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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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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. |
format | Online Article Text |
id | pubmed-9569306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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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