Abstract:Extreme acidophiles play central roles in the geochemical cycling of diverse elements in low pH environments. This has been harnessed in biotechnologies such as biomining, where microorganisms facilitate the recovery of economically important metals such as gold. By generating both extreme acidity and a chemical oxidant (ferric iron) many species of prokaryotes that thrive in low pH environments not only catalyze mineral dissolution but also trigger both community and individual level adaptive changes. These c… Show more
“…The strategy used aims to bypass the fragmentation of most drafts (steps 1–3), the poor annotation of MGE-related contigs (steps 4–6), and the difficulties of fully reconstructing the elements present in the dataset (step 7). For this purpose, we used information available on several integrated MGEs (iMGEs) that have been identified and described to a different extent in A. ferrooxidans 16 , 20 , 22 , 23 , 27 , 33 . Moreover, candidate MGEs derived from applying existing MGE prediction resources to two available complete A. ferrooxidans genome sequences (NC_011761, NC_011206) were used 33 , 40 .…”
The recent revision of the Acidithiobacillia class using genomic taxonomy methods has shown that, in addition to the existence of previously unrecognized genera and species, some species of the class harbor levels of divergence that are congruent with ongoing differentiation processes. In this study, we have performed a subspecies-level analysis of sequenced strains of Acidithiobacillus ferrooxidans to prove the existence of distinct sublineages and identify the discriminant genomic/genetic characteristics linked to these sublineages, and to shed light on the processes driving such differentiation. Differences in the genomic relatedness metrics, levels of synteny, gene content, and both integrated and episomal mobile genetic elements (MGE) repertoires support the existence of two subspecies-level taxa within A. ferrooxidans. While sublineage 2A harbors a small plasmid related to pTF5, this episomal MGE is absent in sublineage 2B strains. Likewise, clear differences in the occurrence, coverage and conservation of integrated MGEs are apparent between sublineages. Differential MGE-associated gene cargo pertained to the functional categories of energy metabolism, ion transport, cell surface modification, and defense mechanisms. Inferred functional differences have the potential to impact long-term adaptive processes and may underpin the basis of the subspecies-level differentiation uncovered within A. ferrooxidans. Genome resequencing of iron- and sulfur-adapted cultures of a selected 2A sublineage strain (CCM 4253) showed that both episomal and large integrated MGEs are conserved over twenty generations in either growth condition. In turn, active insertion sequences profoundly impact short-term adaptive processes. The ISAfe1 element was found to be highly active in sublineage 2A strain CCM 4253. Phenotypic mutations caused by the transposition of ISAfe1 into the pstC2 encoding phosphate-transport system permease protein were detected in sulfur-adapted cultures and shown to impair growth on ferrous iron upon the switch of electron donor. The phenotypic manifestation of the △pstC2 mutation, such as a loss of the ability to oxidize ferrous iron, is likely related to the inability of the mutant to secure the phosphorous availability for electron transport-linked phosphorylation coupled to iron oxidation. Depletion of the transpositional △pstC2 mutation occurred concomitantly with a shortening of the iron-oxidation lag phase at later transfers on a ferrous iron-containing medium. Therefore, the pstII operon appears to play an essential role in A. ferrooxidans when cells oxidize ferrous iron. Results highlight the influence of insertion sequences and both integrated and episomal mobile genetic elements in the short- and long-term adaptive processes of A. ferrooxidans strains under changing growth conditions.
“…The strategy used aims to bypass the fragmentation of most drafts (steps 1–3), the poor annotation of MGE-related contigs (steps 4–6), and the difficulties of fully reconstructing the elements present in the dataset (step 7). For this purpose, we used information available on several integrated MGEs (iMGEs) that have been identified and described to a different extent in A. ferrooxidans 16 , 20 , 22 , 23 , 27 , 33 . Moreover, candidate MGEs derived from applying existing MGE prediction resources to two available complete A. ferrooxidans genome sequences (NC_011761, NC_011206) were used 33 , 40 .…”
The recent revision of the Acidithiobacillia class using genomic taxonomy methods has shown that, in addition to the existence of previously unrecognized genera and species, some species of the class harbor levels of divergence that are congruent with ongoing differentiation processes. In this study, we have performed a subspecies-level analysis of sequenced strains of Acidithiobacillus ferrooxidans to prove the existence of distinct sublineages and identify the discriminant genomic/genetic characteristics linked to these sublineages, and to shed light on the processes driving such differentiation. Differences in the genomic relatedness metrics, levels of synteny, gene content, and both integrated and episomal mobile genetic elements (MGE) repertoires support the existence of two subspecies-level taxa within A. ferrooxidans. While sublineage 2A harbors a small plasmid related to pTF5, this episomal MGE is absent in sublineage 2B strains. Likewise, clear differences in the occurrence, coverage and conservation of integrated MGEs are apparent between sublineages. Differential MGE-associated gene cargo pertained to the functional categories of energy metabolism, ion transport, cell surface modification, and defense mechanisms. Inferred functional differences have the potential to impact long-term adaptive processes and may underpin the basis of the subspecies-level differentiation uncovered within A. ferrooxidans. Genome resequencing of iron- and sulfur-adapted cultures of a selected 2A sublineage strain (CCM 4253) showed that both episomal and large integrated MGEs are conserved over twenty generations in either growth condition. In turn, active insertion sequences profoundly impact short-term adaptive processes. The ISAfe1 element was found to be highly active in sublineage 2A strain CCM 4253. Phenotypic mutations caused by the transposition of ISAfe1 into the pstC2 encoding phosphate-transport system permease protein were detected in sulfur-adapted cultures and shown to impair growth on ferrous iron upon the switch of electron donor. The phenotypic manifestation of the △pstC2 mutation, such as a loss of the ability to oxidize ferrous iron, is likely related to the inability of the mutant to secure the phosphorous availability for electron transport-linked phosphorylation coupled to iron oxidation. Depletion of the transpositional △pstC2 mutation occurred concomitantly with a shortening of the iron-oxidation lag phase at later transfers on a ferrous iron-containing medium. Therefore, the pstII operon appears to play an essential role in A. ferrooxidans when cells oxidize ferrous iron. Results highlight the influence of insertion sequences and both integrated and episomal mobile genetic elements in the short- and long-term adaptive processes of A. ferrooxidans strains under changing growth conditions.
“…They are major participants in key metabolic pathways (carbon fixation, nitrogen metabolism, ferrous iron oxidation and sulfur metabolism). High-resolution targeted metagenomics technology has been used to analyze the changes in the community structure during adaptation to extreme acidity and high concentrations of gold concentrate pulp for a long time [48]. The genomes of the dominant strains in this community (A. ferrooxidans etc.)…”
Bio-mining microorganisms are a key factor affecting the metal recovery rate of bio-leaching, which inevitably produces an extremely acidic environment. As a powerful tool for exploring the adaptive mechanisms of microorganisms in extreme environments, omics technologies can greatly aid our understanding of bio-mining microorganisms and their communities on the gene, mRNA, and protein levels. These omics technologies have their own advantages in exploring microbial diversity, adaptive evolution, changes in metabolic characteristics, and resistance mechanisms of single strains or their communities to extreme environments. These technologies can also be used to discover potential new genes, enzymes, metabolites, metabolic pathways, and species. In addition, integrated multi-omics analysis can link information at different biomolecular levels, thereby obtaining more accurate and complete global adaptation mechanisms of bio-mining microorganisms. This review introduces the current status and future trends in the application of omics technologies in the study of bio-mining microorganisms and their communities in extreme environments.
“…Wet treatment can reduce crushing costs and avoid secondary dust pollution, but the operation is complicated and inefficient [7,8]. The microbial treatment cycle is long and easily affected by the environment [9]. The production temperature of fire treatment is as high as 1000 • C, the production investment is significant, and the energy consumption is excessive.…”
The recovery of copper from circuit boards is currently a hot topic. However, recycling copper from circuit boards economically and environmentally is still a considerable challenge. In this study, a simple hydrothermal method was used to synthesize MoS2 with nano-flower-like morphology using sodium molybdate dihydrate and thiourea as molybdenum and sulfur sources. The metal copper in the chip was successfully dissolved under the action of free radicals produced by ultrasound. The results show that under the catalytic action of hydrothermal synthesis MoS2, the concentration of Cu2+ dissolved by ultrasonic treatment for 10 h is 39.46 mg/L. In contrast, the concentration of Cu2+ dissolved by commercial MoS2 is only 2.20 mg/L under the same condition. The MoS2 is polarized by external mechanical forces and reacts with water to produce H+ and free electrons e−, which can combine with O2 and OH− to produce ·OH and ·O2− free radicals. Elemental Cu is converted to Cu2+ by the attack of these two free radicals.
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