Exploring the potential of co-fermenting sewage sludge and lipids in a resource recovery scenario

In this study, co-fermentation of primary sludge (PS) or waste activated sludge (WAS) with lipids was explored to improve volatile fatty acid production. PS and WAS were used as base substrate to facilitate lipid fermentation at 20 °C under semi-aerobic conditions. Mono-fermentation tests showed higher VFA yields for PS (32-89 mgCOD gVS-1) than for WAS (20-41 mgCOD gVS-1) where propionate production was favoured. The principal component analysis showed that the base substrate had a notable influence on co-fermentation yields and profile. Co-fermentation with WAS resulted in a greater extent of oleic acid degradation (up to 4.7%) and evidence of chain elongation producing valerate. The occurrence of chain elongation suggests that co-fermentation can be engineered to favour medium-chain fatty acids without the addition of external commodity chemicals. BMP tests showed that neither mono-fermentation nor co-fermentation had an impact on downstream anaerobic digestion

Impact of Storage Conditions on the Methanogenic Activity of Anaerobic Digestion Inocula

The impact of storage temperature (4, 22 and 37 ◦C) and storage time (7, 14 and 21 days) on anaerobic digestion inocula was investigated through specific methanogenic activity assays. Experimental results showed that methanogenic activity decreased over time with storage, regardless of storage temperature. However, the rate at which the methanogenic activity decreased was two and five times slower at 4 ◦C than at 22 and 37 ◦C, respectively. The inoculum stored at 4 ◦C and room temperature (22 ◦C) maintained methanogenic activity close to that of fresh inoculum for 14 days (<10% difference). However, a storage temperature of 4 ◦C is preferred because of the slower decrease in activity with lengthier storage time. From this research, it was concluded that inoculum storage time should generally be kept to a minimum, but that storage at 4 ◦C could help maintain methanogenic activity for longe

“Candidatus Dechloromonas phosphoritropha” and “Ca. D. phosphorivorans”, novel polyphosphate accumulating organisms abundant in wastewater treatment systems

Members of the genus Dechloromonas are often abundant in enhanced biological phosphorus removal (EBPR) systems and are recognized putative polyphosphate accumulating organisms (PAOs), but their role in phosphate removal is still unclear. Here, we used 16S rRNA gene sequencing and fluorescence in situ hybridization (FISH) to investigate the abundance and distribution of Dechloromonas spp. in Danish and global wastewater treatment plants. The two most abundant species worldwide revealed in situ dynamics of important intracellular storage polymers, measured by FISH-Raman in activated sludge from four full-scale EBPR plants and from a lab-scale reactor fed with different substrates. Moreover, seven distinct Dechloromonas species were determined from a set of ten high-quality metagenome-assembled genomes (MAGs) from Danish EBPR plants, each encoding the potential for polyphosphate (poly-P), glycogen, and polyhydroxyalkanoates (PHA) accumulation. The two species exhibited an in situ phenotype in complete accordance with the metabolic information retrieved by the MAGs, with dynamic levels of poly-P, glycogen, and PHA during feast-famine anaerobic–aerobic cycling, legitimately placing these microorganisms among the important PAOs. They are potentially involved in denitrification showing niche partitioning within the genus and with other important PAOs. As no isolates are available for the two species, we propose the names Candidatus Dechloromonas phosphoritropha and Candidatus Dechloromonas phosphorivorans

Metagenome from a Spirulina digesting biogas reactor: analysis via binning of contigs and classification of short reads

Nolla Ardevol V, Peces M, Strous M, Tegetmeyer H. Metagenome from a Spirulina digesting biogas reactor: analysis via binning of contigs and classification of short reads. BMC Microbiology. 2015;15(1): 277.Background Anaerobic digestion is a biological process in which a consortium of microorganisms transforms a complex substrate into methane and carbon dioxide. A good understanding of the interactions between the populations that form this consortium can contribute to a successful anaerobic digestion of the substrate. In this study we combine the analysis of the biogas production in a laboratory anaerobic digester fed with the microalgae Spirulina, a protein rich substrate, with the analysis of the metagenome of the consortium responsible for digestion, obtained by high-throughput DNA sequencing. The obtained metagenome was also compared with a metagenome from a full scale biogas plant fed with cellulose rich material. Results The optimal organic loading rate for the anaerobic digestion of Spirulina was determined to be 4.0 g Spirulina L−1 day−1 with a specific biogas production of 350 mL biogas g Spirulina −1 with a methane content of 68 %. Firmicutes dominated the microbial consortium at 38 % abundance followed by Bacteroidetes, Chloroflexi and Thermotogae. Euryarchaeota represented 3.5 % of the total abundance. The most abundant organism (14.9 %) was related to Tissierella, a bacterium known to use proteinaceous substrates for growth. Methanomicrobiales and Methanosarcinales dominated the archaeal community. Compared to the full scale cellulose-fed digesters, Pfam domains related to protein degradation were more frequently detected and Pfam domains related to cellulose degradation were less frequent in our sample. Conclusions The results presented in this study suggest that Spirulina is a suitable substrate for the production of biogas. The proteinaceous substrate appeared to have a selective impact on the bacterial community that performed anaerobic digestion. A direct influence of the substrate on the selection of specific methanogenic populations was not observed

Advances in anaerobic membrane bioreactor technology for municipal wastewater treatment: A 2020 updated review

The application of anaerobic membrane bioreactors (AnMBR) for mainstream municipal sewage treatment is almost ready for full-scale implementation. However, some challenges still need to be addressed to make AnMBR technically and economically feasible. This article presents an updated review of five challenges that currently hinder the implementation of AnMBR technology for mainstream sewage treatment: (i) membrane fouling, (ii) process configuration, (iii) process temperature, (iv) sewage sulphate concentration, and (v) sewage low organics concentration. The gel layer appears to be the main responsible for membrane fouling and flux decline being molecules size and morphology critical properties for its formation. The review also discusses the advantages and disadvantages of five novel AnMBR configurations aiming to optimise fouling control. These include the integration of membrane technology with CSTR or upflow digesters, and the utilisation of scouring particles. Psychrophilic temperatures and high sulphate concentrations are two other limiting factors due to their impact on methane yields and membrane performance. Besides the methane dissolved in the effluent and the competition for organic matter between sulphate reducing bacteria and methanogens, the review examines the impact of temperature on microbial kinetics and community, and their combined effect on AnMBR performance. Finally, the review evaluates the possibility to pre-concentrate municipal sewage by forward osmosis. Sewage pre-concentration is an opportunity to reduce the volumetric flow rate and the dissolved methane losses. Overall, the resolution of these challenges requires a compromise solution considering membrane filtration, anaerobic digestion performance and economic feasibility

Quantification of Biologically and Chemically Bound Phosphorus in Activated Sludge from Full-Scale Plants with Biological P-Removal

[Image: see text] Phosphorus (P) is present in activated sludge from wastewater treatment plants in the form of metal salt precipitates, extracellular polymeric substances, or bound into the biomass, for example, as intracellular polyphosphate (poly-P). Several methods for a reliable quantification of the different P-fractions have recently been developed, and this study combines them to obtain a comprehensive P mass-balance of activated sludge from four enhanced biological phosphate removal (EBPR) plants. Chemical characterization by ICP-OES and sequential P fractionation showed that chemically bound P constituted 38–69% of total P, most likely in the form of Fe, Mg, or Al minerals. Raman microspectroscopy, solution state (31)P NMR, and (31)P MAS NMR spectroscopy applied before and after anaerobic P-release experiments, were used to quantify poly-P, which constituted 22–54% of total P and was found in approximately 25% of all bacterial cells. Raman microspectroscopy in combination with fluorescence in situ hybridization was used to quantify poly-P in known polyphosphate-accumulating organisms (PAO) (Tetrasphaera, Candidatus Accumulibacter, and Dechloromonas) and other microorganisms known to possess high level of poly-P, such as the filamentous Ca. Microthrix. Interestingly, only 1–13% of total P was stored by unidentified PAO, highlighting that most PAOs in the full-scale EBPR plants investigated are known