Enhanced removal of aqueous acetaminophen by a laccase-catalyzed oxidative coupling reaction under a dual-pH optimization strategy
Creators
- 1. Key Lab for Industrial Biocatalysis, Ministry of Education, Department of Chemical Engineering, Tsinghua University, Beijing, 100084 (China)
Description
Highlights: • Acetaminophen was rapidly and effectively removed by a laccase-catalyzed oxidative coupling reaction. • Initial laccase activity was increased approximately 2.9-fold by a dual-pH optimizing strategy. • The kinetics showed that higher enzyme activity accelerated the precipitation of polymerized products. Acetaminophen is one kind of pharmaceutical contaminant that has been detected in municipal water and is hard to digest. A laccase-catalyzed oxidative coupling reaction is a potential method of removing acetaminophen from water. In the present study, the kinetics of radical polymerization combined with precipitation was studied, and the dual-pH optimization strategy (the enzyme solution at pH 7.4 being added to the substrate solution at pH 4.2) was proposed to enhance the removal efficiency of acetaminophen. The reaction kinetics that consisted of the laccase-catalyzed oxidation, radical polymerization and precipitation were studied by UV in situ, LC-MS and DLS (dynamic light scattering) in situ. The results showed that the laccase-catalyzed oxidation is the rate-limiting step in the whole process. The higher rate of enzyme-catalyzed oxidation under a dual-pH optimization strategy led to much faster formation of the dimer, trimer and tetramer. Similarly, the formation of polymerized products that could precipitate naturally from water was faster. Under the dual-pH optimization strategy, the initial laccase activity was increased approximately 2.9-fold, and the activity remained higher for > 250 s, during which approximately 63.7% of the total acetaminophen was transformed into biologically inactive polymerized products, and part of these polymerized products precipitated from the water. Laccase belongs to the family of multi-copper oxidases, and the present study provides a universal method to improve the activity of multi-copper oxidases for the high-performance removal of phenol and its derivatives.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2017.10.191Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2017.10.191;
- PII
- S0048969717329029;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 616
- Journal Page Range
- p. 1270-1278
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53016785
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- COPPER; DIMERS; DRUGS; ENZYME ACTIVITY; LIGHT SCATTERING; OPTIMIZATION; OXIDASES; OXIDATION; PH VALUE; PHENOL; POLYMERIZATION; PRECIPITATION; REACTION KINETICS; ULTRAVIOLET RADIATION; WATER; WATER POLLUTION ABATEMENT
- Descriptors DEC
- AROMATICS; CHEMICAL REACTIONS; ELECTROMAGNETIC RADIATION; ELEMENTS; ENZYMES; HYDROCARBONS; HYDROGEN COMPOUNDS; HYDROXY COMPOUNDS; KINETICS; METALS; ORGANIC COMPOUNDS; OXIDOREDUCTASES; OXYGEN COMPOUNDS; PHENOLS; POLLUTION ABATEMENT; PROTEINS; RADIATIONS; SCATTERING; SEPARATION PROCESSES; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier B.V. All rights reserved.