反硝化
化学
亚硝酸盐
反硝化细菌
斯氏假单胞菌
电子转移
碳纤维
氮气
无机化学
环境化学
硝酸盐
材料科学
光化学
细菌
有机化学
生物
复合数
复合材料
遗传学
作者
Qiansheng Li,Hong Lü,Tian Tian,Ze Fu,Yi Tao Dai,Pei-Wen Li,Jiti Zhou
标识
DOI:10.1021/acs.est.3c08625
摘要
Bulk carbon-based materials can enhance anaerobic biodenitrification when they are present in extracellular matrices. However, little information is available on the effect of nitrogen and iron co-doped carbon dots (N, Fe-CDs) with sizes below 10 nm on this process. This work demonstrated that Fe–NX formed in N, Fe-CDs and their low surface potentials facilitated electron transfer. N, Fe-CDs exhibited good biocompatibility and were effectively absorbed by Pseudomonas stutzeri ATCC 17588. Intracellular N, Fe-CDs played a dominant role in enhancing anaerobic denitrification. During this process, the nitrate removal rate was significantly increased by 40.60% at 11 h with little nitrite and N2O accumulation, which was attributed to the enhanced activities of the electron transport system and various denitrifying reductases. Based on proteomics and metabolomic analysis, N, Fe-CDs effectively regulated carbon/nitrogen/sulfur metabolism to induce more electron generation, less nitrite/N2O accumulation, and higher levels of nitrogen removal. This work reveals the mechanism by which N, Fe-CDs enhance anaerobic denitrification and broaden their potential application in nitrogen removal.
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