-
1
-
-
84883471045
-
Industry backs biocatalysis for greener manufacturing
-
Aldridge S. Industry backs biocatalysis for greener manufacturing. Nat Biotechnol 2013, 31:95.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 95
-
-
Aldridge, S.1
-
2
-
-
84895740421
-
Reduction: enantioselective bioreduction of carbon-carbon double bonds
-
Elsevier Science, Oxford
-
Toogood H.S., Mansell D., Gardiner J.M., Scrutton N.S. Reduction: enantioselective bioreduction of carbon-carbon double bonds. Comprehensive Chirality 2011, vol 7:216. Elsevier Science, Oxford.
-
(2011)
Comprehensive Chirality
, vol.7
, pp. 216
-
-
Toogood, H.S.1
Mansell, D.2
Gardiner, J.M.3
Scrutton, N.S.4
-
3
-
-
84887122693
-
Reduction of CC double bonds
-
Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany
-
Bougioukou D.J., Stewart J.D. Reduction of CC double bonds. Enzyme Catalysis in Organic Synthesis 2012, 1111-1163. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany.
-
(2012)
Enzyme Catalysis in Organic Synthesis
, pp. 1111-1163
-
-
Bougioukou, D.J.1
Stewart, J.D.2
-
4
-
-
0035937122
-
Enoate reductases of Clostridia
-
Rohdich F., Wiese A., Feicht R., Simon H., Bacher A. Enoate reductases of Clostridia. J Biol Chem 2001, 276:5779.
-
(2001)
J Biol Chem
, vol.276
, pp. 5779
-
-
Rohdich, F.1
Wiese, A.2
Feicht, R.3
Simon, H.4
Bacher, A.5
-
5
-
-
0018485158
-
Purification and some properties of a hitherto-unknown enzyme reducing the carbon-carbon double bond of α,β-unsaturated carboxylate anions
-
Tischer W., Bader J., Simon H. Purification and some properties of a hitherto-unknown enzyme reducing the carbon-carbon double bond of α,β-unsaturated carboxylate anions. Eur J Biochem 1979, 97:103.
-
(1979)
Eur J Biochem
, vol.97
, pp. 103
-
-
Tischer, W.1
Bader, J.2
Simon, H.3
-
6
-
-
84865794039
-
Nicotinamide-dependent ene reductases as alternative biocatalysts for the reduction of activated alkenes
-
Durchschein K., Wallner S., Macheroux P., Schwab W., Winkler T., Kreis W., Faber K. Nicotinamide-dependent ene reductases as alternative biocatalysts for the reduction of activated alkenes. Eur J Org Chem 2012, 2012:4963.
-
(2012)
Eur J Org Chem
, vol.2012
, pp. 4963
-
-
Durchschein, K.1
Wallner, S.2
Macheroux, P.3
Schwab, W.4
Winkler, T.5
Kreis, W.6
Faber, K.7
-
7
-
-
84874620748
-
Biocatalytic asymmetric alkene reduction: crystal structure and characterization of a double bond reductase from Nicotiana tabacum
-
Mansell D.J., Toogood H.S., Waller J., Hughes J.M.X., Levy C.W., Gardiner J.M., Scrutton N.S. Biocatalytic asymmetric alkene reduction: crystal structure and characterization of a double bond reductase from Nicotiana tabacum. ACS Catal 2013, 3:370.
-
(2013)
ACS Catal
, vol.3
, pp. 370
-
-
Mansell, D.J.1
Toogood, H.S.2
Waller, J.3
Hughes, J.M.X.4
Levy, C.W.5
Gardiner, J.M.6
Scrutton, N.S.7
-
8
-
-
84857540559
-
Biotechnological development of a practical synthesis of ethyl (S)-2-ethoxy-3-(p-methoxyphenyl)propanoate (EEHP): over 100-fold productivity increase from yeast whole cells to recombinant isolated enzymes
-
Bechtold M., Brenna E., Femmer C., Gatti F.G., Panke S., Parmeggiani F., Sacchetti A. Biotechnological development of a practical synthesis of ethyl (S)-2-ethoxy-3-(p-methoxyphenyl)propanoate (EEHP): over 100-fold productivity increase from yeast whole cells to recombinant isolated enzymes. Org Process Res Dev 2012, 16:269.
-
(2012)
Org Process Res Dev
, vol.16
, pp. 269
-
-
Bechtold, M.1
Brenna, E.2
Femmer, C.3
Gatti, F.G.4
Panke, S.5
Parmeggiani, F.6
Sacchetti, A.7
-
9
-
-
84858065745
-
Ene reductase-catalysed synthesis of (R)-profen derivatives
-
Pietruszka J., Schölzel M. Ene reductase-catalysed synthesis of (R)-profen derivatives. Adv Synth Catal 2012, 354:751.
-
(2012)
Adv Synth Catal
, vol.354
, pp. 751
-
-
Pietruszka, J.1
Schölzel, M.2
-
10
-
-
79959624812
-
Chemoenzymatic one-pot synthesis of γ-butyrolactones
-
Korpak M., Pietruszka J. Chemoenzymatic one-pot synthesis of γ-butyrolactones. Adv Synth Catal 2011, 353:1420.
-
(2011)
Adv Synth Catal
, vol.353
, pp. 1420
-
-
Korpak, M.1
Pietruszka, J.2
-
11
-
-
84884196400
-
Unusual reactions mediated by FMN-dependent ene- and nitro-reductases
-
Durchschein K., Hall M., Faber K. Unusual reactions mediated by FMN-dependent ene- and nitro-reductases. Green Chem 2013, 15:1764.
-
(2013)
Green Chem
, vol.15
, pp. 1764
-
-
Durchschein, K.1
Hall, M.2
Faber, K.3
-
12
-
-
84895752343
-
Enoate reductases for reduction of electron deficient alkenes
-
John Wiley & Sons, Ltd., Chichester, UK
-
Hall M., Winkler C.K., Tasnadi G., Faber K., Brenna E., Gatti F.G., Parmeggiani F., Buzzini P., Goretti M., Ponzoni C., Caselli E., et al. Enoate reductases for reduction of electron deficient alkenes. Practical Methods for Biocatalysis and Biotransformations 2012, vol 2. John Wiley & Sons, Ltd., Chichester, UK.
-
(2012)
Practical Methods for Biocatalysis and Biotransformations
, vol.2
-
-
Hall, M.1
Winkler, C.K.2
Tasnadi, G.3
Faber, K.4
Brenna, E.5
Gatti, F.G.6
Parmeggiani, F.7
Buzzini, P.8
Goretti, M.9
Ponzoni, C.10
Caselli, E.11
-
13
-
-
84863891471
-
Stereocontrol strategies in the asymmetric bioreduction of alkenes
-
Oberdorfer G., Gruber K., Faber K., Hall M. Stereocontrol strategies in the asymmetric bioreduction of alkenes. Synlett 2012, 23:1857.
-
(2012)
Synlett
, vol.23
, pp. 1857
-
-
Oberdorfer, G.1
Gruber, K.2
Faber, K.3
Hall, M.4
-
14
-
-
78149436277
-
Biocatalytic reductions and chemical versatility of the Old Yellow Enzyme family of flavoprotein oxidoreductases
-
Toogood H.S., Gardiner J.M., Scrutton N.S. Biocatalytic reductions and chemical versatility of the Old Yellow Enzyme family of flavoprotein oxidoreductases. ChemCatChem 2010, 2:892.
-
(2010)
ChemCatChem
, vol.2
, pp. 892
-
-
Toogood, H.S.1
Gardiner, J.M.2
Scrutton, N.S.3
-
15
-
-
84875513954
-
Comparative characterization of novel ene-reductases from cyanobacteria
-
Fu Y., Castiglione K., Weuster-Botz D. Comparative characterization of novel ene-reductases from cyanobacteria. Biotechnol Bioeng 2013, 110:1293.
-
(2013)
Biotechnol Bioeng
, vol.110
, pp. 1293
-
-
Fu, Y.1
Castiglione, K.2
Weuster-Botz, D.3
-
16
-
-
84870799068
-
A novel ene-reductase from Synechococcus sp., PCC 7942 for the asymmetric reduction of alkenes
-
Fu Y., Hoelsch K., Weuster-Botz D. A novel ene-reductase from Synechococcus sp., PCC 7942 for the asymmetric reduction of alkenes. Process Biochem 2012, 47:1988.
-
(2012)
Process Biochem
, vol.47
, pp. 1988
-
-
Fu, Y.1
Hoelsch, K.2
Weuster-Botz, D.3
-
17
-
-
84860835013
-
Biochemical characterization and substrate profiling of a new NADH-dependent enoate reductase from Lactobacillus casei
-
Gao X., Ren J., Wu Q., Zhu D. Biochemical characterization and substrate profiling of a new NADH-dependent enoate reductase from Lactobacillus casei. Enzyme Microb Technol 2012, 51:26.
-
(2012)
Enzyme Microb Technol
, vol.51
, pp. 26
-
-
Gao, X.1
Ren, J.2
Wu, Q.3
Zhu, D.4
-
18
-
-
84864579521
-
Asymmetric bioreduction of activated alkenes by a novel isolate of Achromobacter species producing enoate reductase
-
Liu Y.-J., Pei X.-Q., Lin H., Gai P., Liu Y.-C., Wu Z.-L. Asymmetric bioreduction of activated alkenes by a novel isolate of Achromobacter species producing enoate reductase. Appl Microbiol Biotechnol 2012, 95:635.
-
(2012)
Appl Microbiol Biotechnol
, vol.95
, pp. 635
-
-
Liu, Y.-J.1
Pei, X.-Q.2
Lin, H.3
Gai, P.4
Liu, Y.-C.5
Wu, Z.-L.6
-
19
-
-
82955233709
-
Enoate reductases from non conventional yeasts: bioconversion, cloning, and functional expression in Saccharomyces cerevisiae
-
Raimondi S., Romano D., Amaretti A., Molinari F., Rossi M. Enoate reductases from non conventional yeasts: bioconversion, cloning, and functional expression in Saccharomyces cerevisiae. J Biotechnol 2011, 156:279.
-
(2011)
J Biotechnol
, vol.156
, pp. 279
-
-
Raimondi, S.1
Romano, D.2
Amaretti, A.3
Molinari, F.4
Rossi, M.5
-
20
-
-
84873096549
-
Pleurotus ostreatus as a source of enoate reductase
-
Skrobiszewski A., Ogórek R., Plaskowska E., Gładkowski W. Pleurotus ostreatus as a source of enoate reductase. Biocatal Agric Biotechnol 2013, 2:26.
-
(2013)
Biocatal Agric Biotechnol
, vol.2
, pp. 26
-
-
Skrobiszewski, A.1
Ogórek, R.2
Plaskowska, E.3
Gładkowski, W.4
-
21
-
-
84895069832
-
An enoate reductase Achr-OYE4 from Achromobacter sp. Ja81: characterization and application in asymmetric bioreduction of CC bonds
-
in press
-
Wang H.-B., Pei X.-Q., Wu Z.-L. An enoate reductase Achr-OYE4 from Achromobacter sp. Ja81: characterization and application in asymmetric bioreduction of CC bonds. Appl Microbiol Biotechnol 2013, in press. 10.1007/s00253-013-4899-5.
-
(2013)
Appl Microbiol Biotechnol
-
-
Wang, H.-B.1
Pei, X.-Q.2
Wu, Z.-L.3
-
22
-
-
0036308448
-
Differential multiplicity of MDR alcohol dehydrogenases: enzyme genes in the human genome versus those in organisms initially studied
-
Nordling E., Persson B., Jörnvall H. Differential multiplicity of MDR alcohol dehydrogenases: enzyme genes in the human genome versus those in organisms initially studied. Cell Mol Life Sci 2002, 59:1070.
-
(2002)
Cell Mol Life Sci
, vol.59
, pp. 1070
-
-
Nordling, E.1
Persson, B.2
Jörnvall, H.3
-
23
-
-
79953142536
-
Cloning and optimizing expression of enoate reductase gene from Clostridium acetobutylicum in Escherichia coli
-
Tong L., Yang L., Qin Z., Jie R., Min W., Qiaqing W., Dunming Z. Cloning and optimizing expression of enoate reductase gene from Clostridium acetobutylicum in Escherichia coli. Chin J Appl Environ Biol 2011, 17:87.
-
(2011)
Chin J Appl Environ Biol
, vol.17
, pp. 87
-
-
Tong, L.1
Yang, L.2
Qin, Z.3
Jie, R.4
Min, W.5
Qiaqing, W.6
Dunming, Z.7
-
24
-
-
84868212387
-
A surprising observation that oxygen can affect the product enantiopurity of an enzyme-catalysed reaction
-
Fryszkowska A., Toogood H.S., Mansell D., Stephens G., Gardiner J.M., Scrutton N.S. A surprising observation that oxygen can affect the product enantiopurity of an enzyme-catalysed reaction. FEBS J 2012, 279:4160.
-
(2012)
FEBS J
, vol.279
, pp. 4160
-
-
Fryszkowska, A.1
Toogood, H.S.2
Mansell, D.3
Stephens, G.4
Gardiner, J.M.5
Scrutton, N.S.6
-
25
-
-
84864625521
-
A substrate-driven approach to determine reactivities of α,β-unsaturated carboxylic esters towards asymmetric bioreduction
-
Tasnádi G., Winkler C.K., Clay D., Sultana N., Fabian W.M.F., Hall M., Ditrich K., Faber K. A substrate-driven approach to determine reactivities of α,β-unsaturated carboxylic esters towards asymmetric bioreduction. Chem Eur J 2012, 18:10362.
-
(2012)
Chem Eur J
, vol.18
, pp. 10362
-
-
Tasnádi, G.1
Winkler, C.K.2
Clay, D.3
Sultana, N.4
Fabian, W.M.F.5
Hall, M.6
Ditrich, K.7
Faber, K.8
-
26
-
-
37049083746
-
Biotransformation of α,β-unsaturated carbonyl compounds: sulfides, sulfoxides, sulfones, nitriles and esters by yeast species: carbonyl group and carbon-carbon double bond reduction
-
Koul S., Crout D.H.G., Errington W., Tax J. Biotransformation of α,β-unsaturated carbonyl compounds: sulfides, sulfoxides, sulfones, nitriles and esters by yeast species: carbonyl group and carbon-carbon double bond reduction. J Chem Soc Perkin Trans 1995, 1:2969.
-
(1995)
J Chem Soc Perkin Trans
, vol.1
, pp. 2969
-
-
Koul, S.1
Crout, D.H.G.2
Errington, W.3
Tax, J.4
-
27
-
-
80052966037
-
Enantioselective CC bond reduction of unsaturated α-chloro esters by old yellow enzymes
-
Brenna E., Fronza G., Fuganti C., Monti D., Parmeggiani F. Enantioselective CC bond reduction of unsaturated α-chloro esters by old yellow enzymes. J Mol Catal B Enzym 2011, 73:17.
-
(2011)
J Mol Catal B Enzym
, vol.73
, pp. 17
-
-
Brenna, E.1
Fronza, G.2
Fuganti, C.3
Monti, D.4
Parmeggiani, F.5
-
28
-
-
84857533719
-
Enoate reductase-mediated preparation of methyl (S)-2-bromobutanoate, a useful key intermediate for the synthesis of chiral active pharmaceutical ingredients
-
Brenna E., Gatti F.G., Manfredi A., Monti D., Parmeggiani F. Enoate reductase-mediated preparation of methyl (S)-2-bromobutanoate, a useful key intermediate for the synthesis of chiral active pharmaceutical ingredients. Org Proc Res Devel 2012, 16:262.
-
(2012)
Org Proc Res Devel
, vol.16
, pp. 262
-
-
Brenna, E.1
Gatti, F.G.2
Manfredi, A.3
Monti, D.4
Parmeggiani, F.5
-
29
-
-
84863960573
-
Reductive dehalogenation of β-haloacrylic ester derivatives mediated by ene-reductases
-
Tasnádi G., Winkler C.K., Clay D., Hall M., Faber K. Reductive dehalogenation of β-haloacrylic ester derivatives mediated by ene-reductases. Catal Sci Technol 2012, 2:1548.
-
(2012)
Catal Sci Technol
, vol.2
, pp. 1548
-
-
Tasnádi, G.1
Winkler, C.K.2
Clay, D.3
Hall, M.4
Faber, K.5
-
30
-
-
84873964850
-
Chemoenzymatic asymmetric synthesis of pregabalin precursors via asymmetric bioreduction of β-cyanoacrylate esters using ene-reductases
-
Winkler C.K., Clay D., Davies S., O'Neill P., McDaid P., Debarge S., Steflik J., Karmilowicz M., Wong J.W., Faber K. Chemoenzymatic asymmetric synthesis of pregabalin precursors via asymmetric bioreduction of β-cyanoacrylate esters using ene-reductases. J Org Chem 2013, 78:1525.
-
(2013)
J Org Chem
, vol.78
, pp. 1525
-
-
Winkler, C.K.1
Clay, D.2
Davies, S.3
O'Neill, P.4
McDaid, P.5
Debarge, S.6
Steflik, J.7
Karmilowicz, M.8
Wong, J.W.9
Faber, K.10
-
31
-
-
84895755827
-
-
Process for the reduction of cinnamaldehyde derivative employing enoate reductases, US Patent US 2012/0301931 A1
-
Hauer B, Stürmer R, Stückler C Process for the reduction of cinnamaldehyde derivative employing enoate reductases, US Patent US 2012/0301931 A1, 2012.
-
(2012)
-
-
Hauer, B.1
Stürmer, R.2
Stückler, C.3
-
32
-
-
79959590674
-
Combination of CC bond formation by Wittig reaction and enzymatic CC bond reduction in a one-pot process in water
-
Kraußer M., Winkler T., Richter N., Dommer S., Fingerhut A., Hummel W., Gröger H. Combination of CC bond formation by Wittig reaction and enzymatic CC bond reduction in a one-pot process in water. ChemCatChem 2011, 3:293.
-
(2011)
ChemCatChem
, vol.3
, pp. 293
-
-
Kraußer, M.1
Winkler, T.2
Richter, N.3
Dommer, S.4
Fingerhut, A.5
Hummel, W.6
Gröger, H.7
-
33
-
-
84864987268
-
A three-enzyme system involving an ene-reductase for generating valuable chiral building blocks
-
Mangan D., Miskelly I., Moody T.S. A three-enzyme system involving an ene-reductase for generating valuable chiral building blocks. Adv Synth Catal 2012, 354:2185.
-
(2012)
Adv Synth Catal
, vol.354
, pp. 2185
-
-
Mangan, D.1
Miskelly, I.2
Moody, T.S.3
-
34
-
-
84856944211
-
Stereochemical outcome of the biocatalysed reduction of activated tetrasubstituted olefins by Old Yellow Enzymes 1-3
-
Brenna E., Gatti F.G., Monti D., Parmeggiani F., Serra S. Stereochemical outcome of the biocatalysed reduction of activated tetrasubstituted olefins by Old Yellow Enzymes 1-3. Adv Synth Catal 2012, 354:105.
-
(2012)
Adv Synth Catal
, vol.354
, pp. 105
-
-
Brenna, E.1
Gatti, F.G.2
Monti, D.3
Parmeggiani, F.4
Serra, S.5
-
35
-
-
79952647597
-
A site-saturated mutagenesis study of pentaerythritol tetranitrate reductase reveals that residues 181 and 184 influence ligand binding, stereochemistry and reactivity
-
Toogood H.S., Fryszkowska A., Hulley M., Sakuma M., Mansell D., Stephens G.M., Gardiner J.M., Scrutton N.S. A site-saturated mutagenesis study of pentaerythritol tetranitrate reductase reveals that residues 181 and 184 influence ligand binding, stereochemistry and reactivity. ChemBioChem 2011, 12:738.
-
(2011)
ChemBioChem
, vol.12
, pp. 738
-
-
Toogood, H.S.1
Fryszkowska, A.2
Hulley, M.3
Sakuma, M.4
Mansell, D.5
Stephens, G.M.6
Gardiner, J.M.7
Scrutton, N.S.8
-
36
-
-
84878104623
-
Electro-enzymatic viologen-mediated substrate reduction using pentaerythritol tetranitrate reductase and a parallel, segmented fluid flow system
-
Fisher K., Mohr S., Mansell D., Goddard N.J., Fielden P.R., Scrutton N.S. Electro-enzymatic viologen-mediated substrate reduction using pentaerythritol tetranitrate reductase and a parallel, segmented fluid flow system. Catal Sci Technol 2013, 3:1505.
-
(2013)
Catal Sci Technol
, vol.3
, pp. 1505
-
-
Fisher, K.1
Mohr, S.2
Mansell, D.3
Goddard, N.J.4
Fielden, P.R.5
Scrutton, N.S.6
-
37
-
-
84874045759
-
Mimicking nature: synthetic nicotinamide cofactors for CC bioreduction using enoate reductases
-
Paul C.E., Gargiulo S., Opperman D.J., Lavandera I., Gotor-Fernández V., Gotor V., Taglieber A., Arends I.W.C.E., Hollmann F. Mimicking nature: synthetic nicotinamide cofactors for CC bioreduction using enoate reductases. Org Lett 2013, 15:180.
-
(2013)
Org Lett
, vol.15
, pp. 180
-
-
Paul, C.E.1
Gargiulo, S.2
Opperman, D.J.3
Lavandera, I.4
Gotor-Fernández, V.5
Gotor, V.6
Taglieber, A.7
Arends, I.W.C.E.8
Hollmann, F.9
-
38
-
-
79954522978
-
A highly efficient ADH-coupled NADH-recycling system for the asymmetric bioreduction of carbon-carbon double bonds using enoate reductases
-
Tauber K., Hall M., Kroutil W., Fabian W.M.F., Faber K., Glueck S.M. A highly efficient ADH-coupled NADH-recycling system for the asymmetric bioreduction of carbon-carbon double bonds using enoate reductases. Biotechnol Bioeng 2011, 108:1462.
-
(2011)
Biotechnol Bioeng
, vol.108
, pp. 1462
-
-
Tauber, K.1
Hall, M.2
Kroutil, W.3
Fabian, W.M.F.4
Faber, K.5
Glueck, S.M.6
-
39
-
-
84886293347
-
Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated CC-bonds using flavin-dependent ene-reductases
-
in press
-
Winkler C.K., Clay D., van Heerden E., Faber K. Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated CC-bonds using flavin-dependent ene-reductases. Biotechnol Bioengin 2013, in press. 10.1002/bit.24981.
-
(2013)
Biotechnol Bioengin
-
-
Winkler, C.K.1
Clay, D.2
van Heerden, E.3
Faber, K.4
-
40
-
-
80053592227
-
Stereopreferences of Old Yellow Enzymes: structure correlations and sequence patterns in enoate reductases
-
Oberdorfer G., Steinkellner G., Stueckler C., Faber K., Gruber K. Stereopreferences of Old Yellow Enzymes: structure correlations and sequence patterns in enoate reductases. ChemCatChem 2011, 3:1562.
-
(2011)
ChemCatChem
, vol.3
, pp. 1562
-
-
Oberdorfer, G.1
Steinkellner, G.2
Stueckler, C.3
Faber, K.4
Gruber, K.5
-
41
-
-
84874216995
-
Revisiting the enantioselective sequence patterns in enoate reductases
-
Classen T., Pietruszka J., Schuback S.M. Revisiting the enantioselective sequence patterns in enoate reductases. ChemCatChem 2012, 5:711.
-
(2012)
ChemCatChem
, vol.5
, pp. 711
-
-
Classen, T.1
Pietruszka, J.2
Schuback, S.M.3
-
42
-
-
84877080894
-
The structure of glycerol trinitrate reductase NerA from Agrobacterium radiobacter reveals the molecular reason for nitro- and ene-reductase activity in OYE homologues
-
Oberdorfer G., Binter A., Wallner S., Durchschein K., Hall M., Faber K., Macheroux P., Gruber K. The structure of glycerol trinitrate reductase NerA from Agrobacterium radiobacter reveals the molecular reason for nitro- and ene-reductase activity in OYE homologues. ChemBioChem 2013, 14:836.
-
(2013)
ChemBioChem
, vol.14
, pp. 836
-
-
Oberdorfer, G.1
Binter, A.2
Wallner, S.3
Durchschein, K.4
Hall, M.5
Faber, K.6
Macheroux, P.7
Gruber, K.8
-
43
-
-
84863655569
-
Structural and catalytic characterization of Pichia stipitis OYE 2.6, a useful biocatalyst for asymmetric alkene reductions
-
Pompeu Y.A., Sullivan B., Walton A.Z., Stewart J.D. Structural and catalytic characterization of Pichia stipitis OYE 2.6, a useful biocatalyst for asymmetric alkene reductions. Adv Synth Catal 2012, 354:1949.
-
(2012)
Adv Synth Catal
, vol.354
, pp. 1949
-
-
Pompeu, Y.A.1
Sullivan, B.2
Walton, A.Z.3
Stewart, J.D.4
-
44
-
-
84868087352
-
Crystal structure determination and mutagenesis analysis of the ene reductase NCR
-
Reich S., Hoeffken H.W., Rosche B., Nestl B.M., Hauer B. Crystal structure determination and mutagenesis analysis of the ene reductase NCR. ChemBioChem 2012, 13:2400.
-
(2012)
ChemBioChem
, vol.13
, pp. 2400
-
-
Reich, S.1
Hoeffken, H.W.2
Rosche, B.3
Nestl, B.M.4
Hauer, B.5
-
45
-
-
84894958761
-
Variations in the stability of NCR ene reductase by rational enzyme loop modulation
-
in press
-
Reich S., Kress N., Nestl B.M., Hauer B. Variations in the stability of NCR ene reductase by rational enzyme loop modulation. J Struct Biol 2013, in press. 10.1016/j.jsb.2013.04.004.
-
(2013)
J Struct Biol
-
-
Reich, S.1
Kress, N.2
Nestl, B.M.3
Hauer, B.4
-
46
-
-
64049109810
-
Biocatalyst identification by anaerobic high-throughput screening of enzyme libraries and anaerobic microorganisms
-
Wiley-VCH, Weinheim
-
Toogood H., Scrutton N.S. Biocatalyst identification by anaerobic high-throughput screening of enzyme libraries and anaerobic microorganisms. Protein Engineering Handbook 2012, vol 3:193. Wiley-VCH, Weinheim.
-
(2012)
Protein Engineering Handbook
, vol.3
, pp. 193
-
-
Toogood, H.1
Scrutton, N.S.2
-
47
-
-
80053287591
-
Active site modifications in pentaerythritol tetranitrate reductase can lead to improved product enantiopurity, decreased by-product formation and altered stereochemical outcome in reactions with α,β-unsaturated nitroolefins
-
Fryszkowska A., Toogood H., Sakuma M., Stephens G.M., Gardiner J.M., Scrutton N.S. Active site modifications in pentaerythritol tetranitrate reductase can lead to improved product enantiopurity, decreased by-product formation and altered stereochemical outcome in reactions with α,β-unsaturated nitroolefins. Catal Sci Technol 2011, 1:948.
-
(2011)
Catal Sci Technol
, vol.1
, pp. 948
-
-
Fryszkowska, A.1
Toogood, H.2
Sakuma, M.3
Stephens, G.M.4
Gardiner, J.M.5
Scrutton, N.S.6
-
48
-
-
84884881164
-
Improved biocatalysts from a synthetic circular permutation library of the flavin-dependent oxidoreductase Old Yellow Enzyme
-
Daugherty A.B., Govindarajan S., Lutz S. Improved biocatalysts from a synthetic circular permutation library of the flavin-dependent oxidoreductase Old Yellow Enzyme. J Am Chem Soc 2013, 135:14425.
-
(2013)
J Am Chem Soc
, vol.135
, pp. 14425
-
-
Daugherty, A.B.1
Govindarajan, S.2
Lutz, S.3
-
49
-
-
71649109063
-
Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases
-
Stueckler C., Reiter T.C., Baudendistel N., Faber K. Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases. Tetrahedron 2010, 66:663.
-
(2010)
Tetrahedron
, vol.66
, pp. 663
-
-
Stueckler, C.1
Reiter, T.C.2
Baudendistel, N.3
Faber, K.4
-
50
-
-
0031149187
-
Large-scale stereoselective enzymatic ketone reduction with in situ product removal via polymeric adsorbent resins
-
Vicenzi J.T., Zmijewski M.J., Reinhard M.R., Landen B.E., Muth W.L., Marler P.G. Large-scale stereoselective enzymatic ketone reduction with in situ product removal via polymeric adsorbent resins. Enzyme Microb Technol 1997, 20:494.
-
(1997)
Enzyme Microb Technol
, vol.20
, pp. 494
-
-
Vicenzi, J.T.1
Zmijewski, M.J.2
Reinhard, M.R.3
Landen, B.E.4
Muth, W.L.5
Marler, P.G.6
|