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Schmitz, A. M.

Publications and source records attributed to Schmitz, A. M..

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Gluconobacter oxydans Knockout Collection Finds Improved Rare Earth Element Extraction

Rare earth elements (REE) are critical components of our technological society and essential for renewable energy technologies. Traditional thermochemical processes to extract REE from mineral ores or recycled materials are costly and environmentally harmful1, and thus more sustainable extraction methods require exploration. Bioleaching offers a promising alternative to conventional REE extraction2-4, and is already used to extract 5% of the worlds gold, and {approx} 15% of the worlds copper supply5,6. However, the performance of REE bioleaching lags far behind thermochemical processes2,7-9. Despite this, to the best of our knowledge no genetic engineering strategies have yet been used to enhance REE bioleaching, and little is known of the genetics that confer this capability. Here we build a whole genome knockout collection for Gluconobacter oxydans B58, one of the most promising organisms for REE bioleaching10, and use it to comprehensively characterize the genomics of REE bioleaching. In total, we find 304 genes that notably alter production of G. oxydans acidic biolixiviant, including 165 that hold up under statistical comparison with wild-type. The two most impactful groups of genes involved in REE bioleaching have opposing influences on acid production and REE bioleaching. Disruption of genes underlying synthesis of the cofactor pyrroloquinoline quinone (PQQ) and the PQQ-dependent membrane-bound glucose dehydrogenase all but eliminates bioleaching. In contrast, disruption of the phosphate-specific transport system accelerates acid production and enhances bioleaching. We identified 6 disruption mutants, that increase bioleaching by at least 11%. Most significantly, disruption of pstC, encoding part of the phosphate-specific transporter, pstSCAB, enhances bioleaching by 18%. Taken together, these results give a comprehensive roadmap for engineering multiple sites in the genome of G. oxydans to further increase its bioleaching efficiency.

genomics

Constraints on the Efficiency of Electromicrobial Production

Electromicrobial production technologies (EMP) aim to combine renewable electricity and microbial metabolism. We have constructed molecular to reactor scale models of EMP systems using H2-oxidation and extracellular electron transfer (EET). We predict the electrical-to-biofuel conversion efficiency could rise to ≥ 52% with in vivo CO2-fixation. H2 and EET-mediated EMP both need reactors with high surface areas. H2-diffusion at ambient pressure requires areas 20 to 2,000 times that of the solar photovoltaic (PV) supplying the system. Agitation can reduce this to less than the PV area, and the power needed becomes negligible when storing ≥ 1.1 megawatts. EET-mediated systems can be built that are ≤ 10 times the PV area and have minimal resistive energy losses if a conductive extracellular matrix (ECM) with a resistivity and height seen in natural conductive biofilms is used. The system area can be reduced to less than the PV area if the ECM conductivity and height are increased to those of conductive artificial polymers. Schemes that use electrochemical CO2-fixation could achieve electrical-to-fuel efficiencies of almost 50% with no complications of O2-sensitivity.Competing Interest StatementThe authors have declared no competing interest.View Full Text

synthetic biology