Laccase-mediated oxidation of totarol
| Autor: | Sandile Ncanana, Sergio Riva, Stephanie G. Burton, Lucia Roncaglia, Lara Baratto |
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| Jazyk: | angličtina |
| Rok vydání: | 2007 |
| Předmět: | |
| Zdroj: | Advanced synthesis & catalysis 349 (2007): 1507–1513. doi:10.1002/adsc.200700005 info:cnr-pdr/source/autori:Ncanana S.; Baratto L.; Roncaglia L.; Riva S.; Burton S.G./titolo:Laccase-mediated oxidation of totarol/doi:10.1002%2Fadsc.200700005/rivista:Advanced synthesis & catalysis (Print)/anno:2007/pagina_da:1507/pagina_a:1513/intervallo_pagine:1507–1513/volume:349 BIOTRANS 2007, 8th International Symposium on Biocatalysis and Biotransformations, Oviedo (Spagna), 2007 info:cnr-pdr/source/autori:Ncanana S., Baratto L., Roncaglia L., Riva S., Burton S./congresso_nome:BIOTRANS 2007, 8th International Symposium on Biocatalysis and Biotransformations/congresso_luogo:Oviedo (Spagna)/congresso_data:2007/anno:2007/pagina_da:/pagina_a:/intervallo_pagine |
| DOI: | 10.1002/adsc.200700005 |
| Popis: | In this study, novel dimers of the biologically active phenolic compound totarol were synthesized using the phenol oxidase enzyme laccase, obtained from Trametes pusbescens, in organic solvent medium. Two dimeric products, linked either by carbon-carbon or by carbon-oxygen bonds, were isolated and characterized. The effect of changes in various parameters such as solvent, temperature, pH and buffer concentration on the conversion of totarol by laccase was investigated. The nature of the organic solvent, in particular, was found to affect the nature and the ratio of the products obtained. |
| Databáze: | OpenAIRE |
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