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Electrogeneration of hydrogen peroxide applied to the peroxide-mediated oxidation of (R)-limonene in organic media
La Rotta Hernández, Camilo Enrique; Werberich, Diogo Simon; Mattos, Marcio Contrucci Saraiva de; D'Elia, Eliane.
  • La Rotta Hernández, Camilo Enrique; Federal University of Rio de Janeiro. Institute of Chemistry. Department of Inorganic Chemistry. Electrochemistry and Electroanalysis Laboratory. Rio de Janeiro. BR
  • Werberich, Diogo Simon; Federal University of Rio de Janeiro. Institute of Chemistry. Department of Inorganic Chemistry. Electrochemistry and Electroanalysis Laboratory. Rio de Janeiro. BR
  • Mattos, Marcio Contrucci Saraiva de; Federal University of Rio de Janeiro. Institute of Chemistry. Department of Organic Chemistry. Rio de Janeiro. BR
  • D'Elia, Eliane; Federal University of Rio de Janeiro. Institute of Chemistry. Department of Inorganic Chemistry. Electrochemistry and Electroanalysis Laboratory. Rio de Janeiro. BR
Electron. j. biotechnol ; 10(4): 521-535, oct. 2007.
Artigo em Inglês | LILACS | ID: lil-504122
ABSTRACT
Horse radish peroxidase (HRP) from Armoracia rusticana catalyses the oxidation of (R)-limonene into the oxidized derivatives carveol and carvone. This study compares the direct addition (DA) of hydrogen peroxide with its continuous electrogeneration (EG) during the enzymatic oxidation of (R)-limonene. Reaction mixtures containing HRP, (R)-limonene as substrate, and hydrogen peroxide, added directly or electrogenerated, in 100 mM sodium-potassium phosphate buffer pH 7.0, at 25ºC were studied. Two electrochemical systems for the hydrogen peroxide electrogeneration were evaluated, both containing as auxiliary electrode (AE) a platinum wire and saturated calomel electrode (SCE) as reference. Reticulated vitreous carbon foam (RVCF) and an electrolytic copper web (CW) were evaluated as working electrodes (WE). Results were compared in terms of hydrogen peroxide electrogeneration, (R)-limonene residual concentration or conversion and product selectivity. Best results in terms of maximum H2O2 concentration (1.2 mM) were obtained using the CW electrode at -620 mV SCE, and continuous aeration. Use of the EG system under optimized conditions, which included the use of acetone (30% v/v) as a cosolvent in a 3 hrs enzymatic reaction, lead to a 45% conversion of (R)-limonene into carveol and carvone (21). In comparison to the results obtained with DA, the use of EG also improved the half-life of the enzyme.
Assuntos
Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Terpenos / Cicloexanos / Eletroquímica / Peroxidase do Rábano Silvestre / Peróxido de Hidrogênio Idioma: Inglês Revista: Electron. j. biotechnol Assunto da revista: Biotecnologia Ano de publicação: 2007 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Federal University of Rio de Janeiro/BR

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Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Terpenos / Cicloexanos / Eletroquímica / Peroxidase do Rábano Silvestre / Peróxido de Hidrogênio Idioma: Inglês Revista: Electron. j. biotechnol Assunto da revista: Biotecnologia Ano de publicação: 2007 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Federal University of Rio de Janeiro/BR