-
1
-
-
0000026228
-
Cyanogenesis in plants
-
Poulton JE. Cyanogenesis in plants. Plant Physiol 1990; 94: 401-5.
-
(1990)
Plant Physiol
, vol.94
, pp. 401-405
-
-
Poulton, J.E.1
-
3
-
-
36549016684
-
An R-selective hydroxynitrile lyase from Arabidopsis thaliana with an alpha/betahydrolase fold
-
Andexer J, von Langermann J, Mell A et al. An R-selective hydroxynitrile lyase from Arabidopsis thaliana with an alpha/betahydrolase fold. Angew Chem Int Ed 2007; 46: 8679-81.
-
(2007)
Angew Chem Int Ed
, vol.46
, pp. 8679-8681
-
-
Andexer, J.1
von Langermann, J.2
Mell, A.3
-
4
-
-
38949170701
-
Ueber die Bildung des Bittermandelöls
-
Wöhler F, Liebig J. Ueber die Bildung des Bittermandelöls. Ann Pharm 1837; 22: 1-24.
-
(1837)
Ann Pharm
, vol.22
, pp. 1-24
-
-
Wöhler, F.1
Liebig, J.2
-
5
-
-
0001516109
-
Enzyme effected asymmetrical synthesis
-
Rosenthaler L. Enzyme effected asymmetrical synthesis. Biochem Zeitschrift 1908; 14: 238-53.
-
(1908)
Biochem Zeitschrift
, vol.14
, pp. 238-253
-
-
Rosenthaler, L.1
-
6
-
-
0029188401
-
Purification and characterization of a novel (R)-mandelonitrile lyase from the fern Phlebodium aureum
-
Wajant H, Forster S, Selmar D, Effenberger F, Pfizenmaier K. Purification and characterization of a novel (R)-mandelonitrile lyase from the fern Phlebodium aureum. Plant Physiol 1995; 109: 1231-8.
-
(1995)
Plant Physiol
, vol.109
, pp. 1231-1238
-
-
Wajant, H.1
Forster, S.2
Selmar, D.3
Effenberger, F.4
Pfizenmaier, K.5
-
7
-
-
84886595474
-
Cleavage and formation of cyanohydrins
-
In: Drauz K, Gröger H, May O, Eds, Weinheim: Wiley-VCH
-
Gruber-Khadjawi M, Fechter MH, Griengl H. Cleavage and formation of cyanohydrins. In: Drauz K, Gröger H, May O, Eds Enzyme Catalysis in Organic Synthesis. Weinheim: Wiley-VCH 2012: pp. 947-990.
-
(2012)
Enzyme Catalysis in Organic Synthesis
, pp. 947-990
-
-
Gruber-Khadjawi, M.1
Fechter, M.H.2
Griengl, H.3
-
8
-
-
84886587518
-
Industrial application and processes using carbon-carbon lyases
-
In: Drauz K, Gröger H, May O, Eds, Weinheim: Wiley-VCH
-
Hilterhaus L, Liese A. Industrial application and processes using carbon-carbon lyases. In: Drauz K, Gröger H, May O, Eds Enzyme Catalysis in Organic Synthesis. Weinheim: Wiley-VCH 2012: pp. 991-1000.
-
(2012)
Enzyme Catalysis in Organic Synthesis
, pp. 991-1000
-
-
Hilterhaus, L.1
Liese, A.2
-
9
-
-
34547131285
-
Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry
-
Purkarthofer T, Skranc W, Schuster C, Griengl H. Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry. Appl Microbiol Biotechnol 2007; 76: 309-20.
-
(2007)
Appl Microbiol Biotechnol
, vol.76
, pp. 309-320
-
-
Purkarthofer, T.1
Skranc, W.2
Schuster, C.3
Griengl, H.4
-
10
-
-
84886582532
-
Hydroxynitrile lyases: From nature to application
-
In: Carreira EM, Yamamoto H, Eds., Amsterdam: Elsevier
-
Winkler M, Glieder A, Steiner K. Hydroxynitrile lyases: from nature to application. In: Carreira EM, Yamamoto H, Eds. Comprehensive Chirality, Synthetic Methods VI-Enzymatic and Semi-Enzymatic. Amsterdam: Elsevier 2012: Vol. 7, pp. 350-71.
-
(2012)
Comprehensive Chirality, Synthetic Methods VI-Enzymatic and Semi-Enzymatic
, vol.7
, pp. 350-371
-
-
Winkler, M.1
Glieder, A.2
Steiner, K.3
-
11
-
-
34547209337
-
Enzyme immobilization: The quest for optimum performance
-
Sheldon RA. Enzyme immobilization: the quest for optimum performance. Adv Synth Catal 2007; 349: 1289-307.
-
(2007)
Adv Synth Catal
, vol.349
, pp. 1289-1307
-
-
Sheldon, R.A.1
-
12
-
-
79251469073
-
Cross-linked enzyme aggregates as industrial biocatalysts
-
Sheldon RA. Cross-linked enzyme aggregates as industrial biocatalysts. Org Proc Res Devel 2011; 15: 213-23.
-
(2011)
Org Proc Res Devel
, vol.15
, pp. 213-223
-
-
Sheldon, R.A.1
-
13
-
-
82355169635
-
Characteristic features and biotechnological applications of cross-linked enzyme aggregates (CLEAs)
-
Sheldon RA. Characteristic features and biotechnological applications of cross-linked enzyme aggregates (CLEAs). Appl Microbiol Biotechnol 2011; 92: 467-77.
-
(2011)
Appl Microbiol Biotechnol
, vol.92
, pp. 467-477
-
-
Sheldon, R.A.1
-
14
-
-
84891527174
-
Industrial Applications of Asymmetric Synthesis using Cross-Linked Enzyme Aggregates
-
In: Carreira EM, Yamamoto H, Eds., Amsterdam: Elsevier
-
Sheldon RA. Industrial Applications of Asymmetric Synthesis using Cross-Linked Enzyme Aggregates. In: Carreira EM, Yamamoto H, Eds. Comprehensive Chirality, Synthetic Methods VI-Enzymatic and Semi-Enzymatic. Amsterdam: Elsevier 2012: Vol. 9, pp. 353-66.
-
(2012)
Comprehensive Chirality, Synthetic Methods VI-Enzymatic and Semi-Enzymatic
, vol.9
, pp. 353-366
-
-
Sheldon, R.A.1
-
16
-
-
21644433892
-
Hydroxynitrile lyases: At the interface of biology and chemistry
-
Sharma M, Sharma NN, Bhalla TC. Hydroxynitrile lyases: at the interface of biology and chemistry. Enz Microbial Technol 2005; 37: 279-94.
-
(2005)
Enz Microbial Technol
, vol.37
, pp. 279-294
-
-
Sharma, M.1
Sharma, N.N.2
Bhalla, T.C.3
-
17
-
-
77955568869
-
Chiral synthesis of pharmaceutical intermediates using oxynitrilases
-
In: Tao J, Lin G-Q, Liese A, Eds., Wiley VCH
-
Lu W-Y, Lin G-Q. Chiral synthesis of pharmaceutical intermediates using oxynitrilases. In: Tao J, Lin G-Q, Liese A, Eds. Biocatalysis for the Pharmaceutical Industry, Wiley VCH 2009: pp. 89-109.
-
(2009)
Biocatalysis for the Pharmaceutical Industry
, pp. 89-109
-
-
Lu, W.-Y.1
Lin, G.-Q.2
-
18
-
-
69749104380
-
How to overcome limitations in biotechnological processes-examples from hydroxynitrile lyase applications
-
Andexer JN, Langermann J, Kragl U, Pohl M. How to overcome limitations in biotechnological processes-examples from hydroxynitrile lyase applications. Trends Biotechnol 2009; 27: 599-607.
-
(2009)
Trends Biotechnol
, vol.27
, pp. 599-607
-
-
Andexer, J.N.1
Langermann, J.2
Kragl, U.3
Pohl, M.4
-
19
-
-
65949118468
-
Enantioselective enzyme-catalysed synthesis of cyanohydrins
-
Holt J, Hanefeld U. Enantioselective enzyme-catalysed synthesis of cyanohydrins. Curr Org Synth 2009; 6: 15-37.
-
(2009)
Curr Org Synth
, vol.6
, pp. 15-37
-
-
Holt, J.1
Hanefeld, U.2
-
20
-
-
10044248344
-
Catalytic promiscuity in biocatalysis: Using old enzymes to form new bonds and follow new pathways
-
Bornscheuer UT, Kazlauskas RJ. Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways. Angew Chem Int Ed 2004; 43: 6032-40.
-
(2004)
Angew Chem Int Ed
, vol.43
, pp. 6032-6040
-
-
Bornscheuer, U.T.1
Kazlauskas, R.J.2
-
21
-
-
0037449629
-
Synthesis and applications of non-racemic cyanohydrins
-
North M. Synthesis and applications of non-racemic cyanohydrins. Tetrahedron-Asymm 2003; 14: 147-76.
-
(2003)
Tetrahedron-Asymm
, vol.14
, pp. 147-176
-
-
North, M.1
-
22
-
-
21144455026
-
Enantioselective C-C bond synthesis catalysed by enzymes
-
Sukumaran J, Hanefeld U. Enantioselective C-C bond synthesis catalysed by enzymes. Chem Soc Rev 2005; 34: 530-42.
-
(2005)
Chem Soc Rev
, vol.34
, pp. 530-542
-
-
Sukumaran, J.1
Hanefeld, U.2
-
23
-
-
80052468032
-
Hydroxynitrile lyases: Insights into biochemistry, discovery, and engineering
-
Dadashipour M, Asano Y. Hydroxynitrile lyases: insights into biochemistry, discovery, and engineering. ACS Catalysis 2011; 1: 1121-49.
-
(2011)
ACS Catalysis
, vol.1
, pp. 1121-1149
-
-
Dadashipour, M.1
Asano, Y.2
-
26
-
-
85189277899
-
-
US 20100143986
-
Gaisberger R, Glieder A, Liu ZB, Pscheidt B. R-HNL random variants and their use for preparing optically pure, sterically hindered cyanohydrins. US 20100143986, 2010.
-
(2010)
R-HNL random variants and their use for preparing optically pure, sterically hindered cyanohydrins
-
-
Gaisberger, R.1
Glieder, A.2
Liu, Z.B.3
Pscheidt, B.4
-
27
-
-
84873495374
-
-
WO9703214
-
Hasslacher M, Schall M, Schwab H, Hayn E, Kohlwein S, Griengl H. (S)-hydroxynitrilelyase from Hevea brasiliensis. WO9703214, 1997.
-
(1997)
S-hydroxynitrilelyase from Hevea brasiliensis
-
-
Hasslacher, M.1
Schall, M.2
Schwab, H.3
Hayn, E.4
Kohlwein, S.5
Griengl, H.6
-
33
-
-
85189270024
-
-
US6861243
-
Schwab H, Glieder A, Kratky C and et al. Genes containing a DNA sequence coding for hydroxynitrile lyase, recombinant proteins derived therefrom and having hydroxynitrile lyase activity, and use thereof. US6861243, 2005.
-
(2005)
Genes containing a DNA sequence coding for hydroxynitrile lyase, recombinant proteins derived therefrom and having hydroxynitrile lyase activity, and use thereof
-
-
Schwab, H.1
Glieder, A.2
Kratky, C.3
-
35
-
-
29344440805
-
Screening for new hydroxynitrilases from plants
-
Asano Y, Tamura K, Doi N and et al. Screening for new hydroxynitrilases from plants. Biosci Biotechnol Biochem 2005; 69: 2349-57.
-
(2005)
Biosci Biotechnol Biochem
, vol.69
, pp. 2349-2357
-
-
Asano, Y.1
Tamura, K.2
Doi, N.3
-
36
-
-
3042752957
-
Screening for hydroxynitrile lyase activity in crude preparations of some edible plants
-
Hernandez L, Luna H, Ruiz-Teran F, Vazquez A. Screening for hydroxynitrile lyase activity in crude preparations of some edible plants. J Mol Catal B-Enzym 2004; 30: 105-8.
-
(2004)
J Mol Catal B-Enzym
, vol.30
, pp. 105-108
-
-
Hernandez, L.1
Luna, H.2
Ruiz-Teran, F.3
Vazquez, A.4
-
39
-
-
0031051520
-
Molecular cloning of acetone cyanohydrin lyase from flax (Linum usitatissimum)-definition of a novel class of hydroxynitrile lyases
-
Trummler K, Wajant H. Molecular cloning of acetone cyanohydrin lyase from flax (Linum usitatissimum)-definition of a novel class of hydroxynitrile lyases. J Biol Chem 1997; 272: 4770-4.
-
(1997)
J Biol Chem
, vol.272
, pp. 4770-4774
-
-
Trummler, K.1
Wajant, H.2
-
40
-
-
0024022058
-
Purification and characterization of acetone cyanohydrin lyase from Linum usitatissimum
-
Xu LL, Singh BK, Conn EE. Purification and characterization of acetone cyanohydrin lyase from Linum usitatissimum. Arch Biochem Biophys 1988; 263: 256-63.
-
(1988)
Arch Biochem Biophys
, vol.263
, pp. 256-263
-
-
Xu, L.L.1
Singh, B.K.2
Conn, E.E.3
-
41
-
-
0027131001
-
Cloning of cDNA of Prunus-serotina (R)-(+)-mandelonitrile lyase and identification of a putative FADbinding site
-
Cheng IP, Poulton JE. Cloning of cDNA of Prunus-serotina (R)-(+)-mandelonitrile lyase and identification of a putative FADbinding site. Plant Cell Physiol 1993; 34: 1139-43.
-
(1993)
Plant Cell Physiol
, vol.34
, pp. 1139-1143
-
-
Cheng, I.P.1
Poulton, J.E.2
-
43
-
-
80054028925
-
Cloning and expression of hydroxynitrile lyase gene from Eriobotrya japonica in Pichia pastoris
-
Zhao GJ, Yang ZQ, Guo YH. Cloning and expression of hydroxynitrile lyase gene from Eriobotrya japonica in Pichia pastoris. J Biosci Bioeng 2011; 112: 321-5.
-
(2011)
J Biosci Bioeng
, vol.112
, pp. 321-325
-
-
Zhao, G.J.1
Yang, Z.Q.2
Guo, Y.H.3
-
44
-
-
58249087170
-
Parameters influencing asymmetric synthesis of (R)-mandelonitrile by a novel (R)-hydroxynitrile lyase from Eriobotrya japonica
-
Ueatrongchit T, Komeda H, Asano Y. Parameters influencing asymmetric synthesis of (R)-mandelonitrile by a novel (R)-hydroxynitrile lyase from Eriobotrya japonica. J Mol Catal BEnzym 2009; 56: 208-14.
-
(2009)
J Mol Catal BEnzym
, vol.56
, pp. 208-214
-
-
Ueatrongchit, T.1
Komeda, H.2
Asano, Y.3
-
45
-
-
1842578074
-
Industrial methods for the production of optically active intermediates
-
Breuer M, Ditrich K, Habicher T and et al. Industrial methods for the production of optically active intermediates. Angew Chem Int Ed 2004; 43: 788-824.
-
(2004)
Angew Chem Int Ed
, vol.43
, pp. 788-824
-
-
Breuer, M.1
Ditrich, K.2
Habicher, T.3
-
47
-
-
2442622502
-
Biocatalytic conversion of unnatural substrates by recombinant almond R-HNL isoenzyme 5
-
Weis R, Poechlauer P, Bona R and et al. Biocatalytic conversion of unnatural substrates by recombinant almond R-HNL isoenzyme 5. J Mol Catal B-Enzym 2004; 29: 211-8.
-
(2004)
J Mol Catal B-Enzym
, vol.29
, pp. 211-218
-
-
Weis, R.1
Poechlauer, P.2
Bona, R.3
-
49
-
-
85189272963
-
-
US7572608
-
Skranc W, Glieder A, Gruber K, Weis R, Luiten R. Rhydroxynitrile lyases having improved substrate tolerance and the use thereof. US7572608, 2009.
-
(2009)
Rhydroxynitrile lyases having improved substrate tolerance and the use thereof
-
-
Skranc, W.1
Glieder, A.2
Gruber, K.3
Weis, R.4
Luiten, R.5
-
50
-
-
85189263224
-
-
JP2012105671
-
Ogura K, Sato E, Mori H, Nogami H, Kato O, Saito T, Kokubu N, Ninomiya Y. Method for producing optically active cyanohydrin and method for producing optically active alpha-hydroxy carboxylic acid. JP2012105671, 2012.
-
(2012)
Method for producing optically active cyanohydrin and method for producing optically active alpha-hydroxy carboxylic acid
-
-
Ogura, K.1
Sato, E.2
Mori, H.3
Nogami, H.4
Kato, O.5
Saito, T.6
Kokubu, N.7
Ninomiya, Y.8
-
52
-
-
13444287971
-
Crosslinked aggregates of (R)-oxynitrilase: A stable, recyclable biocatalyst for enantioselective hydrocyanation
-
van Langen LM, Selassa RP, van Rantwijk F, Sheldon RA. Crosslinked aggregates of (R)-oxynitrilase: a stable, recyclable biocatalyst for enantioselective hydrocyanation. Org Lett 2005; 7: 327-9.
-
(2005)
Org Lett
, vol.7
, pp. 327-329
-
-
van Langen, L.M.1
Selassa, R.P.2
van Rantwijk, F.3
Sheldon, R.A.4
-
53
-
-
33847174501
-
Synthesis of optically active cyanohydrins from aromatic ketones: Evidence of an increased substrate range and inverted stereoselectivity for the hydroxynitrile lyase from Linum usitatissimum
-
Roberge C, Fleitz F, Pollard D, Devine P. Synthesis of optically active cyanohydrins from aromatic ketones: evidence of an increased substrate range and inverted stereoselectivity for the hydroxynitrile lyase from Linum usitatissimum. Tetrahedron Asymm 2007; 18: 208-14.
-
(2007)
Tetrahedron Asymm
, vol.18
, pp. 208-214
-
-
Roberge, C.1
Fleitz, F.2
Pollard, D.3
Devine, P.4
-
54
-
-
85189270295
-
(R)-and (S)-cyanohydrin formation from pyridine-3-carboxaldehyde using CLEA-immobilized hydroxynitrile lyases
-
In: Whittall J, Sutton PJ, Eds., Wiley
-
Roberge C, Fleitz F, Devine P. (R)-and (S)-cyanohydrin formation from pyridine-3-carboxaldehyde using CLEA-immobilized hydroxynitrile lyases. In: Whittall J, Sutton PJ, Eds. Practical Methods for Biocatalysis and Biotransformations. Wiley: 2010; pp. 114-8.
-
(2010)
Practical Methods for Biocatalysis and Biotransformations
, pp. 114-118
-
-
Roberge, C.1
Fleitz, F.2
Devine, P.3
-
56
-
-
0032509115
-
2+-containing hydroxynitrile lyase from flax (Linum usitatissimum) in Pichia pastoris-utilization of the recombinant enzyme for enzymatic analysis and site-directed mutagenesis
-
2+-containing hydroxynitrile lyase from flax (Linum usitatissimum) in Pichia pastoris-utilization of the recombinant enzyme for enzymatic analysis and site-directed mutagenesis. Plant Sci 1998; 139: 19-27.
-
(1998)
Plant Sci
, vol.139
, pp. 19-27
-
-
Trummler, K.1
Roos, J.2
Schwaneberg, U.3
-
57
-
-
53849118481
-
Efficient biocatalytic synthesis of (R)-pantolactone
-
Pscheidt B, Liu ZB, Gaisberger R and et al. Efficient biocatalytic synthesis of (R)-pantolactone. Adv Synth Catal 2008; 350: 1943-8.
-
(2008)
Adv Synth Catal
, vol.350
, pp. 1943-1948
-
-
Pscheidt, B.1
Liu, Z.B.2
Gaisberger, R.3
-
59
-
-
0348225177
-
One-pot chemoenzymatic synthesis of protected cyanohydrins
-
Purkarthofer T, Skranc W, Weber H and et al. One-pot chemoenzymatic synthesis of protected cyanohydrins. Tetrahedron 2004; 60: 735-9.
-
(2004)
Tetrahedron
, vol.60
, pp. 735-739
-
-
Purkarthofer, T.1
Skranc, W.2
Weber, H.3
-
60
-
-
85189271707
-
-
US6909011
-
Skranc W, Poechlauer P, Wirth I, Neuhofer R, Mayrhofer H. Process for preparing protected enantiomer-enriched cyanohydrins by in-situ derivatization. US6909011, 2005.
-
(2005)
Process for preparing protected enantiomer-enriched cyanohydrins by in-situ derivatization
-
-
Skranc, W.1
Poechlauer, P.2
Wirth, I.3
Neuhofer, R.4
Mayrhofer, H.5
-
61
-
-
67349252054
-
Uneven twins: Comparison of two enantiocomplementary hydroxynitrile lyases with alpha/beta-hydrolase fold
-
Guterl JK, Andexer JN, Sehl Tandfk, et al. Uneven twins: comparison of two enantiocomplementary hydroxynitrile lyases with alpha/beta-hydrolase fold. J Biotechnol 2009; 141: 166-73.
-
(2009)
J Biotechnol
, vol.141
, pp. 166-173
-
-
Guterl, J.K.1
Andexer, J.N.2
Sehl, T.3
-
62
-
-
84865568695
-
Hydroxynitrile lyases with alpha/beta-hydrolase fold: Two enzymes with almost identical 3D structures but opposite enantioselectivities and different reaction mechanisms
-
Andexer JN, Staunig N, Eggert T and et al. Hydroxynitrile lyases with alpha/beta-hydrolase fold: two enzymes with almost identical 3D structures but opposite enantioselectivities and different reaction mechanisms. Chem Bio Chem 2012; 13: 1932-9.
-
(2012)
Chem Bio Chem
, vol.13
, pp. 1932-1939
-
-
Andexer, J.N.1
Staunig, N.2
Eggert, T.3
-
63
-
-
84859587203
-
Tailoring a stabilized variant of hydroxynitrile lyase from Arabidopsis thaliana
-
Okrob D, Metzner J, Wiechert W, Gruber K, Pohl M. Tailoring a stabilized variant of hydroxynitrile lyase from Arabidopsis thaliana. Chem Bio Chem 2012; 13: 797-802.
-
(2012)
Chem Bio Chem
, vol.13
, pp. 797-802
-
-
Okrob, D.1
Metzner, J.2
Wiechert, W.3
Gruber, K.4
Pohl, M.5
-
64
-
-
80052804714
-
Hydroxynitrile lyase from Arabidopsis thaliana: Identification of reaction parameters for enantiopure cyanohydrin synthesis by pure and immobilized catalyst
-
Okrob E, Paravidino M, Orru RVA and et al. Hydroxynitrile lyase from Arabidopsis thaliana: identification of reaction parameters for enantiopure cyanohydrin synthesis by pure and immobilized catalyst. Adv Synth Catal 2011; 353: 2399-408.
-
(2011)
Adv Synth Catal
, vol.353
, pp. 2399-2408
-
-
Okrob, E.1
Paravidino, M.2
Orru, R.V.A.3
-
65
-
-
84863745102
-
Synthesis of chiral cyanohydrins by recombinant Escherichia coli cells in a micro-aqueous reaction system
-
Scholz KE, Okrob D, Kopka B and et al. Synthesis of chiral cyanohydrins by recombinant Escherichia coli cells in a micro-aqueous reaction system. Appl Environ Microbiol 2012; 78: 5025-7.
-
(2012)
Appl Environ Microbiol
, vol.78
, pp. 5025-5027
-
-
Scholz, K.E.1
Okrob, D.2
Kopka, B.3
-
66
-
-
79955766024
-
Synthesis of (R)-beta-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system
-
Fuhshuku K, Asano Y. Synthesis of (R)-beta-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system. J Biotechnol 2011; 153: 153-9.
-
(2011)
J Biotechnol
, vol.153
, pp. 153-159
-
-
Fuhshuku, K.1
Asano, Y.2
-
67
-
-
0002545280
-
Alpha-hydroxynitrile lyase in Hevea brasiliensis and its significance for rapid cyanogenesis
-
Selmar D, Lieberei R, Biehl B, Conn EE. Alpha-hydroxynitrile lyase in Hevea brasiliensis and its significance for rapid cyanogenesis. Physiol Plantarum 1989; 75: 97-101.
-
(1989)
Physiol Plantarum
, vol.75
, pp. 97-101
-
-
Selmar, D.1
Lieberei, R.2
Biehl, B.3
Conn, E.E.4
-
68
-
-
0027325846
-
Aliphatic (S)-cyanohydrins by enzyme-catalyzed synthesis
-
Klempier N, Griengl H, Hayn M. Aliphatic (S)-cyanohydrins by enzyme-catalyzed synthesis. Tetrahedron Lett 1993; 34: 4769-72.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 4769-4772
-
-
Klempier, N.1
Griengl, H.2
Hayn, M.3
-
69
-
-
0028247273
-
Purification, characterization, and cloning of alpha-hydroxynitrile lyase from cassava (Manihot esculenta Crantz)
-
Hughes J, Decarvalho JPC, Hughes MA. Purification, characterization, and cloning of alpha-hydroxynitrile lyase from cassava (Manihot esculenta Crantz). Arch Biochem Biophys 1994; 311: 496-502.
-
(1994)
Arch Biochem Biophys
, vol.311
, pp. 496-502
-
-
Hughes, J.1
Decarvalho, J.P.C.2
Hughes, M.A.3
-
70
-
-
85189259008
-
-
US6337196
-
Kirchner G, Wirth I, Werenka C, Griengl H, Schmidt M. Enzymatic processes for preparing (S)-cyanohydrins. US6337196, 2002.
-
(2002)
Enzymatic processes for preparing (S)-cyanohydrins
-
-
Kirchner, G.1
Wirth, I.2
Werenka, C.3
Griengl, H.4
Schmidt, M.5
-
73
-
-
84889290871
-
Biocatalysis in biphasic systems: Oxynitrilases
-
In: Carrea G, Riva S, Eds., Weinheim: Wiley-VCH
-
Avi M, Griengl H. Biocatalysis in biphasic systems: Oxynitrilases. In: Carrea G, Riva S, Eds. Organic Synthesis with Enzymes in Non-Aqueous Media. Weinheim: Wiley-VCH 2008: pp. 211-26.
-
(2008)
Organic Synthesis with Enzymes in Non-Aqueous Media
, pp. 211-226
-
-
Avi, M.1
Griengl, H.2
-
74
-
-
77956938375
-
Efficient production of active form of recombinant cassava hydroxynitrile lyase using Escherichia coli in low-temperature culture
-
Semba H, Ichige E, Imanaka T, Atomi H, Aoyagi H. Efficient production of active form of recombinant cassava hydroxynitrile lyase using Escherichia coli in low-temperature culture. Methods Mol Biol 2010; 643: 133-44.
-
(2010)
Methods Mol Biol
, vol.643
, pp. 133-144
-
-
Semba, H.1
Ichige, E.2
Imanaka, T.3
Atomi, H.4
Aoyagi, H.5
-
75
-
-
57649200475
-
Improvement of a stereoselective biocatalytic synthesis by substrate and enzyme engineering: 2-hydroxy-(4 '-oxocyclohexyl)acetonitrile as the model
-
Avi M, Wiedner R, Griengl H, Schwab H. Improvement of a stereoselective biocatalytic synthesis by substrate and enzyme engineering: 2-hydroxy-(4 '-oxocyclohexyl)acetonitrile as the model. Chem Eur J 2008; 14: 11415-22.
-
(2008)
Chem Eur J
, vol.14
, pp. 11415-11422
-
-
Avi, M.1
Wiedner, R.2
Griengl, H.3
Schwab, H.4
-
76
-
-
0037416489
-
Substrate specificity of mutants of the hydroxynitrile lyase from Manihot esculenta
-
Bühler H, Effenberger F, Förster S, Roos J, Wajant H. Substrate specificity of mutants of the hydroxynitrile lyase from Manihot esculenta. ChemBioChem 2003; 4: 211-6.
-
(2003)
ChemBioChem
, vol.4
, pp. 211-216
-
-
Bühler, H.1
Effenberger, F.2
Förster, S.3
Roos, J.4
Wajant, H.5
-
77
-
-
0036136695
-
Structure determinants of substrate specificity of hydroxynitrile lyase from Manihot esculenta
-
Lauble H, Miehlich B, Förster S and et al. Structure determinants of substrate specificity of hydroxynitrile lyase from Manihot esculenta. Protein Sci 2002; 11: 65-71.
-
(2002)
Protein Sci
, vol.11
, pp. 65-71
-
-
Lauble, H.1
Miehlich, B.2
Förster, S.3
-
79
-
-
79951945914
-
Comparative expression of wild-type and highly soluble mutant His103Leu of hydroxynitrile lyase from Manihot esculenta in prokaryotic and eukaryotic expression systems
-
Dadashipour M, Fukuta Y, Asano Y. Comparative expression of wild-type and highly soluble mutant His103Leu of hydroxynitrile lyase from Manihot esculenta in prokaryotic and eukaryotic expression systems. Protein Expr Purif 2011; 77: 92-7.
-
(2011)
Protein Expr Purif
, vol.77
, pp. 92-97
-
-
Dadashipour, M.1
Fukuta, Y.2
Asano, Y.3
-
80
-
-
79960321967
-
Functional expression of a plant hydroxynitrile lyase in Escherichia coli by directed evolution: Creation and characterization of highly in vivo soluble mutants
-
Asano Y, Dadashipour M, Yamazaki M, Doi N, Komeda H. Functional expression of a plant hydroxynitrile lyase in Escherichia coli by directed evolution: creation and characterization of highly in vivo soluble mutants. Prot Eng Des Sel 2011; 24: 607-16.
-
(2011)
Prot Eng Des Sel
, vol.24
, pp. 607-616
-
-
Asano, Y.1
Dadashipour, M.2
Yamazaki, M.3
Doi, N.4
Komeda, H.5
-
81
-
-
77956021391
-
Switching from an esterase to a hydroxynitrile lyase mechanism requires only two amino acid substitutions
-
Padhi SK, Fujii R, Legatt G and et al. Switching from an esterase to a hydroxynitrile lyase mechanism requires only two amino acid substitutions. Chem Biol 2010; 17: 863-71.
-
(2010)
Chem Biol
, vol.17
, pp. 863-871
-
-
Padhi, S.K.1
Fujii, R.2
Legatt, G.3
-
83
-
-
60849116707
-
Synthesis of aliphatic (S)-alpha-hydroxycarboxylic amides using a one-pot bienzymatic cascade of immobilised oxynitrilase and nitrile hydratase
-
van Pelt S, van Rantwijk F, Sheldon RA. Synthesis of aliphatic (S)-alpha-hydroxycarboxylic amides using a one-pot bienzymatic cascade of immobilised oxynitrilase and nitrile hydratase. Adv Synth Catal 2009; 351: 397-404.
-
(2009)
Adv Synth Catal
, vol.351
, pp. 397-404
-
-
van Pelt, S.1
van Rantwijk, F.2
Sheldon, R.A.3
-
84
-
-
34547191782
-
A hydroxynitrile lyase in organic solvent-free systems to overcome thermodynamic limitations
-
von Langermann J, Mell A, Paetzold E, Daußmann T, Kragl U. A hydroxynitrile lyase in organic solvent-free systems to overcome thermodynamic limitations. Adv Synth Catal 2007; 349: 1418-24.
-
(2007)
Adv Synth Catal
, vol.349
, pp. 1418-1424
-
-
von Langermann, J.1
Mell, A.2
Paetzold, E.3
Daußmann, T.4
Kragl, U.5
-
85
-
-
84855654946
-
Conversion of sterically demanding alpha, alpha-disubstituted phenylacetonitriles by the arylacetonitrilase from Pseudomonas fluorescens EBC191
-
Baum S, Williamson DS, Sewell T, Stolz A. Conversion of sterically demanding alpha, alpha-disubstituted phenylacetonitriles by the arylacetonitrilase from Pseudomonas fluorescens EBC191. Appl Environ Microbiol 2012; 78: 48-57.
-
(2012)
Appl Environ Microbiol
, vol.78
, pp. 48-57
-
-
Baum, S.1
Williamson, D.S.2
Sewell, T.3
Stolz, A.4
-
86
-
-
84856835101
-
Application of a recombinant Escherichia coli whole-cell catalyst expressing hydroxynitrile lyase and nitrilase activities in ionic liquids for the production of (S)-mandelic acid and (S)-mandeloamide
-
Baum S, van Rantwijk F, Stolz A. Application of a recombinant Escherichia coli whole-cell catalyst expressing hydroxynitrile lyase and nitrilase activities in ionic liquids for the production of (S)-mandelic acid and (S)-mandeloamide. Adv Synth Catal 2012; 354: 113-22.
-
(2012)
Adv Synth Catal
, vol.354
, pp. 113-122
-
-
Baum, S.1
van Rantwijk, F.2
Stolz, A.3
-
87
-
-
84858151784
-
Asymmetric synthesis of both the enantiomers of antidepressant venlafaxine and its analogues
-
Bhuniya R, Nanda S. Asymmetric synthesis of both the enantiomers of antidepressant venlafaxine and its analogues. Tetrahedron Lett 2012; 53: 1990-2.
-
(2012)
Tetrahedron Lett
, vol.53
, pp. 1990-1992
-
-
Bhuniya, R.1
Nanda, S.2
-
88
-
-
85189258295
-
-
EP0326063
-
Niedermayer U, Kragl U, Kula M-R, Wandrey C, Makryaleas K, Drauz K. Enzymatisches Verfahren zur Herstellung von optisch aktiven Cyanhydrinen. EP0326063, 1994.
-
(1994)
Enzymatisches Verfahren zur Herstellung von optisch aktiven Cyanhydrinen
-
-
Niedermayer, U.1
Kragl, U.2
Kula, M.-R.3
Wandrey, C.4
Makryaleas, K.5
Drauz, K.6
|