College of Life Sciences, Jilin Agricultural University, Changchun 130118, China.
School of Grain Science and Technology, Jilin Business and Technology College, Changchun 130507, China.
Molecules. 2024 Nov 15;29(22):5405. doi: 10.3390/molecules29225405.
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 (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 () gene (logFC = 2.11, < 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 -knockout strain (CT-ΔSDRz) and an -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 DH5α after 12 h. Recombinant SDRz (rSDRz) was successfully produced, showing significant enzymatic activity (1.267 ± 0.04 mmol·L·min protein), with kinetic parameters Vmax = 2.870 ± 0.0156 mmol·L⁻·min⁻ protein and Km = 1.805 ± 0.0128 mM·mL. 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.
染料废水污染,特别是持久性和毒性多环有机污染物,如苯胺蓝,对环境构成了重大挑战。苯胺蓝是一种三苯甲烷染料,广泛应用于纺织、皮革、造纸和制药行业,由于其复杂的结构和潜在的生物累积性,处理起来极具难度。在这项研究中,我们探索了 (CT1) 高效降解苯胺蓝的能力,重点研究了潜在的酶促机制和降解途径。通过原核转录组分析,我们鉴定出一个显著上调的短链脱氢酶 () 基因 (logFC = 2.11, < 0.05),该基因在降解过程中起着关键作用。SDRz 酶具有高度保守的基序和典型的短链脱氢酶结构。使用 -敲除菌株 (CT-ΔSDRz) 和 -表达菌株 (E-SDRz) 进行功能验证,证实 SDRz 是苯胺蓝降解所必需的。与 CT1 菌株相比,12 小时后,-敲除菌株 CT-ΔSDRz 的降解效率降低了 1.27 倍;而表达菌株 E-SDRz 的降解效率则提高了 1.24 倍,与 DH5α 相比。成功生产了重组 SDRz (rSDRz),表现出显著的酶活性 (1.267 ± 0.04 mmol·L·min protein),动力学参数 Vmax = 2.870 ± 0.0156 mmol·L⁻·min⁻ protein 和 Km = 1.805 ± 0.0128 mM·mL。在最佳条件下,rSDRz 对苯胺蓝的降解效率达到 62.17%。气相色谱-质谱联用 (GC-MS) 分析鉴定了降解途径中的几种中间代谢物,包括苯乙醛、α,α-二苯基、2-氨基-4-甲基二苯甲酮、苯、1-二甲基氨基-4-苯甲基、苯磺酸、甲酯,进一步阐明了生物降解机制。这些发现强调了 SDRz 作为苯胺蓝生物降解过程中的关键酶,为开发先进的生物修复策略提供了有价值的见解和坚实的理论基础,以解决染料废水污染问题。