NANOWIRED FORMATE DEHYDROGENASE SYSTEM FOR REDUCTION OF CARBON DIOXIDE TO FORMATE
Disclosed herein are systems, methods and compositions of matter for engineered formate dehydrogenases electrocatalytically driven in reverse to fix CO 2 to formate, an electrode interface composed of self-assembled monolayers (SAM), and a nanowire link between the electrode and the enzyme's iron sulfur (FeS) cluster (engineered) to specifically link the iron sulfur cluster to the electrode. Engineering the interface between the enzyme and the electrode enables a high degree of activity and function compared to just an enzyme immobilized on the electrode. This interface enables specific orientational control of the enzyme and allows for separation of the enzyme from the electrode surface to allow retention of its native hydrodynamic radius. The transfer of electrons via the nanowire to the FeS cluster allows the enzyme to utilize its native electron transfer pathways. Moreover, wiring the FeS cluster directly to the electrode avoids the kinetic bottleneck of a soluble mediator and thus allows the wired enzyme to function more efficiently.
1 . A method for the reduction of carbon dioxide to formate comprising linking a FeS cluster within an engineered formate dehydrogenase enzyme to a thiolate linker on a first end and linking the thiolate linker on a second end to an electrode wherein the linked enzyme is exposed to carbon dioxide.
2 . The method of claim 1 wherein formate is produced at a rate of 0.16 mg of formate per hour.
3 . The method of claim 1 wherein formate is produced at a rate of 0.16 mg of formate per hour for 5 hours.
4 . The method of claim 1 wherein the electrode comprises gold.
5 . The method of claim 1 wherein the engineered formate dehydrogenase enzyme comprises a mutation from cysteine to glycine.
6 . The method of claim 5 wherein the mutation from cysteine to glycine is in a cysteine that binds to the FeS cluster in the corresponding native formate dehydrogenase enzyme.
7 . A system for the reduction of carbon dioxide to formate comprising a FeS cluster within an engineered formate dehydrogenase enzyme linked to a thiolate linker on a first end and wherein the thiolate linker is linked on a second end to an electrode.
8 . The system of claim 7 wherein formate is produced at a rate of 0.16 mg of formate per hour.
9 . The system of claim 7 wherein formate is produced at a rate of 0.16 mg of formate per hour for 5 hours.
10 . The system of claim 7 wherein the electrode comprises gold.
11 . The system of claim 7 wherein the engineered formate dehydrogenase enzyme comprises a mutation from cysteine to glycine.
12 . The system of claim 11 wherein the mutation from cysteine to glycine is in a cysteine that binds to the FeS cluster in the corresponding native formate dehydrogenase enzyme.
13 . A composition of matter comprising a FeS cluster within an engineered formate dehydrogenase enzyme linked to a thiolate linker on a first end and wherein the thiolate linker is linked on a second end to an electrode.
14 . The composition of matter of claim 13 wherein the FeS cluster is linked to a thiolate linker on a first end through a glycine residue resulting from mutating a cysteine that binds to the FeS cluster in the corresponding native formate dehydrogenase enzyme.
15 . The composition of matter of claim 13 wherein the electrode comprises gold.