2009
DOI: 10.1007/s10924-009-0125-z
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Removal of Linear and Branched p-Alkylphenols from Aqueous Solution by Combined Use of melB Tyrosinase and Chitosan Beads

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Cited by 15 publications
(30 citation statements)
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“…A reverse phase column, Inertsil ODS‐3 (5 μm, 4.6 mm i.d. × 15 cm), was used 15–17. The aliquots (0.3 cm 3 ) taken from the reaction solutions were immersed in hot water at 80–85°C for 5 min to deactivate tyrosinase and centrifuged at 4000 rpm for 10 min.…”
Section: Methodsmentioning
confidence: 99%
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“…A reverse phase column, Inertsil ODS‐3 (5 μm, 4.6 mm i.d. × 15 cm), was used 15–17. The aliquots (0.3 cm 3 ) taken from the reaction solutions were immersed in hot water at 80–85°C for 5 min to deactivate tyrosinase and centrifuged at 4000 rpm for 10 min.…”
Section: Methodsmentioning
confidence: 99%
“…Therefore, enzymatic treatments have been more frequently used as an alternative procedure. In fact, oxidoreductases such as peroxidase13, 14 and tyrosinase15, 16 have been used to catalyze detoxication or transformation of bisphenol A (BPA) and its derivatives13, 14, 16 as well as alkylphenols and chlorophenols 15, 17. Tyrosinase has the catalysis to convert phenolic compounds into the corresponding quinone derivatives.…”
Section: Introductionmentioning
confidence: 99%
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“…Taking into account these issues, there is the need to develop a new, ecological and auto-sustainable way for the treatment of phenolic effluents. A promising process appears to be the enzymatic oxidation (Durán and Esposito 2000;Faria et al 2007), particularly by polyphenol oxidase (PPO) that is more commonly referred to as tyrosinase (Martin et al 2008;Romanovskaya et al 2009;Yamada et al 2009). Another enzyme equally efficient in the oxidation of phenols is the polyphenol peroxidase (Campeanu et al 1999), but it has the disadvantage of requiring hydrogen peroxide instead of atmospheric oxygen as a substrate (Ikehata and Nicell 2000a, b;López-Molina et al 2003).…”
Section: Introductionmentioning
confidence: 99%