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Changing the tracks: screening for electron transfer proteins to support hydrogen production

ABSTRACT: Ferredoxins are essential electron transferring proteins in organisms. Twelve plant-type ferredoxins in the green alga Chlamydomonas reinhardtii determine the fate of electrons, generated in multiple metabolic processes. The two hydrogenases HydA1 and HydA2 of. C. reinhardtii compete for e...

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Detalles Bibliográficos
Autores principales: Günzel, Alexander, Engelbrecht, Vera, Happe, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569306/
https://www.ncbi.nlm.nih.gov/pubmed/36038787
http://dx.doi.org/10.1007/s00775-022-01956-1
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author Günzel, Alexander
Engelbrecht, Vera
Happe, Thomas
author_facet Günzel, Alexander
Engelbrecht, Vera
Happe, Thomas
author_sort Günzel, Alexander
collection PubMed
description ABSTRACT: Ferredoxins are essential electron transferring proteins in organisms. Twelve plant-type ferredoxins in the green alga Chlamydomonas reinhardtii determine the fate of electrons, generated in multiple metabolic processes. The two hydrogenases HydA1 and HydA2 of. C. reinhardtii compete for electrons from the photosynthetic ferredoxin PetF, which is the first stromal mediator of the high-energy electrons derived from the absorption of light energy at the photosystems. While being involved in many chloroplast-located metabolic pathways, PetF shows the highest affinity for ferredoxin-NADP(+) oxidoreductase (FNR), not for the hydrogenases. Aiming to identify other potential electron donors for the hydrogenases, we screened as yet uncharacterized ferredoxins Fdx7, 8, 10 and 11 for their capability to reduce the hydrogenases. Comparing the performance of the Fdx in presence and absence of competitor FNR, we show that Fdx7 has a higher affinity for HydA1 than for FNR. Additionally, we show that synthetic FeS-cluster-binding maquettes, which can be reduced by NADPH alone, can also be used to reduce the hydrogenases. Our findings pave the way for the creation of tailored electron donors to redirect electrons to enzymes of interest. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00775-022-01956-1.
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spelling pubmed-95693062022-10-17 Changing the tracks: screening for electron transfer proteins to support hydrogen production Günzel, Alexander Engelbrecht, Vera Happe, Thomas J Biol Inorg Chem Original Paper ABSTRACT: Ferredoxins are essential electron transferring proteins in organisms. Twelve plant-type ferredoxins in the green alga Chlamydomonas reinhardtii determine the fate of electrons, generated in multiple metabolic processes. The two hydrogenases HydA1 and HydA2 of. C. reinhardtii compete for electrons from the photosynthetic ferredoxin PetF, which is the first stromal mediator of the high-energy electrons derived from the absorption of light energy at the photosystems. While being involved in many chloroplast-located metabolic pathways, PetF shows the highest affinity for ferredoxin-NADP(+) oxidoreductase (FNR), not for the hydrogenases. Aiming to identify other potential electron donors for the hydrogenases, we screened as yet uncharacterized ferredoxins Fdx7, 8, 10 and 11 for their capability to reduce the hydrogenases. Comparing the performance of the Fdx in presence and absence of competitor FNR, we show that Fdx7 has a higher affinity for HydA1 than for FNR. Additionally, we show that synthetic FeS-cluster-binding maquettes, which can be reduced by NADPH alone, can also be used to reduce the hydrogenases. Our findings pave the way for the creation of tailored electron donors to redirect electrons to enzymes of interest. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00775-022-01956-1. Springer International Publishing 2022-08-29 2022 /pmc/articles/PMC9569306/ /pubmed/36038787 http://dx.doi.org/10.1007/s00775-022-01956-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Günzel, Alexander
Engelbrecht, Vera
Happe, Thomas
Changing the tracks: screening for electron transfer proteins to support hydrogen production
title Changing the tracks: screening for electron transfer proteins to support hydrogen production
title_full Changing the tracks: screening for electron transfer proteins to support hydrogen production
title_fullStr Changing the tracks: screening for electron transfer proteins to support hydrogen production
title_full_unstemmed Changing the tracks: screening for electron transfer proteins to support hydrogen production
title_short Changing the tracks: screening for electron transfer proteins to support hydrogen production
title_sort changing the tracks: screening for electron transfer proteins to support hydrogen production
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569306/
https://www.ncbi.nlm.nih.gov/pubmed/36038787
http://dx.doi.org/10.1007/s00775-022-01956-1
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