Effect of Lactate on the Microbial Community and Process Performance of an EBPR System.

Front Microbiol

Sanitary Engineering Chair Group, Department of Environmental Engineering and Water Technology, UNESCO-IHE Institute for Water Education, Delft, Netherlands.

Published: February 2019

Accumulibacter phosphatis is in general presented as the dominant organism responsible for the biological removal of phosphorus in activated sludge wastewater treatment plants. Lab-scale enhanced biological phosphorus removal (EBPR) studies, usually use acetate as carbon source. However, the complexity of the carbon sources present in wastewater could allow other potential poly-phosphate accumulating organism (PAOs), such as putative fermentative PAOs (e.g., ), to proliferate in coexistence or competition with . Accumulibacter. This research assessed the effects of lactate on microbial selection and process performance of an EBPR lab-scale study. The addition of lactate resulted in the coexistence of . Accumulibacter and in a single EBPR reactor. An increase in anaerobic glycogen consumption from 1.17 to 2.96 C-mol/L and anaerobic PHV formation from 0.44 to 0.87 PHV/PHA C-mol/C-mol corresponded to the increase in the influent lactate concentration. The dominant metabolism shifted from a polyphosphate-accumulating metabolism (PAM) to a glycogen accumulating metabolism (GAM) without EBPR activity. However, despite the GAM, traditional glycogen accumulating organisms (GAOs; Competibacter phosphatis and ) were not detected. Instead, the 16s RNA amplicon analysis showed that the genera was the dominant organism, while a quantification based on FISH-biovolume indicated that . Accumulibacter remained the dominant organism, indicating certain discrepancies between these microbial analytical methods. Despite the discrepancies between these microbial analytical methods, neither . Accumulibacter nor performed biological phosphorus removal by utilizing lactate as carbon source.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387944PMC
http://dx.doi.org/10.3389/fmicb.2019.00125DOI Listing

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