Non-photochemical reduction of thylakoid photosynthetic redox carriers in vitro: relevance to cyclic electron flow around photosystem I?
Non-photochemical (dark) increases in chlorophyll a fluorescence yield associated with non-photochemical reduction of redox carriers (Fnpr) have been attributed to the reduction of plastoquinone (PQ) related to cyclic electron flow (CEF) around photosystem I. In vivo, this rise in fluorescence is as...
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description | Non-photochemical (dark) increases in chlorophyll a fluorescence yield associated with non-photochemical reduction of redox carriers (Fnpr) have been attributed to the reduction of plastoquinone (PQ) related to cyclic electron flow (CEF) around photosystem I. In vivo, this rise in fluorescence is associated with activity of the chloroplast plastoquinone reductase (plastid
plastoquinone oxidoreductase) complex. In contrast, this signal measured in isolated thylakoids has been attributed to the activity of the protein gradient regulation-5 (PGR5)/PGR5-like (PGRL1)-associated CEF pathway. Here, we report a systematic experimentation on the origin of Fnpr in isolated thylakoids. Addition of NADPH and ferredoxin to isolated spinach thylakoids resulted in the reduction of the PQ pool, but neither its kinetics nor its inhibitor sensitivities matched those of Fnpr. Notably, Fnpr was more rapid than PQ reduction, and completely insensitive to inhibitors of the PSII QB site and oxygen evolving complex as well as inhibitors of the cytochrome b6f complex. We thus conclude that Fnpr in isolated thylakoids is not a result of redox equilibrium with bulk PQ. Redox titrations and fluorescence emission spectra imply that Fnpr is dependent on the reduction of a low potential redox component (Em about − 340 mV) within photosystem II (PSII), and is likely related to earlier observations of low potential variants of QA within a subpopulation of PSII that is directly reducible by ferredoxin. The implications of these results for our understanding of CEF and other photosynthetic processes are discussed. |
doi_str_mv | 10.1016/j.bbabio.2014.09.005 |
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plastoquinone oxidoreductase) complex. In contrast, this signal measured in isolated thylakoids has been attributed to the activity of the protein gradient regulation-5 (PGR5)/PGR5-like (PGRL1)-associated CEF pathway. Here, we report a systematic experimentation on the origin of Fnpr in isolated thylakoids. Addition of NADPH and ferredoxin to isolated spinach thylakoids resulted in the reduction of the PQ pool, but neither its kinetics nor its inhibitor sensitivities matched those of Fnpr. Notably, Fnpr was more rapid than PQ reduction, and completely insensitive to inhibitors of the PSII QB site and oxygen evolving complex as well as inhibitors of the cytochrome b6f complex. We thus conclude that Fnpr in isolated thylakoids is not a result of redox equilibrium with bulk PQ. Redox titrations and fluorescence emission spectra imply that Fnpr is dependent on the reduction of a low potential redox component (Em about − 340 mV) within photosystem II (PSII), and is likely related to earlier observations of low potential variants of QA within a subpopulation of PSII that is directly reducible by ferredoxin. The implications of these results for our understanding of CEF and other photosynthetic processes are discussed.</description><identifier>ISSN: 0006-3002</identifier><identifier>ISSN: 0005-2728</identifier><identifier>EISSN: 1879-2650</identifier><identifier>DOI: 10.1016/j.bbabio.2014.09.005</identifier><identifier>PMID: 25251244</identifier><language>eng</language><publisher>Netherlands: Elsevier</publisher><subject>Antimycin A - pharmacology ; Chlorophyll - chemistry ; Chlorophyll - metabolism ; Chloroplasts - drug effects ; Chloroplasts - metabolism ; Cytochrome b6f Complex - antagonists & inhibitors ; Cytochrome b6f Complex - metabolism ; Diuron - pharmacology ; Electron Transport - drug effects ; Enzyme Inhibitors - pharmacology ; Ferredoxin-NADP Reductase - antagonists & inhibitors ; Ferredoxin-NADP Reductase - metabolism ; Ferredoxins - metabolism ; Ferredoxins - pharmacology ; Fluorescence ; Kinetics ; NAD - metabolism ; NAD - pharmacology ; Onium Compounds - pharmacology ; Oxidation-Reduction - drug effects ; Photosynthesis ; Photosynthetic Reaction Center Complex Proteins - metabolism ; Photosystem I Protein Complex - metabolism ; Plant Proteins - metabolism ; Plastoquinone - metabolism ; Quinone Reductases - metabolism ; Spectrometry, Fluorescence ; Spinacia oleracea - metabolism ; Thylakoids - drug effects ; Thylakoids - metabolism</subject><ispartof>Biochimica et biophysica acta, 2014-12, Vol.1837 (12), p.1944-1954</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-da5dfca1823cfdd376f7a76976589adcd22e314c831846128ed22b72d169f473</citedby><cites>FETCH-LOGICAL-c446t-da5dfca1823cfdd376f7a76976589adcd22e314c831846128ed22b72d169f473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25251244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1227316$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Fisher, Nicholas</creatorcontrib><creatorcontrib>Kramer, David M</creatorcontrib><title>Non-photochemical reduction of thylakoid photosynthetic redox carriers in vitro: relevance to cyclic electron flow around photosystem I?</title><title>Biochimica et biophysica acta</title><addtitle>Biochim Biophys Acta</addtitle><description>Non-photochemical (dark) increases in chlorophyll a fluorescence yield associated with non-photochemical reduction of redox carriers (Fnpr) have been attributed to the reduction of plastoquinone (PQ) related to cyclic electron flow (CEF) around photosystem I. In vivo, this rise in fluorescence is associated with activity of the chloroplast plastoquinone reductase (plastid
plastoquinone oxidoreductase) complex. In contrast, this signal measured in isolated thylakoids has been attributed to the activity of the protein gradient regulation-5 (PGR5)/PGR5-like (PGRL1)-associated CEF pathway. Here, we report a systematic experimentation on the origin of Fnpr in isolated thylakoids. Addition of NADPH and ferredoxin to isolated spinach thylakoids resulted in the reduction of the PQ pool, but neither its kinetics nor its inhibitor sensitivities matched those of Fnpr. Notably, Fnpr was more rapid than PQ reduction, and completely insensitive to inhibitors of the PSII QB site and oxygen evolving complex as well as inhibitors of the cytochrome b6f complex. We thus conclude that Fnpr in isolated thylakoids is not a result of redox equilibrium with bulk PQ. Redox titrations and fluorescence emission spectra imply that Fnpr is dependent on the reduction of a low potential redox component (Em about − 340 mV) within photosystem II (PSII), and is likely related to earlier observations of low potential variants of QA within a subpopulation of PSII that is directly reducible by ferredoxin. The implications of these results for our understanding of CEF and other photosynthetic processes are discussed.</description><subject>Antimycin A - pharmacology</subject><subject>Chlorophyll - chemistry</subject><subject>Chlorophyll - metabolism</subject><subject>Chloroplasts - drug effects</subject><subject>Chloroplasts - metabolism</subject><subject>Cytochrome b6f Complex - antagonists & inhibitors</subject><subject>Cytochrome b6f Complex - metabolism</subject><subject>Diuron - pharmacology</subject><subject>Electron Transport - drug effects</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Ferredoxin-NADP Reductase - antagonists & inhibitors</subject><subject>Ferredoxin-NADP Reductase - metabolism</subject><subject>Ferredoxins - metabolism</subject><subject>Ferredoxins - pharmacology</subject><subject>Fluorescence</subject><subject>Kinetics</subject><subject>NAD - metabolism</subject><subject>NAD - pharmacology</subject><subject>Onium Compounds - pharmacology</subject><subject>Oxidation-Reduction - drug effects</subject><subject>Photosynthesis</subject><subject>Photosynthetic Reaction Center Complex Proteins - metabolism</subject><subject>Photosystem I Protein Complex - metabolism</subject><subject>Plant Proteins - metabolism</subject><subject>Plastoquinone - metabolism</subject><subject>Quinone Reductases - metabolism</subject><subject>Spectrometry, Fluorescence</subject><subject>Spinacia oleracea - metabolism</subject><subject>Thylakoids - drug effects</subject><subject>Thylakoids - metabolism</subject><issn>0006-3002</issn><issn>0005-2728</issn><issn>1879-2650</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kctu3CAUhlGVqpmmfYMqQlllY5ebsZ1NFEW9RIraTfYIH7DM1IYJ4DTzBn3sMp00K9A53_kP4kPoEyU1JVR-3tbDoAcXakaoqElfE9K8QRvatX3FZENO0IYQIitOCDtF71PalkvDSf8OnbKGNZQJsUF_fgRf7aaQA0x2caBnHK1ZIbvgcRhxnvaz_hWcwf-gtPd5stnBgQrPGHSMzsaEncdPLsdwVRqzfdIeLM4Bwx7mApcSlKbH4xx-Yx3D6l8DU7YLvrv-gN6Oek7248t5hh6-fnm4_V7d__x2d3tzX4EQMldGN2YETTvGYTSGt3JsdSv7VjZdrw0YxiynAjpOOyEp62ypDC0zVPajaPkZujjGhpSdSuCyhQmC9-WBijLWcioLdHmEdjE8rjZltbgEdp61t2FNisqmfF7f8UOeOKIQQ0rRjmoX3aLjXlGiDp7UVh09qYMnRXpVPJWx85cN67BY8zr0Xwz_C1cFky8</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Fisher, Nicholas</creator><creator>Kramer, David M</creator><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>20141201</creationdate><title>Non-photochemical reduction of thylakoid photosynthetic redox carriers in vitro: relevance to cyclic electron flow around photosystem I?</title><author>Fisher, Nicholas ; Kramer, David M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-da5dfca1823cfdd376f7a76976589adcd22e314c831846128ed22b72d169f473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antimycin A - pharmacology</topic><topic>Chlorophyll - chemistry</topic><topic>Chlorophyll - metabolism</topic><topic>Chloroplasts - drug effects</topic><topic>Chloroplasts - metabolism</topic><topic>Cytochrome b6f Complex - antagonists & inhibitors</topic><topic>Cytochrome b6f Complex - metabolism</topic><topic>Diuron - pharmacology</topic><topic>Electron Transport - drug effects</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Ferredoxin-NADP Reductase - antagonists & inhibitors</topic><topic>Ferredoxin-NADP Reductase - metabolism</topic><topic>Ferredoxins - metabolism</topic><topic>Ferredoxins - pharmacology</topic><topic>Fluorescence</topic><topic>Kinetics</topic><topic>NAD - metabolism</topic><topic>NAD - pharmacology</topic><topic>Onium Compounds - pharmacology</topic><topic>Oxidation-Reduction - drug effects</topic><topic>Photosynthesis</topic><topic>Photosynthetic Reaction Center Complex Proteins - metabolism</topic><topic>Photosystem I Protein Complex - metabolism</topic><topic>Plant Proteins - metabolism</topic><topic>Plastoquinone - metabolism</topic><topic>Quinone Reductases - metabolism</topic><topic>Spectrometry, Fluorescence</topic><topic>Spinacia oleracea - metabolism</topic><topic>Thylakoids - drug effects</topic><topic>Thylakoids - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fisher, Nicholas</creatorcontrib><creatorcontrib>Kramer, David M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Biochimica et biophysica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fisher, Nicholas</au><au>Kramer, David M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-photochemical reduction of thylakoid photosynthetic redox carriers in vitro: relevance to cyclic electron flow around photosystem I?</atitle><jtitle>Biochimica et biophysica acta</jtitle><addtitle>Biochim Biophys Acta</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>1837</volume><issue>12</issue><spage>1944</spage><epage>1954</epage><pages>1944-1954</pages><issn>0006-3002</issn><issn>0005-2728</issn><eissn>1879-2650</eissn><abstract>Non-photochemical (dark) increases in chlorophyll a fluorescence yield associated with non-photochemical reduction of redox carriers (Fnpr) have been attributed to the reduction of plastoquinone (PQ) related to cyclic electron flow (CEF) around photosystem I. In vivo, this rise in fluorescence is associated with activity of the chloroplast plastoquinone reductase (plastid
plastoquinone oxidoreductase) complex. In contrast, this signal measured in isolated thylakoids has been attributed to the activity of the protein gradient regulation-5 (PGR5)/PGR5-like (PGRL1)-associated CEF pathway. Here, we report a systematic experimentation on the origin of Fnpr in isolated thylakoids. Addition of NADPH and ferredoxin to isolated spinach thylakoids resulted in the reduction of the PQ pool, but neither its kinetics nor its inhibitor sensitivities matched those of Fnpr. Notably, Fnpr was more rapid than PQ reduction, and completely insensitive to inhibitors of the PSII QB site and oxygen evolving complex as well as inhibitors of the cytochrome b6f complex. We thus conclude that Fnpr in isolated thylakoids is not a result of redox equilibrium with bulk PQ. Redox titrations and fluorescence emission spectra imply that Fnpr is dependent on the reduction of a low potential redox component (Em about − 340 mV) within photosystem II (PSII), and is likely related to earlier observations of low potential variants of QA within a subpopulation of PSII that is directly reducible by ferredoxin. The implications of these results for our understanding of CEF and other photosynthetic processes are discussed.</abstract><cop>Netherlands</cop><pub>Elsevier</pub><pmid>25251244</pmid><doi>10.1016/j.bbabio.2014.09.005</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antimycin A - pharmacology Chlorophyll - chemistry Chlorophyll - metabolism Chloroplasts - drug effects Chloroplasts - metabolism Cytochrome b6f Complex - antagonists & inhibitors Cytochrome b6f Complex - metabolism Diuron - pharmacology Electron Transport - drug effects Enzyme Inhibitors - pharmacology Ferredoxin-NADP Reductase - antagonists & inhibitors Ferredoxin-NADP Reductase - metabolism Ferredoxins - metabolism Ferredoxins - pharmacology Fluorescence Kinetics NAD - metabolism NAD - pharmacology Onium Compounds - pharmacology Oxidation-Reduction - drug effects Photosynthesis Photosynthetic Reaction Center Complex Proteins - metabolism Photosystem I Protein Complex - metabolism Plant Proteins - metabolism Plastoquinone - metabolism Quinone Reductases - metabolism Spectrometry, Fluorescence Spinacia oleracea - metabolism Thylakoids - drug effects Thylakoids - metabolism |
title | Non-photochemical reduction of thylakoid photosynthetic redox carriers in vitro: relevance to cyclic electron flow around photosystem I? |
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