电合成
化学
细胞外
固氮
固碳
氮气
固氮酶
碳纤维
生物化学
纳米技术
材料科学
有机化学
电极
物理化学
复合材料
复合数
电化学
光合作用
作者
Jiaping Hu,Cuiping Zeng,Guangli Liu,Haiping Luo
标识
DOI:10.1016/j.biortech.2024.131390
摘要
This study investigated the molecular mechanism behind the highly efficient performance of nitrogen-doped carbon dots (NCDs)-assisted microbial electrosynthesis systems (MESs). The impact of NCDs (C:N precursor = 1:0.5–1:3) on acetogens were examined in the biocathode. The highest electrocatalytic performance was observed with NCDs1:1. The maximum acetate production rate of 1.9 ± 0.1 mM d−1 was achieved in NCDs1:1 modified MESs, which was 26.7–216.7 % higher than other MESs (0.6–1.5 mM d−1). With NCDs1:1 modified, the biocathode exhibited a 125.3–186.8 % increase in the abundance of Sporomusa, and 38.5–104.6 % increase in cytochrome expression (cydAB, cybH). Transcriptome confirmed that cytochromes played a crucial role in the extracellular electron uptake (EEU) of NCDs1:1-modified Sporomusa. NCDs1:1 enhanced EEU efficiency, thereby increasing the two H+-pumping steps and accelerating microbial CO2 fixation. These results provide valuable insights into increasing CO2 fixation by maximizing EEU efficiency in acetogens.
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