Mechanism of polycyclic aromatic hydrocarbons degradation in the rhizosphere of Phragmites australis: Organic acid co-metabolism, iron-driven, and microbial response

文献类型: 外文期刊

第一作者: Zhang, Ni-chen

作者: Zhang, Ni-chen;Chao, Yuan-qing;Qiu, Rong-liang;Zhang, Ni-chen;Lin, Qing-qi;Qiu, Rong-liang;A, Dan;Lin, Qing-qi;Qiu, Rong-liang;Li, Ya-ying;Li, Hai-Yan;Li, Hai-Yan;Li, Charles

作者机构:

关键词: Co -metabolic degradation; Iron -driven; Microbial community; Polycyclic aromatic hydrocarbons; Root organic exudates

期刊名称:ENVIRONMENTAL POLLUTION ( 影响因子:8.9; 五年影响因子:9.5 )

ISSN: 0269-7491

年卷期: 2023 年 327 卷

页码:

收录情况: SCI

摘要: Microbial co-metabolism is crucial for the efficient biodegradation of polycyclic aromatic hydrocarbons (PAHs); however, their intrinsic mechanisms remain unclear. To explore the co-metabolic degradation of PAHs, root organic acids (ROAs) (phenolic ROAs: caffeic acid [CA] and ferulic acid [FA]; non-phenolic ROAs: oxalic acid [OA]) were exogenously added as co-metabolic substrates under high (HFe) and low (LFe) iron levels in this study. The results demonstrated that more than 90% of PAHs were eliminated from the rhizosphere of Phragmites australis. OA can promote the enrichment of unrelated degrading bacteria and non-specific dioxygenases. FA with a monohydroxy structure can activate hydroxylase; however, it relies on phytosiderophores released by plants (such as OA) to adapt to stress. Therefore, non-specific co-metabolism occurred in these units. The best performance for PAH removal was observed in the HFe-CA unit because: (a) HFe concentrations enriched the Fereducing and denitrifying bacteria and promoted the rate-limiting degradation for PAHs as the enzyme cofactor; (b) CA with a dihydroxyl structure enriched the related degrading bacteria, stimulated specific dioxygenase, and activated Fe to concentrate around the rhizosphere simultaneously to perform the specific cometabolism. Understanding the co-metabolic degradation of PAHs will help improve the efficacy of rhizosphere-mediated remediation.

分类号:

  • 相关文献
作者其他论文 更多>>