TY - JOUR
T1 - Understanding the biodegradation pathways of azo dyes by immobilized white-rot fungus, Trametes hirsuta D7, using UPLC-PDA-FTICR MS supported by in silico simulations and toxicity assessment
AU - Alam, Rafiqul
AU - Mahmood, Raisul Awal
AU - Islam, Syful
AU - Ardiati, Fenny Clara
AU - Solihat, Nissa Nurfajrin
AU - Alam, Md Badrul
AU - Lee, Sang Han
AU - Yanto, Dede Heri Yuli
AU - Kim, Sunghwan
N1 - Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2023/2
Y1 - 2023/2
N2 - No biodegradation methods are absolute in the treatment of all textile dyes, which leads to structure-dependent degradation. In this study, biodegradation of three azo dyes, reactive black 5 (RB5), acid blue 113 (AB113), and acid orange 7 (AO7), was investigated using an immobilized fungus, Trametes hirsuta D7. The degraded metabolites were identified using UPLC-PDA-FTICR MS and the biodegradation pathway followed was proposed. RB5 (92%) and AB113 (97%) were effectively degraded, whereas only 30% of AO7 was degraded. Molecular docking simulations were performed to determine the reason behind the poor degradation of AO7. Weak binding affinity, deficiency in H-bonding interactions, and the absence of interactions between the azo (-N[dbnd]N-) group and active residues of the model laccase enzyme were responsible for the low degradation efficiency of AO7. Furthermore, cytotoxicity and genotoxicity assays confirmed that the fungus-treated dye produced non-toxic metabolites. The observations of this study will be useful for understanding and further improving enzymatic dye biodegradation.
AB - No biodegradation methods are absolute in the treatment of all textile dyes, which leads to structure-dependent degradation. In this study, biodegradation of three azo dyes, reactive black 5 (RB5), acid blue 113 (AB113), and acid orange 7 (AO7), was investigated using an immobilized fungus, Trametes hirsuta D7. The degraded metabolites were identified using UPLC-PDA-FTICR MS and the biodegradation pathway followed was proposed. RB5 (92%) and AB113 (97%) were effectively degraded, whereas only 30% of AO7 was degraded. Molecular docking simulations were performed to determine the reason behind the poor degradation of AO7. Weak binding affinity, deficiency in H-bonding interactions, and the absence of interactions between the azo (-N[dbnd]N-) group and active residues of the model laccase enzyme were responsible for the low degradation efficiency of AO7. Furthermore, cytotoxicity and genotoxicity assays confirmed that the fungus-treated dye produced non-toxic metabolites. The observations of this study will be useful for understanding and further improving enzymatic dye biodegradation.
KW - Biodegradation
KW - Molecular docking
KW - T. hirsuta D7
KW - Toxicity assessment
KW - UPLC-PDA-FTICR MS
UR - http://www.scopus.com/inward/record.url?scp=85143721740&partnerID=8YFLogxK
U2 - 10.1016/j.chemosphere.2022.137505
DO - 10.1016/j.chemosphere.2022.137505
M3 - Article
C2 - 36509189
AN - SCOPUS:85143721740
SN - 0045-6535
VL - 313
JO - Chemosphere
JF - Chemosphere
M1 - 137505
ER -