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BACKGROUND The utilization of different kinds of ion exchange membrane is a common practice in bioelectrochemical systems such as two‐chambered microbial fuel cells (MFCs). However, little is known about the effect of membrane materials on the anodic microbial community diversity. RESULTS The effect of two cationic and one anionic exchange membranes (Nafion N‐117, Ultrex CMI‐7000, and Ultrex AMI‐7000) on the microbial community dynamics of Eubacteria and Archaea has been assessed in two‐chambered MFCs. The experimental results indicated that the eubacterial community in the anodic chamber was not affected by the membrane materials, being predominantly populations of Bacteroidetes (Porphyromonadaceae) and β‐proteobacteria (Alcaligenaceae and Comamonadaceae). On the other hand, the archaeal counterpart appears to be highly dependent on the type of membrane used, as was evidenced by the selective enrichment of Methanosarcina sp. in the MFC equipped with the membrane Nafion N‐117 which was the MFC that showed the highest current production. CONCLUSIONS The results obtained in the present study suggest that membrane materials affect archaeal diversity whereas both anodofilic eubacteria and methanogenic archaea populations could play an important role in the overall MFC process performance. © 2014 Society of Chemical Industry

The anaerobic ammonium oxidation (anammox) consists on the biological conversion of ammonium (NH4+) into dinitrogen gas under absence of oxygen. Nitrite (NO2-) is a substrate of the anammox reaction, but also an inhibitor at high concentrations. This study investigates the effect of nitrite on the microbial community during the batch enrichment of anammox sludge. Six inoculums collected from different environments were enriched after a conditioning pretreatment and under controlled conditions during 4 months. Concerning the mineral medium used, two different nitrite supply strategies were applied; i.e., (i) initially low concentration at 25 mg NO2-–N/L and progressive increase to 150 mg NO2-–N/L, and (ii) constant high concentration at 150 mg NO2-–N/L. All tested inoculums developed anammox activity but only when the enrichment was started at low nitrite concentration. In such case, the specific ammonium conversion rates finally obtained ranged from 21 ±1 to 118 ±1 mg NH4+–N/g VS/d (VS, volatile solids). Abundance of the functional gene encoding for the enzyme hydrazine oxidoreductase (hzo) was assessed using the real-time quantitative polymerase chain reaction (q-PCR) showing positive correlation with the anammox activity finally reported. In addition, high-throughput DNA sequencing helped to elucidate the underlying microbial community dynamics. The raw inoculum source, the conditioning pretreatment, and the cultivation conditions applied were jointly determinants of the final microbial community structure of the enrichments despite a clear convergence at the end of the experimental period. On the other hand, the cultivation conditions alone determined the selection of anammox species belonging to the genus Candidatus Brocadia.Postprint (updated version

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