-
1
-
-
0034833453
-
Highly active oligomeric (salen)co catalysts for asymmetric epoxide ring-opening reactions
-
Ready J.M., and Jacobsen E.N. Highly active oligomeric (salen)co catalysts for asymmetric epoxide ring-opening reactions. J. Am. Chem. Soc. 123 (2001) 2687-2688
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 2687-2688
-
-
Ready, J.M.1
Jacobsen, E.N.2
-
3
-
-
0029664614
-
Asp333, Asp495, and His523 form the catalytic triad of rat soluble epoxide hydrolase
-
Arand M., Wagner H., and Oesch F. Asp333, Asp495, and His523 form the catalytic triad of rat soluble epoxide hydrolase. J. Biol. Chem. 271 (1996) 4223-4229
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 4223-4229
-
-
Arand, M.1
Wagner, H.2
Oesch, F.3
-
4
-
-
0033545515
-
Epoxide hydrolases from yeasts and other sources: versatile tools in biocatalysis
-
Weijers C.A.G.M., and de Bont J.A.M. Epoxide hydrolases from yeasts and other sources: versatile tools in biocatalysis. J. Mol. Catal. B Enzym. 6 (1999) 199-214
-
(1999)
J. Mol. Catal. B Enzym.
, vol.6
, pp. 199-214
-
-
Weijers, C.A.G.M.1
de Bont, J.A.M.2
-
5
-
-
0035710814
-
Microbial epoxide hydrolases for preparative biotransformations
-
Steinreiber A., and Faber K. Microbial epoxide hydrolases for preparative biotransformations. Curr. Opin. Biotechnol. 12 (2001) 552-558
-
(2001)
Curr. Opin. Biotechnol.
, vol.12
, pp. 552-558
-
-
Steinreiber, A.1
Faber, K.2
-
6
-
-
0032530570
-
Fungal epoxide hydrolases: new tools for the synthesis of enantiopure epoxide and diols
-
Archelas A. Fungal epoxide hydrolases: new tools for the synthesis of enantiopure epoxide and diols. J. Mol. Catal., B Enzym. 5 (1998) 79-85
-
(1998)
J. Mol. Catal., B Enzym.
, vol.5
, pp. 79-85
-
-
Archelas, A.1
-
7
-
-
0030569736
-
Enantioselective hydrolysis of p-nitrostyrene oxide by an epoxide hydrolase preparation from Aspergillus niger
-
Nellaiah H., Morisseau C., Archelas A., Furstoss R., and Baratti J.C. Enantioselective hydrolysis of p-nitrostyrene oxide by an epoxide hydrolase preparation from Aspergillus niger. Biotechnol. Bioeng. 49 (1996) 70-77
-
(1996)
Biotechnol. Bioeng.
, vol.49
, pp. 70-77
-
-
Nellaiah, H.1
Morisseau, C.2
Archelas, A.3
Furstoss, R.4
Baratti, J.C.5
-
8
-
-
0032546059
-
Microbiological transformations 40. Use of fungal epoxide hydrolases for the synthesis of enantiopure alkyl epoxides
-
Moussou P., Archelas A., and Furstoss R. Microbiological transformations 40. Use of fungal epoxide hydrolases for the synthesis of enantiopure alkyl epoxides. Tetrahedron 54 (1998) 1563-1572
-
(1998)
Tetrahedron
, vol.54
, pp. 1563-1572
-
-
Moussou, P.1
Archelas, A.2
Furstoss, R.3
-
9
-
-
0033565356
-
Purification and characterization of a highly enantioselective epoxide hydrolase from Aspergillus niger
-
Morisseau C., Archelas A., Guitton C., Faucher D., Furstoss R., and Baratti J.C. Purification and characterization of a highly enantioselective epoxide hydrolase from Aspergillus niger. Eur. J. Biochem. 263 (1999) 386-395
-
(1999)
Eur. J. Biochem.
, vol.263
, pp. 386-395
-
-
Morisseau, C.1
Archelas, A.2
Guitton, C.3
Faucher, D.4
Furstoss, R.5
Baratti, J.C.6
-
10
-
-
0033570996
-
Cloning and molecular characterization of a soluble epoxide hydrolase from Aspergillus niger that is related to mammalian microsomal epoxide hydrolase
-
Arand M., Hemmer H., Durk H., Baratti J., Archelas A., Furstoss R., and Oesch F. Cloning and molecular characterization of a soluble epoxide hydrolase from Aspergillus niger that is related to mammalian microsomal epoxide hydrolase. Biochem. J. 344 Pt. 1 (1999) 273-280
-
(1999)
Biochem. J.
, vol.344
, Issue.PART 1
, pp. 273-280
-
-
Arand, M.1
Hemmer, H.2
Durk, H.3
Baratti, J.4
Archelas, A.5
Furstoss, R.6
Oesch, F.7
-
11
-
-
1242270555
-
Fungal epoxdie hydrolases: new landmarks in sequence-activity space
-
Smit M.S. Fungal epoxdie hydrolases: new landmarks in sequence-activity space. Trends Biotechnol. 22 (2004) 123-129
-
(2004)
Trends Biotechnol.
, vol.22
, pp. 123-129
-
-
Smit, M.S.1
-
12
-
-
33644769395
-
Enzymatic resolution of racemic phenyloxirane by a novel epoxide hydrolase from Aspergillus niger SQ-6 and its fed-batch fermentation
-
Liu Y.., Sha Q., Wu S., Wang J., Yang L., and Sun W. Enzymatic resolution of racemic phenyloxirane by a novel epoxide hydrolase from Aspergillus niger SQ-6 and its fed-batch fermentation. J. Ind. Microbiol. Biotechnol. 33 (2006) 274-282
-
(2006)
J. Ind. Microbiol. Biotechnol.
, vol.33
, pp. 274-282
-
-
Liu, Y..1
Sha, Q.2
Wu, S.3
Wang, J.4
Yang, L.5
Sun, W.6
-
13
-
-
0034651639
-
Structure of Aspergillus niger epoxide hydrolase at 1.8 A resolution: implications for the structure and function of the mammalian microsomal class of epoxide hydrolases
-
Zou J., Hallberg B.M., Bergfors T., Oesch F., Arand M., Mowbray S.L., and Jones T.A. Structure of Aspergillus niger epoxide hydrolase at 1.8 A resolution: implications for the structure and function of the mammalian microsomal class of epoxide hydrolases. Structure. Fold. Des. 8 (2000) 111-122
-
(2000)
Structure. Fold. Des.
, vol.8
, pp. 111-122
-
-
Zou, J.1
Hallberg, B.M.2
Bergfors, T.3
Oesch, F.4
Arand, M.5
Mowbray, S.L.6
Jones, T.A.7
-
14
-
-
0037073334
-
Enzymatic transformations. Part 53: Epoxide hydrolase-catalysed resolution of key synthons for azole antifungal agents
-
Monfort N., Archelas A., and Furstoss R. Enzymatic transformations. Part 53: Epoxide hydrolase-catalysed resolution of key synthons for azole antifungal agents. Tetrahedron: Asymmetry 13 (2003) 2399-2401
-
(2003)
Tetrahedron: Asymmetry
, vol.13
, pp. 2399-2401
-
-
Monfort, N.1
Archelas, A.2
Furstoss, R.3
-
15
-
-
0029856005
-
Microbiological transformations. 33. Fungal epoxide hydrolases applied to the synthesis of enantiopure para-substituted styrene oxides. A mechanistic approach
-
Pedragosa-Moreau S., Morisseau C., Zylber J., Archelas A., Baratti J., and Furstoss R. Microbiological transformations. 33. Fungal epoxide hydrolases applied to the synthesis of enantiopure para-substituted styrene oxides. A mechanistic approach. J. Org. Chem. 61 (1996) 7402-7407
-
(1996)
J. Org. Chem.
, vol.61
, pp. 7402-7407
-
-
Pedragosa-Moreau, S.1
Morisseau, C.2
Zylber, J.3
Archelas, A.4
Baratti, J.5
Furstoss, R.6
-
17
-
-
0027692823
-
Identification and characterization of MPG1, a gene involved in pathogenicity from the rice blast fungus Magnaporthe grisea
-
Talbot N.J., Ebbole D.J., and Hamer J.E. Identification and characterization of MPG1, a gene involved in pathogenicity from the rice blast fungus Magnaporthe grisea. Plant Cell 5 (1993) 1575-1590
-
(1993)
Plant Cell
, vol.5
, pp. 1575-1590
-
-
Talbot, N.J.1
Ebbole, D.J.2
Hamer, J.E.3
-
18
-
-
0023691425
-
Genetic applications of an inverse polymerase chain reaction
-
Ochman H., Gerber A.S., and Hartl D.L. Genetic applications of an inverse polymerase chain reaction. Genetics 120 (1988) 621-623
-
(1988)
Genetics
, vol.120
, pp. 621-623
-
-
Ochman, H.1
Gerber, A.S.2
Hartl, D.L.3
-
19
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
20
-
-
0034124265
-
Purification, molecular cloning and ethylene-inducible expression of a soluble-type epoxide hydrolase from soybean (Glycine max [L.] Merr.)
-
Arahira M., Nong V.H., Udaka K., and Fukazawa C. Purification, molecular cloning and ethylene-inducible expression of a soluble-type epoxide hydrolase from soybean (Glycine max [L.] Merr.). Eur. J. Biochem. 267 (2000) 2649-2657
-
(2000)
Eur. J. Biochem.
, vol.267
, pp. 2649-2657
-
-
Arahira, M.1
Nong, V.H.2
Udaka, K.3
Fukazawa, C.4
-
22
-
-
0029090931
-
Isolation of a highly enantioselective epoxide hydrolase from Rhodococcus sp. NCIMB 11216
-
Mischitz M., Faber K., and Willetts A. Isolation of a highly enantioselective epoxide hydrolase from Rhodococcus sp. NCIMB 11216. Biotechnol. Lett. 17 (1995) 893-898
-
(1995)
Biotechnol. Lett.
, vol.17
, pp. 893-898
-
-
Mischitz, M.1
Faber, K.2
Willetts, A.3
-
23
-
-
0025183708
-
Basic local alignment search tool
-
Altschul S.F., Gish W., Miller W., Myers E.W., and Lipman D.J. Basic local alignment search tool. J. Mol. Biol. 215 (1990) 403-410
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
24
-
-
0036428553
-
Brassica napus soluble epoxide hydrolase (BNSEH1)
-
Bellevik S., Zhang J., and Meijer J. Brassica napus soluble epoxide hydrolase (BNSEH1). Eur. J. Biochem. 269 (2002) 5295-5302
-
(2002)
Eur. J. Biochem.
, vol.269
, pp. 5295-5302
-
-
Bellevik, S.1
Zhang, J.2
Meijer, J.3
-
25
-
-
2442731907
-
Catalytic triad of microsomal epoxide hydrolase: replacement of Glu404 with Asp leads to a strongly increased turnover rate
-
Arand M., Muller F., Mecky A., Hinz W., Urban P., Pompon D., Kellner R., and Oesch F. Catalytic triad of microsomal epoxide hydrolase: replacement of Glu404 with Asp leads to a strongly increased turnover rate. Biochem. J. 337 Pt. 1 (1999) 37-43
-
(1999)
Biochem. J.
, vol.337
, Issue.PART 1
, pp. 37-43
-
-
Arand, M.1
Muller, F.2
Mecky, A.3
Hinz, W.4
Urban, P.5
Pompon, D.6
Kellner, R.7
Oesch, F.8
-
26
-
-
14844314796
-
Soybean epoxide hydrolase: identification of the catalytic residues and probing of the reaction mechanism with secondary kinetic isotope effects
-
Blee E., Summerer S., Flenet M., Rogniaux H., Van D.A., and Schuber F. Soybean epoxide hydrolase: identification of the catalytic residues and probing of the reaction mechanism with secondary kinetic isotope effects. J. Biol. Chem. 280 (2005) 6479-6487
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 6479-6487
-
-
Blee, E.1
Summerer, S.2
Flenet, M.3
Rogniaux, H.4
Van, D.A.5
Schuber, F.6
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