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Volumn 119, Issue 6, 2015, Pages 487-493

Identification of fungal ene-reductase activity by means of a functional screening

Author keywords

Biocatalysis; Bioreduction; Carbon carbon double bond; Filamentous fungi; , unsaturated compounds

Indexed keywords

ALKENE; ENZYME ACTIVITY; IDENTIFICATION METHOD; ISOLATED POPULATION; MOLECULAR ANALYSIS; REDUCTION;

EID: 84929516304     PISSN: 18786146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.funbio.2015.01.006     Document Type: Article
Times cited : (14)

References (20)
  • 2
    • 32944459987 scopus 로고    scopus 로고
    • Comparative characterization and expression analysis of the four Old Yellow Enzyme homologues from Shewanella oneidensis indicate differences in physiological function
    • Brigé A., Van Den Hemel D., Carpentier W., De Smet L., Van Beeumen J.J. Comparative characterization and expression analysis of the four Old Yellow Enzyme homologues from Shewanella oneidensis indicate differences in physiological function. Biochemical Journal 2006, 394:335-344.
    • (2006) Biochemical Journal , vol.394 , pp. 335-344
    • Brigé, A.1    Van Den Hemel, D.2    Carpentier, W.3    De Smet, L.4    Van Beeumen, J.J.5
  • 3
    • 1842453221 scopus 로고    scopus 로고
    • Gongronella butleri, Schizosaccharomyces octosporus and Diplogelasinospora grovesii: novel microorganisms useful for the stereoselective reduction of ketones
    • Carballeira J.D., Valmaseda M., Alvarez E., Sinisterra-Gago J.V. Gongronella butleri, Schizosaccharomyces octosporus and Diplogelasinospora grovesii: novel microorganisms useful for the stereoselective reduction of ketones. Enzyme and Microbial Technology 2004, 34:611-623.
    • (2004) Enzyme and Microbial Technology , vol.34 , pp. 611-623
    • Carballeira, J.D.1    Valmaseda, M.2    Alvarez, E.3    Sinisterra-Gago, J.V.4
  • 4
    • 0036846969 scopus 로고    scopus 로고
    • Fulfilling the promise of biotechnology
    • Colwell R.R. Fulfilling the promise of biotechnology. Biotechnology Advances 2002, 20:215-228.
    • (2002) Biotechnology Advances , vol.20 , pp. 215-228
    • Colwell, R.R.1
  • 6
    • 71549138353 scopus 로고    scopus 로고
    • Stereochemical course of baker's yeast mediated reduction of the tri- and tetrasubstituted double bonds of substituted cinnamaldehydes
    • Fronza G., Fuganti C., Serra S. Stereochemical course of baker's yeast mediated reduction of the tri- and tetrasubstituted double bonds of substituted cinnamaldehydes. The European Journal of Organic Chemistry 2009, 6160-6171.
    • (2009) The European Journal of Organic Chemistry , pp. 6160-6171
    • Fronza, G.1    Fuganti, C.2    Serra, S.3
  • 8
    • 0032479878 scopus 로고    scopus 로고
    • Product distribution in the microbial biogeneration of raspberry ketone from 4-hydroxybenzalacetone
    • Fuganti C., Zucchi G. Product distribution in the microbial biogeneration of raspberry ketone from 4-hydroxybenzalacetone. Journal of Molecular Catalysis B: Enzymatic 1998, 4:289-293.
    • (1998) Journal of Molecular Catalysis B: Enzymatic , vol.4 , pp. 289-293
    • Fuganti, C.1    Zucchi, G.2
  • 9
    • 84860835013 scopus 로고    scopus 로고
    • Biochemical characterization and substrate profiling of a new NADH-dependent enoate reductase from Lactobacillus casei
    • Gao X., Ren J., Wu Q., Zhu D. Biochemical characterization and substrate profiling of a new NADH-dependent enoate reductase from Lactobacillus casei. Enzyme and Microbial Technology 2012, 51:26-34.
    • (2012) Enzyme and Microbial Technology , vol.51 , pp. 26-34
    • Gao, X.1    Ren, J.2    Wu, Q.3    Zhu, D.4
  • 10
    • 24944546402 scopus 로고    scopus 로고
    • Biotechnology a sustainable alternative for chemical industry
    • Gavrilescu M., Chisti Y. Biotechnology a sustainable alternative for chemical industry. Biotechnology Advances 2005, 23:471-499.
    • (2005) Biotechnology Advances , vol.23 , pp. 471-499
    • Gavrilescu, M.1    Chisti, Y.2
  • 13
    • 33845196229 scopus 로고    scopus 로고
    • Asymmetric whole-cell bioreduction of an α, β-unsaturated aldehyde (citral): competing prim-alcohol dehydrogenase and C-C lyase activities
    • Hall M., Hauer B., Stuermer R., Kroutil W., Faber K. Asymmetric whole-cell bioreduction of an α, β-unsaturated aldehyde (citral): competing prim-alcohol dehydrogenase and C-C lyase activities. Tetrahedron Asymmetry 2006, 17:3058-3062.
    • (2006) Tetrahedron Asymmetry , vol.17 , pp. 3058-3062
    • Hall, M.1    Hauer, B.2    Stuermer, R.3    Kroutil, W.4    Faber, K.5
  • 14
    • 0029557273 scopus 로고
    • Structure-function relations for old yellow enzyme
    • Karplus P.A., Fox K.M., Massey V. Structure-function relations for old yellow enzyme. FASEB Journal 1995, 9:1518-1526.
    • (1995) FASEB Journal , vol.9 , pp. 1518-1526
    • Karplus, P.A.1    Fox, K.M.2    Massey, V.3
  • 15
    • 0035910865 scopus 로고    scopus 로고
    • Asymmetric reduction of nitroalkenes with baker's yeast
    • Kawai Y., Inaba Y., Tokitoh N. Asymmetric reduction of nitroalkenes with baker's yeast. Tetrahedron Asymmetry 2001, 12:309-318.
    • (2001) Tetrahedron Asymmetry , vol.12 , pp. 309-318
    • Kawai, Y.1    Inaba, Y.2    Tokitoh, N.3
  • 18
    • 0027401725 scopus 로고
    • Old yellow enzyme. The discovery of multiple isozyme and a family of related proteins
    • Stott K., Saito K., Thiele D.J., Massey V. Old yellow enzyme. The discovery of multiple isozyme and a family of related proteins. Journal of Biological Chemistry 1993, 268:6097-6106.
    • (1993) Journal of Biological Chemistry , vol.268 , pp. 6097-6106
    • Stott, K.1    Saito, K.2    Thiele, D.J.3    Massey, V.4
  • 19
    • 34047189417 scopus 로고    scopus 로고
    • Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family
    • Stuermer R., Hauer B., Hall M., Faber K. Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family. Current Opinion in Chemical Biology 2007, 11:203-213.
    • (2007) Current Opinion in Chemical Biology , vol.11 , pp. 203-213
    • Stuermer, R.1    Hauer, B.2    Hall, M.3    Faber, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.