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Cyclic electron flow within PSII functions in intact chloroplasts from spinach [Spinacia oleracea] leaves

"Using thylakoid membranes, we previously demon strated that accumulated electrons in the photosynthetic electron transport system induces the electron flow from the acceptor side of PSII to its donor side only in the presence of a pH gradient (DpH) across the thylakoid membranes. This electron...

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Published in:Plant and cell physiology 2002-08, Vol.43 (8), p.951-957
Main Authors: "Miyake, C. (Kyushu Univ., Fukuoka (Japan)), Yonekura, K, Kobayashi, Y, Yokota, A.
Format: Article
Language:English
Subjects:
AEF
APX
Asc
Fm
MDA
NPQ
PFD
SOD
WWC
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cited_by cdi_FETCH-LOGICAL-c461t-452be49c296e6a7cb32b824ebe371779d7cdc3950e3885758b7466953f94c98b3
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container_title Plant and cell physiology
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creator "Miyake, C. (Kyushu Univ., Fukuoka (Japan))
Yonekura, K
Kobayashi, Y
Yokota, A.
description "Using thylakoid membranes, we previously demon strated that accumulated electrons in the photosynthetic electron transport system induces the electron flow from the acceptor side of PSII to its donor side only in the presence of a pH gradient (DpH) across the thylakoid membranes. This electron flow has been referred to as cyclic electron flow within PSII (CEF-PSII) [Miyake and Yokota (2001) Plant Cell Physiol. 42: 508]. In the present study, we examined whether CEF-PSII operates in isolated intact chloroplasts from spinach leaves, by correlating the quantum yield of PSII [F(PSII)] with the activity of the linear electron flow [V(O sub2)j. The addition of the protonophore nigericin to the intact chloroplasts decreased F(PSII), but increased V(O sub2), and relative electron flux in PSII (F(PSII) * PFD and V(O sub2) were proportional to one another. F(PSII) * PFD at a given V(O sub2) was much higher in the presence of ApH than that in its absence. These effects of nigericin on the relationship between F(PSII) * PFD and V(O sub2) are consistent with those previously observed in thyl-akoid membranes, indicating the occurrence of CEF-PSII also in intact chloroplasts. In the presence of DpH, CEF-PSII accounted for the excess electron flux in PSII that could not be attributed to photosynthetic linear electron flow. The activity of CEF-PSII increased with increased light intensity and almost corresponded to that of the water-water cycle (WWC), implying that CEF-PSII can dissipate excess photon energy in cooperation with WWC to protect PSII from photoinhibition under limited photo-synthesis conditions"
doi_str_mv 10.1093/pcp/pcf113
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(Kyushu Univ., Fukuoka (Japan)) ; Yonekura, K ; Kobayashi, Y ; Yokota, A.</creator><creatorcontrib>"Miyake, C. (Kyushu Univ., Fukuoka (Japan)) ; Yonekura, K ; Kobayashi, Y ; Yokota, A.</creatorcontrib><description>"Using thylakoid membranes, we previously demon strated that accumulated electrons in the photosynthetic electron transport system induces the electron flow from the acceptor side of PSII to its donor side only in the presence of a pH gradient (DpH) across the thylakoid membranes. This electron flow has been referred to as cyclic electron flow within PSII (CEF-PSII) [Miyake and Yokota (2001) Plant Cell Physiol. 42: 508]. In the present study, we examined whether CEF-PSII operates in isolated intact chloroplasts from spinach leaves, by correlating the quantum yield of PSII [F(PSII)] with the activity of the linear electron flow [V(O sub2)j. The addition of the protonophore nigericin to the intact chloroplasts decreased F(PSII), but increased V(O sub2), and relative electron flux in PSII (F(PSII) * PFD and V(O sub2) were proportional to one another. F(PSII) * PFD at a given V(O sub2) was much higher in the presence of ApH than that in its absence. These effects of nigericin on the relationship between F(PSII) * PFD and V(O sub2) are consistent with those previously observed in thyl-akoid membranes, indicating the occurrence of CEF-PSII also in intact chloroplasts. In the presence of DpH, CEF-PSII accounted for the excess electron flux in PSII that could not be attributed to photosynthetic linear electron flow. The activity of CEF-PSII increased with increased light intensity and almost corresponded to that of the water-water cycle (WWC), implying that CEF-PSII can dissipate excess photon energy in cooperation with WWC to protect PSII from photoinhibition under limited photo-synthesis conditions"</description><identifier>ISSN: 0032-0781</identifier><identifier>EISSN: 1471-9053</identifier><identifier>DOI: 10.1093/pcp/pcf113</identifier><identifier>PMID: 12198198</identifier><language>eng</language><publisher>Japan: Oxford University Press</publisher><subject>a pH gradient across thylakoid membranes ; AEF ; alternative electron flow ; APX ; Asc ; Asc peroxidase ; ascorbate ; BIOCHEMICAL PATHWAYS ; CEF-PSII ; Chlorophyll - metabolism ; CHLOROPLASTS ; Chloroplasts - drug effects ; Chloroplasts - metabolism ; Chloroplasts - radiation effects ; cyclic electron flow within PSII ; defined as (F′m–Fs)/F′m ; defined as Fm/Fm′–1 ; Electron Transport - drug effects ; Electron Transport - radiation effects ; Fm ; Fm after illumination ; Hydrogen-Ion Concentration ; Ionophores - pharmacology ; Je(PSII) ; Keywords: Alternative electron flow — Chloroplasts — Cyclic electron flow — Photoinhibition — PSII — Water–water cycle ; LEAVES ; Light ; Light-Harvesting Protein Complexes ; maximal yield of Chl fluorescence after dark adaptation ; MDA ; minimal Chl fluorescence after dark adaptation ; monodehydroascorbate radical ; Nigericin - pharmacology ; non-photochemical quenching coefficient of Chl fluorescence ; NPQ ; Oxygen - metabolism ; PCO cycle ; PCR cycle ; PFD ; photorespiratory carbon-oxidation cycle ; Photosynthesis - drug effects ; Photosynthesis - physiology ; Photosynthesis - radiation effects ; photosynthetic carbon-reduction cycle ; Photosynthetic Reaction Center Complex Proteins - drug effects ; Photosynthetic Reaction Center Complex Proteins - metabolism ; Photosynthetic Reaction Center Complex Proteins - radiation effects ; photosynthetically active photon flux density ; PHOTOSYSTEMS ; Plant Leaves - drug effects ; Plant Leaves - metabolism ; Plant Leaves - radiation effects ; plastoquinol ; plastoquinone ; PQH2 ; SOD ; SPINACIA OLERACEA ; Spinacia oleracea - drug effects ; Spinacia oleracea - metabolism ; Spinacia oleracea - radiation effects ; superoxide dismutase ; the electron flux in PSII ; the molar ratio of PSII to PSI in thylakoid membranes ; the quantum yield of electron transport in PSII at steady state ; the rate of O2 uptake ; the water–water cycle ; V(O2) ; Water - pharmacology ; Water - physiology ; WWC ; yield of steady-state Chl fluorescence ; ΔpH ; Φ(PSII)</subject><ispartof>Plant and cell physiology, 2002-08, Vol.43 (8), p.951-957</ispartof><rights>Copyright Oxford University Press(England) Aug 15, 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-452be49c296e6a7cb32b824ebe371779d7cdc3950e3885758b7466953f94c98b3</citedby><cites>FETCH-LOGICAL-c461t-452be49c296e6a7cb32b824ebe371779d7cdc3950e3885758b7466953f94c98b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12198198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>"Miyake, C. (Kyushu Univ., Fukuoka (Japan))</creatorcontrib><creatorcontrib>Yonekura, K</creatorcontrib><creatorcontrib>Kobayashi, Y</creatorcontrib><creatorcontrib>Yokota, A.</creatorcontrib><title>Cyclic electron flow within PSII functions in intact chloroplasts from spinach [Spinacia oleracea] leaves</title><title>Plant and cell physiology</title><addtitle>Plant Cell Physiol</addtitle><description>"Using thylakoid membranes, we previously demon strated that accumulated electrons in the photosynthetic electron transport system induces the electron flow from the acceptor side of PSII to its donor side only in the presence of a pH gradient (DpH) across the thylakoid membranes. This electron flow has been referred to as cyclic electron flow within PSII (CEF-PSII) [Miyake and Yokota (2001) Plant Cell Physiol. 42: 508]. In the present study, we examined whether CEF-PSII operates in isolated intact chloroplasts from spinach leaves, by correlating the quantum yield of PSII [F(PSII)] with the activity of the linear electron flow [V(O sub2)j. The addition of the protonophore nigericin to the intact chloroplasts decreased F(PSII), but increased V(O sub2), and relative electron flux in PSII (F(PSII) * PFD and V(O sub2) were proportional to one another. F(PSII) * PFD at a given V(O sub2) was much higher in the presence of ApH than that in its absence. These effects of nigericin on the relationship between F(PSII) * PFD and V(O sub2) are consistent with those previously observed in thyl-akoid membranes, indicating the occurrence of CEF-PSII also in intact chloroplasts. In the presence of DpH, CEF-PSII accounted for the excess electron flux in PSII that could not be attributed to photosynthetic linear electron flow. The activity of CEF-PSII increased with increased light intensity and almost corresponded to that of the water-water cycle (WWC), implying that CEF-PSII can dissipate excess photon energy in cooperation with WWC to protect PSII from photoinhibition under limited photo-synthesis conditions"</description><subject>a pH gradient across thylakoid membranes</subject><subject>AEF</subject><subject>alternative electron flow</subject><subject>APX</subject><subject>Asc</subject><subject>Asc peroxidase</subject><subject>ascorbate</subject><subject>BIOCHEMICAL PATHWAYS</subject><subject>CEF-PSII</subject><subject>Chlorophyll - metabolism</subject><subject>CHLOROPLASTS</subject><subject>Chloroplasts - drug effects</subject><subject>Chloroplasts - metabolism</subject><subject>Chloroplasts - radiation effects</subject><subject>cyclic electron flow within PSII</subject><subject>defined as (F′m–Fs)/F′m</subject><subject>defined as Fm/Fm′–1</subject><subject>Electron Transport - drug effects</subject><subject>Electron Transport - radiation effects</subject><subject>Fm</subject><subject>Fm after illumination</subject><subject>Hydrogen-Ion Concentration</subject><subject>Ionophores - pharmacology</subject><subject>Je(PSII)</subject><subject>Keywords: Alternative electron flow — Chloroplasts — Cyclic electron flow — Photoinhibition — PSII — Water–water cycle</subject><subject>LEAVES</subject><subject>Light</subject><subject>Light-Harvesting Protein Complexes</subject><subject>maximal yield of Chl fluorescence after dark adaptation</subject><subject>MDA</subject><subject>minimal Chl fluorescence after dark adaptation</subject><subject>monodehydroascorbate radical</subject><subject>Nigericin - pharmacology</subject><subject>non-photochemical quenching coefficient of Chl fluorescence</subject><subject>NPQ</subject><subject>Oxygen - metabolism</subject><subject>PCO cycle</subject><subject>PCR cycle</subject><subject>PFD</subject><subject>photorespiratory carbon-oxidation cycle</subject><subject>Photosynthesis - drug effects</subject><subject>Photosynthesis - physiology</subject><subject>Photosynthesis - radiation effects</subject><subject>photosynthetic carbon-reduction cycle</subject><subject>Photosynthetic Reaction Center Complex Proteins - drug effects</subject><subject>Photosynthetic Reaction Center Complex Proteins - metabolism</subject><subject>Photosynthetic Reaction Center Complex Proteins - radiation effects</subject><subject>photosynthetically active photon flux density</subject><subject>PHOTOSYSTEMS</subject><subject>Plant Leaves - drug effects</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Leaves - radiation effects</subject><subject>plastoquinol</subject><subject>plastoquinone</subject><subject>PQH2</subject><subject>SOD</subject><subject>SPINACIA OLERACEA</subject><subject>Spinacia oleracea - drug effects</subject><subject>Spinacia oleracea - metabolism</subject><subject>Spinacia oleracea - radiation effects</subject><subject>superoxide dismutase</subject><subject>the electron flux in PSII</subject><subject>the molar ratio of PSII to PSI in thylakoid membranes</subject><subject>the quantum yield of electron transport in PSII at steady state</subject><subject>the rate of O2 uptake</subject><subject>the water–water cycle</subject><subject>V(O2)</subject><subject>Water - pharmacology</subject><subject>Water - physiology</subject><subject>WWC</subject><subject>yield of steady-state Chl fluorescence</subject><subject>ΔpH</subject><subject>Φ(PSII)</subject><issn>0032-0781</issn><issn>1471-9053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNpd0d-LFSEUB3CJor1tvfReSA89BFP-GEd9jEu1d9loY4uiCHG8Z7pu3nFSp23_-6y5FASKB_1wOHxF6D4lTynR_NnkproHSvkNtKKtpI0mgt9EK0I4a4hU9AjdyfmSkFpzchsdUUa1qmuF_PraBe8wBHAlxREPIV7hK192fsTnF5sNHubRFR_HjOuNH4t1BbtdiClOweaS8ZDiHufJj9bt8OeLP4W3OAZI1oH9ggPYH5DvoluDDRnuHc5j9P7li3frk-bszavN-vlZ49qOlqYVrIdWO6Y76Kx0PWe9Yi30wCWVUm-l2zquBQGulJBC9bLtOi34oFunVc-P0eOl75Ti9xlyMXufHYRgR4hzNpIRXqOiFT76D17GOY11NsMIFUJzISp6siCXYs4JBjMlv7fp2lBifqdvavpmSb_ih4eOc7-H7T96iLuCZgE-F_j5992mb6aTXApz8vGTUez1aUvUW_Oh-geLH2w09mvy2Zyes_qthFDZMv4Lp06Ygg</recordid><startdate>20020801</startdate><enddate>20020801</enddate><creator>"Miyake, C. (Kyushu Univ., Fukuoka (Japan))</creator><creator>Yonekura, K</creator><creator>Kobayashi, Y</creator><creator>Yokota, A.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>FBQ</scope><scope>BSCLL</scope><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>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20020801</creationdate><title>Cyclic electron flow within PSII functions in intact chloroplasts from spinach [Spinacia oleracea] leaves</title><author>"Miyake, C. (Kyushu Univ., Fukuoka (Japan)) ; Yonekura, K ; Kobayashi, Y ; Yokota, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-452be49c296e6a7cb32b824ebe371779d7cdc3950e3885758b7466953f94c98b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>a pH gradient across thylakoid membranes</topic><topic>AEF</topic><topic>alternative electron flow</topic><topic>APX</topic><topic>Asc</topic><topic>Asc peroxidase</topic><topic>ascorbate</topic><topic>BIOCHEMICAL PATHWAYS</topic><topic>CEF-PSII</topic><topic>Chlorophyll - metabolism</topic><topic>CHLOROPLASTS</topic><topic>Chloroplasts - drug effects</topic><topic>Chloroplasts - metabolism</topic><topic>Chloroplasts - radiation effects</topic><topic>cyclic electron flow within PSII</topic><topic>defined as (F′m–Fs)/F′m</topic><topic>defined as Fm/Fm′–1</topic><topic>Electron Transport - drug effects</topic><topic>Electron Transport - radiation effects</topic><topic>Fm</topic><topic>Fm after illumination</topic><topic>Hydrogen-Ion Concentration</topic><topic>Ionophores - pharmacology</topic><topic>Je(PSII)</topic><topic>Keywords: Alternative electron flow — Chloroplasts — Cyclic electron flow — Photoinhibition — PSII — Water–water cycle</topic><topic>LEAVES</topic><topic>Light</topic><topic>Light-Harvesting Protein Complexes</topic><topic>maximal yield of Chl fluorescence after dark adaptation</topic><topic>MDA</topic><topic>minimal Chl fluorescence after dark adaptation</topic><topic>monodehydroascorbate radical</topic><topic>Nigericin - pharmacology</topic><topic>non-photochemical quenching coefficient of Chl fluorescence</topic><topic>NPQ</topic><topic>Oxygen - metabolism</topic><topic>PCO cycle</topic><topic>PCR cycle</topic><topic>PFD</topic><topic>photorespiratory carbon-oxidation cycle</topic><topic>Photosynthesis - drug effects</topic><topic>Photosynthesis - physiology</topic><topic>Photosynthesis - radiation effects</topic><topic>photosynthetic carbon-reduction cycle</topic><topic>Photosynthetic Reaction Center Complex Proteins - drug effects</topic><topic>Photosynthetic Reaction Center Complex Proteins - metabolism</topic><topic>Photosynthetic Reaction Center Complex Proteins - radiation effects</topic><topic>photosynthetically active photon flux density</topic><topic>PHOTOSYSTEMS</topic><topic>Plant Leaves - drug effects</topic><topic>Plant Leaves - metabolism</topic><topic>Plant Leaves - radiation effects</topic><topic>plastoquinol</topic><topic>plastoquinone</topic><topic>PQH2</topic><topic>SOD</topic><topic>SPINACIA OLERACEA</topic><topic>Spinacia oleracea - drug effects</topic><topic>Spinacia oleracea - metabolism</topic><topic>Spinacia oleracea - radiation effects</topic><topic>superoxide dismutase</topic><topic>the electron flux in PSII</topic><topic>the molar ratio of PSII to PSI in thylakoid membranes</topic><topic>the quantum yield of electron transport in PSII at steady state</topic><topic>the rate of O2 uptake</topic><topic>the water–water cycle</topic><topic>V(O2)</topic><topic>Water - pharmacology</topic><topic>Water - physiology</topic><topic>WWC</topic><topic>yield of steady-state Chl fluorescence</topic><topic>ΔpH</topic><topic>Φ(PSII)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>"Miyake, C. (Kyushu Univ., Fukuoka (Japan))</creatorcontrib><creatorcontrib>Yonekura, K</creatorcontrib><creatorcontrib>Kobayashi, Y</creatorcontrib><creatorcontrib>Yokota, A.</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Plant and cell physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>"Miyake, C. (Kyushu Univ., Fukuoka (Japan))</au><au>Yonekura, K</au><au>Kobayashi, Y</au><au>Yokota, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyclic electron flow within PSII functions in intact chloroplasts from spinach [Spinacia oleracea] leaves</atitle><jtitle>Plant and cell physiology</jtitle><addtitle>Plant Cell Physiol</addtitle><date>2002-08-01</date><risdate>2002</risdate><volume>43</volume><issue>8</issue><spage>951</spage><epage>957</epage><pages>951-957</pages><issn>0032-0781</issn><eissn>1471-9053</eissn><abstract>"Using thylakoid membranes, we previously demon strated that accumulated electrons in the photosynthetic electron transport system induces the electron flow from the acceptor side of PSII to its donor side only in the presence of a pH gradient (DpH) across the thylakoid membranes. This electron flow has been referred to as cyclic electron flow within PSII (CEF-PSII) [Miyake and Yokota (2001) Plant Cell Physiol. 42: 508]. In the present study, we examined whether CEF-PSII operates in isolated intact chloroplasts from spinach leaves, by correlating the quantum yield of PSII [F(PSII)] with the activity of the linear electron flow [V(O sub2)j. The addition of the protonophore nigericin to the intact chloroplasts decreased F(PSII), but increased V(O sub2), and relative electron flux in PSII (F(PSII) * PFD and V(O sub2) were proportional to one another. F(PSII) * PFD at a given V(O sub2) was much higher in the presence of ApH than that in its absence. These effects of nigericin on the relationship between F(PSII) * PFD and V(O sub2) are consistent with those previously observed in thyl-akoid membranes, indicating the occurrence of CEF-PSII also in intact chloroplasts. In the presence of DpH, CEF-PSII accounted for the excess electron flux in PSII that could not be attributed to photosynthetic linear electron flow. The activity of CEF-PSII increased with increased light intensity and almost corresponded to that of the water-water cycle (WWC), implying that CEF-PSII can dissipate excess photon energy in cooperation with WWC to protect PSII from photoinhibition under limited photo-synthesis conditions"</abstract><cop>Japan</cop><pub>Oxford University Press</pub><pmid>12198198</pmid><doi>10.1093/pcp/pcf113</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0032-0781
ispartof Plant and cell physiology, 2002-08, Vol.43 (8), p.951-957
issn 0032-0781
1471-9053
language eng
recordid cdi_proquest_miscellaneous_72031131
source Oxford Journals Online
subjects a pH gradient across thylakoid membranes
AEF
alternative electron flow
APX
Asc
Asc peroxidase
ascorbate
BIOCHEMICAL PATHWAYS
CEF-PSII
Chlorophyll - metabolism
CHLOROPLASTS
Chloroplasts - drug effects
Chloroplasts - metabolism
Chloroplasts - radiation effects
cyclic electron flow within PSII
defined as (F′m–Fs)/F′m
defined as Fm/Fm′–1
Electron Transport - drug effects
Electron Transport - radiation effects
Fm
Fm after illumination
Hydrogen-Ion Concentration
Ionophores - pharmacology
Je(PSII)
Keywords: Alternative electron flow — Chloroplasts — Cyclic electron flow — Photoinhibition — PSII — Water–water cycle
LEAVES
Light
Light-Harvesting Protein Complexes
maximal yield of Chl fluorescence after dark adaptation
MDA
minimal Chl fluorescence after dark adaptation
monodehydroascorbate radical
Nigericin - pharmacology
non-photochemical quenching coefficient of Chl fluorescence
NPQ
Oxygen - metabolism
PCO cycle
PCR cycle
PFD
photorespiratory carbon-oxidation cycle
Photosynthesis - drug effects
Photosynthesis - physiology
Photosynthesis - radiation effects
photosynthetic carbon-reduction cycle
Photosynthetic Reaction Center Complex Proteins - drug effects
Photosynthetic Reaction Center Complex Proteins - metabolism
Photosynthetic Reaction Center Complex Proteins - radiation effects
photosynthetically active photon flux density
PHOTOSYSTEMS
Plant Leaves - drug effects
Plant Leaves - metabolism
Plant Leaves - radiation effects
plastoquinol
plastoquinone
PQH2
SOD
SPINACIA OLERACEA
Spinacia oleracea - drug effects
Spinacia oleracea - metabolism
Spinacia oleracea - radiation effects
superoxide dismutase
the electron flux in PSII
the molar ratio of PSII to PSI in thylakoid membranes
the quantum yield of electron transport in PSII at steady state
the rate of O2 uptake
the water–water cycle
V(O2)
Water - pharmacology
Water - physiology
WWC
yield of steady-state Chl fluorescence
ΔpH
Φ(PSII)
title Cyclic electron flow within PSII functions in intact chloroplasts from spinach [Spinacia oleracea] leaves
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