The Mechanism of Aniline Blue Degradation by Short-Chain Dehydrogenase (SDRz) in Comamonas testosteroni

Dye wastewater pollution, particularly from persistent and toxic polycyclic organic pollutants, such as aniline blue, poses a significant environmental challenge. Aniline blue, a triphenylmethane dye widely used in the textile, leather, paper, and pharmaceutical industries, is notoriously difficult to treat owing to its complex structure and potential for bioaccumulation. In this study, we explored the capacity of <i>Comamonas testosteroni</i> (CT1) to efficiently degrade aniline blue, focusing on the underlying enzymatic mechanisms and degradation pathways. Through prokaryotic transcriptome analysis, we identified a significantly upregulated short-chain dehydrogenase (<i>SDRz</i>) gene (log<sub>2</sub>FC = 2.11, <i>p</i> < 0.05) that plays a crucial role in the degradation process. The SDRz enzyme possessed highly conserved motifs and a typical short-chain dehydrogenase structure. Functional validation using an <i>SDRz</i>-knockout strain (CT-ΔSDRz) and an <i>SDRz</i>-expressioning strains (E-SDRz) confirmed that SDRz is essential for aniline blue degradation. The knockout strain CT-ΔSDRz exhibited a 1.27-fold reduction in the degradation efficiency, compared to CT1 strain after 12 h; while the expression strain E-SDRz showed a 1.24-fold increase compared to <i>Escherichia coli</i> DH5α after 12 h. Recombinant SDRz (rSDRz) was successfully produced, showing significant enzymatic activity (1.267 ± 0.04 mmol·L<sup>-1</sup>·min<sup>-1</sup> protein), with kinetic parameters Vmax = 2.870 ± 0.0156 mmol·L⁻<sup>1</sup>·min⁻<sup>1</sup> protein and Km = 1.805 ± 0.0128 mM·mL<sup>-1</sup>. Under optimal conditions, the rSDRz achieved a degradation efficiency of 62.17% for aniline blue. Gas chromatography-mass spectrometry (GC-MS) analysis identified several intermediate metabolites in the degradation pathway, including benzeneacetaldehyde, a, a-diphenyl, 2-amino-4-methylbenzophenone, benzene, 1-dimethylamino-4-phenylmethyl, benzenesulfonic acid, methyl ester, further elucidating the biodegradation mechanism. These findings highlight SDRz as a critical enzyme in the biodegradation of aniline blue, offering valuable insights and a robust theoretical foundation for developing advanced bioremediation strategies to address dye wastewater pollution.

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Publication Details

Journal
Molecules
Published
2024-11-15
DOI
https://doi.org/10.3390/molecules29225405
Citations
5
Primary Topic
Enzyme-mediated dye degradation
Type
article
Field-Weighted Citation Impact
3.00

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article

The Mechanism of Aniline Blue Degradation by Short-Chain Dehydrogenase (SDRz) in Comamonas testosteroni

Chuanzhi Zhang, Yong Huang, Edmund Maser, Elshan Musazade et al.
5 citations
Molecules
Enzyme-mediated dye degradation
3.00
article

The Mechanism of Aniline Blue Degradation by Short-Chain Dehydrogenase (SDRz) in Comamonas testosteroni

Chuanzhi Zhang, Yong Huang, Edmund Maser, Elshan Musazade, Lei He, Guangming Xiong, Lijing Yu, Jinyuan Zhang, Jiaxin He, Liquan Guo, Miao Xu
article en
5 citations

Abstract

Dye wastewater pollution, particularly from persistent and toxic polycyclic organic pollutants, such as aniline blue, poses a significant environmental challenge. Aniline blue, a triphenylmethane dye widely used in the textile, leather, paper, and pharmaceutical industries, is notoriously difficult to treat owing to its complex structure and potential for bioaccumulation. In this study, we explored the capacity of <i>Comamonas testosteroni</i> (CT1) to efficiently degrade aniline blue, focusing on the underlying enzymatic mechanisms and degradation pathways. Through prokaryotic transcriptome analysis, we identified a significantly upregulated short-chain dehydrogenase (<i>SDRz</i>) gene (log<sub>2</sub>FC = 2.11, <i>p</i> < 0.05) that plays a crucial role in the degradation process. The SDRz enzyme possessed highly conserved motifs and a typical short-chain dehydrogenase structure. Functional validation using an <i>SDRz</i>-knockout strain (CT-ΔSDRz) and an <i>SDRz</i>-expressioning strains (E-SDRz) confirmed that SDRz is essential for aniline blue degradation. The knockout strain CT-ΔSDRz exhibited a 1.27-fold reduction in the degradation efficiency, compared to CT1 strain after 12 h; while the expression strain E-SDRz showed a 1.24-fold increase compared to <i>Escherichia coli</i> DH5α after 12 h. Recombinant SDRz (rSDRz) was successfully produced, showing significant enzymatic activity (1.267 ± 0.04 mmol·L<sup>-1</sup>·min<sup>-1</sup> protein), with kinetic parameters Vmax = 2.870 ± 0.0156 mmol·L⁻<sup>1</sup>·min⁻<sup>1</sup> protein and Km = 1.805 ± 0.0128 mM·mL<sup>-1</sup>. Under optimal conditions, the rSDRz achieved a degradation efficiency of 62.17% for aniline blue. Gas chromatography-mass spectrometry (GC-MS) analysis identified several intermediate metabolites in the degradation pathway, including benzeneacetaldehyde, a, a-diphenyl, 2-amino-4-methylbenzophenone, benzene, 1-dimethylamino-4-phenylmethyl, benzenesulfonic acid, methyl ester, further elucidating the biodegradation mechanism. These findings highlight SDRz as a critical enzyme in the biodegradation of aniline blue, offering valuable insights and a robust theoretical foundation for developing advanced bioremediation strategies to address dye wastewater pollution.

MoleculesVol. 29(22)
University Hospital Schleswig-Holstein (DE), Jilin Province Science and Technology Department (CN), Jilin Agricultural University (CN), Jilin Business and Technology College, Changchun University (CN), University of Lübeck (DE)
Interreg South Baltic, European Commission, People's Government of Jilin Province, European Regional Development Fund, Interreg
Clean water and sanitation
Openalex Percentile: Top 9%
Enzyme-mediated dye degradation
3.00
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