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. 2019 Mar 4;13(7):1688–1699. doi: 10.1038/s41396-019-0379-y

Table 1.

Net anaerobic HONO and NO emissions from different Proteobacteria in the presence of initial nitrite or nitrate

Proteobacteria Strains Genes encoding nitrogen oxide reductases converting Maximum flux (ng m−2 s−1)
NO3 to NO2 NO2 to NO NO2 to NH4+ NO to N2O N2O to N2 Nitrite Nitrate
narG napA nirK nirS nirBDC/nrfAB norBC nosZ HONO NO HONO NO
Nitrate reducer Escherichia coli K-12 + + +a 575 ± 115 165 ± 33 697 ± 139 258 ± 52
Denitrifiers Pseudomonas G-179 + + + −12 ± 2 96 ± 19 11 ± 2 39 ± 8
Bradyrhizobium japonicum + + + + −31 ± 6 −13 ± 3 14 ± 3 16 ± 3
Rhodanobacter denitrificans + + + + 4 ± 1 5 ± 1 0.1 ± 0 0 ± 0.1
Pseudomonas stutzeri JM-300 + + + + + −37 ± 7 −31 ± 6 0.7 ± 0.1 0.6 ± 0.1

+ and − indicate that the bacteria have or do not have the specific denitrification-associated gene, respectively. Nitrogen mass-based maximum fluxes of HONO and NO were calculated by the differences between the maximum flux from pure cell culture and sterilized background medium, and can be attributed to the direct effect of the bacteria. Values are the maximum fluxes ± relative errors. Relative errors were calculated based on 20% of the flux value, which were derived from four replications of sterilized background measurement.

aAlternative nitrite reductases, see Fig. 3