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Volumn 35, Issue 9, 2012, Pages 1515-1522

Isolation of enantioselective α-hydroxyacid dehydrogenases based on a high-throughput screening method

Author keywords

Hydroxyacid; Hydroxyacid dehydrogenase; Enantioselectivity; High throughput screening; Pseudomonas aeruginosa

Indexed keywords

2 ,4-DINITROPHENYLHYDRAZINE; COLORIMETRIC METHODS; ENANTIOSELECTIVE; HIGH-THROUGHPUT; HIGH-THROUGHPUT SCREENING; HYDROXYACIDS; POTENTIAL APPLICATIONS; PSEUDOMONAS AERUGINOSA; SPECTROPHOTOMETRIC MEASUREMENTS;

EID: 84870327274     PISSN: 16157591     EISSN: 16157605     Source Type: Journal    
DOI: 10.1007/s00449-012-0741-1     Document Type: Article
Times cited : (11)

References (28)
  • 1
    • 0036782116 scopus 로고    scopus 로고
    • Putting chirality to work: The strategy of chiral switches
    • Agranat I, Caner H, Caldwell J (2002) Putting chirality to work: the strategy of chiral switches. Nat Rev Drug Discov 1:753-768
    • (2002) Nat Rev Drug Discov , vol.1 , pp. 753-768
    • Agranat, I.1    Caner, H.2    Caldwell, J.3
  • 2
    • 0242424115 scopus 로고    scopus 로고
    • A transient intermediate in the reaction catalyzed by (s)-mandelate dehydrogenase from pseudomonas putida
    • Dewanti AR, Mitra B (2003) A transient intermediate in the reaction catalyzed by (S)-mandelate dehydrogenase from Pseudomonas putida. Biochemistry 42:12893-12901
    • (2003) Biochemistry , vol.42 , pp. 12893-12901
    • Dewanti, A.R.1    Mitra, B.2
  • 3
    • 4143117810 scopus 로고    scopus 로고
    • Role of glycine 81 in (s)-mandelate dehydrogenase from pseudomonas putida in substrate specificity and oxidase activity
    • Dewanti AR, Xu Y, Mitra B (2004) Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase activity. Biochemistry 43:10692-10700
    • (2004) Biochemistry , vol.43 , pp. 10692-10700
    • Dewanti, A.R.1    Xu, Y.2    Mitra, B.3
  • 4
    • 85005697480 scopus 로고
    • Dehydrogenases for the synthesis of chiral compounds
    • Hummel W, Kula MR (1989) Dehydrogenases for the synthesis of chiral compounds. Eur J Biochem 184:1-13
    • (1989) Eur J Biochem , vol.184 , pp. 1-13
    • Hummel, W.1    Kula, M.R.2
  • 5
    • 43549084542 scopus 로고    scopus 로고
    • A new family of d-2-hydroxyacid dehydrogenases that comprises d-mandelate dehydrogenases and 2-ketopantoate reductases
    • Wada Y, Iwai S, Tamura Y, Ando T, Shinoda T, Arai K, Taguchi H (2008) A new family of D-2-hydroxyacid dehydrogenases that comprises D-mandelate dehydrogenases and 2-ketopantoate reductases. Biosci Biotechnol Biochem 72:1087-1094
    • (2008) Biosci Biotechnol Biochem , vol.72 , pp. 1087-1094
    • Wada, Y.1    Iwai, S.2    Tamura, Y.3    Ando, T.4    Shinoda, T.5    Arai, K.6    Taguchi, H.7
  • 6
    • 78449259734 scopus 로고    scopus 로고
    • Biocatalysis -Key to sustainable industrial chemistry
    • Wohlgemuth R (2011) Biocatalysis -key to sustainable industrial chemistry. Curr Opin Biotechnol 21:713-724
    • (2011) Curr Opin Biotechnol , vol.21 , pp. 713-724
    • Wohlgemuth, R.1
  • 7
    • 38349029126 scopus 로고    scopus 로고
    • Deracemization of secondary alcohols through a concurrent tandem biocatalytic oxidation and reduction
    • Voss CV, Gruber CC, Kroutil W (2008) Deracemization of secondary alcohols through a concurrent tandem biocatalytic oxidation and reduction. Angew Chem Int Edit 47:741-745
    • (2008) Angew Chem Int Edit , vol.47 , pp. 741-745
    • Voss, C.V.1    Gruber, C.C.2    Kroutil, W.3
  • 8
    • 0028970755 scopus 로고
    • R-(-)-mandelic acid production from racemic mandelic acids using pseudomonas polycolor ifo 3918 and micrococcus freudenreichii ferm-p 13221
    • Takahashi E, Nakamichi K, Furui M (1995) R-(-)-mandelic acid production from racemic mandelic acids using Pseudomonas polycolor IFO 3918 and Micrococcus freudenreichii FERM-P 13221. J Ferment Bioeng 80:247-250
    • (1995) J Ferment Bioeng , vol.80 , pp. 247-250
    • Takahashi, E.1    Nakamichi, K.2    Furui, M.3
  • 10
    • 0027050187 scopus 로고
    • Highly efficient conversion of (r)-mandelic acid to its (r)-(-)-enantiomer by combination of enzyme-mediated oxidation and reduction
    • Tsuchiya S, Miyamoto K, Ohta H (1992) Highly efficient conversion of (R)-mandelic acid to its (R)-(-)-enantiomer by combination of enzyme-mediated oxidation and reduction. Biotechnol Lett 14:1137-1142
    • (1992) Biotechnol Lett , vol.14 , pp. 1137-1142
    • Tsuchiya, S.1    Miyamoto, K.2    Ohta, H.3
  • 11
    • 0026741055 scopus 로고
    • Enantioselective oxidation of mandelic acid using a phenylmalonate metabolizing pathway of a soil bacterium: Alcaligenes bronchisepticus ku 1201
    • Miyamoto K, Ohta H (1992) Enantioselective oxidation of mandelic acid using a phenylmalonate metabolizing pathway of a soil bacterium: Alcaligenes bronchisepticus KU 1201. Biotechnol Lett 14:363-366
    • (1992) Biotechnol Lett , vol.14 , pp. 363-366
    • Miyamoto, K.1    Ohta, H.2
  • 12
    • 0029053853 scopus 로고
    • R-(-)-mandelic acid production from racemic mandelic acids by pseudomonas polycolor with asymmetric degrading activity
    • Takahashi E, Nakamichi K, Furui M, Mori T (1995) R-(-)-mandelic acid production from racemic mandelic acids by Pseudomonas polycolor with asymmetric degrading activity. J Ferment Bioeng 79:439-442
    • (1995) J Ferment Bioeng , vol.79 , pp. 439-442
    • Takahashi, E.1    Nakamichi, K.2    Furui, M.3    Mori, T.4
  • 13
    • 47349083412 scopus 로고    scopus 로고
    • Preparation of (r)-(-)-mandelic acid and its derivatives from racemates by enantioselective degradation with a newly isolated bacterial strain alcaligenes sp
    • He Y-C, Xu J-H, Pan J, Ouyang L-M, 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. Bioproc Biosyst Eng 31:445-451
    • (2008) ECU0401. Bioproc Biosyst Eng , vol.31 , pp. 445-451
    • He, Y.-C.1    Xu, J.-H.2    Pan, J.3    Ouyang, L.-M.4    Xu, Y.5
  • 14
    • 20444431209 scopus 로고    scopus 로고
    • Preparation of (s)-mandelic acids by enantioselective degradation of racemates with a new isolate pseudomonas putida ecu1009
    • Huang H-R, Xu J-H, Xu Y, Pan J, Liu X (2005) Preparation of (S)-mandelic acids by enantioselective degradation of racemates with a new isolate Pseudomonas putida ECU1009. Tetrahedron Asymmetry 16:2113-2117
    • (2005) Tetrahedron Asymmetry , vol.16 , pp. 2113-2117
    • Huang, H.-R.1    Xu, J.-H.2    Xu, Y.3    Pan, J.4    Liu, X.5
  • 15
    • 0026349486 scopus 로고
    • Analysis of keto acids as their methyl esters of 2,4- dinitrophenylhydrazone derivatives by gas chromatography and gas chromatography-mass spectrometry
    • Navarro-Gonzalez R, Negron-Mendoza A, Albarran G (1991) Analysis of keto acids as their methyl esters of 2,4-dinitrophenylhydrazone derivatives by gas chromatography and gas chromatography-mass spectrometry. J Chromatogr A 587:247-254
    • (1991) J Chromatogr A , vol.587 , pp. 247-254
    • Navarro-Gonzalez, R.1    Negron-Mendoza, A.2    Albarran, G.3
  • 17
    • 20644469267 scopus 로고
    • Quantitative analyses of biochemical kinetic resolutions of enantiomers
    • Chen CS, Fujimoto Y, Girdaukas G, Sih CJ (1982) Quantitative analyses of biochemical kinetic resolutions of enantiomers. J Am Chem Soc 104:7294-7299
    • (1982) J Am Chem Soc , vol.104 , pp. 7294-7299
    • Chen, C.S.1    Fujimoto, Y.2    Girdaukas, G.3    Sih, C.J.4
  • 18
    • 84870314630 scopus 로고    scopus 로고
    • Analysis of the content of benzoylformic acid in mixture by colorimetry
    • Li GY, Huang KL, Jiang YR, Ding P (2007) Analysis of the content of benzoylformic acid in mixture by colorimetry. J Anal Sci 23:734-736
    • (2007) J Anal Sci , vol.23 , pp. 734-736
    • Li, G.Y.1    Huang, K.L.2    Jiang, Y.R.3    Ding, P.4
  • 19
    • 33846197938 scopus 로고    scopus 로고
    • Biocatalysis for pharmaceutical intermediates: The future is now
    • Pollard DJ, Woodley JM (2007) Biocatalysis for pharmaceutical intermediates: the future is now. Trends Biotechnol 25:66-73
    • (2007) Trends Biotechnol , vol.25 , pp. 66-73
    • Pollard, D.J.1    Woodley, J.M.2
  • 20
    • 0035915157 scopus 로고    scopus 로고
    • A highthroughput-screening method for the identification of active and enantioselective hydrolases
    • Baumann M, Sturmer R, Bornscheuer UT (2001) A highthroughput-screening method for the identification of active and enantioselective hydrolases. Angew Chem Int Edit 40:4201-4204
    • (2001) Angew Chem Int Edit , vol.40 , pp. 4201-4204
    • Baumann, M.1    Sturmer, R.2    Bornscheuer, U.T.3
  • 21
    • 67651091590 scopus 로고    scopus 로고
    • A new highthroughput screening method for determining active and enantioselective hydrolases
    • Wang B, Tang XL, Ren GF, Liu J, Yu HW (2009) A new highthroughput screening method for determining active and enantioselective hydrolases. Biochem Eng J 46:345-349
    • (2009) Biochem Eng J , vol.46 , pp. 345-349
    • Wang, B.1    Tang, X.L.2    Ren, G.F.3    Liu, J.4    Yu, H.W.5
  • 22
    • 1642351056 scopus 로고    scopus 로고
    • High-throughput screening method for the identification of active and enantioselective omegatransaminases
    • Hwang BY, Kim BG (2004) High-throughput screening method for the identification of active and enantioselective omegatransaminases. Enzyme Microb Technol 34:429-436
    • (2004) Enzyme Microb Technol , vol.34 , pp. 429-436
    • Hwang, B.Y.1    Kim, B.G.2
  • 23
    • 79955103831 scopus 로고    scopus 로고
    • Ferrous and ferric ions-based high-throughput screening strategy for nitrile hydratase and amidase
    • Lin Z-J, Zheng R-C, Lei L-H, Zheng Y-G, Shen Y-C (2011) Ferrous and ferric ions-based high-throughput screening strategy for nitrile hydratase and amidase. J Microbiol Methods 85:214-220
    • (2011) J Microbiol Methods , vol.85 , pp. 214-220
    • Lin, Z.-J.1    Zheng, R.-C.2    Lei, L.-H.3    Zheng, Y.-G.4    Shen, Y.-C.5
  • 24
    • 33846598795 scopus 로고    scopus 로고
    • A screening system for active and enantioselective amidase based on its acyl transfer activity
    • Zheng R-C, Zheng Y-G, Shen Y-C (2007) A screening system for active and enantioselective amidase based on its acyl transfer activity. Appl Microbiol Biotechnol 74:256-262
    • (2007) Appl Microbiol Biotechnol , vol.74 , pp. 256-262
    • Zheng, R.-C.1    Zheng, Y.-G.2    Shen, Y.-C.3
  • 25
    • 18144431361 scopus 로고    scopus 로고
    • Rapid and sensitive method for the determination of acetaldehyde in fuel ethanol by high-performance liquid chromatography with uv-vis detection
    • Saczk AA, Okumura LL, Firmino de Oliveira M, Boldrin Zanoni MV, Ramos Stradiotto N (2005) Rapid and sensitive method for the determination of acetaldehyde in fuel ethanol by high-performance liquid chromatography with UV-Vis detection. Anal Bioanal Chem 381:1619-1624
    • (2005) Anal Bioanal Chem , vol.381 , pp. 1619-1624
    • Saczk, A.A.1    Okumura, L.L.2    Firmino De Oliveira, M.3    Boldrin Zanoni, M.V.4    Ramos Stradiotto, N.5
  • 26
    • 1642575160 scopus 로고    scopus 로고
    • Validated hplc determination of 2-[(dimethylamino)methyl]cyclohexanone, an impurity in tramadol, using a precolumn derivatisation reaction with 2,4-dinitrophenylhydrazine
    • Medvedovici A, Albu F, Farca A, David V (2004) Validated HPLC determination of 2-[(dimethylamino)methyl]cyclohexanone, an impurity in Tramadol, using a precolumn derivatisation reaction with 2,4- dinitrophenylhydrazine. J Pharm Biomed Anal 34:67-74
    • (2004) J Pharm Biomed Anal , vol.34 , pp. 67-74
    • Medvedovici, A.1    Albu, F.2    Farca, A.3    David, V.4
  • 28
    • 0042998220 scopus 로고    scopus 로고
    • Visualization of enzyme-catalyzed reactions using ph indicators: Rapid screening of hydrolase libraries and estimation of the enantioselectivity
    • Moris-Varas F, Shah A, Aikens J, Nadkarni NP, Rozzell JD, Demirjian DC (1999) Visualization of enzyme-catalyzed reactions using pH indicators: rapid screening of hydrolase libraries and estimation of the enantioselectivity. Bioorg Med Chem 7:2183-2188
    • (1999) Bioorg Med Chem , vol.7 , pp. 2183-2188
    • Moris-Varas, F.1    Shah, A.2    Aikens, J.3    Nadkarni, N.P.4    Rozzell, J.D.5    Demirjian, D.C.6


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