微生物と電気の力でアンモニウムの再生に成功~サステイナブルな窒素循環社会の実現に期待~

2026-09-15 北海道大学

北海道大学大学院工学研究院の研究グループは、微生物と電気化学反応を組み合わせ、地下水や河川水に含まれる低濃度の硝酸(約1 mM)をアンモニウムイオンへ変換・回収する新しい生物電気化学プロセスを開発した。従来のバイオフィルムを利用する方法では、微生物への電子供給が限られることが課題だった。そこで本研究では、溶液中を自由に移動する水溶性電子伝達体を利用し、微生物全体へ効率的に電子を供給する仕組みを構築した。その結果、硝酸からアンモニウムへの再生速度は従来法の最大8倍以上に向上し、実際の地下水・河川水でも同様の性能を確認した。また、金属触媒を用いる方法より少ないエネルギーで変換できることも示された。本技術は、環境中の硝酸汚染を低減すると同時に、窒素をアンモニウムとして回収・再利用することで、窒素資源の循環利用を実現する技術として期待される。

微生物と電気の力でアンモニウムの再生に成功~サステイナブルな窒素循環社会の実現に期待~
環境中へ大量に散逸する硝酸(NO3–)を生物電気化学的にNH4+へ戻し、再生肥料化する。

<関連情報>

水溶性電子伝達体を用いた生物電気化学プロセスによる硝酸のアンモニウム再生 Soluble-electron mediator assisted bioelectrochemical reduction of nitrate to ammonium for nitrogen recovery

Yunjeong Choi, Nichika Takahashi, Satoshi Okabe, Mamoru Oshiki
Chemical Engineering Journal  Available online: 7 September 2026
DOI:https://doi.org/10.1016/j.cej.2026.181710

Highlights

  • First demonstration of soluble-mediator-assisted bioelectrochemical NO3− reduction to NH4+
  • High NO3− reduction activity; 10.9 mmol-N L−1 day−1 and Ks = 0.19 mM
  • Efficient NO3− reduction in natural water matrices at 1 mM NO3−
  • Faradaic efficiency in natural water matrices; 50–59%
  • Electricity consumption in natural water matrices; 188–192 kWh kg-NO3−-N−1

Abstract

Bioelectrochemical reduction of dilute nitrate (NO3−; sub-mM) to ammonium (NH4+) is a promising route toward circular nitrogen management from nitrate-contaminated groundwater and surface waters. However, conventional bioelectrochemical systems (BES) rely on extracellular electron transfer through electrode-attached biofilms, restricting catalysis to a few electroactive bacteria in direct contact with the electrode. Here, we developed a soluble-mediator-assisted BES in which a diffusible mediator shuttles electrons to suspended cells throughout the catholyte, enabling weakly electroactive bacteria to serve as nitrate-reduction catalysts. Three biocatalysts (Escherichia coli, Shewanella oneidensis, and Candidatus Brocadia sinica), nine soluble mediators spanning viologens, quinones, and phenazines, cathodic potentials from −0.3 to −0.9 V, and pH 6.5 to 8.5 were screened, and NO3− reduction to NH4+ was confirmed using a 15NO3− tracer. With E. coli cells and methyl viologen, NO3− was reduced to NH4+ at a maximum volumetric rate of 10.9 mmol-N L−1 day−1 and a low NO3−-affinity constant (Ks = 0.19 mM). This rate was 8-fold higher than previously reported biofilm-based systems, and NO3− reduction was repeated over three successive NO3− additions during 48 h of operation. Furthermore, the soluble-mediator-assisted BES showed high performance even in natural groundwater and surface water, with a Faradaic efficiency of 50–59% and an electricity consumption of 188–192 kWh kg-NO3−-N−1, substantially lower than metal-catalyst systems at comparable NO3− concentration. These findings demonstrate that soluble-mediator-assisted BESs provide an energy-efficient platform for converting NO3− in natural water into a recoverable NH4+ form, with full nitrogen recovery additionally requiring downstream NH4+ concentration or separation.

1202農芸化学
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