Methanotrophs Contribute to Nitrogen Fixation in Emergent Macrophytes

Root-associated aerobic methanotroph plays an important role in reducing methane emissions from wetlands. In this study, we examined the activity of methane-dependent nitrogen fixation and active nitrogen-fixing bacterial communities on the roots of Typha angustifolia and Scirpus triqueter using a (15)N-N(2) feeding experiment and a cDNA-based clone library sequence of the nifH gene, respectively. A (15)N-N(2) feeding experiment showed that the N(2) fixation rate of S. triqueter (1.74 μmol h(–1) g(–1) dry weight) was significantly higther than that of T. angustifolia (0.48 μmol h(–1) g(–1) dry weight). The presence of CH(4) significantly increased the incorporation of (15)N-labeled N(2) into the roots of both plants, and the rate of CH(4)-dependent N(2) fixation of S. triqueter (5.6 μmol h(–1) g(–1) dry weight) was fivefold higher than that of T. angustifolia (0.94 μmol h(–1) g(–1) dry weight). The active root-associated diazotrophic communities differed between the plant species. Diazotrophic Methylosinus of the Methylocystaceae was dominant in S. triqueter, while Rhizobium of the Rhizobiaceae was dominant in T. angustifolia. However, there were no significant differences in the copy numbers of nifH between plant species. These results suggest that N(2) fixation was enhanced by the oxidation of CH(4) in the roots of macrophytes grown in natural wetlands and that root-associated Methylocystacea, including Methylosinus, contribute to CH(4) oxidation-dependent N(2) fixation.