-
1
-
-
33744933430
-
Environmental biocatalysis: From remediation with enzymes to novel green processes
-
16647150 10.1016/j.tibtech.2006.04.002 1:CAS:528:DC%2BD28XlsFKksbo%3D
-
Alcalde M, Ferrer M, Plou FJ, Ballesteros A (2006) Environmental biocatalysis: from remediation with enzymes to novel green processes. Trends Biotechnol 24:281-287
-
(2006)
Trends Biotechnol
, vol.24
, pp. 281-287
-
-
Alcalde, M.1
Ferrer, M.2
Plou, F.J.3
Ballesteros, A.4
-
2
-
-
0035404556
-
Organization and regulation of meta cleavage pathway gene for toluene and o-xylene derivative degradation in Pseudomonas stutzeri OX1
-
11425758 10.1128/AEM.67.7.3304-3308.2001 1:CAS:528:DC%2BD3MXkvFSms70%3D
-
Arenghi FLD, Berlanda D, Galli E, Sello G, Barbieri P (2001) Organization and regulation of meta cleavage pathway gene for toluene and o-xylene derivative degradation in Pseudomonas stutzeri OX1. Appl Environ Microbiol 67:3304-3308
-
(2001)
Appl Environ Microbiol
, vol.67
, pp. 3304-3308
-
-
Arenghi, F.L.D.1
Berlanda, D.2
Galli, E.3
Sello, G.4
Barbieri, P.5
-
3
-
-
2342602915
-
Bacterial monooxygenase mediated preparation of chiral oxiranes: Study of the effects of substituent nature and position
-
10.1016/j.tetasy.2004.04.005 1:CAS:528:DC%2BD2cXktVeks7Y%3D
-
Bernasconi S, Orsini F, Sello G, Di Gennaro P (2004) Bacterial monooxygenase mediated preparation of chiral oxiranes: study of the effects of substituent nature and position. Tetrahedron Asymmetry 15:1603-1606
-
(2004)
Tetrahedron Asymmetry
, vol.15
, pp. 1603-1606
-
-
Bernasconi, S.1
Orsini, F.2
Sello, G.3
Di Gennaro, P.4
-
4
-
-
33750709966
-
Development of bioconversion processes by biocatalysts based on Pseudomonas oxygenases to produce oxygenated compounds
-
1:CAS:528:DC%2BD2MXjslemtw%3D%3D
-
Bestetti G, Di Gennaro P, Galli E, Bernasconi S, Orsini F, Sello G (2003) Development of bioconversion processes by biocatalysts based on Pseudomonas oxygenases to produce oxygenated compounds. Recent Res Dev Appl Microbiol Biotechnol 1:197-217
-
(2003)
Recent Res Dev Appl Microbiol Biotechnol
, vol.1
, pp. 197-217
-
-
Bestetti, G.1
Di Gennaro, P.2
Galli, E.3
Bernasconi, S.4
Orsini, F.5
Sello, G.6
-
5
-
-
0034026210
-
Metabolic engineering and directed evolution for production of pharmaceuticals
-
10753771 10.1016/S0958-1669(00)00081-1 1:CAS:528:DC%2BD3cXisFyns7s%3D
-
Chartrain M, Salmon PM, Robinson DK, Buckland BC (2000) Metabolic engineering and directed evolution for production of pharmaceuticals. Curr Opin Biotechnol 11:209-214
-
(2000)
Curr Opin Biotechnol
, vol.11
, pp. 209-214
-
-
Chartrain, M.1
Salmon, P.M.2
Robinson, D.K.3
Buckland, B.C.4
-
6
-
-
0027390501
-
q/Ptrp-lac plasmids and trasposons that confer conditional phenotypes
-
10.1016/0378-1119(93)90533-9
-
q/Ptrp-lac plasmids and trasposons that confer conditional phenotypes. Gene 23:17-24
-
(1993)
Gene
, vol.23
, pp. 17-24
-
-
De Lorenzo, V.1
Eltis, L.2
Kessler, B.3
Timmis, K.N.4
-
7
-
-
38049087012
-
Biocatalytic reductions: From lab curiosity to first choice
-
10.1021/ar7001073
-
De Wildeman SMA, Sonke T, Schoemaker HE, May O (2007) Biocatalytic reductions: from lab curiosity to first choice. Chem Res 40:1260-1266
-
(2007)
Chem Res
, vol.40
, pp. 1260-1266
-
-
De Wildeman, S.M.A.1
Sonke, T.2
Schoemaker, H.E.3
May, O.4
-
8
-
-
0030974130
-
Production of substituted naphthalene dihydrodiols by engineered Escherichia coli containing the cloned naphthalene 1,2-dioxygenase gene from Pseudomonas fluorescens N3
-
9765814 10.1016/S0923-2508(97)81591-4 1:STN:280:DyaK1cvjvV2msw%3D%3D
-
Di Gennaro P, Galli E, Albini G, Pelizzoni F, Sello G, Bestetti G (1997) Production of substituted naphthalene dihydrodiols by engineered Escherichia coli containing the cloned naphthalene 1,2-dioxygenase gene from Pseudomonas fluorescens N3. Res Microbiol 148:355-364
-
(1997)
Res Microbiol
, vol.148
, pp. 355-364
-
-
Di Gennaro, P.1
Galli, E.2
Albini, G.3
Pelizzoni, F.4
Sello, G.5
Bestetti, G.6
-
9
-
-
0033017776
-
A new biocatalyst for production of optically pure aryl epoxides by styrene monooxygenase from Pseudomonas fluorescens ST
-
10347083
-
Di Gennaro P, Colmegna A, Galli E, Sello G, Pelizzoni F, Bestetti G (1999) A new biocatalyst for production of optically pure aryl epoxides by styrene monooxygenase from Pseudomonas fluorescens ST. Appl Environ Microbiol 65:2794-2797
-
(1999)
Appl Environ Microbiol
, vol.65
, pp. 2794-2797
-
-
Di Gennaro, P.1
Colmegna, A.2
Galli, E.3
Sello, G.4
Pelizzoni, F.5
Bestetti, G.6
-
10
-
-
0033946313
-
Development of biocatalysts carrying naphthalene dioxygenase and dihydrodiol dehydrogenase genes inducible in aerobic and anaerobic conditions
-
10919518 10.1016/S0923-2508(00)00161-3 1:STN:280:DC%2BD3M%2Fit1ymtQ%3D%3D
-
Di Gennaro P, Galli E, Orsini F, Pelizzoni F, Sello G, Bestetti G (2000) Development of biocatalysts carrying naphthalene dioxygenase and dihydrodiol dehydrogenase genes inducible in aerobic and anaerobic conditions. Res Microbiol 151(5):383-391
-
(2000)
Res Microbiol
, vol.151
, Issue.5
, pp. 383-391
-
-
Di Gennaro, P.1
Galli, E.2
Orsini, F.3
Pelizzoni, F.4
Sello, G.5
Bestetti, G.6
-
11
-
-
44649116398
-
Novel auto-inducing expression systems for the development of whole-cell biocatalysts
-
18465124 10.1007/s00253-008-1460-z 1:CAS:528:DC%2BD1cXmsFKnsrs%3D
-
Di Gennaro P, Ferrara S, Bestetti G, Sello G, Solera D, Galli E, Renzi F, Bertoni G (2008) Novel auto-inducing expression systems for the development of whole-cell biocatalysts. Appl Microbiol Biotechnol 79:617-625
-
(2008)
Appl Microbiol Biotechnol
, vol.79
, pp. 617-625
-
-
Di Gennaro, P.1
Ferrara, S.2
Bestetti, G.3
Sello, G.4
Solera, D.5
Galli, E.6
Renzi, F.7
Bertoni, G.8
-
12
-
-
0033636716
-
Chemical biotechnology. A happy marriage between chemistry and biotechnology: Asymmetric synthesis via green chemistry
-
11102783 10.1016/S0958-1669(00)00157-9 1:CAS:528:DC%2BD3MXisFGn
-
Faber K, Patel R (2000) Chemical biotechnology. A happy marriage between chemistry and biotechnology: asymmetric synthesis via green chemistry. Curr Opin Biotechnol 11:517-551
-
(2000)
Curr Opin Biotechnol
, vol.11
, pp. 517-551
-
-
Faber, K.1
Patel, R.2
-
13
-
-
20544439844
-
The substrate spectrum of mandelate racemase: Minimum structural requirements for substrates and substrate model
-
10.1002/adsc.200505012 1:CAS:528:DC%2BD2MXlsV2gs7s%3D
-
Felfer U, Gorlup M, Koegl MF, Wagner U, Larissegger-Schnell B, Faber K, Kroutil W (2005) The substrate spectrum of mandelate racemase: minimum structural requirements for substrates and substrate model. Adv Synth Catal 347:951-961
-
(2005)
Adv Synth Catal
, vol.347
, pp. 951-961
-
-
Felfer, U.1
Gorlup, M.2
Koegl, M.F.3
Wagner, U.4
Larissegger-Schnell, B.5
Faber, K.6
Kroutil, W.7
-
14
-
-
0018848378
-
Construction of a partial diploid for the degradative pathway encoded by the TOL plasmid from Pseudomonas putida mt-2: Evidence for the positive nature of the regulation by the xylR gene
-
6929031 10.1007/BF00267445 1:CAS:528:DyaL3cXhslOhsb0%3D
-
Franklin FC, Williams PA (1980) Construction of a partial diploid for the degradative pathway encoded by the TOL plasmid from Pseudomonas putida mt-2: evidence for the positive nature of the regulation by the xylR gene. Mol Gen Genet 177:321-328
-
(1980)
Mol Gen Genet
, vol.177
, pp. 321-328
-
-
Franklin, F.C.1
Williams, P.A.2
-
15
-
-
0032710935
-
Whole microbial cell processes for manufacturing amino acids, vitamins or ribonucleotides
-
10600687 10.1016/S0958-1669(99)00041-5 1:CAS:528:DyaK1MXotFSls7w%3D
-
Hashimoto S, Ozaki A (1999) Whole microbial cell processes for manufacturing amino acids, vitamins or ribonucleotides. Curr Opin Biotechnol 10:604-608
-
(1999)
Curr Opin Biotechnol
, vol.10
, pp. 604-608
-
-
Hashimoto, S.1
Ozaki, A.2
-
16
-
-
18044398220
-
Directed evolution of biocatalytic processes
-
15857779 10.1016/j.bioeng.2004.09.003 1:CAS:528:DC%2BD2MXjs1Ogsr0%3D
-
Hibbert EG, Baganz F, Hailes HC, Ward JM, Lye GJ, Woodley JM, Dalby PA (2005) Directed evolution of biocatalytic processes. Biomol Eng 22:11-19
-
(2005)
Biomol Eng
, vol.22
, pp. 11-19
-
-
Hibbert, E.G.1
Baganz, F.2
Hailes, H.C.3
Ward, J.M.4
Lye, G.J.5
Woodley, J.M.6
Dalby, P.A.7
-
17
-
-
84858437641
-
Resting cells of recombinant E. coli show high epoxidation yields on energy source and high sensitivity to product inhibition
-
22170310 10.1002/bit.24404 1:CAS:528:DC%2BC3MXhs1OiurvM
-
Julsing MK, Kuhn D, Schmid A, Buhler B (2012) Resting cells of recombinant E. coli show high epoxidation yields on energy source and high sensitivity to product inhibition. Biotechnol Bioeng 109(5):1109-1119
-
(2012)
Biotechnol Bioeng
, vol.109
, Issue.5
, pp. 1109-1119
-
-
Julsing, M.K.1
Kuhn, D.2
Schmid, A.3
Buhler, B.4
-
18
-
-
56749102605
-
Asymmetric synthesis of optically pure pharmacologically relevant amines employing omega-transaminases
-
10.1002/adsc.200800496 1:CAS:528:DC%2BD1cXhsFSntrjO
-
Koszelewski D, Lavandera I, Clay D, Rozzel I, Kroutil W (2008) Asymmetric synthesis of optically pure pharmacologically relevant amines employing omega-transaminases. Adv Synth Catal 350:2761-2766
-
(2008)
Adv Synth Catal
, vol.350
, pp. 2761-2766
-
-
Koszelewski, D.1
Lavandera, I.2
Clay, D.3
Rozzel, I.4
Kroutil, W.5
-
21
-
-
67549130333
-
One-pot multienzymatic synthesis of 12-ketoursodeoxycholic acid: Subtle cofactor specificities rule the reaction equilibria of five biocatalysts working in a row
-
10.1002/adsc.200800727 1:CAS:528:DC%2BD1MXos1aru7o%3D
-
Monti D, Ferrandi EE, Zanellato I, Hua L, Polentini F, Carrea G, Riva S (2009) One-pot multienzymatic synthesis of 12-ketoursodeoxycholic acid: subtle cofactor specificities rule the reaction equilibria of five biocatalysts working in a row. Adv Synth Catal 351:1303-1311
-
(2009)
Adv Synth Catal
, vol.351
, pp. 1303-1311
-
-
Monti, D.1
Ferrandi, E.E.2
Zanellato, I.3
Hua, L.4
Polentini, F.5
Carrea, G.6
Riva, S.7
-
22
-
-
0034609021
-
Production of enantiopure styrene oxide by recombinant Escherichia coli synthesizing a two-component styrene monooxygenase
-
10820335 10.1002/(SICI)1097-0290(20000705)69:1<91: AID-BIT11>3.0.CO;2-X 1:CAS:528:DC%2BD3cXkt1WrtL4%3D
-
Panke S, Wubbolts MG, Witholt B (2000) Production of enantiopure styrene oxide by recombinant Escherichia coli synthesizing a two-component styrene monooxygenase. Biotechnol Bioeng 69:91-100
-
(2000)
Biotechnol Bioeng
, vol.69
, pp. 91-100
-
-
Panke, S.1
Wubbolts, M.G.2
Witholt, B.3
-
23
-
-
34147104660
-
Carbon metabolism and product inibition determine the epoxydation efficiency of solvent tolerant Pseudomonas sp. strain VLB129â̂ †C
-
17514751 10.1002/bit.21496 1:CAS:528:DC%2BD2sXhtlWmtL3I
-
Park JB, Buhler B, Panke S, Witholt B, Schmid A (2007) Carbon metabolism and product inibition determine the epoxydation efficiency of solvent tolerant Pseudomonas sp. strain VLB129â̂†C. Biotechnol Bioeng 98(6):1219-1229
-
(2007)
Biotechnol Bioeng
, vol.98
, Issue.6
, pp. 1219-1229
-
-
Park, J.B.1
Buhler, B.2
Panke, S.3
Witholt, B.4
Schmid, A.5
-
24
-
-
0343417027
-
Synthesis of enantiomerically pure forms of trans-3-phenylglycidic acid
-
10.1016/S0040-4039(96)02426-4 1:CAS:528:DyaK2sXhtVKmt7w%3D
-
Plucinska K, Kasprzykowski F, Kozian E (1997) Synthesis of enantiomerically pure forms of trans-3-phenylglycidic acid. Tetrahedron Lett 38(5):861-864
-
(1997)
Tetrahedron Lett
, vol.38
, Issue.5
, pp. 861-864
-
-
Plucinska, K.1
Kasprzykowski, F.2
Kozian, E.3
-
26
-
-
0035843170
-
Industrial biocatalysis today and tomorrow
-
11196655 10.1038/35051736 1:CAS:528:DC%2BD3MXlvFWhug%3D%3D
-
Schmid A, Dordick JS, Hauer B, Kiener A, Wubbolts MG, Witholt B (2001) Industrial biocatalysis today and tomorrow. Nature 409:258-268
-
(2001)
Nature
, vol.409
, pp. 258-268
-
-
Schmid, A.1
Dordick, J.S.2
Hauer, B.3
Kiener, A.4
Wubbolts, M.G.5
Witholt, B.6
-
27
-
-
34547224693
-
Stereo-complementary two-step cascades using a two-enzyme system leading to enantiopure epoxides
-
10.1002/adsc.200700027 1:CAS:528:DC%2BD2sXntVSjurw%3D
-
Seisser B, Lavandera I, Faber K, Lutje Spelberg JH, Kroutil W (2007) Stereo-complementary two-step cascades using a two-enzyme system leading to enantiopure epoxides. Adv Synth Catal 349:1399-1404
-
(2007)
Adv Synth Catal
, vol.349
, pp. 1399-1404
-
-
Seisser, B.1
Lavandera, I.2
Faber, K.3
Lutje Spelberg, J.H.4
Kroutil, W.5
-
28
-
-
41449102433
-
Biocatalyst expressing cis-naphthalene dihydrodiol dehydrogenase from Pseudomonas fluorescens N3 catalyzes alcohol and 1,2-diol dehydrogenase reactions
-
10.1016/j.molcatb.2007.10.014
-
Sello G, Bernasconi S, Orsini F, Mattavelli P, Di Gennaro P, Bestetti G (2008) Biocatalyst expressing cis-naphthalene dihydrodiol dehydrogenase from Pseudomonas fluorescens N3 catalyzes alcohol and 1,2-diol dehydrogenase reactions. J Mol Cat B Enzym 52:67-73
-
(2008)
J Mol Cat B Enzym
, vol.52
, pp. 67-73
-
-
Sello, G.1
Bernasconi, S.2
Orsini, F.3
Mattavelli, P.4
Di Gennaro, P.5
Bestetti, G.6
-
29
-
-
65349128162
-
Multienzymatic preparation of (-)-[3-(oxiran-2-yl) phenyl] methanol and (-)-3-(oxyran-2-yl) benzoic acid
-
10.1016/j.tetasy.2009.03.023 1:CAS:528:DC%2BD1MXltl2ksrw%3D
-
Sello G, Bernasconi S, Orsini F, Di Gennaro P (2009) Multienzymatic preparation of (-)-[3-(oxiran-2-yl) phenyl] methanol and (-)-3-(oxyran-2-yl) benzoic acid. Tetrahedron Asymmetry 20:563-565
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 563-565
-
-
Sello, G.1
Bernasconi, S.2
Orsini, F.3
Di Gennaro, P.4
-
30
-
-
54249116802
-
Orchestration of concurrent oxidation and reduction cycles for stereoinversion and deracemization of sec-alcohols
-
18821754 10.1021/ja804816a 1:CAS:528:DC%2BD1cXhtFOiu7jL
-
Voss CV, Gruber CC, Faber K, Knaus T, Macheroux P, Kroutil W (2008) Orchestration of concurrent oxidation and reduction cycles for stereoinversion and deracemization of sec-alcohols. J Am Chem Soc 130:13969-13972
-
(2008)
J Am Chem Soc
, vol.130
, pp. 13969-13972
-
-
Voss, C.V.1
Gruber, C.C.2
Faber, K.3
Knaus, T.4
MacHeroux, P.5
Kroutil, W.6
-
31
-
-
0000493625
-
Enzyme-catalyzed organic synthesis: NAD(P)H cofactor regeneration using ethanol/alcohol dehydrogenase/aldehyde dehydrogenase and methano/alcohol dehydrogenase/aldehyde dehydrogenase/formate dehydrogenase
-
10.1021/jo00135a037 1:CAS:528:DyaL38Xkt1Sjtbg%3D
-
Wong CH, Whitesides GM (1982) Enzyme-catalyzed organic synthesis: NAD(P)H cofactor regeneration using ethanol/alcohol dehydrogenase/aldehyde dehydrogenase and methano/alcohol dehydrogenase/aldehyde dehydrogenase/formate dehydrogenase. J Org Chem 47:2816-2818
-
(1982)
J Org Chem
, vol.47
, pp. 2816-2818
-
-
Wong, C.H.1
Whitesides, G.M.2
-
32
-
-
0021943518
-
Improved M13 phage cloning vectors and host strains: Nucleotide sequences of the M13mp18 and pUC19 vectors
-
10.1016/0378-1119(85)90120-9
-
Yanish-Perron C, Vieira J, Messing J (1985) Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene 33:103-119
-
(1985)
Gene
, vol.33
, pp. 103-119
-
-
Yanish-Perron, C.1
Vieira, J.2
Messing, J.3
|