Transfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesis

In a discovery of the transfer of chloroplast biosynthesis activity to an inorganic material, ferredoxin-NADP+ reductase (FNR), the pivotal redox flavoenzyme of photosynthetic CO2 assimilation, binds tightly within the pores of indium tin oxide (ITO) to produce an electrode for direct studies of the...

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Main Authors: Siritanaratkul, B, Megarity, C, Roberts, T, Samuels, T, Winkler, M, Warner, J, Happe, T, Armstrong, F
Format: Journal article
Jezik:English
Izdano: Royal Society of Chemistry 2017
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author Siritanaratkul, B
Megarity, C
Roberts, T
Samuels, T
Winkler, M
Warner, J
Happe, T
Armstrong, F
author_facet Siritanaratkul, B
Megarity, C
Roberts, T
Samuels, T
Winkler, M
Warner, J
Happe, T
Armstrong, F
author_sort Siritanaratkul, B
collection OXFORD
description In a discovery of the transfer of chloroplast biosynthesis activity to an inorganic material, ferredoxin-NADP+ reductase (FNR), the pivotal redox flavoenzyme of photosynthetic CO2 assimilation, binds tightly within the pores of indium tin oxide (ITO) to produce an electrode for direct studies of the redox chemistry of the FAD active site, and fast, reversible and diffusion-controlled interconversion of NADP+ and NADPH in solution. The dynamic electrochemical properties of FNR and NADP(H) are thus revealed in a special way that enables facile coupling of selective, enzyme-catalysed organic synthesis to a controllable power source, as demonstrated by efficient synthesis of l-glutamate from 2-oxoglutarate and NH4+.
first_indexed 2024-03-07T02:17:21Z
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publishDate 2017
publisher Royal Society of Chemistry
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spelling oxford-uuid:a2b8028d-f53e-46a5-823b-0b3f9a69f5f72022-03-27T02:21:57ZTransfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesisJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a2b8028d-f53e-46a5-823b-0b3f9a69f5f7EnglishSymplectic Elements at OxfordRoyal Society of Chemistry2017Siritanaratkul, BMegarity, CRoberts, TSamuels, TWinkler, MWarner, JHappe, TArmstrong, FIn a discovery of the transfer of chloroplast biosynthesis activity to an inorganic material, ferredoxin-NADP+ reductase (FNR), the pivotal redox flavoenzyme of photosynthetic CO2 assimilation, binds tightly within the pores of indium tin oxide (ITO) to produce an electrode for direct studies of the redox chemistry of the FAD active site, and fast, reversible and diffusion-controlled interconversion of NADP+ and NADPH in solution. The dynamic electrochemical properties of FNR and NADP(H) are thus revealed in a special way that enables facile coupling of selective, enzyme-catalysed organic synthesis to a controllable power source, as demonstrated by efficient synthesis of l-glutamate from 2-oxoglutarate and NH4+.
spellingShingle Siritanaratkul, B
Megarity, C
Roberts, T
Samuels, T
Winkler, M
Warner, J
Happe, T
Armstrong, F
Transfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesis
title Transfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesis
title_full Transfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesis
title_fullStr Transfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesis
title_full_unstemmed Transfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesis
title_short Transfer of photosynthetic NADP+/NADPH recycling activity to a porous metal oxide for highly specific, electrochemically-driven organic synthesis
title_sort transfer of photosynthetic nadp nadph recycling activity to a porous metal oxide for highly specific electrochemically driven organic synthesis
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