Function Of Extracellular Polymeric Substances Research Articles

Functions of extracellular polymeric substances in partitioning suspended and sinking particles in the upper oceans of two open ocean systems

AbstractMarine particle dynamics and carbon export, involving extracellular polymeric substances (EPS) like transparent exopolymer particles (TEP) and Coomassie Brilliant Blue‐stained particles (CSP), are poorly understood. Although TEP adhesive properties may enhance carbon export by facilitating aggregate formation, their low density can also enhance particle suspension. Factors influencing TEP regulation of particle dynamics remain unclear. To investigate EPS contributions to particle dynamics, we investigated ratios of TEP to particulate organic carbon (POC) and of CSP to POC in suspended and sinking particles collected with marine snow catchers. Samples were collected in a subarctic region near Hokkaido during a spring phytoplankton bloom and in the oligotrophic, subtropical Kuroshio region. At Hokkaido, the mean TEP : POC ratio of sinking particles (0.075 μg Xeq. : μg C) was > 30× lower than in suspended particles (2.3), consistent with a model prediction of selective retention of buoyant TEP‐rich particles in the upper water column. In the Kuroshio region, sinking particles also contained fewer TEP than suspended particles; however, the TEP : POC ratio of sinking particles (1.0) was > 10× higher than at Hokkaido, suggesting that TEP constitute a significant carbon component of sinking particles. These findings indicate that TEP facilitate aggregation of high‐density particles and particle sinking in the Kuroshio region. Distributions of CSP : POC ratios between suspended and sinking particles resembled TEP : POC ratios in both regions, implying a significant contribution of CSP to particle dynamics. We propose that EPS have divergent effects on suspension and sinking of marine particles, which vary with particle composition and biogeochemical conditions.

Combining sulfite and freezing/thawing pretreatment to simultaneously improves methanogenesis, dewaterability, and pathogen inactivation of waste activated sludge: Depicting sulfite migration during ice crystal growth

Harmless treatment of waste activated sludge (WAS) is the primary goal for sludge management while bioresource recovery is raising wide scholarly and industrial interest due to the abundant resource potential in WAS. This study employed sulfite and freezing/thawing to pretreat WAS for its versatility in simultaneously enhancing methane production, improving dewaterability, and inactivating pathogenic microorganisms. The addition of 100 mg S/L of sulfite and subsequent freezing/thawing significantly promoted the release of organics from a low organic-contained WAS (volatile solid/total solid = 0.4), leading to a substantial increase in methane production by 10.99 %. The combined pretreatment significantly reduced the capillary suction time of sludge by 77.24 % and effectively inactivated pathogenic microorganisms to below detectable levels. From a micro level, sulfur aggregation was observed around sludge particles, which can be attributed to the process of ice formation. During this process, sulfite was continuously transferred to the aqueous phase surrounding the particles where were froze even slower. Moreover, the formation of capillary water ice crystals further compromised the protective function of extracellular polymeric substances (EPS) on sludge cells. Economic, and environmental analyses suggest this combined sulfite and freezing/thawing pretreatment has a potential for efficient sludge treatment towards energy recovery and safe disposal with high environmental and economic value.

Aerobic biodegradation of quinoline under denitrifying conditions in membrane-aerated biofilm reactor

Aerobic denitrification is being investigated as a novel biological nitrogen removal process, yet the knowledge on aerobic denitrification is limited to pure culture isolations and its occurrence in bioreactors remains unclear. This study investigated the feasibility and capacity of applying aerobic denitrification in membrane aerated biofilm reactor (MABR) for biological treatment of quinoline-laden wastewater. Stable and efficient removals of quinoline (91.5 ± 5.2%) and nitrate (NO3−) (86.5 ± 9.3%) were obtained under different operational conditions. Enhanced formation and function of extracellular polymeric substances (EPS) were observed at increasing quinoline loadings. MABR biofilm was highly enriched with aerobic quinoline-degrading bacteria, with a predominance of Rhodococcus (26.9 ± 3.7%) and secondary abundance of Pseudomonas (1.7 ± 1.2%) and Comamonas (0.94 ± 0.9%). Metagenomic analysis indicated that Rhodococcus contributed significantly to both aromatic degradation (24.5 ± 21.3%) and NO3− reduction (4.5 ± 3.9%), indicating its key role in aerobic denitrifying quinoline biodegradation. At increasing quinoline loadings, abundances of aerobic quinoline degradation gene oxoO and denitrifying genes of napA, nirS and nirK increased; there was a significant positive correlation of oxoO with nirS and nirK (p < 0.05). Aerobic quinoline degradation was likely initiated by hydroxylation, encoded by oxoO, followed by stepwise oxidations through 5,6-dihydroxy-1H-2-oxoquinoline or 8-hydroxycoumarin pathway. The results advance our understanding of quinoline degradation during biological nitrogen removal, and highlight the potential implementation of aerobic denitrification driven quinoline biodegradation in MABR for simultaneous removal of nitrogen and recalcitrant organic carbon from coking, coal gasification and pharmaceutical wastewaters.

A Review of the Role of Extracellular Polymeric Substances (EPS) in Wastewater Treatment Systems.

A review of the characterization and functions of extracellular polymeric substances (EPS) of microbial aggregates in biological wastewater treatment systems is presented in this paper. EPS represent the complex high-molecular-weight mixture of polymers excreted by microorganisms generated from cell lysis as well as adsorbed inorganic and organic matter from wastewater. EPS exhibit a three-dimensional, gel-like, highly hydrated matrix that facilitates microbial attachment, embedding, and immobilization. EPS play multiple roles in containments removal, and the main components of EPS crucially influence the properties of microbial aggregates, such as adsorption ability, stability, and formation capacity. Moreover, EPS are important to sludge bioflocculation, settleability, and dewatering properties and could be used as carbon and energy sources in wastewater treatment. However, due to the complex structure of EPS, related knowledge is incomplete, and further research is necessary to understand fully the precise roles in biological treatment processes.

Understanding and mitigating the distinctive stresses induced by diverse microplastics on anaerobic hydrogen-producing granular sludge

This work comparatively studied the different stress responses of anaerobic hydrogen-producing granular sludge (HPG) to several typical MPs in wastewater, i.e., polyethylene (PE), polyethylene terephthalate (PET), and polyvinyl chloride (PVC) MPs. A new approach to mitigating the inhibition caused by MPs based on biochar was then proposed. The results displayed that microbe in HPG had diverse tolerances to PE-MPs, PET-MPs and PVC-MPs, with the hydrogen production downgraded to 82.0 ± 3.2 %, 72.3 ± 2.5 % and 66.6 ± 2.3 % (p < 0.05) of control respectively, due to the distinct leachates toxicities and oxidative stress level induced by different MPs. The discrepant mitigation reflected in the hydrogen yields of biochar-based HPGs raised back to 88.7 ± 1.4 %, 85.3 ± 3.8 % and 88.5 ± 3.5 % of control. The MPs induced disintegrated granule morphology, fragile microbial viability and impaired defensive function of extracellular polymeric substances were restored by biochar. The effective mitigation was revealed to be due to the strong adsorption of MPs by biochar, reducing direct contact between microbes and MPs. Biochar addition also enhanced protection for HPG by increasing EPS secretion and weakened the oxidative damage to anaerobes induced by MPs. Biochar manifested the disparate adsorption properties of three MPs. The most superior mitigation in HPG contaminated by PVC-MPs was attributed to the strongest affinity of biochar to PVC-MPs and effective alleviation of PVC leachates toxicity.

Spatiotemporal variation of extracellular polymeric substances (EPS) associated with the microphytobenthos of tidal flats in the Yellow Sea

The physical functions of extracellular polymeric substances (EPS), viz., by-product of microphytobenthos (MPB), in tidal flat system are well documented, but some ecological aspects remain unknown. We investigated MPB biomass (Chl-a), EPS, diatom assemblage, and erodibility in two contrasting tidal flat environments (megatidal vs. macrotidal flat) in the Yellow Sea. Thick biofilms were observed when MPB bloomed, with high Chl-a and increased EPS concentrations. Among diatom genera, Navicula was the most dominant taxa found over the year (mean 41%) in both areas. Compared with non-bloom periods, the erodibility decreased by 54–73% as biofilm thickened during the blooms. It was attributed to the elevated abundance of large-sized (>40 μm) Navicula, which was expected to secrete large amounts of EPS. Overall, we successfully demonstrated spatiotemporal differences of sediment stabilization that significantly related to ecological variations of MPB, and identified the key diatom genus as a “sediment stabilizer” in the typical tidal flats of the Yellow Sea.

Quantitative assessment of extraction methods for bound extracellular polymeric substances (B-EPSs) produced by Microcystis sp. and Scenedesmus sp.

Extracellular polymeric substances (EPSs) play a significant role in the growth and survival of microorganisms. They have been applied in various fields, such as animal feed, pharmaceuticals and cosmetics, due to their physicochemical characteristics (e.g., high contents of polysaccharides and proteins, properties of antivirus, antitumor and antioxidant). However, lack of standard evaluation methods for efficient extraction restricts further investigation on the characteristics or functions of EPSs and their commercial applications. In this study, the Bound-EPS (B-EPS) Extraction Efficiency Evaluation Model (B-E4 Model) was developed to assess various extraction methods for two microalgae (i.e., the prokaryotic Microcystis sp. and the eukaryotic Scenedesmus sp.), including heating, centrifugation, ultrasound, ethylenediaminetetraacetic acid, cation-exchange resin or sodium hydroxide. The evaluation parameter k, was introduced to represent the extraction yields of B-EPSs, which was normalized to the per unit mass of released intracellular organics. This study revealed that heating at 70 °C for 10 min led to the highest extraction efficiency for both Microcystis sp. and Scenedesmus sp., with k values of 12.34 ± 1.48 and 6.02 ± 0.14, respectively. Moreover, model predictions for cell rupture were in close agreement with the results of flow cytometry analysis obtained in this study and the literature. Moreover, to test the applicability of B-E4 Model established in this study, it was utilized to evaluate the extraction efficiencies of various methods applied in a previous study on the microalgae Neocystis mucosa SX, and cation-exchange resin treating for 6 h was found to be the optimal method. The B-E4 model developed in this study was proven to be a powerful tool for optimizing the microalgal B-EPS extraction procedures.

Generation behavior of extracellular polymeric substances and its correlation with extraction efficiency of valuable metals and change of process parameters during bioleaching of spent petroleum catalyst

The vital functions of extracellular polymeric substances (EPS) have been well recognized in bioleaching of sulfide ores. However, no report is available about the role of EPS in bioleaching of spent catalyst. To completely and deeply understand the functions of EPS in bioleaching of spent catalyst, the generation behavior of EPS at various pulp densities during bioleaching was characterized by three-dimensional excitation-emission matrix (3DEEM), and its relevance with bioleaching performance and process parameters were analyzed using mathematical means. The results showed that the EPS contain humus-like substances as main component (>70%) and protein-like substances as minor component (<30%). Both total EPS and humus-like substances mainly keep growing over the whole duration of bioleaching at low pulp density of 5.0% or lower; whereas total EPS and humus-like fraction keep declining at high pulp density of 7.5% or higher. Among the total EPS and its components, humus-like substances only have a positive significant correlation with bioleaching efficiencies of both Co and Mo and affect bioleaching process more greatly due to greater correlation coefficient. Biofilm appears at the spent catalyst surface under 2.5% of pulp density mediated by EPS while no biofilm occurs at 10% of pulp density due to shortage of EPS, accounting for the great difference in bioleaching efficiencies between high and low pulp densities which are 48.3% for Mo and 50.0% for Co at 10% of pulp density as well as 75.9% for Mo and 78.8% for Co at 2.5% of pulp density, respectively.

Green Synthesis of Iron Nanoparticles for Investigation of Biofilm Inhibition Property

AbstractGreen metal nanoparticles (NPs) have emerged as efficient biofilm inhibitors.Citrus macroptera(CM) fruit extract mediated iron (Fe) NPs,i. e., CM‐FeNPs were thus synthesized for studying biofilm inhibition property. The shape (spherical), size (12 nm), and crystallinity (α‐Fe0bcc) of the CM‐FeNPs were confirmed by studying mainly Transmission Electron microscopy (TEM) and X‐ray Diffractometer (X‐RD) tools. The particles inhibit biofilm growth of a bacteriaPseudomonas aeruginosa(P. aeruginosa) by inhibiting the functions of extracellular polymeric substances (EPS) and virulence factors to ∼80 %. Scanning Electron microscopy (SEM) images of the bacteria in presence of the CM‐FeNPs (4600 nM) in combination with azithromycin (AZI) evidence the inhibition of biofilm growth &gt;80 %. Molecular docking studies support experimental findings and result significant negative binding energies (e. g., isoplatydesmine/LasR: −8.25 kcal/mole, isoplatydesmine/MvfR: −7.56 kcal/mole) from bioactive molecules/biofilm proteins interactions. Thus, CM‐FeNPs could be considered as potential biofilm inhibitors, and as an alternative to antibiotic drugs.

Simvastatin decreases the silver resistance of E. faecalis through compromising the entrapping function of extracellular polymeric substances against silver.

Enterococcus faecalis (E. faecalis) is a Gram-positive bacterium closely related to many refractory infections of human and shows the resistant ability against the antibacterial effects of silver. Simvastatin is a semisynthetic compound derived from lovastatin and a hydroxymethyl glutaryl coenzyme A(HMG-COA) reductase inhibitor showing certain inhibitive effects on bacteria. The main purpose of this study was to establish and characterize the Ag+/silver nanoparticles (AgNPs)-resistant E. faecalis, and further evaluate the function of extracellular polymeric substances (EPS) in the silver resistance and the effect of simvastatin on the silver-resistance of E. faecalis. The results showed that the established silver-resistant E. faecalis had strong resistance against both Ag+ and AgNPs and simvastatin could decrease the silver-resistance of both original and Ag+/AgNPs-resistant E. faecalis. The Transmission electron microscopy (TEM), High-angle annular dark-field (HAADF) and mapping images showed that the silver ions or particles aggregated and confined in the EPS on surface areas of the cell membrane when the silver-resistant E. faecalis were incubated with Ag+ or AgNPs. When the simvastatin was added, the silver element was not confined in the EPS and entered the bacteria. These findings may indicate that the silver resistance of E. faecalis was derived from the entrapping function of EPS, but simvastatin could compromise the function of EPS to decrease the silver resistant ability of E. faecalis.

Functional exploration of extracellular polymeric substances (EPS) in the bioleaching of obsolete electric vehicle LiNixCoyMn1-x-yO2 Li-ion batteries

As a fairly new concept, the recovery of valuable metals from urban mining by using bioleaching has become a hotspot. However, the function of extracellular polymeric substances (EPS) in the bioleaching of urban mining gains little attention. The current study used spent EV LIBs to represent urban mining products and systematically explored the function and role of EPS in the attachment of cells to the cathodes, formation of aggregates (cell-EPS-cathode), variation in the electrical and surface properties of the aggregates, concentration of both Fe2+ and Fe3+ surrounding the aggregates, electron transfer inside the aggregates and metals released from the aggregates. The results indicated that a strong adhesion of cells to the cathodes occurs mediated by EPS via both hydrophobic force as a main role and electrostatic force as a minor role. Second, the EPS not only adsorb Fe3+ but also more strongly adsorb Fe2+ to concentrate the Fe2+/Fe3+ cycle inside the aggregates, witnessing stronger reductive attack on the high valence state of metals as a contact reductive mechanism. Third, the retention or addition of EPS elevated the electronic potential and reduced the electronic resistance to lift the corrosion electric current, thereby boosting the electron transfer and metal dissolution.

Insight into the roles of tightly and loosely bound extracellular polymeric substances on a granular sludge in ammonium nitrogen removal

To explicitly understand the function of extracellular polymeric substances in the treatment of ammonium-nitrogen-rich wastewater using aerobic granular sludge, the three forms of nitrogen (ammonium, nitrite and nitrate nitrogen) contained in tightly and loosely bound extracellular polymeric substances were analyzed. The three forms of nitrogen were monitored in the tightly and loosely bound extracellular polymeric substances in aerobic granular sludge after adsorption. The ammonium nitrogen contained in the extracellular polymeric substances was distributed in both the tightly and loosely bound forms and decreased gradually as the aeration time increased. Ammonium nitrogen remained in the tightly bound extracellular polymeric substances even after aeration was complete. The nitrite and nitrate nitrogen species in the extracellular polymeric substances were mainly present in the loosely bound extracellular polymeric substances. The sources of the three nitrogen forms detected in the extracellular polymeric substances differed relative to the different nitrogen forms.

Characterization, structure, and function of extracellular polymeric substances (EPS) of microbial biofilm in biological wastewater treatment systems: a review

AbstractA review concerning the definition, extraction, characterization, production, and functions of extracellular polymeric substances (EPS) of microbial aggregates in biological wastewater treatment reactors is given in this paper. EPS are a complex high-molecular-weight mixture of polymers excreted by microorganisms, produced from cell lysis and adsorbed organic matter from wastewater. The EPS fill and form the space between the biofilm constituents, e.g. prokaryotic and eukaryotic microorganisms which inhabit the aggregates. It seems that the EPS matrix may serve as a multipurpose functional element of microbial communities, including adhesion, structure, protection, recognition, and physiology. Due to the metabolic activity of the cells, gradients develop and create different habitats within small distances, allowing a wide variety of organisms to settle and grow in the aggregate. As many of these organisms produce their specific EPS, it is not surprising that an extremely wide variety of microbial...

Identification of the function of extracellular polymeric substances (EPS) in denitrifying phosphorus removal sludge in the presence of copper ion

Industrial wastewater containing heavy metals that enters municipal wastewater treatment plants inevitably has a toxic impact on biological treatment processes. In this study, the impact of Cu(II) (0, 1.5, 2, 2.5, 3 mg/L) on the performance of denitrifying phosphorus removal (DPR) and microbial community structures was investigated. Particularly, the dynamic change in the amount and composition of extracellular polymeric substances (EPS), and the role of EPS in P removal, were assessed using three-dimensional excitation–emission matrix fluorescence spectroscopy combined with parallel factor (PARAFAC) analysis. The results showed that, after long-term adjustment, the P removal efficiency was maintained at 95 ± 2.7% at Cu(II) addition up to 2.5 mg/L, but deteriorated when the Cu(II) addition was 3 mg/L. The EPS content, including proteins and humic substances, increased with increasing Cu(II) additions at concentrations ≤2.5 mg/L. This property of EPS was beneficial for protecting phosphate-accumulating organisms (PAOs) against heavy metals, as both proteins and humic substances are strong ligands for Cu(II). Therefore, the PAOs abundance was still relatively high (67 ± 3%) when Cu(II) accumulation in sludge was up to 10 mg/g SS. PARAFAC confirmed that aromatic proteins could be transformed into soluble microbial byproduct-like material when microorganisms were subjected to Cu(II) stress, owing to their strong metal ion complexing capacity. The increase in the percentage of humic-like substances enhanced the detoxification function of the sludge EPS. EPS accounted for approximately 26–47% of P removed by adsorption when Cu(II) additions were between 0 and 2.5 mg/L. The EPS function, including binding toxic heavy metals and P storage, enhanced the operating stability of DPR systems. This study provides us with a better understanding of (1) the tolerance of DPR sludge to copper toxicity and (2) the function of sludge EPS in the presence of heavy metals in biological P removal systems.

The effect of extracellular polymeric substances on the adhesion of bacteria to clay minerals and goethite

The functions of extracellular polymeric substances (EPS) during the adhesion of Bacillus subtilis to kaolinite, montmorillonite, and goethite were examined by a direct comparison of the adhesion behaviors of native and EPS-free cells via cation exchange resin (CER) treatment using batch experiments, attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy, and potentiometric titration. The EPS removal had no apparent influence on bacterial adhesion when the wet bacteria/mineral mass ratio was low (<0.4 for the clay mineral systems and <1.8 for the goethite system). With higher mass ratios, the absence of EPS reduced adhesion to clay minerals but enhanced adhesion to goethite. The ATR-FTIR spectra suggested that protein conformational changes were involved in the adhesion of bacteria to clay minerals, whereas additional chemical interactions such as POFe bonds were important for adhesion to goethite. In addition to electrostatic forces (repulsion for clays and attraction for goethite), absence of chemical interactions may also cause the relatively much weaker bacterial adhesion to clay minerals than to goethite. The absence of EPS did not change the interaction mode of the adhesion to clay minerals but enhanced the chemical interactions via carboxyl groups for bacteria–goethite adhesion. The potentiometric titration results coupled with the ATR-FTIR spectra showed a significant increase in site concentrations of the CER-treated bacteria as compared to the native cells. Changes in surface site concentrations and chemical interactions that were accompanied by the EPS removal may reasonably explain the influences of EPS on bacterial adhesion to different minerals.

Digging into the extracellular matrix of a complex microbial community using a combined metagenomic and metaproteomic approach

Knowledge about identity and function of extracellular polymeric substances (EPS) in complex microbial communities is sparse, although these components have a large influence on the function of the microbial communities. We investigated the presence of selected genes potentially involved in EPS production in a 145 Mbp metagenome prepared by Illumina sequencing from a full-scale wastewater treatment plant carrying out enhanced biological phosphorus removal (EBPR). A range of genes involved in alginate production was identified and assigned mainly to bacteria from the phylum Bacteroidetes. Furthermore, several proteins in the EPS matrix were extracted, purified and identified by mass spectrometry. By using the metagenome as a reference for the metaproteomic analysis, more proteins were identified compared to using only publicly available databases. This illustrates the low degree of similarity between the bacteria in the EBPR community and the sequenced bacteria in the public databases. Hence, the combination of metagenomics and metaproteomics presented here is needed to investigate the identity of the proteins in the EPS matrix.

Lack of Influence of Extracellular Polymeric Substances (EPS) Level on Hydroxyl Radical Mediated Disinfection of Escherichia coli

Photolysis of nitrate, a prevalent constituent in agriculturally impacted waters, may influence pathogen attenuation in such systems through production of hydroxyl radical ((•)OH). This study focuses on the efficacy of (•)OH generated during nitrate photolysis in promoting E. coli die-off as a function of extracellular polymeric substances (EPS) coverage. EPS levels of four E. coli isolates were systematically altered through a sonication extraction method and photochemical batch experiments with a solar simulator examined isolate viability loss as a function of time in nitrate solutions. E. coli viability loss over time exhibited two regimes: an initial induction time, t(s), with little decay was followed by rapid exponential decay characterized by a first-order disinfection rate constant, k. Increasing steady-state (•)OH concentrations enhanced E. coli viability loss, increasing values of k and decreasing t(s) values, both of which were quantified with a multitarget bacterial disinfection model. Notably, at a given steady-state (•)OH concentration, values of t(s) and k were independent of EPS levels, nor did they vary among the different E. coli strains considered. Results herein show that while (•)OH generated via nitrate photolysis enhances rates of disinfection in surface water, the mechanism by which (•)OH kills E. coli is relatively insensitive to common bacterial variables.

Multiple Fluorescence Labeling and Two Dimensional FTIR–13C NMR Heterospectral Correlation Spectroscopy to Characterize Extracellular Polymeric Substances in Biofilms Produced during Composting

Knowledge on the structure and function of extracellular polymeric substances (EPS) in biofilms is essential for understanding biodegradation processes. Herein, a novel method based on multiple fluorescence labeling and two-dimensional (2D) FTIR-(13)C NMR heterospectral correlation spectroscopy was developed to gain insight on the composition, architecture, and function of EPS in biofilms during composting. Compared to other environmental biofilms, biofilms in the thermophilic (>55 °C) and cooling (mature) stage of composting have distinct characteristics. The results of multiple fluorescence labeling demonstrated that biofilms were distributed in clusters during the thermophilic stage (day 14), and dead cells were detected. In the mature stage (day 26), the biofilm formed a continuous layer with a thickness of approximately 20-100 μm around the compost, and recolonization of cells at the surface of the compost was easily observed. Through 2D FTIR-(13)C NMR correlation heterospectral spectroscopy, the following trend in the ease of the degradation of organic compounds was observed: heteropolysaccharides > cellulose > amide I in proteins. And proteins and cellulose showed significantly more degradation than heteropolysaccharides. In summary, the combination of multiple fluorescence labeling and 2D correlation spectroscopy is a promising approach for the characterization of EPS in biofilms.

Nutrient removal, microbial community and sludge settlement in anaerobic/aerobic sequencing batch reactors without enhanced biological phosphorus removal

Nutrient removal, microbial community and sludge settlement were examined in two 3-litre laboratory-scale anaerobic/aerobic sequencing batch reactors (SBRs). One SBR was operated at 10 degrees C and the other SBR at 20 degrees C. Different from conventional enhanced biological phosphorus removal, most of the soluble sodium acetate was removed in the aerobic phase and no organic carbon uptake or biological phosphorus release occurred in the anaerobic phase. In this type of anaerobic/aerobic SBR, the phosphorus removal and sludge settlement seemed to be unstable, and the dominant microorganism was Zoogloea sp. Although no excess biological phosphorus removal occurred, extracellular phosphorus precipitation contributed a significant proportion to total phosphorus removed. Sludge volume index decreased with increasing phosphorus contents in the biomass under all conditions. The functions of extracellular polymeric substances in sludge settlement and phosphorus removal depended on the environmental conditions applied.

Extracellular polymeric substances mediate bioleaching/biocorrosion via interfacial processes involving iron(III) ions and acidophilic bacteria

Extracellular polymeric substances seem to play a pivotal role in biocorrosion of metals and bioleaching, biocorrosion of metal sulfides for the winning of precious metals as well as acid rock drainage. For better control of both processes, the structure and function of extracellular polymeric substances of corrosion-causing or leaching bacteria are of crucial importance. Our research focused on the extremophilic bacteria Acidithiobacillus ferrooxidans and Leptospirillum ferrooxidans, because of the “simplicity” and knowledge about the interactions of these bacteria with their substrate/substratum and their environment. For this purpose, the composition of the corresponding extracellular polymeric substances and their functions were analyzed. The extracellular polymeric substances of both species consist mainly of neutral sugars and lipids. The functions of the exopolymers seem to be: (i) to mediate attachment to a (metal) sulfide surface, and (ii) to concentrate iron(III) ions by complexation through uronic acids or other residues at the mineral surface, thus, allowing an oxidative attack on the sulfide. Consequently, dissolution of the metal sulfide is enhanced, which may result in an acceleration of 20- to 100-fold of the bioleaching process over chemical leaching. Experiments were performed to elucidate the importance of the iron(III) ions complexed by extracellular polymeric substances for strain-specific differences in oxidative activity for pyrite. Strains of A. ferrooxidans with a high amount of iron(III) ions in their extracellular polymeric substances possess greater oxidation activity than those with fewer iron(III) ions. These data provide insight into the function of and consequently the advantages that extracellular polymeric substances provide to bacteria. The role of extracellular polymeric substances for attachment under the conditions of a space station and resulting effects like biofouling, biocorrosion, malodorous gases, etc. will be discussed.