Cargando…

A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP

[Image: see text] The importance of energized nanoconfinement for facilitating the study and execution of enzyme cascades that feature multiple exchangeable cofactors is demonstrated by experiments with carboxylic acid reductase (CAR), an enzyme that requires both NADPH and ATP during a single catal...

Descripción completa

Detalles Bibliográficos
Autores principales: Megarity, Clare F., Weald, Thomas R. I., Heath, Rachel S., Turner, Nicholas J., Armstrong, Fraser A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361290/
https://www.ncbi.nlm.nih.gov/pubmed/35966600
http://dx.doi.org/10.1021/acscatal.2c00999
_version_ 1784764501517664256
author Megarity, Clare F.
Weald, Thomas R. I.
Heath, Rachel S.
Turner, Nicholas J.
Armstrong, Fraser A.
author_facet Megarity, Clare F.
Weald, Thomas R. I.
Heath, Rachel S.
Turner, Nicholas J.
Armstrong, Fraser A.
author_sort Megarity, Clare F.
collection PubMed
description [Image: see text] The importance of energized nanoconfinement for facilitating the study and execution of enzyme cascades that feature multiple exchangeable cofactors is demonstrated by experiments with carboxylic acid reductase (CAR), an enzyme that requires both NADPH and ATP during a single catalytic cycle. Conversion of cinnamic acid to cinnamaldehyde by a package of four enzymes loaded into and trapped in the random nanopores of an indium tin oxide (ITO) electrode is driven and monitored through the simultaneous delivery of electrical and chemical energy. The electrical energy is transduced by ferredoxin NADP(+) reductase, which undergoes rapid, direct electron exchange with ITO and regenerates NADP(H). The chemical energy provided by phosphoenolpyruvate, a fuel contained in the bulk solution, is cotransduced by adenylate kinase and pyruvate kinase, which efficiently convert the AMP product back into ATP that is required for the next cycle. The use of the two-kinase system allows the recycling process to be dissected to evaluate the separate roles of AMP removal and ATP supply during presteady-state and steady-state catalysis.
format Online
Article
Text
id pubmed-9361290
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-93612902022-08-10 A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP Megarity, Clare F. Weald, Thomas R. I. Heath, Rachel S. Turner, Nicholas J. Armstrong, Fraser A. ACS Catal [Image: see text] The importance of energized nanoconfinement for facilitating the study and execution of enzyme cascades that feature multiple exchangeable cofactors is demonstrated by experiments with carboxylic acid reductase (CAR), an enzyme that requires both NADPH and ATP during a single catalytic cycle. Conversion of cinnamic acid to cinnamaldehyde by a package of four enzymes loaded into and trapped in the random nanopores of an indium tin oxide (ITO) electrode is driven and monitored through the simultaneous delivery of electrical and chemical energy. The electrical energy is transduced by ferredoxin NADP(+) reductase, which undergoes rapid, direct electron exchange with ITO and regenerates NADP(H). The chemical energy provided by phosphoenolpyruvate, a fuel contained in the bulk solution, is cotransduced by adenylate kinase and pyruvate kinase, which efficiently convert the AMP product back into ATP that is required for the next cycle. The use of the two-kinase system allows the recycling process to be dissected to evaluate the separate roles of AMP removal and ATP supply during presteady-state and steady-state catalysis. American Chemical Society 2022-07-08 2022-08-05 /pmc/articles/PMC9361290/ /pubmed/35966600 http://dx.doi.org/10.1021/acscatal.2c00999 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Megarity, Clare F.
Weald, Thomas R. I.
Heath, Rachel S.
Turner, Nicholas J.
Armstrong, Fraser A.
A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP
title A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP
title_full A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP
title_fullStr A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP
title_full_unstemmed A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP
title_short A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP
title_sort nanoconfined four-enzyme cascade simultaneously driven by electrical and chemical energy, with built-in rapid, confocal recycling of nadp(h) and atp
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361290/
https://www.ncbi.nlm.nih.gov/pubmed/35966600
http://dx.doi.org/10.1021/acscatal.2c00999
work_keys_str_mv AT megarityclaref ananoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT wealdthomasri ananoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT heathrachels ananoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT turnernicholasj ananoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT armstrongfrasera ananoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT megarityclaref nanoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT wealdthomasri nanoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT heathrachels nanoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT turnernicholasj nanoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp
AT armstrongfrasera nanoconfinedfourenzymecascadesimultaneouslydrivenbyelectricalandchemicalenergywithbuiltinrapidconfocalrecyclingofnadphandatp