Abstract

During the process of circulating aquaculture, high concentrations of nitrate will accumulate. A simultaneous denitrification and fermentation process is described to remove nitrate from a recirculating aquaculture system using endogenous carbon on a biofilm. 15N isotope technology was used to assess the nitrate removal, mainly through heterotrophic denitrification. The nitrate removal rate could be as high as 98.97%, with a final concentration of nitrate below 1 mg/L. The denitrification process obeys a Michaelis–Menten-type enzyme kinetic model, with a half saturation constant of 99.91 mg/L and a maximum nitrate removal rate of 0.39 mg L−1 h−1 at 28 °C. The functional genes narG and narH for nitrate removal were obtained from Nitrospirae spp. at proportions of 39.13% and 26.16%, respectively. The acetate, propionate and iso-valerate produced by anaerobic fermentation provided the principal electron donors for denitrification.

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