This study presents the effect of aqueous Pb(II) and nutrient concentrations on the Pb(II)-removal, biomass viability, active species identities, and population distribution of an industrial Pb(II) resistant microbial consortium. The studied consortium has previously shown to be highly effective at precipitating Pb(II) from solution. At all conditions tested (80 and 500 ppm Pb(II), and varying nutrients conditions) it was found that circa 50% of Pb(II) was removed within the first 3 h, with the absence of any visual changes, followed by a slower rate of Pb(II) removal accompanied by the formation of a dark precipitate. The Pb(II) removal was found to be independent of microbial growth, while growth was observed dependent on the concentration of Pb(II), nutrients, and nitrates in the system. SEM analysis indicated viable bacilli embedded in precipitate. These findings indicate that precipitation occurs on the surface of the biomass as opposed to an internal excretion mechanism. BLAST (Basic Local Alignment Search Tool) results indicated Klebsiella pneumoniae as the active species responsible for Pb(II) bioprecipitation for both the 80 and 500 ppm isolated colonies, while a diverse population distribution of organisms was observed for the streak plate analyses. A quicker microbial generation rate was observed than what was expected for Klebsiella pneumoniae, indicating that the overall consortial population contributed to the growth rates observed. This study provided insights into the factors affecting Pb(II) bio-removal and bioprecipitation by the investigated industrially obtained consortium, thereby providing invaluable knowledge required for industrial application.
The study aimed to quantify the lead(II) bio-precipitation effectiveness, and the produced precipitate identities, of industrial consortia under aerobic and anaerobic batch conditions. The consortia were obtained from an automotive battery recycling plant and an operational lead mine in South Africa. The experiments were performed in the complex growth medium Luria-Bertani broth containing 80 ppm lead(II). The precipitation and corresponding removal of lead(II) were successfully achieved for both aerobic (yellow/brown precipitate) and anaerobic (dark grey/black precipitate) conditions. The removal of lead(II) followed similar trends for both aeration conditions, with the majority of lead(II) removed within the initial 48 h, followed by a marked decline in removal rate for the remainder of the experiments. The final lead(II) removal ranged between 78.11 ± 4.02% and 88.76 ± 3.98% recorded after 144 h. The precipitates were analysed using XPS which indicated the presence of exclusively PbO and elemental lead in the aerobic precipitates, while PbO, PbS, and elemental lead were present in the anaerobic precipitates. The results indicated an oxidationreduction mechanism with lead(II) as an electron acceptor in both aerobic and anaerobic conditions, while a sulphide-liberation catabolism of sulphur-containing amino acids was evident exclusively in the anaerobic runs. This study provides the first report of bacterial bio-reduction in aqueous lead(II) to elemental lead through a dissimilatory lead reduction mechanism. It further provides support for the application of bioremediation for the removal and recovery of lead from industrial waste streams through the application of bacterial biocatalysts for direct elemental lead recovery.
The main objective of this study was to achieve the continuous biorecovery and bioreduction of Pb(II) using an industrially obtained consortia as a biocatalyst. An upflow anaerobic sludge blanket reactor was used in the treatment process. The bioremediation technique that was applied made use of a yeast extract as the microbial substrate and Pb(NO3)2 as the source of Pb(II). The UASB reactor exhibited removal efficiencies of between 90 and 100% for the inlet Pb concentrations from 80 to 2000 ppm and a maximum removal rate of 1948.4 mg/(L·d) was measured. XRD and XPS analyses of the precipitate revealed the presence of Pb0, PbO, PbS and PbSO4. Supporting experimental work carried out included growth measurements, pH, oxidation–reduction potentials and nitrate levels.
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