Batch enrichment of anammox bacteria and study of the underlying microbial community dynamics

•Effect of nitrite supply during batch enrichment of anammox sludge was investigated.•Anammox activity was only developed when starting at low nitrite concentration.•Final abundance of the hzo gene and anammox activity were positively correlated.•Inoculum and enrichment conditions determined final m...

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Published inChemical engineering journal (Lausanne, Switzerland : 1996) Vol. 297; pp. 217 - 228
Main Authors Connan, Romain, Dabert, Patrick, Khalil, Hassan, Bridoux, Gilbert, Béline, Fabrice, Magrí, Albert
Format Journal Article Publication
LanguageEnglish
Published Elsevier B.V 01.08.2016
Elsevier
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Summary:•Effect of nitrite supply during batch enrichment of anammox sludge was investigated.•Anammox activity was only developed when starting at low nitrite concentration.•Final abundance of the hzo gene and anammox activity were positively correlated.•Inoculum and enrichment conditions determined final microbial community structure.•Enrichment conditions prompted selection of anammox species belonging to Ca. Brocadia. 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 4months. Concerning the mineral medium used, two different nitrite supply strategies were applied; i.e., (i) initially low concentration at 25mgNO2−–N/L and progressive increase to 150mgNO2−–N/L, and (ii) constant high concentration at 150mgNO2−–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±1mgNH4+–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.
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ISSN:1385-8947
1873-3212
DOI:10.1016/j.cej.2016.03.154