Biological Nitrogen Removal Database

A manually curated data resource for microbial nitrogen removal


Marine systems


Experimental setup


Influent:Marine water

Denitrification system:Marine Recirculating aquaculture systems (RAS)

Denitrifying reactor:nan

Medium:PHBV granules

Culture taken from:Marinobacter hydrocarbonoclasticus

Organism (s) cultured:nan

Respiration:Aerobic

Electron donor:PHBV

Electron acceptor:Nitrate


Experimental Information


Input NO3-N (mg/l):nan

Nitrate removal rate (mg NO3-N/l/h):nan

Denitrification rate (gNO3-N removed/m3/day):nan

Microorganisms identified:Marinobacter hydrocarbonoclasticus RAD-2

Molecular tools:16S rRNA gene


Information about Article


Major findings:Marinobacter hydrocarbonoclasticus RAD-2, was isolated from a long-term PHBV-supported denitrification reactor that operated under alternate aerobic/anoxic conditions for marine RAS-effluent treatment. Have the ability to utilize of various biodegradable polymers as sole carbon

Authors:Kong et al., 2018

Title:Denitrification-Potential Evaluation and Nitrate-Removal-Pathway Analysis of Aerobic Denitrifier Strain Marinobacter hydrocarbonoclasticus RAD-2.

Pubmed link:None

Full research link:Link

Abstract:An aerobic denitrifier was isolated from a long-term poly (3-hydroxybutyrate-co-3-hydroxyvalerate) PHBV-supported denitrification reactor that operated under alternate aerobic/anoxic conditions. The strain was identified as Marinobacter hydrocarbonoclasticus RAD-2 based on 16S rRNA-sequence phylogenetic analysis. Morphology was observed by scanning electron microscopy (SEM), and phylogenetic characteristics were analyzed with the API 20NE test. Strain RAD-2 showed efficient aerobic denitrification ability when using NO3?-N or NO2?-N as its only nitrogen source, while heterotrophic nitrification was not detected. The average NO3?-N and NO2?-N removal rates were 6.47 mg/(L·h)and 6.32 mg/(L·h), respectively. Single-factor experiments indicated that a 5:10 C/N ratio, 25–40 °C temperature, and 100–150 rpm rotation speed were the optimal conditions for aerobic denitrification. Furthermore, the denitrifying gene napA had the highest expression on a transcriptional level, followed by the denitrifying genes nirS and nosZ. The norB gene was found to have significantly low expression during the experiment. Overall, great aerobic denitrification ability makes the RAD-2 strain a potential alternative in enhancing nitrate management for marine recirculating aquaculture system (RAS) practices. View Full-Text