Rational redesign of the ferredoxin-NADP + -oxido-reductase/ferredoxin-interaction for photosynthesis-dependent H 2 -production
Utilization of electrons from the photosynthetic water splitting reaction for the generation of biofuels, commodities as well as application in biotransformations requires a partial rerouting of the photosynthetic electron transport chain. Due to its rather negative redox potential and its bifurcati...
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description | Utilization of electrons from the photosynthetic water splitting reaction for the generation of biofuels, commodities as well as application in biotransformations requires a partial rerouting of the photosynthetic electron transport chain. Due to its rather negative redox potential and its bifurcational function, ferredoxin at the acceptor side of Photosystem 1 is one of the focal points for such an engineering. With hydrogen production as model system, we show here the impact and potential of redox partner design involving ferredoxin (Fd), ferredoxin-oxido-reductase (FNR) and [FeFe]‑hydrogenase HydA1 on electron transport in a future cyanobacterial design cell of Synechocystis PCC 6803. X-ray-structure-based rational design and the allocation of specific interaction residues by NMR-analysis led to the construction of Fd- and FNR-mutants, which in appropriate combination enabled an about 18-fold enhanced electron flow from Fd to HydA1 (in competition with equimolar amounts of FNR) in in vitro assays. The negative impact of these mutations on the Fd-FNR electron transport which indirectly facilitates H
production (with a contribution of ≤42% by FNR variants and ≤23% by Fd-variants) and the direct positive impact on the Fd-HydA1 electron transport (≤23% by Fd-mutants) provide an excellent basis for the construction of a hydrogen-producing design cell and the study of photosynthetic efficiency-optimization with cyanobacteria. |
doi_str_mv | 10.1016/j.bbabio.2018.01.006 |
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production (with a contribution of ≤42% by FNR variants and ≤23% by Fd-variants) and the direct positive impact on the Fd-HydA1 electron transport (≤23% by Fd-mutants) provide an excellent basis for the construction of a hydrogen-producing design cell and the study of photosynthetic efficiency-optimization with cyanobacteria.</description><identifier>ISSN: 0005-2728</identifier><identifier>DOI: 10.1016/j.bbabio.2018.01.006</identifier><identifier>PMID: 29378161</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Binding Sites ; Cloning, Molecular ; Electron Transport ; Electrons ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Ferredoxin-NADP Reductase - chemistry ; Ferredoxin-NADP Reductase - genetics ; Ferredoxin-NADP Reductase - metabolism ; Ferredoxins - chemistry ; Ferredoxins - genetics ; Ferredoxins - metabolism ; Gene Expression ; Hydrogen - metabolism ; Hydrogenase - chemistry ; Hydrogenase - genetics ; Hydrogenase - metabolism ; Kinetics ; Metabolic Engineering - methods ; Models, Molecular ; Mutagenesis, Site-Directed ; Oxidation-Reduction ; Photosynthesis - genetics ; Photosystem I Protein Complex - genetics ; Photosystem I Protein Complex - metabolism ; Protein Binding ; Protein Conformation, alpha-Helical ; Protein Conformation, beta-Strand ; Protein Interaction Domains and Motifs ; Recombinant Proteins - chemistry ; Recombinant Proteins - genetics ; Recombinant Proteins - metabolism ; Synechocystis - enzymology ; Synechocystis - genetics ; Thermodynamics</subject><ispartof>Biochimica et biophysica acta. Bioenergetics, 2018-04, Vol.1859 (4), p.253</ispartof><rights>Copyright © 2018. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29378161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wiegand, K</creatorcontrib><creatorcontrib>Winkler, M</creatorcontrib><creatorcontrib>Rumpel, S</creatorcontrib><creatorcontrib>Kannchen, D</creatorcontrib><creatorcontrib>Rexroth, S</creatorcontrib><creatorcontrib>Hase, T</creatorcontrib><creatorcontrib>Farès, C</creatorcontrib><creatorcontrib>Happe, T</creatorcontrib><creatorcontrib>Lubitz, W</creatorcontrib><creatorcontrib>Rögner, M</creatorcontrib><title>Rational redesign of the ferredoxin-NADP + -oxido-reductase/ferredoxin-interaction for photosynthesis-dependent H 2 -production</title><title>Biochimica et biophysica acta. Bioenergetics</title><addtitle>Biochim Biophys Acta Bioenerg</addtitle><description>Utilization of electrons from the photosynthetic water splitting reaction for the generation of biofuels, commodities as well as application in biotransformations requires a partial rerouting of the photosynthetic electron transport chain. Due to its rather negative redox potential and its bifurcational function, ferredoxin at the acceptor side of Photosystem 1 is one of the focal points for such an engineering. With hydrogen production as model system, we show here the impact and potential of redox partner design involving ferredoxin (Fd), ferredoxin-oxido-reductase (FNR) and [FeFe]‑hydrogenase HydA1 on electron transport in a future cyanobacterial design cell of Synechocystis PCC 6803. X-ray-structure-based rational design and the allocation of specific interaction residues by NMR-analysis led to the construction of Fd- and FNR-mutants, which in appropriate combination enabled an about 18-fold enhanced electron flow from Fd to HydA1 (in competition with equimolar amounts of FNR) in in vitro assays. The negative impact of these mutations on the Fd-FNR electron transport which indirectly facilitates H
production (with a contribution of ≤42% by FNR variants and ≤23% by Fd-variants) and the direct positive impact on the Fd-HydA1 electron transport (≤23% by Fd-mutants) provide an excellent basis for the construction of a hydrogen-producing design cell and the study of photosynthetic efficiency-optimization with cyanobacteria.</description><subject>Binding Sites</subject><subject>Cloning, Molecular</subject><subject>Electron Transport</subject><subject>Electrons</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Ferredoxin-NADP Reductase - chemistry</subject><subject>Ferredoxin-NADP Reductase - genetics</subject><subject>Ferredoxin-NADP Reductase - metabolism</subject><subject>Ferredoxins - chemistry</subject><subject>Ferredoxins - genetics</subject><subject>Ferredoxins - metabolism</subject><subject>Gene Expression</subject><subject>Hydrogen - metabolism</subject><subject>Hydrogenase - chemistry</subject><subject>Hydrogenase - genetics</subject><subject>Hydrogenase - metabolism</subject><subject>Kinetics</subject><subject>Metabolic Engineering - methods</subject><subject>Models, Molecular</subject><subject>Mutagenesis, Site-Directed</subject><subject>Oxidation-Reduction</subject><subject>Photosynthesis - genetics</subject><subject>Photosystem I Protein Complex - genetics</subject><subject>Photosystem I Protein Complex - metabolism</subject><subject>Protein Binding</subject><subject>Protein Conformation, alpha-Helical</subject><subject>Protein Conformation, beta-Strand</subject><subject>Protein Interaction Domains and Motifs</subject><subject>Recombinant Proteins - chemistry</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - metabolism</subject><subject>Synechocystis - enzymology</subject><subject>Synechocystis - genetics</subject><subject>Thermodynamics</subject><issn>0005-2728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtLAzEYRbNQbK3-A5HsJdM8ZiYzy1IfFYqK6Lokky82pU2GJAW78q87RQVXl3s5nMVF6IrRglFWTzeF1kq7UHDKmoKygtL6BI0ppRXhkjcjdJ7Shg5oycUZGvFWyIbVbIy-XlV2wastjmAguQ-Pg8V5DdhCHKbw6Tx5mt2-4BtMhmICGdZ9l1WC6T_E-QxRdUcXtiHifh1ySAc_mJJLxEAP3oDPeIE5Jn0MR8cAX6BTq7YJLn9zgt7v797mC7J8fnicz5akZ7TJRFCpuxIk1QwqrU0N0spGVJpzqTohpBqw0rIWhClZK0FqTqHkjFvVqLYVE3T94-33egdm1Ue3U_Gw-ntCfAPyJWJg</recordid><startdate>201804</startdate><enddate>201804</enddate><creator>Wiegand, K</creator><creator>Winkler, M</creator><creator>Rumpel, S</creator><creator>Kannchen, D</creator><creator>Rexroth, S</creator><creator>Hase, T</creator><creator>Farès, C</creator><creator>Happe, T</creator><creator>Lubitz, W</creator><creator>Rögner, M</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>201804</creationdate><title>Rational redesign of the ferredoxin-NADP + -oxido-reductase/ferredoxin-interaction for photosynthesis-dependent H 2 -production</title><author>Wiegand, K ; Winkler, M ; Rumpel, S ; Kannchen, D ; Rexroth, S ; Hase, T ; Farès, C ; Happe, T ; Lubitz, W ; Rögner, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p108t-307bc4e70b1e5bbd6e7f7835b227ac337a1084f19e3d4197e7b20e4212fa8a993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Binding Sites</topic><topic>Cloning, Molecular</topic><topic>Electron Transport</topic><topic>Electrons</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Ferredoxin-NADP Reductase - chemistry</topic><topic>Ferredoxin-NADP Reductase - genetics</topic><topic>Ferredoxin-NADP Reductase - metabolism</topic><topic>Ferredoxins - chemistry</topic><topic>Ferredoxins - genetics</topic><topic>Ferredoxins - metabolism</topic><topic>Gene Expression</topic><topic>Hydrogen - metabolism</topic><topic>Hydrogenase - chemistry</topic><topic>Hydrogenase - genetics</topic><topic>Hydrogenase - metabolism</topic><topic>Kinetics</topic><topic>Metabolic Engineering - methods</topic><topic>Models, Molecular</topic><topic>Mutagenesis, Site-Directed</topic><topic>Oxidation-Reduction</topic><topic>Photosynthesis - genetics</topic><topic>Photosystem I Protein Complex - genetics</topic><topic>Photosystem I Protein Complex - metabolism</topic><topic>Protein Binding</topic><topic>Protein Conformation, alpha-Helical</topic><topic>Protein Conformation, beta-Strand</topic><topic>Protein Interaction Domains and Motifs</topic><topic>Recombinant Proteins - chemistry</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - metabolism</topic><topic>Synechocystis - enzymology</topic><topic>Synechocystis - genetics</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wiegand, K</creatorcontrib><creatorcontrib>Winkler, M</creatorcontrib><creatorcontrib>Rumpel, S</creatorcontrib><creatorcontrib>Kannchen, D</creatorcontrib><creatorcontrib>Rexroth, S</creatorcontrib><creatorcontrib>Hase, T</creatorcontrib><creatorcontrib>Farès, C</creatorcontrib><creatorcontrib>Happe, T</creatorcontrib><creatorcontrib>Lubitz, W</creatorcontrib><creatorcontrib>Rögner, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Biochimica et biophysica acta. Bioenergetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wiegand, K</au><au>Winkler, M</au><au>Rumpel, S</au><au>Kannchen, D</au><au>Rexroth, S</au><au>Hase, T</au><au>Farès, C</au><au>Happe, T</au><au>Lubitz, W</au><au>Rögner, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rational redesign of the ferredoxin-NADP + -oxido-reductase/ferredoxin-interaction for photosynthesis-dependent H 2 -production</atitle><jtitle>Biochimica et biophysica acta. Bioenergetics</jtitle><addtitle>Biochim Biophys Acta Bioenerg</addtitle><date>2018-04</date><risdate>2018</risdate><volume>1859</volume><issue>4</issue><spage>253</spage><pages>253-</pages><issn>0005-2728</issn><abstract>Utilization of electrons from the photosynthetic water splitting reaction for the generation of biofuels, commodities as well as application in biotransformations requires a partial rerouting of the photosynthetic electron transport chain. Due to its rather negative redox potential and its bifurcational function, ferredoxin at the acceptor side of Photosystem 1 is one of the focal points for such an engineering. With hydrogen production as model system, we show here the impact and potential of redox partner design involving ferredoxin (Fd), ferredoxin-oxido-reductase (FNR) and [FeFe]‑hydrogenase HydA1 on electron transport in a future cyanobacterial design cell of Synechocystis PCC 6803. X-ray-structure-based rational design and the allocation of specific interaction residues by NMR-analysis led to the construction of Fd- and FNR-mutants, which in appropriate combination enabled an about 18-fold enhanced electron flow from Fd to HydA1 (in competition with equimolar amounts of FNR) in in vitro assays. The negative impact of these mutations on the Fd-FNR electron transport which indirectly facilitates H
production (with a contribution of ≤42% by FNR variants and ≤23% by Fd-variants) and the direct positive impact on the Fd-HydA1 electron transport (≤23% by Fd-mutants) provide an excellent basis for the construction of a hydrogen-producing design cell and the study of photosynthetic efficiency-optimization with cyanobacteria.</abstract><cop>Netherlands</cop><pmid>29378161</pmid><doi>10.1016/j.bbabio.2018.01.006</doi></addata></record> |
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subjects | Binding Sites Cloning, Molecular Electron Transport Electrons Escherichia coli - genetics Escherichia coli - metabolism Ferredoxin-NADP Reductase - chemistry Ferredoxin-NADP Reductase - genetics Ferredoxin-NADP Reductase - metabolism Ferredoxins - chemistry Ferredoxins - genetics Ferredoxins - metabolism Gene Expression Hydrogen - metabolism Hydrogenase - chemistry Hydrogenase - genetics Hydrogenase - metabolism Kinetics Metabolic Engineering - methods Models, Molecular Mutagenesis, Site-Directed Oxidation-Reduction Photosynthesis - genetics Photosystem I Protein Complex - genetics Photosystem I Protein Complex - metabolism Protein Binding Protein Conformation, alpha-Helical Protein Conformation, beta-Strand Protein Interaction Domains and Motifs Recombinant Proteins - chemistry Recombinant Proteins - genetics Recombinant Proteins - metabolism Synechocystis - enzymology Synechocystis - genetics Thermodynamics |
title | Rational redesign of the ferredoxin-NADP + -oxido-reductase/ferredoxin-interaction for photosynthesis-dependent H 2 -production |
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