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Preparation and Optimisation of Cross-Linked Enzyme Aggregates Using Native Isolate White Rot Fungi Trametes versicolor and Fomes fomentarius for the Decolourisation of Synthetic Dyes

Bibliographic Data

ID15498196
AuthorsMartina Vršanská (0000-0002-4689-1561, Mendel University in Brno), Stanislava Voběrková (0000-0001-7099-7692, Mendel University in Brno), Ana Maria Jimenez Jimenez (0000-0003-1736-492X, Brno University of Technology), Ana Jiménez Jiménez (Mendel University in Brno), Vladislav Strmiska (0000-0002-7036-1640, Mendel University in Brno), Vojtěch Adam (0000-0002-8527-286X, Central European Institute of Technology, corresponding author)
Year2017
Volume15
Issue1
Pages23-23
Publication date2017-12-23
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph15010023
PMID29295505
OpenAlexW2779956700
LanguageEN
Citations received1
References cited61

The key to obtaining an optimum performance of an enzyme is often a question of devising a suitable enzyme and optimisation of conditions for its immobilization. In this study, laccases from the native isolates of white rot fungi Fomes fomentarius and/or Trametes versicolor , obtained from Czech forests, were used. From these, cross-linked enzyme aggregates (CLEA) were prepared and characterised when the experimental conditions were optimized. Based on the optimization steps, saturated ammonium sulphate solution (75 wt.%) was used as the precipitating agent, and different concentrations of glutaraldehyde as a cross-linking agent were investigated. CLEA aggregates formed under the optimal conditions showed higher catalytic efficiency and stabilities (thermal, pH, and storage, against denaturation) as well as high reusability compared to free laccase for both fungal strains. The best concentration of glutaraldehyde seemed to be 50 mM and higher efficiency of cross-linking was observed at a low temperature 4 °C. An insignificant increase in optimum pH for CLEA laccases with respect to free laccases for both fungi was observed. The results show that the optimum temperature for both free laccase and CLEA laccase was 35 °C for T. versicolor and 30 °C for F. fomentarius . The CLEAs retained 80% of their initial activity for Trametes and 74% for Fomes after 70 days of cultivation. Prepared cross-linked enzyme aggregates were also investigated for their decolourisation activity on malachite green, bromothymol blue, and methyl red dyes. Immobilised CLEA laccase from Trametes versicolor showed 95% decolourisation potential and CLEA from Fomes fomentarius demonstrated 90% decolourisation efficiency within 10 h for all dyes used. These results suggest that these CLEAs have promising potential in dye decolourisation

Biology · Botany · Chromatography · Enzyme · Fomes · Glutaraldehyde · Laccase · Mycelium · Trametes versicolor · Biochemical and biochemical processes · Chemistry · Enzyme-mediated dye degradation · Microbial Metabolism and Applications · Organic Chemistry

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Unique citing works1
Citations per year0.2
Citation span2021 - 2021 (1)
Citation velocityhistorical
Highly citedNo
Citation typesNeutral: 1

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