Artículo

Médici, R.; Garaycoechea, J.I.; Dettorre, L.A.; Iribarren, A.M.; Lewkowicz, E.S. "Biocatalysed halogenation of nucleobase analogues" (2011) Biotechnology Letters. 33(10):1999-2003
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Abstract:

The synthesis of halogenated nucleosides and nucleobases is of interest due to their chemical and pharmacological applications. Herein, the enzymatic halogenation of nucleobases and analogues catalysed by microorganisms and by chloroperoxidase from Caldariomyces fumago has been studied. This latter enzyme catalysed the chlorination and bromination of indoline and uracil. Pseudomonas, Citrobacter, Aeromonas, Streptomyces, Xanthomonas, and Bacillus genera catalysed the chlorination and/or bromination of indole and indoline. Different products were obtained depending on the substrate, the biocatalyst and the halide used. In particular, 85% conversion from indole to 5-bromoindole was achieved using Streptomyces cetonii. © 2011 Springer Science+Business Media B.V.

Registro:

Documento: Artículo
Título:Biocatalysed halogenation of nucleobase analogues
Autor:Médici, R.; Garaycoechea, J.I.; Dettorre, L.A.; Iribarren, A.M.; Lewkowicz, E.S.
Filiación:Biotransformation Laboratory, Universidad Nacional de Quilmes, R. S. Peña 352 Bernal, 1876 Buenos Aires, Argentina
INGEBI, CONICET, Vuelta de Obligado 2490, 1428 Buenos Aires, Argentina
Palabras clave:Enzymatic halogenation; Haloperoxidases; Nucleobases; Whole cell biocatalysts; 5-Bromoindole; Aeromonas; Caldariomyces; Chloroperoxidase; Enzymatic halogenation; Haloperoxidases; Nucleobases; Whole cell biocatalysts; Xanthomonas; Bacteriology; Biocatalysts; Catalysis; Chlorination; Enzymes; Bacteria; chloride peroxidase; chlorodimedone; cyclohexanone derivative; drug derivative; halogenated hydrocarbon; indole derivative; indoline; uracil; article; Ascomycetes; bacterium; biocatalysis; enzymology; halogenation; metabolism; Ascomycota; Bacteria; Biocatalysis; Chloride Peroxidase; Cyclohexanones; Halogenation; Hydrocarbons, Halogenated; Indoles; Uracil; Aeromonas; Citrobacter; Leptoxyphium fumago; Pseudomonas; Streptomyces; Xanthomonas
Año:2011
Volumen:33
Número:10
Página de inicio:1999
Página de fin:2003
DOI: http://dx.doi.org/10.1007/s10529-011-0655-z
Título revista:Biotechnology Letters
Título revista abreviado:Biotechnol. Lett.
ISSN:01415492
CODEN:BILED
CAS:chloride peroxidase, 9055-20-3; indoline, 496-15-1; uracil, 66-22-8; Chloride Peroxidase, 1.11.1.10; Cyclohexanones; Hydrocarbons, Halogenated; Indoles; Uracil, 66-22-8; chlorodimedone, 7298-89-7; indoline, 496-15-1
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01415492_v33_n10_p1999_Medici

Referencias:

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Citas:

---------- APA ----------
Médici, R., Garaycoechea, J.I., Dettorre, L.A., Iribarren, A.M. & Lewkowicz, E.S. (2011) . Biocatalysed halogenation of nucleobase analogues. Biotechnology Letters, 33(10), 1999-2003.
http://dx.doi.org/10.1007/s10529-011-0655-z
---------- CHICAGO ----------
Médici, R., Garaycoechea, J.I., Dettorre, L.A., Iribarren, A.M., Lewkowicz, E.S. "Biocatalysed halogenation of nucleobase analogues" . Biotechnology Letters 33, no. 10 (2011) : 1999-2003.
http://dx.doi.org/10.1007/s10529-011-0655-z
---------- MLA ----------
Médici, R., Garaycoechea, J.I., Dettorre, L.A., Iribarren, A.M., Lewkowicz, E.S. "Biocatalysed halogenation of nucleobase analogues" . Biotechnology Letters, vol. 33, no. 10, 2011, pp. 1999-2003.
http://dx.doi.org/10.1007/s10529-011-0655-z
---------- VANCOUVER ----------
Médici, R., Garaycoechea, J.I., Dettorre, L.A., Iribarren, A.M., Lewkowicz, E.S. Biocatalysed halogenation of nucleobase analogues. Biotechnol. Lett. 2011;33(10):1999-2003.
http://dx.doi.org/10.1007/s10529-011-0655-z