Decolorization and Detoxification of Synthetic Dyes by Mexican Strains of Trametes sp

Laccases have attracted a great deal of interest because of their remarkable ability for the degradation of synthetic dyes present in wastewaters. New laccase producing sources with robust operational and functional properties are being continuously explored. In this work, the potential for the deco...

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Bibliographic Details
Published in:International journal of environmental research and public health 2019-11, Vol.16 (23), p.4610
Main Authors: Levin, Laura N, Hernández-Luna, Carlos E, Niño-Medina, Guillermo, García-Rodríguez, Juan Pablo, López-Sadin, Iosvany, Méndez-Zamora, Gerardo, Gutiérrez-Soto, Guadalupe
Format: Article
Language:English
Subjects:
Biodegradation
Biodegradation, Environmental
Catalysts
Coloring Agents - chemistry
Coloring Agents - metabolism
Coloring Agents - toxicity
Decoloring
Decolorization
Detoxification
Dyes
Effluent treatment
Electrophoresis
Enzymes
Ethanol
Evaluation
Fungi
Gel electrophoresis
Gels
Hydrogen peroxide
Inactivation, Metabolic
Laccase
Laccase - metabolism
Lignin
Ligninolytic enzymes
Metabolites
Oxidation
Polyacrylamide
Proteins
Raphanus - drug effects
Toxicity
Trametes - enzymology
Waste Water - chemistry
Wastewater treatment
Water Decolorization - methods
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Summary:Laccases have attracted a great deal of interest because of their remarkable ability for the degradation of synthetic dyes present in wastewaters. New laccase producing sources with robust operational and functional properties are being continuously explored. In this work, the potential for the decolorization and detoxification of synthetic dyes was evaluated in two Mexican strains of the genus . The decolorization capacity of LE130 and sp. LA1 was tested in solid and liquid media. The phytotoxicity of the degradation products was determined using and seeds. In solid media, both strains showed a higher decolorization capacity ( ≤ 0.05) than ATCC 24725, which is known to be very efficient in lignin and dye-degradation. They produced laccase as the main ligninolytic enzyme; LE130 secreted a single isoform of 43.9 kDa, while sp. LA1 produced three isoforms of 67.3, 58.6 and 52.7 kDa, respectively. sp. LA1 culture fluids were capable of decolorizing and detoxifying chemically diverse dyes (anthraquinonic dye Remazol Brilliant Blue R, azoic Reactive Black 5 and triphenylmethane Crystal Violet) without the addition of redox mediators. Therefore, this could be considered as a new laccase source which could be potentially competitive in the bioremediation of dye-containing wastewaters.
ISSN:1660-4601
1661-7827
1660-4601
DOI:10.3390/ijerph16234610