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Pyrene hydrogel for promoting direct bioelectrochemistry: ATP-independent electroenzymatic reduction of N-2

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dc.creator Sahin, Selmihan
dc.creator Minteer, Shelley D.
dc.creator ABDELLAOUI, Sofiene
dc.creator YUAN, Mengwei
dc.creator CAI, Rong
dc.creator LİM, Koun
dc.creator Hickey, David P.
dc.creator Patterson, Ashlea R.
dc.date 2018-06-20T21:00:00Z
dc.date.accessioned 2020-10-06T12:03:19Z
dc.date.available 2020-10-06T12:03:19Z
dc.identifier fb9ac456-70de-4d86-824b-9fcdec229252
dc.identifier 10.1039/c8sc01638k
dc.identifier https://avesis.sdu.edu.tr/publication/details/fb9ac456-70de-4d86-824b-9fcdec229252/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/76921
dc.description Enzymatic bioelectrocatalysis often requires an artificial redox mediator to observe significant electron transfer rates. The use of such mediators can add a substantial overpotential and obfuscate the protein's native kinetics, which limits the voltage of a biofuel cell and alters the analytical performance of biosensors. Herein, we describe a material for facilitating direct electrochemical communication with redox proteins based on a novel pyrene-modified linear poly(ethyleneimine). This method was applied for promoting direct bioelectrocatalytic reduction of O-2 by laccase and, by immobilizing the catalytic subunit of nitrogenase (MoFe protein), to demonstrate the ATP-independent direct electroenzymatic reduction of N-2 to NH3.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Pyrene hydrogel for promoting direct bioelectrochemistry: ATP-independent electroenzymatic reduction of N-2
dc.type info:eu-repo/semantics/article


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