Publications
43
| Citation | Title | ||
|---|---|---|---|
| Qiu et al., 2019, Environmental Science & Technology | Metabolic Traits of Candidatus Accumulibacter clade IIF Strain SCELSE-1 Using Amino Acids As Carbon Sources for Enhanced Biological Phosphorus Removal | ||
| Li et al., 2019, Applied and Environmental Microbiology | Population Structure and Morphotype Analysis of “ Candidatus Accumulibacter” Using Fluorescence In Situ Hybridization-Staining-Flow Cytometry | ||
| Srinivasan et al., 2019, | Oligotyping and Genome-Resolved Metagenomics Reveal DistinctCandidatusAccumulibacter Communities in Full-Scale Side-Stream versus Conventional Enhanced Biological Phosphorus Removal (EBPR) Configurations | ||
| Zeng et al., 2018, Journal of Environmental Sciences | Community structures and population dynamics of “Candidatus Accumulibacter” in activated sludges of wastewater treatment plants using ppk1 as phylogenetic marker | ||
| Wang et al., 2018, Frontiers in Microbiology | Effect of Salt on the Metabolism of ‘Candidatus Accumulibacter’ Clade I and II | ||
| Nittami et al., 2017, Applied Microbiology and Biotechnology | Effects of different carbon sources on enhanced biological phosphorus removal and “Candidatus Accumulibacter” community composition under continuous aerobic condition | ||
| Zeng et al., 2017, Enzyme and Microbial Technology | Interaction of “ Candidatus Accumulibacter” and nitrifying bacteria to achieve energy-efficient denitrifying phosphorus removal via nitrite pathway from sewage | ||
| Rubio-Rincón et al., 2017, Water Research | Cooperation between Candidatus Competibacter and Candidatus Accumulibacter clade I, in denitrification and phosphate removal processes | ||
| Welles et al., 2017, Frontiers in Microbiology | Metabolic Response of “Candidatus Accumulibacter Phosphatis” Clade II C to Changes in Influent P/C Ratio | ||
| Zeng et al., 2016, Bioresource Technology | Denitrifying phosphorus removal from municipal wastewater and dynamics of “Candidatus Accumulibacter” and denitrifying bacteria based on genes of ppk1, narG, nirS and nirK |