4.7 Article

Molecular docking and molecular dynamics simulation approaches for evaluation of laccase-mediated biodegradation of various industrial dyes

Journal

JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
Volume 40, Issue 23, Pages 12461-12471

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/07391102.2021.1971564

Keywords

Laccase; molecular docking; molecular dynamic simulation; pigment red23; fuchsin base; and Sudan IV

Funding

  1. DST FIST grant [SR/FST/LS-I/2018/131]

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By utilizing molecular docking, this research identifies three dyes that show stable interaction with laccase, indicating the potential role of laccase in degrading these toxic dyes. The study provides a molecular understanding of the expression of laccase and its bioremediation function in degrading pigments red 23, fuchsin base, and Sudan IV.
Dyes are being increasingly utilized across the globe, but there is no appropriate method of bio-remediation for their full mineralization from the environment. Laccases are key enzymes that help microbes to degrade dyes as well as their intermediate metabolites. Various dyes have been reported to be degraded by bacteria, but it is still unclear how these enzymes function during dye degradation. To effectively eradicate toxic dyes from the system, it is essential to understand the molecular function of enzymes. As a result, the interaction of laccase with different toxic dyes was investigated using molecular docking. Based on the highest binding energy we have screened ten dyes with positive interaction with laccase. Evaluating the MD simulation results, three out of ten dyes were more stable as potential targets for degradation by laccase of Bacillus subtilis. As a result, subsequent research focused solely on the results of three substrates: pigment red, fuchsin base, and Sudan IV. Analysis of MD simulation revealed that pigments red 23, fuchsin base, and Sudan IV form hydrogen and hydrophobic bond as well as Vander Waals interactions with the active site of laccase to keep it stable in aqueous solution. The conformation of laccase is greatly altered by the inclusion of all three substrates in the active site. The MD simulation findings show that laccase complexes remain stable throughout the catalytic reaction. Therefore, this research provides a molecular understanding of laccase expression and its role in the bioremediation of the pigments red 23, fuchsin base, and Sudan IV.

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