Methods for catalyzing CH insertion reactions using heme enzymes are described. The present disclosure provides a method for producing a CH insertion product comprising providing an substrate having an sp.sup.3-hybridized CH bond, a carbene precursor such as a diazo reagent, and a heme enzyme, and admixing the components in a reaction for a time sufficient to produce the CH insertion product. Heme enzyme variants useful for carrying out in vivo and in vitro CH insertion reactions, as well as expression vectors and host cells expressing the heme enzymes, are also described.

A method for manufacturing a modified porous organic framework includes steps as follows. A mixed solution is provided. The mixed solution includes a porous organic framework, a plurality of group donors and a solvent. The porous organic framework includes a plurality of first ligands. Each of the first ligands includes at least one tetrazine group. Each of the group donors includes a reactive group and a modifying group covalently connected with each other. The reactive groups are alkenyl groups, alkynyl groups, aldehyde groups, ketone groups or a combination thereof. A modifying step is conducted, wherein at least one of the reactive groups of the group donors is reacted with at least one of the tetrazine groups of the first ligands, so that at least one of the modifying groups of the group donors is covalently connected with the porous organic framework, whereby the modified porous organic framework is obtained.

A hierarchical catalyst composition comprising a continuous or particulate macroporous scaffold in which is incorporated mesoporous aggregates of magnetic nanoparticles, wherein an enzyme is embedded in mesopores of the mesoporous aggregates of magnetic nanoparticles. Methods for synthesizing the hierarchical catalyst composition are also described. Also described are processes that use the recoverable hierarchical catalyst composition for depolymerizing lignin, remediation of water contaminated with aromatic substances, polymerizing monomers by a free-radical mechanism, epoxidation of alkenes, halogenation of phenols, inhibiting growth and function of microorganisms in a solution, and carbon dioxide conversion to methanol. Further described are methods for increasing the space time yield and/or total turnover number of a liquid-phase chemical reaction that includes magnetic particles to facilitate the chemical reaction, the method comprising subjecting the chemical reaction to a plurality of magnetic fields of selected magnetic strength, relative position in the chemical reaction, and relative motion.

The present invention relates to methods for improving carbon capture using entrained catalytic-particles within an amine solvent. The particles are functionalized and appended with a CO.sub.2 hydration catalyst to enhance the kinetics of CO.sub.2 hydration and improve overall mass transfer of CO.sub.2 from an acid gas.

A composition comprising mesoporous aggregates of magnetic nanoparticles and free-radical producing enzyme (i.e., enzyme-bound mesoporous aggregates), wherein the mesoporous aggregates of magnetic nanoparticles have mesopores in which the free-radical-producing enzyme is embedded. Methods for synthesizing the enzyme-bound mesoporous aggregates are also described. Processes that use said enzyme-bound mesoporous aggregates for depolymerizing lignin, removing aromatic contaminants from water, and polymerizing monomers polymerizable by a free-radical reaction are also described.

A composition comprising mesoporous aggregates of magnetic nanoparticles and free-radical producing enzyme (i.e., enzyme-bound mesoporous aggregates), wherein the mesoporous aggregates of magnetic nanoparticles have mesopores in which the free-radical-producing enzyme is embedded. Methods for synthesizing the enzyme-bound mesoporous aggregates are also described. Processes that use said enzyme-bound mesoporous aggregates for depolymerizing lignin, removing aromatic contaminants from water, and polymerizing monomers polymerizable by a free-radical reaction are also described.

Photocatalytic device to dissociate an aqueous phase to product hydrogen gas, said device being set up in such a way that at least one photocatalytic system in contact with said aqueous phase can be irradiated by a light source to producethrough an oxidation reaction in said aqueous phaseoxygen gas, electrons and protons at a means of electron capture, said device comprising: a first zone comprising said aqueous phase, and a means for reducing said protons set up to carry out a reduction reaction on said protons by said electrons in order to generate hydrogen gas.
said device being characterised in that said means for proton reduction is a proton exchange interface with a front side facing said means of electron capture, and a back side, with only said back side of said proton exchange interface bearing at least one catalyst and/or at least one catalytic system.

The introduction of graphene as a carrier for enzymes and catalysts is disclosed.

In accordance with one embodiment, a mixture for forming polymer-encapsulated whole cells includes: at least one polymer precursor; at least one initiator; and a plurality of whole cells. In further embodiments, a product includes a structure comprising a plurality of whole cells encapsulated by a polymer network, where polymer(s) of the polymer network are cross-linked. The whole cells may include live whole cells, dried whole cells, and/or reconstituted whole cells, and have a characteristic to convert a chemical reactant to a product, where the chemical reactant is a gas (e.g., C1-C3 carbon gases such as methane, carbon dioxide, ethane, etc.) and the product is a liquid (e.g. methanol, etc.). For example, the whole cells may include organisms such as methanotrophic organisms and/or acetogenic anaerobes.

Aspects of the disclosure relate to an efficient entirely man-made nanobio hybrid fabricated through cell-free expression of transmembrane proton pump followed by assembly of the synthetic protein architecture with semiconductor nanoparticles for photocatalytic H.sub.2 evolution. The system produces H.sub.2 at a turnover rate of 240 ?mol of H.sub.2 (?mol protein).sup.?1 h.sup.?1 under green and 17.74 mmol of H.sub.2 (?mol protein).sup.?1 h.sup.?1 under white light at ambient conditions, in water at neutral pH with methanol as a sacrificial electron donor. Robsutness and flexibility of this approach allows for systemic manipulation at nanoparticle-bio interface toward directed evolution of energy materials and devices.