메뉴 건너뛰기




Volumn 95, Issue 3, 2012, Pages 635-645

Asymmetric bioreduction of activated alkenes by a novel isolate of Achromobacter species producing enoate reductase

Author keywords

Achromobacter sp.; Activated alkene; Asymmetric reduction; Baclofen; Enoate reductase; Old yellow enzyme

Indexed keywords

ACHROMOBACTER SP.; ASYMMETRIC REDUCTION; BACLOFEN; ENOATE REDUCTASE; OLD YELLOW ENZYMES;

EID: 84864579521     PISSN: 01757598     EISSN: 14320614     Source Type: Journal    
DOI: 10.1007/s00253-012-4064-6     Document Type: Article
Times cited : (22)

References (33)
  • 1
    • 0030844225 scopus 로고    scopus 로고
    • Enantioselective synthesis of ß-substituted butyric acid derivatives via orthoester claisen rearrangement of enzymatically resolved allylic alcohols: Application to the synthesis of (R)-(-)-baclofen
    • Brenna E, Caraccia N, Fuganti C, Fuganti D, Grasselli P (1997) Enantioselective synthesis of ß-substituted butyric acid derivatives via orthoester claisen rearrangement of enzymatically resolved allylic alcohols: application to the synthesis of (R)-(-)-baclofen. Tetrahedron: Asymmetry 8:3801-3805
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 3801-3805
    • Brenna, E.1    Caraccia, N.2    Fuganti, C.3    Fuganti, D.4    Grasselli, P.5
  • 2
    • 82355190997 scopus 로고    scopus 로고
    • Productivity enhancement of C0C bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymes
    • Brenna E, Gatti FG, Monti D, Parmeggiani F, Sacchetti A (2012) Productivity enhancement of C0C bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymes. Chem Commun 48:79-81
    • (2012) Chem Commun , vol.48 , pp. 79-81
    • Brenna, E.1    Gatti, F.G.2    Monti, D.3    Parmeggiani, F.4    Sacchetti, A.5
  • 3
    • 0027742495 scopus 로고
    • Condensation of arylacetonitriles with glyoxylic acid. Facile synthesis of arylmaleic acid derivatives
    • Dean WD, Blum DM (1993) Condensation of arylacetonitriles with glyoxylic acid. Facile synthesis of arylmaleic acid derivatives. J Org Chem 58:7916-7917
    • (1993) J Org Chem , vol.58 , pp. 7916-7917
    • Dean, W.D.1    Blum, D.M.2
  • 4
    • 77950299892 scopus 로고    scopus 로고
    • Biodegradation of mtbe by Achromobacter xylosoxidans MCM1/1 induces synthesis of proteins that may be related to cell survival
    • Eixarch H, Constanti M (2010) Biodegradation of mtbe by Achromobacter xylosoxidans MCM1/1 induces synthesis of proteins that may be related to cell survival. Process Biochem 45:794-798
    • (2010) Process Biochem , vol.45 , pp. 794-798
    • Eixarch, H.1    Constanti, M.2
  • 5
    • 44949240574 scopus 로고    scopus 로고
    • Highly enantioselective reduction of ß,ß-disubstituted aromatic nitroalkenes catalyzed by Clostridium sporogenes
    • Fryszkowska A, Fisher K, Gardiner JM, Stephens GM (2008) Highly enantioselective reduction of ß,ß-disubstituted aromatic nitroalkenes catalyzed by Clostridium sporogenes. J Org Chem 73:4295-4298
    • (2008) J Org Chem , vol.73 , pp. 4295-4298
    • Fryszkowska, A.1    Fisher, K.2    Gardiner, J.M.3    Stephens, G.M.4
  • 6
    • 75149145899 scopus 로고    scopus 로고
    • A short, chemoenzymatic route to chiral beta-aryl-gamma-amino acids using reductases from anaerobic bacteria
    • Fryszkowska A, Fisher K, Gardiner JM, Stephens GM (2010) A short, chemoenzymatic route to chiral beta-aryl-gamma-amino acids using reductases from anaerobic bacteria. Org Biomol Chem 8:533-535
    • (2010) Org Biomol Chem , vol.8 , pp. 533-535
    • Fryszkowska, A.1    Fisher, K.2    Gardiner, J.M.3    Stephens, G.M.4
  • 7
    • 0035911387 scopus 로고    scopus 로고
    • Asymmetric acyloin condensation catalysed by phenylpyruvate decarboxylase. Part 2: Substrate specificity and purification of the enzyme
    • Guo Z, Goswami A, Nanduri VB, Patel RN (2001) Asymmetric acyloin condensation catalysed by phenylpyruvate decarboxylase. Part 2: substrate specificity and purification of the enzyme. Tetrahedron: Asymmetry 12:571-577
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 571-577
    • Guo, Z.1    Goswami, A.2    Nanduri, V.B.3    Patel, R.N.4
  • 8
    • 33746409555 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of the C-C double bond of 1-and 1,2-methylated maleimides with cultured suspension cells of Marchantia polymorpha
    • Hegazy MEF, Shishido K, Hirata T (2006) Asymmetric hydrogenation of the C-C double bond of 1-and 1,2-methylated maleimides with cultured suspension cells of Marchantia polymorpha. Tetrahedron: Asymmetry 17:1859-1862
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1859-1862
    • Hegazy, M.E.F.1    Shishido, K.2    Hirata, T.3
  • 9
    • 84986409354 scopus 로고
    • Synthesis of optically-active natural carotenoids and structurally related compounds. 1. Synthesis of chiral key compound (4R,6R)-4-hydroxy-2,2,6- trimethylcyclohexanone
    • Leuenberger HGW, Boguth W, Widmer E, Zell R (1976) Synthesis of optically-active natural carotenoids and structurally related compounds. 1. Synthesis of chiral key compound (4R,6R)-4-hydroxy-2,2,6-trimethylcyclohexanone. Helv Chim Acta 59:1832-1849
    • (1976) Helv Chim Acta , vol.59 , pp. 1832-1849
    • Leuenberger, H.G.W.1    Boguth, W.2    Widmer, E.3    Zell, R.4
  • 10
    • 67649271051 scopus 로고    scopus 로고
    • Biodegradation and detoxification of endosulfan in aqueous medium and soil by Achromobacter xylosoxidans strain CS5
    • Li W, Dai Y, Xue B, Li Y, Peng X, Zhang J, Yan Y (2009) Biodegradation and detoxification of endosulfan in aqueous medium and soil by Achromobacter xylosoxidans strain CS5. J Hazard Mater 167:209-216
    • (2009) J Hazard Mater , vol.167 , pp. 209-216
    • Li, W.1    Dai, Y.2    Xue, B.3    Li, Y.4    Peng, X.5    Zhang, J.6    Yan, Y.7
  • 12
    • 79954589570 scopus 로고    scopus 로고
    • Enantioselective bioreduction of 2-fluoro-2-alken-1-ols mediated by Saccharomyces cerevisiae
    • Luo F, Lu D, Gong Y (2011) Enantioselective bioreduction of 2-fluoro-2-alken-1-ols mediated by Saccharomyces cerevisiae. J Mol Catal B: Enzym 70:101-107
    • (2011) J Mol Catal B: Enzym , vol.70 , pp. 101-107
    • Luo, F.1    Lu, D.2    Gong, Y.3
  • 13
    • 0034934039 scopus 로고    scopus 로고
    • Simple synthesis of arylsuccinic acids
    • Makosza M, Marcinowicz A (2001) Simple synthesis of arylsuccinic acids. Synthesis: 1311-1312
    • (2001) Synthesis , pp. 1311-1312
    • Makosza, M.1    Marcinowicz, A.2
  • 14
    • 54249149436 scopus 로고    scopus 로고
    • Organocatalytic asymmetric transfer hydrogenation of ß- nitroacrylates: Accessing ß2-amino acids
    • Martin NJA, Cheng X, List B (2008) Organocatalytic asymmetric transfer hydrogenation of ß-nitroacrylates: accessing ß2-amino acids. J Am Chem Soc 130:13862-13863
    • (2008) J Am Chem Soc , vol.130 , pp. 13862-13863
    • Martin, N.J.A.1    Cheng, X.2    List, B.3
  • 15
    • 84985520823 scopus 로고
    • Simple method for the esterification of carboxylic acids
    • Neises B, Steglich W (1978) Simple method for the esterification of carboxylic acids. Angew Chem Int Ed 17:522-524
    • (1978) Angew Chem Int Ed , vol.17 , pp. 522-524
    • Neises, B.1    Steglich, W.2
  • 16
    • 0001393485 scopus 로고
    • Asymmetric reduction of nitro olefins by fermenting bakers-yeast
    • Ohta H, Kobayashi N, Ozaki K (1989) Asymmetric reduction of nitro olefins by fermenting bakers-yeast. J Org Chem 54:1802-1804
    • (1989) J Org Chem , vol.54 , pp. 1802-1804
    • Ohta, H.1    Kobayashi, N.2    Ozaki, K.3
  • 18
    • 0034139797 scopus 로고    scopus 로고
    • Recent advances in GABA(B) receptors: From pharmacology to molecular biology
    • Ong J, Kerr DI (2000) Recent advances in GABA(B) receptors: from pharmacology to molecular biology. Acta Pharmacologica Sinica 21:111-123
    • (2000) Acta Pharmacologica Sinica , vol.21 , pp. 111-123
    • Ong, J.1    Kerr, D.I.2
  • 19
    • 33847801898 scopus 로고
    • Reagent for the alpha, beta reduction of conjugated nitrile
    • Profitt JA, Watt DS, Corey EJ (1975) Reagent for the alpha, beta reduction of conjugated nitrile. J Org Chem 40:127-128
    • (1975) J Org Chem , vol.40 , pp. 127-128
    • Profitt, J.A.1    Watt, D.S.2    Corey, E.J.3
  • 20
    • 33846485125 scopus 로고    scopus 로고
    • Polishing a diamond in the rough "Cu-H" catalysis with silanes
    • Rendler S, Oestreich M (2007) Polishing a diamond in the rough: "Cu-H" catalysis with silanes. Angew Chem Int Ed 46:498-504
    • (2007) Angew Chem Int Ed , vol.46 , pp. 498-504
    • Rendler, S.1    Oestreich, M.2
  • 21
    • 4143140137 scopus 로고    scopus 로고
    • Asymmetric reduction of a,ß-unsaturated carbonyl compounds with reductases from Nicotiana tabacum
    • Shimoda K, Kubota N, Hamada H (2004) Asymmetric reduction of a,ß-unsaturated carbonyl compounds with reductases from Nicotiana tabacum. Tetrahedron: Asymmetry 15:2443-2446
    • (2004) Tetrahedron: Asymmetry , vol.15 , pp. 2443-2446
    • Shimoda, K.1    Kubota, N.2    Hamada, H.3
  • 22
    • 77953130369 scopus 로고    scopus 로고
    • Efficient asymmetric hydrogenation of the C-C double bond of 2-methyl-and 2,3-dimethyl-Nphenylalkylmaleimides by Aspergillus fumigatus
    • Sortino M, Alicia Zacchino S (2010) Efficient asymmetric hydrogenation of the C-C double bond of 2-methyl-and 2,3-dimethyl-Nphenylalkylmaleimides by Aspergillus fumigatus. Tetrahedron: Asymmetry 21:535-539
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 535-539
    • Sortino, M.1    Alicia Zacchino, S.2
  • 23
    • 66149165730 scopus 로고    scopus 로고
    • Highly enantioselective reduction of the C-C double bond of N-phenyl-2-methyland N-phenyl-2,3-dimethyl-maleimides by fungal strains
    • Sortino MA, Cechinel Filho V, Zacchino SA (2009) Highly enantioselective reduction of the C-C double bond of N-phenyl-2-methyland N-phenyl-2,3-dimethyl- maleimides by fungal strains. Tetrahedron: Asymmetry 20:1106-1108
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1106-1108
    • Sortino, M.A.1    Cechinel Filho, V.2    Zacchino, S.A.3
  • 25
    • 34047189417 scopus 로고    scopus 로고
    • Asymmetric bioreduction of activated C0C bonds using enoate reductases from the old yellow enzyme family
    • Stuermer R, Hauer B, Hall M, Faber K (2007) Asymmetric bioreduction of activated C0C bonds using enoate reductases from the old yellow enzyme family. Curr Opin Chem Biol 11:203-213
    • (2007) Curr Opin Chem Biol , vol.11 , pp. 203-213
    • Stuermer, R.1    Hauer, B.2    Hall, M.3    Faber, K.4
  • 26
    • 0037424371 scopus 로고    scopus 로고
    • Enantioselective synthesis of (R)-(-)-baclofen via Ru(II)-BINAP catalyzed asymmetric hydrogenation
    • Thakur VV, Nikalje MD, Sudalai A (2003) Enantioselective synthesis of (R)-(-)-baclofen via Ru(II)-BINAP catalyzed asymmetric hydrogenation. Tetrahedron: Asymmetry 14:581-586
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 581-586
    • Thakur, V.V.1    Nikalje, M.D.2    Sudalai, A.3
  • 27
    • 78149436277 scopus 로고    scopus 로고
    • Biocatalytic reductions and chemical versatility of the old yellow enzyme family of flavoprotein oxidoreductases
    • Toogood HS, Gardiner JM, Scrutton NS (2010) Biocatalytic reductions and chemical versatility of the old yellow enzyme family of flavoprotein oxidoreductases. Chemcatchem 2:892-914
    • (2010) Chemcatchem , vol.2 , pp. 892-914
    • Toogood, H.S.1    Gardiner, J.M.2    Scrutton, N.S.3
  • 28
    • 33846559758 scopus 로고    scopus 로고
    • Degradation of p-nitrophenol by Achromobacter xylosoxidans Ns isolated from wetland sediment
    • Wan N, Gu J-D, Yan Y (2007) Degradation of p-nitrophenol by Achromobacter xylosoxidans Ns isolated from wetland sediment. Int Biodeterior Biodegrad 59:90-96
    • (2007) Int Biodeterior Biodegrad , vol.59 , pp. 90-96
    • Wan, N.1    Gu, J.-D.2    Yan, Y.3
  • 29
    • 0038796436 scopus 로고
    • On a new oxidation enzyme and its absorption spectrum
    • Warburg O, Christian W (1932) On a new oxidation enzyme and its absorption spectrum. Biochem Z 254:438-458
    • (1932) Biochem Z , vol.254 , pp. 438-458
    • Warburg, O.1    Christian, W.2
  • 30
    • 0035987236 scopus 로고    scopus 로고
    • New uses for an old enzyme'-The old yellow enzyme family of flavoenzymes
    • Williams RE, Bruce NC (2002) 'New uses for an old enzyme'-the old yellow enzyme family of flavoenzymes. Microbiology 148:1607-1614
    • (2002) Microbiology , vol.148 , pp. 1607-1614
    • Williams, R.E.1    Bruce, N.C.2
  • 31
    • 0001279038 scopus 로고    scopus 로고
    • Preparation of genomic DNA from bacteria
    • In Ausubel FM, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (eds) Wiley, New York
    • Wilson K (1997) Preparation of genomic DNA from bacteria. In: Ausubel FM, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (eds) Current protocols in molecular biology. Wiley, New York, pp 241-245
    • (1997) Current Protocols in Molecular Biology , pp. 241-245
    • Wilson, K.1
  • 32
    • 33947577467 scopus 로고    scopus 로고
    • Aerobic degradation of bisphenol a by Achromobacter xylosoxidans strain B-16 isolated from compost leachate of municipal solid waste
    • Zhang C, Guangming Z, Li Y, Jian Y, Jianbing L, Guohe H, Beidou X, Hongliang L (2007) Aerobic degradation of bisphenol a by Achromobacter xylosoxidans strain B-16 isolated from compost leachate of municipal solid waste. Chemosphere 68:181-190
    • (2007) Chemosphere , vol.68 , pp. 181-190
    • Zhang, C.1    Guangming, Z.2    Li, Y.3    Jian, Y.4    Jianbing, L.5    Guohe, H.6    Beidou, X.7    Hongliang, L.8
  • 33
    • 53949083087 scopus 로고    scopus 로고
    • Anaerobic reduction of hexavalent chromium by bacterial cells of Achromobacter sp strain Ch1
    • Zhu W, Chai L, Ma Z, Wang Y, Mao H, Zhao K (2008) Anaerobic reduction of hexavalent chromium by bacterial cells of Achromobacter sp strain Ch1. Microbiol Res 163:616-623
    • (2008) Microbiol Res , vol.163 , pp. 616-623
    • Zhu, W.1    Chai, L.2    Ma, Z.3    Wang, Y.4    Mao, H.5    Zhao, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.