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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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 |
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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 |
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