|
[1] 郑裕国,薛亚平,柳志强,等.腈转化酶在精细化学品生产中的应用.生物工程学报,2009, 25(12):1795-1807. Zheng Y G,Xue Y P,Liu Z Q,et al. Applications of nitrile converting enzymes in the production of fine chemicals. Chinese Journal of Biotechnology,2009,25(12):1795-1807.
[2] Mayaux J F,Cerbelaud E,Soubrier F,et al. Purification, cloning and primary structure of a new enantiomer-selective amidase from a Rhodococcus Strain - structural evidence for a conserved genetic coupling with nitrile hydratase. Journal of Bacteriology,1991,173(21):6694-6704.
[3] Martinkova L,Kren V. Nitrile- and amide-converting microbial enzymes: Stereo-,regio- and chemoselectivity. Biocatalysis and Biotransformation,2002,20(2):73-93.
[4] Lorenz P,Eck J. Screening for novel industrial biocatalysts. Engineering in Life Sciences,2004,4(6):501-504.
[5] Schmid A,Dordick J S,Hauer B,et al. Industrial biocatalysis today and tomorrow. Nature,2001, 409(6817):258-268.
[6] Kobayashi M,Komeda H,Nagasawa T,et al. Amidase coupled with low-molecular-mass nitrile hydratase from Rhodococcus Rhodochrous J1 - sequencing and expression of the gene and purification and characterization of the gene-product. European Journal of Biochemistry,1993, 217(1):327-336.
[7] Ciskanik L M,Wilczek J M,Fallon R D. Purification and characterization of an enantioselective amidase from Pseudomonas Chlororaphis B23. Applied and Environmental Microbiology,1995,61(3):998-1003.
[8] Petre D,Cerbelaud E,Yeh P. Enantioselective amidases and uses thereof. US 5766918,1998.
[9] Hermes H F M,Tandler R F,Sonke T,et al. Purification and characterization of an L-amino amidase from Mycobacterium Neoaurum ATCC 25795. Applied and Environmental Microbiology,1994,60(1):153-159.
[10] Hirrlinger B,Stolz A,Knackmuss H J. Purification and properties of an amidase from Rhodococcus erythropolis MP50 which enantioselectively hydrolyzes 2-arylpropionamides. Journal of Bacteriology,1996,178(12):3501-3507.
[11] Yamamoto K,Otsubo K,Matsuo A,et al. Production of R-(-)-ketoprofen from an amide compound by Comamonas acidovorans KPO-2771-4. Applied and Environmental Microbiology,1996,62(1):152-155.
[12] Yang Z Y,Ni Y,Lu Z Y,et al. Industrial production of S-2,2-dimethylcyclopropanecarboxamide with a novel recombinant R-amidase from Delftia tsuruhatensis. Process Biochemistry,2011,46(1):182-187.
[13] Ozaki A,Kawasaki H,Yagasaki M,et al. Enzymatic production of D-alanine from DL-alaninamide by novel D-alaninamide specific amide hydrolase. Bioscience Biotechnology and Biochemistry,1992,56(12):1980-1984.
[14] Prelog V. Specification of the stereospecificity of some oxidoreductases by diamond lattice sections. Pure Appl. Chem,1964,9(9):119-130.
[15] Kazlauskas R J,Weissfloch A N E,Rappaport A T,et al. A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosa. Journal of Organic Chemistry,1991,56(8):2656-2665.
[16] Ma D Y,Wang D X,Pan J,et al. Nitrile biotransformations for the synthesis of highly enantioenriched beta-hydroxy and beta-amino acid and amide derivatives: A general and simple but powerful and efficient benzyl protection strategy to increase enantioselectivity of the amidase. Journal of Organic Chemistry,2008,73(11):4087-4091.
[17] Wu Z L,Li Z Y. Enantioselective hydrolysis of various racemic alpha-substituted arylacetonitriles using Rhodococcus sp. CGMCC 0497. Tetrahedron-Asymmetry,2001,12(23):3305-3312.
[18] Phillips R S. Temperature modulation of the stereochemistry of enzymatic catalysis:Prospects for exploitation. Trends in Biotechnology,1996,14(1):13-16.
[19] Phillips R S. Temperature effects on stereochemistry of enzymatic-reactions. Enzyme and Microbial Technology,1992,14(5):417-419.
[20] Jin S J,Zheng R C, Zheng Y G,et al. R-enantioselective hydrolysis of 2, 2-dimethylcyclopropanecarboxamide by amidase from a newly isolated strain Brevibacterium epidermidis ZJB-07021. Journal of Applied Microbiology,2008,105(4):1150-1157.
[21] Zheng R C,Wang Y S,Liu Z Q,et al. Isolation and characterization of Delftia tsuruhatensis ZJB-05174, capable of R-enantioselective degradation of 2,2-dimethylcyclopropanecarboxamide. Research in Microbiology,2007,158(3):258-264.
[22] Yeom S J,Kim H J,Oh D K. Enantioselective production of 2, 2-dimethylcyclopropane carboxylic acid from 2, 2-dimethylcyclopropane carbonitrile using the nitrile hydratase and amidase of Rhodococcus erythropolis ATCC 25544. Enzyme and Microbial Technology,2007,41(6-7):842-848.
[23] 彭立凤, 赵汝淇.有机介质中酶催化活性和选择性的调控.生物技术通报,1999,15(6):28-32. Peng L F,Zhao R Q. Accommodation and control of enzymatic activity and selectivity in organic solvents. Biotechnology Bulletin,1999,15(6):28-32.
[24] 郑仁朝.立体选择性酰胺酶的筛选及其动力学拆分制备(S)-(+)-2,2-二甲基环丙烷甲酰胺的研究. 杭州:浙江工业大学,生物与环境工程学院,2007. Zheng R C. Screening for enantioselective amidase: Kinetic resolution of racemate to (S)-(+)-2,2-dimethylcyclopropane carboxamide. Hangzhou:Zhejiang University of Technology,College of Biological and Environmental Engineering,2007.
[25] Gilligan T,Yamada H,Nagasawa T. Production of S-(+)-2-phenylpropionic acid from (R,S)-2-phenylpropionitrile by the combination of nitrile hydratase and stereoselective amidase in Rhodococcus equi TG328. Applied Microbiology and Biotechnology,1993,39(6):720-725.
[26] Shaw N M,Naughton A,Robins K,et al. Selection, purification, characterisation, and cloning of a novel heat-stable stereo-specific amidase from Klebsiella oxytoca, and its application in the synthesis of enantiomerically pure (R)- and (S)-3,3,3-trifluoro-2-hydroxy-2-methylpropionic acids and (S)-3,3,3-trifluoro-2-hydroxy-2-methylpropionamide. Organic Process Research & Development,2002,6(4):497-504.
[27] Ewert C,Lutz-Wahl S,Fischer L. Enantioselective conversion of alpha-arylnitriles by Klebsiella oxytoca. Tetrahedron-Asymmetry,2008,19(22):2573-2578.
[28] Snell D,Colby J. Enantioselective hydrolysis of racemic ibuprofen amide to S-(+)-ibuprofen by Rhodococcus AJ270. Enzyme and Microbial Technology,1999,24(3-4):160-163.
[29] Eichhorn E,Roduit J P,Shaw N,et al. Preparation of (S)-piperazine-2-carboxylic acid, (R)-piperazine-2-carboxylic acid, and (S)-piperidine-2-carboxylic acid by kinetic resolution of the corresponding racemic carboxamides with stereoselective amidases in whole bacterial cells. Tetrahedron-Asymmetry,1997,8(15):2533-2536.
[30] Layh N,Stolz A,Bohme J,et al. Enantioselective hydrolysis of racemic naproxen nitrile and naproxen amide to S-naproxen by new bacterial isolates. Journal of Biotechnology,1994,33(2):175-182.
[31] Komeda H,Asano Y. Gene cloning, nucleotide sequencing, and purification and characterization of the D-stereospecific amino-acid amidase from Ochrobactrum anthropi SV3. European Journal of Biochemistry,2000,267(7):2028-2035.
[32] Vandentweel W J J,Vandooren T J G M,Dejonge P H,et al. Ochrobactrum Anthropi NCIMB 40321 - a new biocatalyst with broad-spectrum L-specific amidase activity. Applied Microbiology and Biotechnology,1993,39(3):296-300.
[33] Hongpattarakere T,Komeda H,Asano Y. Purification, characterization, gene cloning and nucleotide sequencing of D-stereospecific amino acid amidase from soil bacterium: Delftia acidovorans. Journal of Industrial Microbiology & Biotechnology,2005,32(11-12):567-576.
[34] Suzuki Y,Ohta H. Identification of a thermostable and enantio selective amidase from the thermoacidophilic archaeon Sulfolobus tokodaii strain 7. Protein Expression and Purification,2006,45(2):368-373.
[35] Wegman M A,Heinemann U,Rantwijk F,et al. Hydrolysis of D,L-phenylglycine nitrile by new bacterial cultures. Journal of Molecular Catalysis B-Enzymatic,2001,11(4-6):249-253.
[36] d’Abusco A S,Ammendola S,Scandurra R,et al. Molecular and biochemical characterization of the recombinant amidase from hyperthermophilic archaeon Sulfolobus solfataricus. Extremophiles,2001,5(3):183-192.
[37] Hensel M,Lutz-Wahl S,Fischer L. Stereoselective hydration of (R, S)-phenylglycine nitrile by new whole cell biocatalysts. Tetrahedron-Asymmetry,2002,13(24):2629-2633.
[38] Komeda H,Harada H,Washika S,et al. A novel R-stereoselective amidase from Pseudomonas sp. MCI3434 acting on piperazine-2-tert-butylcarboxamide. European Journal of Biochemistry,2004,271(8):1580-1590.
[39] Komeda H,Harada H,Washika S,et al. S-Stereoselective piperazine-2-tert-butylcarboxamide hydrolase from Pseudomonas azotoformans IAM 1603 is a novel L-amino acid amidase. European Journal of Biochemistry,2004,271(8):1465-1475.
[40] 吕志堂, 徐长源, 郭晓东,等.假单胞菌 X1 的培养及哌嗪-2-甲酰胺的拆分条件优化.中国医药工业杂志,2009(005):341-344. Lü Z T,Xu C Y,Guo X D,et al. Optimization of culture conditions of pseudomonas sp. X1 and resolution of piperazine-2-carboxaminde. Chinese Journal of Pharmaceuticals,2009(005):341-344.
[41] Komeda H,Asano Y. A novel D-stereoselective amino acid amidase from Brevibacterium iodinum: gene cloning, expression and characterization. Enzyme and Microbial Technology,2008,43(3):276-283.
[42] Baek D H,Kwon S J,Hong S P,et al. Characterization of a thermostable D-stereospecific alanine amidase from Brevibacillus borstelensis BCS-1. Applied and Environmental Microbiology,2003,69(2):980-986.
[43] Krieg L,Ansorge-Schumacher M B,Kula M.R. Screening for amidases: Isolation and characterization of a novel D-amidase from Variovorax paradoxus. Advanced Synthesis & Catalysis,2002,344(9):965-973.
[44] Bianchi D,Battistel E,Cesti P,et al. Substrate-specificity and stereoselectivity of hydrolytic enzymes from Brevibacterium imperiale B222. Applied Microbiology and Biotechnology,1993,40(1):53-56.
[45] Bauer R,Hirrlinger B,Layh N,et al. Enantioselective hydrolysis of racemic 2-phenylpropionitrile and other (R,S)-2-arylpropionitriles by a new bacterial isolate, Agrobacterium tumefaciens Strain D3. Applied Microbiology and Biotechnology,1994,42(1):1-7.
[46] Komeda H,Hariyama N,Asano Y. L-Stereoselective amino acid amidase with broad substrate specificity from Brevundimonas diminuta: characterization of a new member of the leucine aminopeptidase family. Applied Microbiology and Biotechnology,2006,70(4):412-421.
[47] Makhongela H S,Glowacka A E,Agarkar V B,et al. A novel thermostable nitrilase superfamily amidase from Geobacillus pallidus showing acyl transfer activity. Applied Microbiology and Biotechnology,2007,75(4):801-811.
[48] Doran J P,Duggan P,Masterson M,et al. Expression and purification of a recombinant enantioselective amidase. Protein Expr Purif,2005,40(1):190-196.
[49] Egorova K,Trauthwein H,Verseck S,et al. Purification and properties of an enantioselective and thermoactive amidase from the thermophilic actinomycete Pseudonocardia thermophila. Applied Microbiology and Biotechnology,2004,65(1):38-45.
[50] Mayaux J F,Cerbelaud E,Soubrier F,et al. Purification, cloning, and primary structure of an enantiomer-selective amidase from Brevibacterium sp. Strain R312 - structural evidence for genetic coupling with nitrile hydratase. Journal of Bacteriology,1990,172(12):6764-6773.
[51] Wang M X,Feng G Q. Enzymatic synthesis of optically active 2-methyl- and 2, 2-dimethylcyclopropanecarboxylic acids and their derivatives. Journal of Molecular Catalysis B-Enzymatic,2002,18(4-6):267-272.
[52] Wu Z L,Li Z Y. Biocatalytic asymmetric hydrolysis of (+/-)-beta-hydroxy nitriles by Rhodococcus sp CGMCC 0497. Journal of Molecular Catalysis B-Enzymatic,2003,22(1-2):105-112.
[53] Banerjee A,Sharma R,Banerjee U C. The nitrile-degrading enzymes: current status and future prospects. Applied Microbiology and Biotechnology,2002,60(1-2):33-44.
[54] Patel R N. Biocatalysis: Synthesis of key Intermediates for development of pharmaceuticals. Acs Catalysis,2011,1(9):1056-1074.
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