Project description:We developed a laboratory-scale model to improve our understanding and capacity to assess the biological risks of genetically engineered bacteria and their genetic elements in the natural environment. Our hypothetical scenario concerns an industrial bioreactor failure resulting in the introduction of genetically engineered bacteria to a downstream municipal wastewater treatment plant (MWWTP). As the first step towards developing a model for this scenario, we sampled microbial communities from the aeration basin of a MWWTP at three seasonal time points. Having established a baseline for community composition, we investigated how the community changed when propagated in the laboratory, including cell culture media conditions that could provide selective pressure in future studies. Specifically, using PhyloChip 16S rRNA gene-targeting microarrays, we compared the compositions of sampled communities to those of inoculates propagated in the laboratory in simulated wastewater conditionally amended with various carbon sources (glucose, chloroacetate, D-threonine) or the ionic liquid 1-ethyl-3-methylimidazolium chloride ([C2mim]Cl). Proteobacteria, Bacteroidetes, and Actinobacteria were predominant in aeration basin and laboratory-cultured populations. Laboratory-cultured populations were enriched in Gammaproteobacteria. Enterobacteriaceae and Aeromonadaceae were enriched by glucose, Pseudomonadaceae by chloroacetate and D-threonine, and Burkholderiaceae by high (50 mM) concentrations of chloroacetate. Microbial populations cultured with chloroacetate and D-threonine were more similar to sampled populations than thoes cultured with glucose or [C2mim]Cl. Although observed relative richness in operational taxonomic units was lower for laboratory cultures than for sampled populations, both flask and reactor systems cultured phylogenetically diverse communities. These results importantly provide a foundation for laboratory models of industrial bioreactor failure scenarios.

Project description:We developed a laboratory-scale model to improve our understanding and capacity to assess the biological risks of genetically engineered bacteria and their genetic elements in the natural environment. Our hypothetical scenario concerns an industrial bioreactor failure resulting in the introduction of genetically engineered bacteria to a downstream municipal wastewater treatment plant (MWWTP). As the first step towards developing a model for this scenario, we sampled microbial communities from the aeration basin of a MWWTP at three seasonal time points. Having established a baseline for community composition, we investigated how the community changed when propagated in the laboratory, including cell culture media conditions that could provide selective pressure in future studies. Specifically, using PhyloChip 16S rRNA gene-targeting microarrays, we compared the compositions of sampled communities to those of inoculates propagated in the laboratory in simulated wastewater conditionally amended with various carbon sources (glucose, chloroacetate, D-threonine) or the ionic liquid 1-ethyl-3-methylimidazolium chloride ([C2mim]Cl). Proteobacteria, Bacteroidetes, and Actinobacteria were predominant in aeration basin and laboratory-cultured populations. Laboratory-cultured populations were enriched in Gammaproteobacteria. Enterobacteriaceae and Aeromonadaceae were enriched by glucose, Pseudomonadaceae by chloroacetate and D-threonine, and Burkholderiaceae by high (50 mM) concentrations of chloroacetate. Microbial populations cultured with chloroacetate and D-threonine were more similar to sampled populations than thoes cultured with glucose or [C2mim]Cl. Although observed relative richness in operational taxonomic units was lower for laboratory cultures than for sampled populations, both flask and reactor systems cultured phylogenetically diverse communities. These results importantly provide a foundation for laboratory models of industrial bioreactor failure scenarios. 46 samples, flask and reactor experiments were conducted in triplicate with two exceptions: [C2mim]Cl_flask and No-Carbon_flask treatments had only one sample (no replicates).

Project description:This work reports the fast and effective bio-fabrication of novel platinum-palladium bimetallic nanoparticles (Pt-Pd BNPs) along with their counterparts Pt and Pd monometallic NPs (MNPs) through aqueous Annona muricata leaf extract. The bio-fabrication of the NPs was achieved within 2 h at 100 °C and pH 7 which was established by the occurrence of dark brown color for Pt MNPs and black color for Pd MNPs and Pt-Pd BNPs. NPs were evaluated for their catalytic activity in the reduction of methyl orange (MO), rhodamine-B (rh-B), and methylene blue (MB) textile dyes in presence of sodium borohydride as a reducing agent. Pt-Pd (1:3) BNPs showed higher MO dye degradation (96.84 ± 2.05% in 50 min) followed by Pd MNPs (97.07 ± 1.46% in 60 min), Pt-Pd (3:1) BNPs (97.34 ± 1.17% in 70 min) and Pt-Pd (1:1) BNPs (98.12 ± 1.04% in 80 min). Pd MNPs showed significant catalytic activity in the reduction of rh-B dye by 97.27 ± 1.14% in 12 min followed by Pt-Pd (3:1) BNPs (96.76 ± 2.17% in 18 min), Pt-Pd (1:3) BNPs (96.53 ± 1.97% in 33 min) and Pt-Pd (1:1) BNPs (97.11 ± 2.09% in 39 min). Pt-Pd (1:3) BNPs also showed higher MB dye degradation (96.95 ± 1.57% in 40 min) followed by Pd MNPs (96.22 ± 2.36% in 55 min), Pt-Pd (3:1) BNPs (97.29 ± 1.22% in 75 min) and Pt-Pd (1:1) BNPs (96.45 ± 2.19% in 105 min). However, Pt MNPs showed no catalytic activity. Standard disc diffusion method was used to evaluate the NPs toxicity towards Escherichia coli and Staphylococcus aureus, which showed no inhibitory zones. NPs showed less toxicity compared to potassium dichromate (control) against Artemia nauplii. Among the NPs studied, Pt-Pd (1:1) BNPs showed less toxicity with 100% mortality only at 100 µg/mL concentration followed by Pt MNPs (≥ 80 µg/mL), Pt-Pd (1:3) BNPs (≥ 60 µg/mL), Pt-Pd (3:1) BNPs (≥ 60 µg/mL) and Pd MNPs (≥ 40 µg/mL) after 72 h exposure. These evaluations support the application of bio-fabricated Pt-Pd BNPs as nano-catalysts in textile dyes degradation.Supplementary informationThe online version contains supplementary material available at 10.1007/s13205-021-02935-0.

Dataset Information

Catalytic Palladium-Based and Iron-Based Membrane Reactors: Novel Strategies of Synthesis.

Publications

Catalytic Palladium-Based and Iron-Based Membrane Reactors: Novel Strategies of Synthesis.

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