-
1
-
-
84926166921
-
-
(Eds.: S. Riva, W.-D. Fessner), Wiley-VCH, Weinheim
-
Cascade Biocatalysis (Eds.:, S. Riva, W.-D. Fessner,), Wiley-VCH, Weinheim, 2014;
-
(2014)
Cascade Biocatalysis
-
-
-
2
-
-
84889432812
-
-
(Ed.: E. Garcia-Junceda) Wiley-VCH, Weinheim.
-
Multi-Step Enzyme Catalysis (Ed.:, E. Garcia-Junceda,) Wiley-VCH, Weinheim, 2008.
-
(2008)
Multi-Step Enzyme Catalysis
-
-
-
4
-
-
84925355800
-
-
J. Muschiol, C. Peters, N. Oberleitner, M. D. Mihovilovic, U. T. Bornscheuer, F. Rudroff, Chem. Commun. 2015, 51, 5798-5811;
-
(2015)
Chem. Commun.
, vol.51
, pp. 5798-5811
-
-
Muschiol, J.1
Peters, C.2
Oberleitner, N.3
Mihovilovic, M.D.4
Bornscheuer, U.T.5
Rudroff, F.6
-
6
-
-
80052812654
-
-
E. Ricca, B. Brucher, J. H. Schrittwieser, Adv. Synth. Catal. 2011, 353, 2239-2262;
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 2239-2262
-
-
Ricca, E.1
Brucher, B.2
Schrittwieser, J.H.3
-
7
-
-
79953313806
-
-
J. H. Schrittwieser, J. Sattler, V. Resch, F. G. Mutti, W. Kroutil, Curr. Opin. Chem. Biol. 2011, 15, 249-256;
-
(2011)
Curr. Opin. Chem. Biol.
, vol.15
, pp. 249-256
-
-
Schrittwieser, J.H.1
Sattler, J.2
Resch, V.3
Mutti, F.G.4
Kroutil, W.5
-
10
-
-
0034731616
-
-
G. Chotani, T. Dodge, A. Hsu, M. Kumar, R. LaDuca, D. Trimbur, W. Weyler, K. Sanford, Biochim. Biophys. Acta Protein Struct. Mol. Enzymol. 2000, 1543, 434-455;
-
(2000)
Biochim. Biophys. Acta Protein Struct. Mol. Enzymol.
, vol.1543
, pp. 434-455
-
-
Chotani, G.1
Dodge, T.2
Hsu, A.3
Kumar, M.4
LaDuca, R.5
Trimbur, D.6
Weyler, W.7
Sanford, K.8
-
11
-
-
78649716727
-
-
J. Keasling, Science 2010, 330, 1355-1358.
-
(2010)
Science
, vol.330
, pp. 1355-1358
-
-
Keasling, J.1
-
12
-
-
77949881748
-
-
The three most frequently occurring functional groups in chemical products are hydroxy (40%), carboxy (22%), and amino functionalities (16%), see:, in contrast, OH and CO2H groups largely dominate in renewable resources, see
-
The three most frequently occurring functional groups in chemical products are hydroxy (40%), carboxy (22%), and amino functionalities (16%), see:, S. M. Glueck, S. Gümüs, W. M. F. Fabian, K. Faber, Chem. Soc. Rev. 2010, 39, 313-328; in contrast, OH and CO2H groups largely dominate in renewable resources, see:
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 313-328
-
-
Glueck, S.M.1
Gümüs, S.2
Fabian, W.M.F.3
Faber, K.4
-
14
-
-
84879237909
-
-
M. Schrewe, N. Ladkau, B. Bühler, A. Schmid, Adv. Synth. Catal. 2013, 355, 1693-1697.
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 1693-1697
-
-
Schrewe, M.1
Ladkau, N.2
Bühler, B.3
Schmid, A.4
-
16
-
-
84891779078
-
-
R. C. Simon, N. Richter, E. Busto, W. Kroutil, ACS Catal. 2014, 4, 129-143.
-
(2014)
ACS Catal.
, vol.4
, pp. 129-143
-
-
Simon, R.C.1
Richter, N.2
Busto, E.3
Kroutil, W.4
-
17
-
-
37049112388
-
-
For instance, see
-
For instance, see:, R. Grigg, T. R. B. Mitchell, S. Sutthivaiyakit, N. Tongpenyai, J. Chem. Soc. Chem. Commun. 1981, 611-612;
-
(1981)
J. Chem. Soc. Chem. Commun.
, pp. 611-612
-
-
Grigg, R.1
Mitchell, T.R.B.2
Sutthivaiyakit, S.3
Tongpenyai, N.4
-
18
-
-
84859221016
-
-
M. Lafrance, M. Roggen, E. M. Carreira, Angew. Chem. Int. Ed. 2012, 51, 3470-3473;
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 3470-3473
-
-
Lafrance, M.1
Roggen, M.2
Carreira, E.M.3
-
19
-
-
84863184863
-
-
Angew. Chem. 2012, 124, 3527-3530;
-
(2012)
Angew. Chem.
, vol.124
, pp. 3527-3530
-
-
-
20
-
-
79961241685
-
-
S. Imm, S. Bähn, M. Zhang, L. Neubert, H. Neumann, F. Klasovsky, J. Pfeffer, T. Haas, M. Beller, Angew. Chem. Int. Ed. 2011, 50, 7599-7603;
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 7599-7603
-
-
Imm, S.1
Bähn, S.2
Zhang, M.3
Neubert, L.4
Neumann, H.5
Klasovsky, F.6
Pfeffer, J.7
Haas, T.8
Beller, M.9
-
21
-
-
81255209712
-
-
Angew. Chem. 2011, 123, 7741-7745.
-
(2011)
Angew. Chem.
, vol.123
, pp. 7741-7745
-
-
-
22
-
-
84937976089
-
-
M. Pickl, M. Fuchs, S. M. Glueck, K. Faber, Appl. Microbiol. Biotechnol. 2015, 99, 6617- 6642.
-
(2015)
Appl. Microbiol. Biotechnol.
, vol.99
, pp. 6617-6642
-
-
Pickl, M.1
Fuchs, M.2
Glueck, S.M.3
Faber, K.4
-
26
-
-
84863959852
-
-
M. Fuchs, K. Tauber, J. Sattler, H. Lechner, J. Pfeffer, W. Kroutil, K. Faber, RSC Adv. 2012, 2, 6262-6265.
-
(2012)
RSC Adv.
, vol.2
, pp. 6262-6265
-
-
Fuchs, M.1
Tauber, K.2
Sattler, J.3
Lechner, H.4
Pfeffer, J.5
Kroutil, W.6
Faber, K.7
-
27
-
-
28644434509
-
-
W. C. Nierman, A. Pain, M. J. Anderson, J. R. Wortman, H. S. Kim, J. Arroyo, M. Berriman, K. Abe, D. B. Archer, C. Bermejo, et al., Nature 2005, 438, 1151-1156.
-
(2005)
Nature
, vol.438
, pp. 1151-1156
-
-
Nierman, W.C.1
Pain, A.2
Anderson, M.J.3
Wortman, J.R.4
Kim, H.S.5
Arroyo, J.6
Berriman, M.7
Abe, K.8
Archer, D.B.9
Bermejo, C.10
-
28
-
-
34547534084
-
-
U. Kaulmann, K. Smithies, M. E. B. Smith, H. C. Hailes, J. M. Ward, Enzyme Microb. Technol. 2007, 41, 628-637.
-
(2007)
Enzyme Microb. Technol.
, vol.41
, pp. 628-637
-
-
Kaulmann, U.1
Smithies, K.2
Smith, M.E.B.3
Hailes, H.C.4
Ward, J.M.5
-
29
-
-
56449120814
-
-
D. Koszelewski, I. Lavandera, D. Clay, G. M. Guebitz, D. Rozzell, W. Kroutil, Angew. Chem. Int. Ed. 2008, 47, 9337-9340;
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 9337-9340
-
-
Koszelewski, D.1
Lavandera, I.2
Clay, D.3
Guebitz, G.M.4
Rozzell, D.5
Kroutil, W.6
-
30
-
-
62949214480
-
-
Angew. Chem. 2008, 120, 9477-9480.
-
(2008)
Angew. Chem.
, vol.120
, pp. 9477-9480
-
-
-
31
-
-
67650433799
-
-
E. W. Van Hellemond, L. Vermote, W. Koolen, T. Sonke, E. Zandvoort, D. P. H. M. Heuts, D. B. Janssen, M. W. Fraaije, Adv. Synth. Catal. 2009, 351, 1523-1530;
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 1523-1530
-
-
Van Hellemond, E.W.1
Vermote, L.2
Koolen, W.3
Sonke, T.4
Zandvoort, E.5
Heuts, D.P.H.M.6
Janssen, D.B.7
Fraaije, M.W.8
-
32
-
-
74349101264
-
-
P. Ferreira, A. Hernandez-Ortega, B. Herguedas, J. Rencoret, A. Gutierrez, M. J. Martinez, J. Jimenez-Barbero, M. Medina, A. T. Martinez, Biochem. J. 2010, 425, 585-593.
-
(2010)
Biochem. J.
, vol.425
, pp. 585-593
-
-
Ferreira, P.1
Hernandez-Ortega, A.2
Herguedas, B.3
Rencoret, J.4
Gutierrez, A.5
Martinez, M.J.6
Jimenez-Barbero, J.7
Medina, M.8
Martinez, A.T.9
-
33
-
-
84943366234
-
-
The same conversion of the model substrate 1-hexanol (3a) to the corresponding amine (3b) was obtained with ω-TA from Vibrio fluvialis.
-
The same conversion of the model substrate 1-hexanol (3a) to the corresponding amine (3b) was obtained with ω-TA from Vibrio fluvialis.
-
-
-
-
34
-
-
80052819261
-
-
M. Fuchs, M. Schober, J. Pfeffer, W. Kroutil, R. Birner-Gruenberger, K. Faber, Adv. Synth. Catal. 2011, 353, 2354-2358.
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 2354-2358
-
-
Fuchs, M.1
Schober, M.2
Pfeffer, J.3
Kroutil, W.4
Birner-Gruenberger, R.5
Faber, K.6
|