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Biodegradation of synthetic dye using partially purified and characterized laccase and its proposed mechanism

  • Z. Ghobadi Nejad
  • S. M. BorgheiEmail author
  • S. Yaghmaei
Original Paper
  • 25 Downloads

Abstract

The supernatant obtained from the extracellular laccase produced by Phanerochaete chrysosporium was used as the enzyme source to conduct a partial purification, characterization and dye decolorization study. The partially purified enzyme was stable in the pH range of 3–5 and showed an optimum activity at pH 4.0, using guaiacol as a substrate. Laccase stability of pH was determined and discovered to retain 100% of its activity at a pH of 4.0 after 2 h. The maximum enzyme activity was obtained between 30 and 50 °C. The maximum velocity and Michaelis constant were calculated as 3.171 µM−1·min and 1628.23 µM, respectively. The enzyme was activated by Fe2+, Zn2+, Ca2+ and Cu2+, while Hg2+, Mn2+, Co2+, Mg2+, Cd2+, Ni2+ reduced the laccase activity. The partially purified enzyme was strongly inhibited by 1 mM of NaN3 and sodium thioglycolate. Among the eight different dyes (Malachite green, Safranin, Crystal violet, Methylene blue, Eriochrome black T, Methyl red, Methyl orange, Rhodamine B and Nigrosin), the enzyme showed highly efficient decolorizing activity (99%) toward Malachite green after treatment for 24 h at 30 °C. Antibacterial results showed that the product obtained by treating the dye with the enzyme is completely non-toxic to Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli. High-performance liquid chromatography and mass spectroscopy analysis of the extracted product confirmed the complete biodegradation of Malachite green and Leucomalachite green. Di-benzyl methane and 4-(dimethylamino) benzaldehyde were the ultimate products identified in this research.

Keywords

Antibacterial activity Decolorization Detoxification Dye Laccase 

Notes

Acknowledgements

This work was supported by the Biotechnology Development Council of the Islamic Republic of Iran (Grant No: 960402). This research was also supported by the Iran National Science Foundation (INSF) (Grant No: 95833882). The authors would like to acknowledge Biochemical and Bioenvironmental Research Center, Sharif University of Technology, for providing valuable help to accomplish the research work. They also thank the Graduate School of the Environment and Energy, Science and Research Branch, Islamic Azad University.

Compliance with ethical standards

Conflict of interest

The authors have no financial conflicts of interest to declare.

Supplementary material

13762_2019_2226_MOESM1_ESM.docx (31 kb)
Supplementary material 1 (DOCX 30 kb)

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Copyright information

© Islamic Azad University (IAU) 2019

Authors and Affiliations

  • Z. Ghobadi Nejad
    • 1
  • S. M. Borghei
    • 2
    • 3
    Email author
  • S. Yaghmaei
    • 3
  1. 1.Department of Natural Resources and Environment, Science and Research BranchIslamic Azad University, TehranTehranIran
  2. 2.Biochemical and Bioenvironmental Research CentreSharif University of TechnologyTehranIran
  3. 3.Department of Chemical and Petroleum EngineeringSharif University of TechnologyTehranIran

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