3981-3990, 1993.
-
(1993)
Biochemistry
, vol.32
, pp. 3981-3990
-
-
Gallo, K.A.1
Knowles, J.R.2
-
130
-
-
0027197398
-
A new amino-acid racemase with threonine alpha-epimerase activity from Pseudomonas putida: Purification and characterization
-
Lim, Y.H. et al., A new amino-acid racemase with threonine alpha-epimerase activity from Pseudomonas putida: purification and characterization, J. Bacteriol., 175, 4213-4217, 1993.
-
(1993)
J. Bacteriol.
, vol.175
, pp. 4213-4217
-
-
Lim, Y.H.1
-
131
-
-
26244463618
-
Discovery of amino acid amides as new substrates for alphaamino-epsilon-caprolactam racemase from Achromobacter obae
-
Asano, Y. and Yamaguchi, S., Discovery of amino acid amides as new substrates for alphaamino-epsilon-caprolactam racemase from Achromobacter obae, J. Mol. Catal. B Enzym., 36, 22-29, 2005.
-
(2005)
J. Mol. Catal. B Enzym.
, vol.36
, pp. 22-29
-
-
Asano, Y.1
Yamaguchi, S.2
-
132
-
-
0035501658
-
Substrate spectrum of mandelate racemase-Part 2. (Hetero)-aryl-substituted mandelate derivatives and modulation of activity
-
Felfer, U. et al., Substrate spectrum of mandelate racemase-Part 2. (Hetero)-aryl-substituted mandelate derivatives and modulation of activity, J. Mol. Catal. B Enzym., 15, 213-222, 2001.
-
(2001)
J. Mol. Catal. B Enzym.
, vol.15
, pp. 213-222
-
-
Felfer, U.1
-
133
-
-
0033408470
-
Deracemization of (+/-)-mandelic acid using a lipase-mandelate racemase two-enzyme system
-
Strauss, U.T. and Faber, K., Deracemization of (+/-)-mandelic acid using a lipase-mandelate racemase two-enzyme system, Tetrahedron Asymmetry, 10, 4079-4081, 1999.
-
(1999)
Tetrahedron Asymmetry
, vol.10
, pp. 4079-4081
-
-
Strauss, U.T.1
Faber, K.2
-
134
-
-
1842689186
-
Mandelate racemase activity in ionic liquids: Scopes and limitations
-
Kaftzik, N. et al., Mandelate racemase activity in ionic liquids: scopes and limitations, J. Mol. Catal. A Chem., 214, 107-112, 2004.
-
(2004)
J. Mol. Catal. A Chem.
, vol.214
, pp. 107-112
-
-
Kaftzik, N.1
-
135
-
-
0032560785
-
Enzymatic synthesis of 4-OH-benzoic acid from phenol and CO2: The first example of a biotechnological application of a carboxylase enzyme
-
Aresta, M. et al., Enzymatic synthesis of 4-OH-benzoic acid from phenol and CO2: the first example of a biotechnological application of a carboxylase enzyme, Tetrahedron, 54, 8841-8846, 1998.
-
(1998)
Tetrahedron
, vol.54
, pp. 8841-8846
-
-
Aresta, M.1
-
136
-
-
0016273515
-
DNA ligase: Structure, mechanism, and function
-
Lehman, I.R., DNA ligase: structure, mechanism, and function, Science, 186, 790-797, 1974.
-
(1974)
Science
, vol.186
, pp. 790-797
-
-
Lehman, I.R.1
-
137
-
-
0026693965
-
Mammalian DNA ligases
-
Lindahl, T. and Barnes, D.E., Mammalian DNA ligases, Annu. Rev. Biochem., 61, 251-281, 1992.
-
(1992)
Annu. Rev. Biochem.
, vol.61
, pp. 251-281
-
-
Lindahl, T.1
Barnes, D.E.2
-
138
-
-
1342310505
-
Dimethyl sulfoxide at 2.5% (v/v) alters the structural cooperativity and unfolding mechanism of dimeric bacterial NAD(+) synthetase
-
Yang, Z.R.W. et al., Dimethyl sulfoxide at 2.5% (v/v) alters the structural cooperativity and unfolding mechanism of dimeric bacterial NAD(+) synthetase, Prot. Sci., 13, 830-841, 2004.
-
(2004)
Prot. Sci.
, vol.13
, pp. 830-841
-
-
Yang, Z.R.W.1
-
139
-
-
23944509003
-
Acetyl-coenzyme A carboxylase: Crucial metabolic enzyme and attractive target for drug discovery
-
Tong, L., Acetyl-coenzyme A carboxylase: crucial metabolic enzyme and attractive target for drug discovery, Cell. Mol. Life Sci., 62, 1784-1803, 2005.
-
(2005)
Cell. Mol. Life Sci.
, vol.62
, pp. 1784-1803
-
-
Tong, L.1
-
140
-
-
0032167489
-
Microbial lipases form versatile tools for biotechnology
-
Jaeger, K.E. and Reetz, M.T., Microbial lipases form versatile tools for biotechnology, Trends Biotechnol., 16, 396-403, 1998.
-
(1998)
Trends Biotechnol.
, vol.16
, pp. 396-403
-
-
Jaeger, K.E.1
Reetz, M.T.2
-
141
-
-
0032897271
-
The realm of microbial lipases in biotechnology
-
Pandey, A. et al., The realm of microbial lipases in biotechnology, Biotechnol. Appl. Biochem., 29, 119-131, 1999.
-
(1999)
Biotechnol. Appl. Biochem.
, vol.29
, pp. 119-131
-
-
Pandey, A.1
-
142
-
-
0000717057
-
Solving pitch problems in pulp and paper processes by the use of enzymes or fungi
-
Farrell, R.L., Hata, K., and Wall, M.B., Solving pitch problems in pulp and paper processes by the use of enzymes or fungi, Adv. Biochem. Eng. Biotechnol., 57, 197-212, 1997.
-
(1997)
Adv. Biochem. Eng. Biotechnol.
, vol.57
, pp. 197-212
-
-
Farrell, R.L.1
Hata, K.2
Wall, M.B.3
-
143
-
-
0001638432
-
Chiral discrimination by hydrolytic enzymes in the synthesis of optically pure materials
-
Parmar, V.S. et al., Chiral discrimination by hydrolytic enzymes in the synthesis of optically pure materials, Proc. Ind. Acad. Sci. Chem. Sci., 108, 575-583, 1996.
-
(1996)
Proc. Ind. Acad. Sci. Chem. Sci.
, vol.108
, pp. 575-583
-
-
Parmar, V.S.1
-
144
-
-
85055499117
-
-
VCH, Weinheim, Germany
-
Rehm, H.J., Reed, G., and Stadler, P., Biotransformations I-Water, Organic Solvents and Other Reaction Media, VCH, Weinheim, Germany, 1998, 8a
-
(1998)
Biotransformations I-Water, Organic Solvents and Other Reaction Media
, pp. 8
-
-
Rehm, H.J.1
Reed, G.2
Stadler, P.3
-
145
-
-
0031459209
-
The lipodygenase sensor, a new approach in essential fatty acid determination in foods
-
Shoemaker, M. et al., The lipodygenase sensor, a new approach in essential fatty acid determination in foods, Biosens. Bioelectron., 12, 1089-1099, 1997.
-
(1997)
Biosens. Bioelectron.
, vol.12
, pp. 1089-1099
-
-
Shoemaker, M.1
-
147
-
-
0031017555
-
Enzymatic transesterification of 3,7-dimethyl-4,7-octadien-1-ol using lipases
-
Izumi, T. et al., Enzymatic transesterification of 3,7-dimethyl-4,7-octadien-1-ol using lipases, J. Chem. Technol. Biotechnol., 68, 57-64, 1997.
-
(1997)
J. Chem. Technol. Biotechnol.
, vol.68
, pp. 57-64
-
-
Izumi, T.1
-
148
-
-
0027135561
-
Extracellular and intracellular lipases from a thermophilic Rhizopus oryzae and factors affecting their production
-
Salleh, A.B. et al., Extracellular and intracellular lipases from a thermophilic Rhizopus oryzae and factors affecting their production, Can. J. Microbiol., 39, 978-981, 1993.
-
(1993)
Can. J. Microbiol.
, vol.39
, pp. 978-981
-
-
Salleh, A.B.1
-
149
-
-
0022595964
-
Activation of Rhizopus delemar lipase-catalyzed hydrolysis of tripropionin by DDT and aldrin: Tightly bound pesticide-lipase complexes
-
Kaneki, H. and Tanaka, M., Activation of Rhizopus delemar lipase-catalyzed hydrolysis of tripropionin by DDT and aldrin: tightly bound pesticide-lipase complexes, Eisei Kagaku-Jap. J. Toxicol. Environ. Health, 32, 1-12, 1986.
-
(1986)
Eisei Kagaku-Jap. J. Toxicol. Environ. Health
, vol.32
, pp. 1-12
-
-
Kaneki, H.1
Tanaka, M.2
-
150
-
-
0026356460
-
Esterolytic and lipolytic enzymes in organic-synthesis
-
Boland, W., Frossl, C., and Lorenz, M., Esterolytic and lipolytic enzymes in organic-synthesis, Synth. Stutt., 1049-1072, 1991.
-
(1991)
Synth. Stutt.
, pp. 1049-1072
-
-
Boland, W.1
Frossl, C.2
Lorenz, M.3
-
151
-
-
0001595852
-
Transesterification
-
Otera, J., Transesterification, Chem. Rev., 93, 1449-1470, 1993.
-
(1993)
Chem. Rev.
, vol.93
, pp. 1449-1470
-
-
Otera, J.1
-
152
-
-
0000760617
-
Lipase-supported synthesis of biologically active compounds
-
Theil, F., Lipase-supported synthesis of biologically active compounds, Chem. Rev., 95, 2203-2227, 1995.
-
(1995)
Chem. Rev.
, vol.95
, pp. 2203-2227
-
-
Theil, F.1
-
153
-
-
0024137153
-
Enzymes in the food-processing industry
-
West, S.I., Enzymes in the food-processing industry, Chem. Br., 24, 1220-1222, 1988.
-
(1988)
Chem. Br.
, vol.24
, pp. 1220-1222
-
-
West, S.I.1
-
154
-
-
0032825993
-
Non-conventional hydrolase chemistry: Amide and carbamate bond formation catalyzed by lipases
-
Gotor, V., Non-conventional hydrolase chemistry: amide and carbamate bond formation catalyzed by lipases, Bioorg. Med. Chem., 7, 2189-2197, 1999.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 2189-2197
-
-
Gotor, V.1
-
155
-
-
2342631985
-
Hydrolysis and synthesis reactions catalysed by Thermomyces lanuginosa lipase in the AOT/isooctane reversed micellar system
-
Fernandes, M.L.M. et al., Hydrolysis and synthesis reactions catalysed by Thermomyces lanuginosa lipase in the AOT/isooctane reversed micellar system, J. Mol. Catal. B Enzym., 30, 43-49, 2004.
-
(2004)
J. Mol. Catal. B Enzym.
, vol.30
, pp. 43-49
-
-
Fernandes, M.L.M.1
-
156
-
-
3142740190
-
Effect of the addition of a nonaqueous polar solvent (Glycerol) on enzymatic catalysis in reverse micelles. Hydrolysis of 2-naphthyl acetate by alpha-chymotrypsin
-
Falcone, R.D. et al., Effect of the addition of a nonaqueous polar solvent (Glycerol) on enzymatic catalysis in reverse micelles. Hydrolysis of 2-naphthyl acetate by alpha-chymotrypsin, Langmuir, 20, 5732-5737, 2004.
-
(2004)
Langmuir
, vol.20
, pp. 5732-5737
-
-
Falcone, R.D.1
-
157
-
-
1542358719
-
Solvent condition in triolein hydrolysis by Rhizopus delemar lipase using an AOT reverse micellar system
-
Naoe, K. et al., Solvent condition in triolein hydrolysis by Rhizopus delemar lipase using an AOT reverse micellar system, Biochem. Eng. J., 18, 49-55, 2004.
-
(2004)
Biochem. Eng. J.
, vol.18
, pp. 49-55
-
-
Naoe, K.1
-
158
-
-
0036644157
-
Optimization of ion-paired lipase for non-aqueous media: Acylation of doxorubicin based on surface models of fatty acid esterification
-
Altreuter, D.H., Dordick, J.S., and Clark, D.S., Optimization of ion-paired lipase for non-aqueous media: acylation of doxorubicin based on surface models of fatty acid esterification, Enzyme Microb. Technol., 31, 10-19, 2002.
-
(2002)
Enzyme Microb. Technol.
, vol.31
, pp. 10-19
-
-
Altreuter, D.H.1
Dordick, J.S.2
Clark, D.S.3
-
159
-
-
0035924035
-
Kinetic studies of lipase-catalyzed esterification in water-in-oil microemulsions and the catalytic behavior of immobilized lipase in MBGs
-
Zhou, G.W. et al., Kinetic studies of lipase-catalyzed esterification in water-in-oil microemulsions and the catalytic behavior of immobilized lipase in MBGs, Colloids Surf. A Physicochem. Eng. Aspects, 194, 41-47, 2001.
-
(2001)
Colloids Surf. A Physicochem. Eng. Aspects
, vol.194
, pp. 41-47
-
-
Zhou, G.W.1
-
160
-
-
0036099668
-
Compressed gases as alternative enzymatic-reaction solvents: A short review
-
Knez, Z. and Habulin, M., Compressed gases as alternative enzymatic-reaction solvents: a short review, J. Supercrit. Fluids, 23, 29-42, 2002.
-
(2002)
J. Supercrit. Fluids
, vol.23
, pp. 29-42
-
-
Knez, Z.1
Habulin, M.2
-
161
-
-
1842638620
-
Synthesis of glycidyl esters catalyzed by lipases in ionic liquids and supercritical carbon dioxide
-
Lozano, P. et al., Synthesis of glycidyl esters catalyzed by lipases in ionic liquids and supercritical carbon dioxide, J. Mol. Catal. A Chem., 214, 113-119, 2004.
-
(2004)
J. Mol. Catal. A Chem.
, vol.214
, pp. 113-119
-
-
Lozano, P.1
-
162
-
-
3042811855
-
Synthesis of biodiesel in supercritical fluids
-
Madras, G., Kolluru, C., and Kumar, R., Synthesis of biodiesel in supercritical fluids, Fuel, 83, 2029-2033, 2004.
-
(2004)
Fuel
, vol.83
, pp. 2029-2033
-
-
Madras, G.1
Kolluru, C.2
Kumar, R.3
-
163
-
-
0037790987
-
Lipase-catalysed hydrolysis of blackcurrant oil in supercritical carbon dioxide
-
Sovova, H. and Zarevucka, M., Lipase-catalysed hydrolysis of blackcurrant oil in supercritical carbon dioxide, Chem. Eng. Sci., 58, 2339-2350, 2003.
-
(2003)
Chem. Eng. Sci.
, vol.58
, pp. 2339-2350
-
-
Sovova, H.1
Zarevucka, M.2
-
164
-
-
1642393268
-
Membrane reactor with immobilized Candida antarctica lipase B for ester synthesis in supercritical carbon dioxide
-
Lozano, P. et al., Membrane reactor with immobilized Candida antarctica lipase B for ester synthesis in supercritical carbon dioxide, J. Supercrit. Fluids, 29, 121-128, 2004.
-
(2004)
J. Supercrit. Fluids
, vol.29
, pp. 121-128
-
-
Lozano, P.1
-
165
-
-
0001997457
-
Pig-liver esterase catalyzed hydrolyzes of racemic alpha-substituted alphahydroxy esters
-
Moorlag, H. et al., Pig-liver esterase catalyzed hydrolyzes of racemic alpha-substituted alphahydroxy esters, J. Org. Chem., 55, 5878-5881, 1990.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 5878-5881
-
-
Moorlag, H.1
-
166
-
-
84989410575
-
Geometric selectivity of pig-liver esterase and its application to the separation of fluorinated bicyclic esters
-
Sicsic, S., Leroy, J., and Wakselman, C., Geometric selectivity of pig-liver esterase and its application to the separation of fluorinated bicyclic esters, Synth. Stutt., 155-156, 1987.
-
(1987)
Synth. Stutt.
, pp. 155-156
-
-
Sicsic, S.1
Leroy, J.2
Wakselman, C.3
-
167
-
-
33845377138
-
Use of enzymatic-hydrolysis of dimethyl malates for a short synthesis of tulipalin-b and of its enantiomer
-
Papageorgiou, C. and Benezra, C., Use of enzymatic-hydrolysis of dimethyl malates for a short synthesis of tulipalin-b and of its enantiomer, J. Org. Chem., 50, 1144-1145, 1985.
-
(1985)
J. Org. Chem.
, vol.50
, pp. 1144-1145
-
-
Papageorgiou, C.1
Benezra, C.2
-
168
-
-
14744305021
-
Effiziente Ganzzell-Biotransformation im zweiphasigen System ionische Flüssigkeit Wasser
-
Pfründer Weuster-Botz, H., et al., Effiziente Ganzzell-Biotransformation im zweiphasigen System ionische Flüssigkeit Wasser, Angew. Chem., 116, 4629-4631, 2004.
-
(2004)
Angew. Chem.
, vol.116
, pp. 4629-4631
-
-
Pfründer Weuster-Botz, H.1
|