PMID- 12691906 OWN - NLM STAT- MEDLINE DCOM- 20030807 LR - 20131121 IS - 0043-1354 (Print) IS - 0043-1354 (Linking) VI - 37 IP - 9 DP - 2003 May TI - Evaluation of the impact of bioaugmentation and biostimulation by in situ hybridization and microelectrode. PG - 2206-16 AB - Three rotating disk biofilm reactors were operated to evaluate whether bioaugmentation and biostimulation can be used to improve the start-up of microbial nitrification. The first reactor was bioaugmented during start-up period with an enrichment culture of nitrifying bacteria, the second reactor received a synthetic medium containing NH(4)(+) and NO(2)(-) to facilitate concomitant proliferation of ammonia- and nitrite-oxidizing bacteria, and the third reactor was used as a control. To evaluate the effectiveness of bioaugmentation and biostimulation approaches, time-dependent developments of nitrifying bacterial community and in situ nitrifying activity in biofilms were monitored by fluorescence in situ hybridization (FISH) technique and microelectrode measurements of NH(4)(+), NO(2)(-), NO(3)(-), and O(2). In situ hybridization results revealed that addition of the enrichment culture of nitrifying bacteria significantly facilitated development of dense nitrifying bacterial populations in the biofilm shortly after, which led to a rapid start-up and enhancement of in situ nitrification activity. The inoculated bacteria could proliferate and/or survive in the biofilm. In addition, the addition of nitrifying bacteria increased the abundance of nitrifying bacteria in the surface of the biofilm, resulting in the higher nitrification rate. On the other hand, the addition of 2.1mM NO(2)(-) did not stimulate the growth of nitrite-oxidizing bacteria and did inhibit the proliferation of ammonia-oxidizing bacteria instead. Thus, the start-up of NO(2)(-) oxidation was unchanged, and the start-up of NH(4)(+) oxidation was delayed. In all the three biofilm reactors, data sets of time series analyses on population dynamics of nitrifying bacteria determined by FISH, in situ nitrifying activities determined by microelectrode measurements, and the reactor performances revealed an approximate agreement between the appearance of nitrifying bacteria and the initiation of nitrification activity, suggesting that the combination of these techniques was a very powerful monitoring tool to evaluate the effectiveness of bioaugmentation and biostimulation strategies. FAU - Satoh, Hisashi AU - Satoh H AD - Department of Environmental and Civil Engineering, Hachinohe Institute of Technology, Aomori 031-8501, Japan. FAU - Okabe, Satoshi AU - Okabe S FAU - Yamaguchi, Yuki AU - Yamaguchi Y FAU - Watanabe, Yoshimasa AU - Watanabe Y LA - eng PT - Journal Article PL - England TA - Water Res JT - Water research JID - 0105072 RN - 0 (DNA Primers) RN - 0 (DNA, Bacterial) RN - N762921K75 (Nitrogen) SB - IM MH - *Biofilms MH - *Bioreactors MH - DNA Primers MH - DNA, Bacterial/analysis MH - Electrodes MH - In Situ Hybridization, Fluorescence MH - *Models, Theoretical MH - Nitrogen/*metabolism MH - Oxidation-Reduction EDAT- 2003/04/15 05:00 MHDA- 2003/08/09 05:00 CRDT- 2003/04/15 05:00 PHST- 2003/04/15 05:00 [pubmed] PHST- 2003/08/09 05:00 [medline] PHST- 2003/04/15 05:00 [entrez] AID - S0043-1354(02)00617-6 [pii] AID - 10.1016/S0043-1354(02)00617-6 [doi] PST - ppublish SO - Water Res. 2003 May;37(9):2206-16. doi: 10.1016/S0043-1354(02)00617-6.