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NTIS 바로가기Bioprocess and biosystems engineering, v.37 no.7, 2014년, pp.1241 - 1248
Zhang, Zhi-Jun , Pan, Jiang , Li, Chun-Xiu , Yu, Hui-Lei , Zheng, Gao-Wei , Ju, Xin , Xu, Jian-He
Recombinant Escherichia coli cells expressing Alcaligenes sp. nitrilase were simply immobilized by direct cross-linking using glutaraldehyde. About 85 % of the total nitrilase activity was recovered under the optimal cross-linking conditions. The thermal stabilities of the cross-linked cells measure...
Microb Cell Fact JS Gong 11 142 2012 10.1186/1475-2859-11-142 Gong JS, Lu ZM, Li H, Shi JS, Zhou ZM, Xu ZH (2012) Nitrilases in nitrile biocatalysis: recent progress and forthcoming research. Microb Cell Fact 11:142-159
Adv Synth Catal H Groger 343 547 2001 10.1002/1615-4169(200108)343:6/7<547::AID-ADSC547>3.0.CO;2-A Groger H (2001) Enzymatic routes to enantiomerically pure aromatic α-hydroxy carboxylic acids: a further example for the diversity of biocatalysis. Adv Synth Catal 343:547-558
Top Catal MX Wang 35 117 2005 10.1007/s11244-005-3817-1 Wang MX (2005) Enantioselective biotransformations of nitriles in organic synthesis. Top Catal 35:117-130
Chimia MX Wang 63 331 2009 10.2533/chimia.2009.331 Wang MX (2009) Progress of enantioselective nitrile biotransformations in organic synthesis. Chimia 63:331-333
Org Lett D Zhu 9 2561 2007 10.1021/ol070962b Zhu D, Ankati H, Mukherjee C, Yang Y, Biehl ER, Hua L (2007) Asymmetric reduction of β-ketonitriles with a recombinant carbonyl reductase and enzymatic transformation to optically pure β-hydroxy carboxylic acids. Org Lett 9:2561-2563
Appl Microbiol Biotechnol X Ju 86 83 2010 10.1007/s00253-009-2286-z Ju X, Yu HL, Pan J, Wei DZ, Xu JH (2010) Bioproduction of chiral mandelate by enantioselective deacylation of α-acetoxyphenylacetic acid using whole cells of newly isolated Pseudomonas sp. ECU1011. Appl Microbiol Biotechnol 86:83-91
Trends Biotechnol MV Golynskiy 28 340 2010 10.1016/j.tibtech.2010.04.003 Golynskiy MV, Seelig B (2010) De Novo enzymes: from computational design to mRNA display. Trends Biotechnol 28:340-345
Bioprocess Biosyst Eng YC He 31 445 2008 10.1007/s00449-007-0181-5 He YC, Xu JH, Pan J, Ouyang LM, Xu Y (2008) Preparation of (R)-(−)-mandelic acid and its derivatives from racemates by enantioselective degradation with a newly isolated bacterial strain Alcaligenes sp. ECU0401. Bioprocess Biosyst Eng 31:445-451
Biosci Biotechnol Biochem S Oda 56 1216 1992 10.1271/bbb.56.1216 Oda S, Kikuchi Y, Nanishi Y (1992) Synthesis of optically active mandelic acid via microbial oxidation of racemic 1-phenyl-1,2-ethanediol. Biosci Biotechnol Biochem 56:1216-1220
J Org Chem MAK Patterson 46 4682 1981 10.1021/jo00336a011 Patterson MAK, Szajewski RP, Whitesides GM (1981) Enzymatic conversion of alpha-keto aldehydes to optically active alpha hydroxy acids using glyoxalase I and II. J Org Chem 46:4682-4685
Enzyme Microb Technol MT Xiao 37 589 2005 10.1016/j.enzmictec.2005.02.018 Xiao MT, Huang YY, Shi XA, Guo YH (2005) Bioreduction of phenylglyoxylic acid to R-(−)-mandelic acid by Saccharomyces cerevisiae FD11b. Enzyme Microb Technol 37:589-596
Biochem Eng J GD Yadav 19 101 2004 10.1016/j.bej.2003.12.004 Yadav GD, Sivakumar P (2004) Enzyme-catalysed optical resolution of mandelic acid via RS(∓)-methyl mandelate in non-aqueous media. Biochem Eng J 19:101-107
Appl Environ Microbiol K Yamamoto 57 3028 1991 10.1128/AEM.57.10.3028-3032.1991 Yamamoto K, Oishi K, Fujimatsu I, Komatsu KI (1991) Production of R-(−)-mandelic acid from mandelonitrile by Alcaligenes faecalis ATCC 8750. Appl Environ Microbiol 57:3028-3032
Appl Microbiol Biotechnol A Banerjee 72 77 2006 10.1007/s00253-005-0255-8 Banerjee A, Kaul P, Banerjee UC (2006) Enhancing the catalytic potential of nitrilase from Pseudomonas putida for stereoselective nitrile hydrolysis. Appl Microbiol Biotechnol 72:77-87
Tetrahedron Asymmetry P Kaul 15 207 2004 10.1016/j.tetasy.2003.10.041 Kaul P, Banerjee A, Mayilraj S, Banerjee UC (2004) Screening for enantioselective nitrilases: kinetic resolution of racemic mandelonitrile to (R)-(−)-mandelic acid by new bacterial isolates. Tetrahedron Asymmetry 15:207-211
Biomacromolecules P Kaul 7 1536 2006 10.1021/bm0507913 Kaul P, Banerjee A, Banerjee UC (2006) Stereoselective nitrile hydrolysis by immobilized whole-cell biocatalyst. Biomacromolecules 7:1536-1541
Bioprocess Biosyst Eng R Singh 27 415 2005 10.1007/s00449-005-0013-4 Singh R, Banerjee A, Kaul P, Barse B, Banerjee UC (2005) Release of an enantioselective nitrilase from Alcaligenes faecalis MTCC 126: a comparative study. Bioprocess Biosyst Eng 27:415-424
BMC Biotechnol H Wang 13 14 2013 10.1186/1472-6750-13-14 Wang H, Sun H, Wei D (2013) Discovery and characterization of a highly efficient enantioselective mandelonitrile hydrolase from Burkholderia cenocepacia J2315 by phylogeny-based enzymatic substrate specificity prediction. BMC Biotechnol 13:14-24
Biochem Eng J YP Xue 53 143 2010 10.1016/j.bej.2010.10.009 Xue YP, Liu ZQ, Xu M, Wang YJ, Zheng YG, Shen YC (2010) Enhanced biotransformation of (R, S)-mandelonitrile to (R)-(−)-mandelic acid with in situ production removal by addition of resin. Biochem Eng J 53:143-149
J In Microbiol Biotechnol YP Xue 38 337 2011 10.1007/s10295-010-0778-6 Xue YP, Xu SZ, Liu ZQ, Zheng YG, Shen YC (2011) Enantioselective biocatalytic hydrolysis of (R, S)-mandelonitrile for production of (R)-(−)-mandelic acid by a newly isolated mutant strain. J In Microbiol Biotechnol 38:337-345
Chin Chem Lett YC He 18 677 2007 10.1016/j.cclet.2007.04.034 He YC, Xu JH, Xu Y, Ouyang LM, Pan J (2007) Biocatalytic synthesis of (R)-(−)-mandelic acid from racemic mandelonitrile by a newly isolated nitrilase-producer Alcaligenes sp. ECU0401. Chin Chem Lett 18:677-680
J Ind Microbiol Biotechnol YC He 37 741 2010 10.1007/s10295-010-0720-y He YC, Zhang ZJ, Xu JH, Liu YY (2010) Biocatalytic synthesis of (R)-(−)-mandelic acid from racemic mandelonitrile by cetyltrimethylammonium bromidepermeabilized cells of Alcaligenes faecalis ECU0401. J Ind Microbiol Biotechnol 37:741-750
Process Biochem ZJ Zhang 45 887 2010 10.1016/j.procbio.2010.02.011 Zhang ZJ, Xu JH, He YC, Ouyang LM, Liu YY, Imanaka T (2010) Efficient production of (R)-(-)-mandelic acid with highly substrate/product tolerant and enantioselective nitrilase of recombinant Alcaligenes sp. Process Biochem 45:887-891
Bioprocess Biosyst Eng ZJ Zhang 34 315 2011 10.1007/s00449-010-0473-z Zhang ZJ, Xu JH, He YC, Ouyang LM, Liu YY (2011) Cloning and biochemical properties of a highly thermostable and enantioselective nitrilase from Alcaligenes sp. ECU0401 and its potential for (R)-(−)-mandelic acid production. Bioprocess Biosyst Eng 34:315-322
J Biotechnol ZJ Zhang 152 24 2011 10.1016/j.jbiotec.2011.01.013 Zhang ZJ, Pan J, Liu JF, Xu JH, He YC, Liu YY (2011) Significant enhancement of (R)-mandelic acid production by relieving substrate inhibition of recombinant nitrilase in toluene-water biphasic system. J Biotechnol 152:24-29
J Mol Catal B Enzym GW Zheng 70 138 2011 10.1016/j.molcatb.2011.02.018 Zheng GW, Yu HL, Li CX, Pan J, Xu JH (2011) Immobilization of Bacillus subtilis esterase by simple cross-linking for enzymatic resolution of dl-menthyl acetate. J Mol Catal B Enzym 70:138-143
Curr Org Chem V Mylerova 7 1279 2003 10.2174/1385272033486486 Mylerova V, Martinkova L (2003) Synthetic applications of nitrile-converting enzymes. Curr Org Chem 7:1279-1295
Biotechnol Bioeng PCJ Roach 85 450 2004 10.1002/bit.10852 Roach PCJ, Ramsden DK, Hughes J, Williams P (2004) Biocatalytic scrubbing of gaseous acrylonitrile using Rhodococcus ruber immobilized in synthetic silicone polymer (ImmobaSil) rings. Biotechnol Bioeng 85:450-455
J Ind Microbiol Biotechnol L Kabaivanova 32 7 2005 10.1007/s10295-004-0189-7 Kabaivanova L, Dobreva E, Dimitrov P, Emanuilova E (2005) Immobilization of cells with nitrilase activity from a thermophilic bacterial strain. J Ind Microbiol Biotechnol 32:7-11
J Mol Catal B Enzym V Vejvoda 39 55 2006 10.1016/j.molcatb.2006.01.027 Vejvoda V, Kaplan O, Benzouska K, Martinkova L (2006) Mild hydrolysis of nitriles by the immobilized nitrilase from Aspergillus niger K10. J Mol Catal B Enzym 39:55-58
Adv Synth Catal P Kaul 349 2167 2007 10.1002/adsc.200700125 Kaul P, Stolz A, Banerjee UC (2007) Cross-linked amorphous nitrilase aggregates for enantioselective nitrile hydrolysis. Adv Synth Catal 349:2167-2176
Bioresour Technol S Kumar 101 6856 2010 10.1016/j.biortech.2010.03.084 Kumar S, Mohan U, Kamble AL, Powar S, Banerjee UC (2010) Cross-linked enzyme aggregates of recombinant Pseudomonas putida nitrilase for enantioselective nitrile hydrolysis. Bioresour Technol 101:6856-6858
Org Process Res Dev RA Sheldon 15 213 2011 10.1021/op100289f Sheldon RA (2011) Cross-linked enzyme aggregates as industrial biocatalysts. Org Process Res Dev 15:213-233
J Mol Catal B Enzym C Mateo 38 154 2006 10.1016/j.molcatb.2005.12.007 Mateo C, Fernandes B, van Rantwijk F, Stolz A, Sheldon RA (2006) Stabilisation of oxygen-labile nitrilases via co-aggregation with poly(ethyleneimine). J Mol Catal B Enzym 38:154-157
Biotechnol Bioeng C Mateo 86 273 2004 10.1002/bit.20033 Mateo C, Palomo JM, van Langen LM, van Rantwijk F, Sheldon RA (2004) A new, mild cross-linking methodology to prepare cross-linked enzyme aggregates. Biotechnol Bioeng 86:273-276
Appl Microbiol Biotechnol JF Liu 89 665 2011 10.1007/s00253-010-2866-y Liu JF, Zhang ZJ, Li AT, Pan J, Xu JH (2011) Significantly enhanced production of recombinant nitrilase by optimization of culture conditions and glycerol feeding. Appl Microbiol Biotechnol 89:665-672
Org Process Res Dev YP Xue 17 213 2013 10.1021/op3001993 Xue YP, Xu M, Chen HS, Liu ZQ, Wang YJ, Zheng YG (2013) A novel integrated bioprocess for efficient production of (R)-(−)-mandelic acid with immobilized Alcaligenes faecalis ZJUTB10. Org Process Res Dev 17:213-220
Biotech SV Pawar 2 319 2012 Pawar SV, Meena VS, Kaushik S, Kamble A, Kumar S, Chisti Y, Banerjee UC (2012) Stereo-selective conversion of mandelonitrile to (R)-(−)-mandelic acid using immobilized cells of recombinant Escherichia coli. 3. Biotech 2:319-326
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