Riboflavin synthesis from gaseous nitrogen and carbon dioxide by a hybrid inorganic-biological system.

Microbes can provide a more sustainable and energy-efficient method of food and nutrient production compared to plant and animal sources, but energy-intensive carbon (e.g., sugars) and nitrogen (e.g., ammonia) inputs are required. Gas-fixing microorganisms that can grow on H2 from renewable water splitting and gaseous CO2 and N2 offer a renewable path to overcoming these limitations but confront challenges owing to the scarcity of genetic engineering in such organisms. Here, we demonstrate that the hydrogen-oxidizing carbon- and nitrogen-fixing microorganism Xanthobacter autotrophicus grown on a CO2/N2/H2 gas mixture can overproduce the vitamin riboflavin (vitamin B2). We identify plasmids and promoters for use in this bacterium and employ a constitutive promoter to overexpress riboflavin pathway enzymes. Riboflavin production is quantified at 15 times that of the wild-type organism. We demonstrate that riboflavin overproduction is maintained when the bacterium is grown under hybrid inorganic-biological conditions, in which H2 from water splitting, along with CO2 and N2, is fed to the bacterium, establishing the viability of the approach to sustainably produce food and nutrients.

Efficient Electrocatalytic Hydrogenation with a Palladium Membrane Reactor.

We report here the benefits of using a palladium membrane reactor to drive hydrogenation chemistry with electricity while bypassing the formation of gaseous H2. This technique uses a palladium membrane to physically separate the electrochemical and hydrogenation chemistry. As a result, hydrogenation can be performed electrochemically with protons but in any organic solvent. In this article, we outline a series of experiments showing how hydrogenation in the palladium membrane reactor proceeds at faster reaction rates and with much higher voltage efficiency than hydrogenation at an electrode. Moreover, the organic reaction chemistry in the membrane reactor can be performed in organic solvents and without contamination by electrolytes. The physical separation of the hydrogenation compartment from the electrolysis compartment therefore broadens the scope of electrolytically-driven reactions that are available, and simplifies reagent handling and purification.

Facets and vertices regulate hydrogen uptake and release in palladium nanocrystals.

Crystal facets, vertices and edges govern the energy landscape of metal surfaces and thus the chemical interactions on the surface1,2. The facile absorption and desorption of hydrogen at a palladium surface provides a useful platform for defining how metal-solute interactions impact properties relevant to energy storage, catalysis and sensing3-5. Recent advances in in operando and in situ techniques have enabled the phase transitions of single palladium nanocrystals to be temporally and spatially tracked during hydrogen absorption6-11. We demonstrate herein that in situ X-ray diffraction can be used to track both hydrogen absorption and desorption in palladium nanocrystals. This ensemble measurement enabled us to delineate distinctive absorption and desorption mechanisms for nanocrystals containing exclusively (111) or (100) facets. We show that the rate of hydrogen absorption is higher for those nanocrystals containing a higher number of vertices, consistent with hydrogen absorption occurring quickly after ß-phase nucleation at lattice-strained vertices9,10. Tracking hydrogen desorption revealed initial desorption rates to be nearly tenfold faster for samples with (100) facets, presumably due to the faster recombination of surface hydrogen atoms. These results inspired us to make nanocrystals with a high number of vertices and (100) facets, which were found to accommodate fast hydrogen uptake and release.