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Anaerobic ammonium oxidation (anammox) bacteria were enriched in continuous packed-bed columns with marine sediment. One column (SB-C) was packed with only marine sediment collected from a shrimp-aquaculture pond, and another column (SB-AMX) was inoculated with marine anammox bacteria (MAB) as a control. These columns were continuously fed with natural or artificial seawater including ammonium (NH 4 + ) and nitrite (NO 2 - ). The SB-AMX showed anammox activities from the beginning and continued for over 200 days. However, the SB-C had no nitrogen removal performance for over 170 days. After adding a bicarbonate solution (KHCO 3 ) to the sediment-only packed column, anammox activity was observed within 13 days. The column exhibited a nitrogen removal efficiency (NRE) of 88% at a nitrogen loading rate (NLR) of 1.0 kg-N·m -3 ·day -1 , which was comparable to the control one. A next-generation sequencing analysis revealed the predominance of MAB related to "Candidatus Scalindua spp.". In addition, the co-occurrence of sulfur-oxidizing denitrifiers was observed, which suggests their symbiotic relationship. This study suggests the applicability of MAB for in-situ bioremediation of nitrogen-contaminated marine sediments and reveals a potential microbial interaction between anammox and sulfur-oxidizing communities responsible for nitrogen and sulfur cycling in marine aquaculture systems., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

Partial nitritation and anammox (PN/A) was applied in a lab-scale membrane bioreactor (MBR) to investigate its technical feasibility for treating ammonium-rich wastewater with low C/N ratio. The bacterial community was analyzed by molecular cloning and 16S rRNA sequence analysis. Partial nitritation (PN) was first realized in MBR by seeding aerobic activated sludge. With dissolved oxygen control, a steady effluent mixture with NO2 (-)-N/NH4 (+)-N ratio of 1.13 ± 0.08 was generated from the PN process. Subsequently, the MBR was seeded with anammox biomass on day 59. After running 300 days, the one-stage PN/A achieved a maximum nitrogen removal rate of 1.45 kg N/m(3)/day at the nitrogen removal efficiency of 89.5 %. Microbial community analysis revealed that Nitrosomonas sp. HKU and Nitrosospira sp. YKU corresponded to nitritation; meanwhile, Candidatus Brocadia TKU sp. accounted for nitrogen removal of the PN/A system. Specifically, Nitrosomonas sp. were enriched in the reactor at the PN/A phase and then conquered Nitrosospira sp. to be the predominant ammonia oxidizers. Nitrite oxidizers and denitrifiers were detected in symbiosis with aforementioned microbes. Denitrification promised potential plus nitrogen depletion. The present one-stage PN/A process allows a significant decrease in operational costs compared with classical nitrification/denitrification.

Anaerobic ammonium oxidation (anammox) bacteria have been detected in variety of marine environment in recent years, however, there have been only a few studies on their characteristics in the culture. The aim of this study is to reveal the effect of temperature on nitrogen removal ability and bacterial community in a culture of marine anammox bacteria (MAAOB). The MAAOB were cultured from the sediment of a sea-based waste disposal site at the North Port of Osaka Bay in Japan. The maximum nitrogen removal rate (NRR) was observed at 25°C in the MAAOB culture, and it decreased both at below 20°C and over 33°C. The activation energy of the MAAOB culture was calculated to be 54.6 kJ mol(-1) in the 5°C to 30°C range. No significant change in bacterial community according with temperature (5-37°C) was confirmed in the results of polymerase chain reaction and denaturing gradient gel electrophoresis (PCR-DGGE). Meanwhile, a number of bacteria related to the oxidation-reduction reaction of sulfur were confirmed and it is speculated that they involved in the activity of MAAOB and nitrogen removal ability in the culture., (Copyright © 2011 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.)

This paper provides the first kinetic parameters for a hydrogen-oxidizing perchlorate-reducing bacterium (PCRB), Dechloromonas sp. PC1. The qmax for perchlorate and chlorate were 3.1 and 6.3 mg/mgDW-day, respectively. The K for perchlorate was 0.14 mg/L, an order of magnitude lower than reported for other PCRB. The yields Y on perchlorate and chlorate were 0.23 and 0.22 mgDW/mg, respectively, and the decay constant b was 0.055/day. The growth-threshold, Smin, for perchlorate was 14 microg/L, suggesting that perchlorate cannot be reduced below this level when perchlorate is the primary electron-acceptor, although it may be possible when oxygen or nitrate is the primary acceptor. Chlorate accumulated at maximum concentrations of 0.6-4.3 mg/L in batch tests with initial perchlorate concentrations ranging from 100 to 600 mg/L. Furthermore, 50 mg/L chlorate inhibited perchlorate reduction with perchlorate at 100 mg/L. This is the first report of chlorate accumulation and inhibition for a pure culture of PCRB. These Chlorate effects are consistent with competitive inhibition between perchlorate and chlorate for the (per)chlorate reductase enzyme.

The hydrogen-based membrane biofilm reactor (MBfR) has been shown to reduce perchlorate to below 4μg/L, but little is known about the microbial ecology of this or other hydrogen-based reactors, especially when influent perchlorate concentrations are much lower than the influent oxygen and nitrate concentrations. Dissimilatory (per)chlorate-reducing bacteria (PCRB) can use oxygen as an electron acceptor, and most can also use nitrate. Since oxygen and nitrate can be reduced concurrently with perchlorate, they may serve as primary electron acceptors, sustaining PCRB when the perchlorate concentrations are very low. We studied five identical MBfRs, all seeded with the same inoculum and initially supplied with oxygen, or oxygen plus nitrate, in the influent. After 20 days, perchlorate was added to four MBfRs at influent concentrations of 100–10,000μg/L, while the fifth was maintained as a control. One day after perchlorate addition, the MBfRs displayed limited perchlorate reduction, suggesting a low initial abundance of PCRB. However, perchlorate reduction improved significantly over time, and denaturing gradient gel electrophoresis (DGGE) analyses suggested an increasing abundance of a single Dechloromonas species. Fluorescence in-situ hybridization (FISH) tests showed that the Dechloromonas species accounted for 14% of the bacterial count in the control MBfR, and 22%, 31%, and 49% in the MBfRs receiving nitrate plus 100, 1000, and 10,000μg/L perchlorate, respectively. The abundance was 34% in the MBfR receiving oxygen plus 1000μg/L perchlorate. These results suggest that oxygen is more favorable than nitrate as a primary electron acceptor for PCRB, that PCRB are present at low levels even without perchlorate, and that the presence of perchlorate, even at low levels relative to nitrate or oxygen, significantly enhances selection for PCRB. [Copyright &y& Elsevier]

An aryl-phosphate ester (APE)-degrading bacterium was isolated from the leachate of a sea-based waste disposal site. The isolated APE-degrading bacterial strain YS-57 grew well in a medium containing glucose and NaCl, and degraded two types of APE:tricresyl phosphate and triphenyl phosphate. The optimal temperature, pH, and NaCl concentration for the growth of strain YS-57 were 30°C, 7.0, and 1.0%, respectively. Strain YS-57 grew at an APE concentration of 25 mg/l without being inhibited. APEs were degraded by the supernatant of the medium in which strain YS-57 was cultured, suggesting that the APE-degrading enzyme was released into the extracellular space in the logarithmic growth phase. The 16S rDNA sequence of strain YS-57 showed 95.6% similarity to that of Roseobacter gallaeciensis and the morphological properties were also comparable. Consequently, strain YS-57 was closely related to the genus Roseobacter. [Copyright &y& Elsevier]

• An unclassified Anammox bacterium responds to N removal in an SBR fed with leachate. • The unclassified Anammox bacterium is distinctly related to known Anammox bacteria. • PN/A was achieved from activated sludge in an SBR without biomass carriers. • SBR performed robust N removal and achieved a peak NRR of 1.91 kg N/m3/d. • SBR likely performed arsenate reduction and degradation of drugs and antibiotics. Treatment of landfill leachate was conducted in a lab-scale sequencing batch reactor (SBR). The SBR was started through inoculating activated sludge with controlling dissolved oxygen of 0.5–1.0 mg/L. Anammox reaction took place within around three months. The SBR established robust nitrogen removal with incremental NLRs of 0.25–2.17 kg N/m3/d. At the final phase, it achieved elevated nitrogen removals of 1.68–1.91 kg N/m3/d. 16S rRNA gene amplicon sequencing analysis revealed Nitrosomonas , unclassified Anammox bacterium, and diverse denitrifying populations coexisted and accounted for 4.02%, 20.05% and 34.69%, respectively. Phylogenic analysis and average nucleotide identity comparison jointly suggested the unclassified Anammox bacterium potentially pertained to a novel Anammox lineage. The functional profiles' prediction suggested sulfate reduction, arsenate reduction and eliminations of antibiotics and drugs likely occurred in the SBR. The finding from this study suggests contribution of unclassified Anammox bacteria in influencing nitrogen budget in natural and engineering systems is currently being underestimated. [ABSTRACT FROM AUTHOR]