Kinetic correlation of recovery from photoinhibition and zeaxanthin epoxidation
The generation of non-photochemical fluorescence quenching under photoinhibitory illumination and its relaxation under subsequent low light illumination in leaves from intermittent-light-grown pea (Pisum sativum L.) plants (IML-plants) has been investigated. In parallel, we studied (i) the activity...
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Veröffentlicht in: | Planta 1996, Vol.198 (2), p.202-210 |
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description | The generation of non-photochemical fluorescence quenching under photoinhibitory illumination and its relaxation under subsequent low light illumination in leaves from intermittent-light-grown pea (Pisum sativum L.) plants (IML-plants) has been investigated. In parallel, we studied (i) the activity of the xanthophyll cycle with emphasis on zeaxanthin formation and reconversion to violaxanthin and (ii) the degradation rate of D1 protein. In comparison to control plants grown in continuous light, IML-plants were much more susceptible to photoinhibition as determined from the increase of slowly (halftimes > 20 min) relaxing quenching (qI) of variable chlorophyll fluorescence. The relaxation (recovery) kinetics of qI (under weak light) in both types of plant depended on the photon flux density, temperature and duration of pre-illumination. The recovery time generally increased with an increasing degree of qI. In IML-plants, relaxation of qI was kinetically closely related to the epoxidation of zeaxanthin. At high degrees of photosystem II inhibition the kinetics resembled those of D1 degradation. The results are discussed in terms of the mechanisms of photosystem II inactivation in vivo. |
doi_str_mv | 10.1007/BF00206245 |
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In parallel, we studied (i) the activity of the xanthophyll cycle with emphasis on zeaxanthin formation and reconversion to violaxanthin and (ii) the degradation rate of D1 protein. In comparison to control plants grown in continuous light, IML-plants were much more susceptible to photoinhibition as determined from the increase of slowly (halftimes > 20 min) relaxing quenching (qI) of variable chlorophyll fluorescence. The relaxation (recovery) kinetics of qI (under weak light) in both types of plant depended on the photon flux density, temperature and duration of pre-illumination. The recovery time generally increased with an increasing degree of qI. In IML-plants, relaxation of qI was kinetically closely related to the epoxidation of zeaxanthin. At high degrees of photosystem II inhibition the kinetics resembled those of D1 degradation. The results are discussed in terms of the mechanisms of photosystem II inactivation in vivo.</description><identifier>ISSN: 0032-0935</identifier><identifier>EISSN: 1432-2048</identifier><identifier>DOI: 10.1007/BF00206245</identifier><identifier>CODEN: PLANAB</identifier><language>eng</language><publisher>Berlin: Springer-Verlag</publisher><subject>Biological and medical sciences ; chlorophyll ; chlorophyll a/b binding protein ; Chlorophylls ; D1 protein ; Epoxidation ; Fluorescence ; Fundamental and applied biological sciences. Psychology ; Kinetics ; Leaves ; light ; light intensity ; lutein ; Metabolism ; Photoinhibition ; photoperiod ; Photosynthesis, respiration. Anabolism, catabolism ; photosystem II ; Pigments ; Pisum sativum ; Plant physiology and development ; Plants ; Xanthophylls</subject><ispartof>Planta, 1996, Vol.198 (2), p.202-210</ispartof><rights>Springer-Verlag 1996</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c304t-e7be8ff6e8ae7c4e7904cd1b4746d83c23eb302be2ffeda8b1b5d48220918333</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23384259$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23384259$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,4010,27900,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2965501$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jahns, P</creatorcontrib><creatorcontrib>Miehe, B</creatorcontrib><title>Kinetic correlation of recovery from photoinhibition and zeaxanthin epoxidation</title><title>Planta</title><description>The generation of non-photochemical fluorescence quenching under photoinhibitory illumination and its relaxation under subsequent low light illumination in leaves from intermittent-light-grown pea (Pisum sativum L.) plants (IML-plants) has been investigated. In parallel, we studied (i) the activity of the xanthophyll cycle with emphasis on zeaxanthin formation and reconversion to violaxanthin and (ii) the degradation rate of D1 protein. In comparison to control plants grown in continuous light, IML-plants were much more susceptible to photoinhibition as determined from the increase of slowly (halftimes > 20 min) relaxing quenching (qI) of variable chlorophyll fluorescence. The relaxation (recovery) kinetics of qI (under weak light) in both types of plant depended on the photon flux density, temperature and duration of pre-illumination. The recovery time generally increased with an increasing degree of qI. In IML-plants, relaxation of qI was kinetically closely related to the epoxidation of zeaxanthin. At high degrees of photosystem II inhibition the kinetics resembled those of D1 degradation. The results are discussed in terms of the mechanisms of photosystem II inactivation in vivo.</description><subject>Biological and medical sciences</subject><subject>chlorophyll</subject><subject>chlorophyll a/b binding protein</subject><subject>Chlorophylls</subject><subject>D1 protein</subject><subject>Epoxidation</subject><subject>Fluorescence</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kinetics</subject><subject>Leaves</subject><subject>light</subject><subject>light intensity</subject><subject>lutein</subject><subject>Metabolism</subject><subject>Photoinhibition</subject><subject>photoperiod</subject><subject>Photosynthesis, respiration. Anabolism, catabolism</subject><subject>photosystem II</subject><subject>Pigments</subject><subject>Pisum sativum</subject><subject>Plant physiology and development</subject><subject>Plants</subject><subject>Xanthophylls</subject><issn>0032-0935</issn><issn>1432-2048</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNpFkE1Lw0AQhhdRsFYv3sUcPAnR2Y8km6MWq2KhB-s5bDazdkubDbtBWn-9ayP2NAPP8w7DS8glhTsKUNw_TgEY5ExkR2REBWcpAyGPyQgg7lDy7JSchbACiLAoRmT-ZlvsrU608x7XqreuTZxJPGr3hX6XGO82Sbd0vbPt0tZ2L6i2Sb5RbVXbL22bYOe2ttlnz8mJUeuAF39zTBbTp8XkJZ3Nn18nD7NUcxB9ikWN0pgcpcJCCyxKELqhtShE3kiuGceaA6uRGYONkjWts0ZIxqCkknM-JrfDWe1dCB5N1Xm7UX5XUah-m6gOTUT5ZpA7FbRaG69abcN_gpV5lgGN2tWgrULv_AFzLgXLysivB26Uq9Snjyc-3lkMApN5KeJbP1wecZE</recordid><startdate>1996</startdate><enddate>1996</enddate><creator>Jahns, P</creator><creator>Miehe, B</creator><general>Springer-Verlag</general><general>Springer</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1996</creationdate><title>Kinetic correlation of recovery from photoinhibition and zeaxanthin epoxidation</title><author>Jahns, P ; Miehe, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c304t-e7be8ff6e8ae7c4e7904cd1b4746d83c23eb302be2ffeda8b1b5d48220918333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Biological and medical sciences</topic><topic>chlorophyll</topic><topic>chlorophyll a/b binding protein</topic><topic>Chlorophylls</topic><topic>D1 protein</topic><topic>Epoxidation</topic><topic>Fluorescence</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Kinetics</topic><topic>Leaves</topic><topic>light</topic><topic>light intensity</topic><topic>lutein</topic><topic>Metabolism</topic><topic>Photoinhibition</topic><topic>photoperiod</topic><topic>Photosynthesis, respiration. Anabolism, catabolism</topic><topic>photosystem II</topic><topic>Pigments</topic><topic>Pisum sativum</topic><topic>Plant physiology and development</topic><topic>Plants</topic><topic>Xanthophylls</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jahns, P</creatorcontrib><creatorcontrib>Miehe, B</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Planta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jahns, P</au><au>Miehe, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetic correlation of recovery from photoinhibition and zeaxanthin epoxidation</atitle><jtitle>Planta</jtitle><date>1996</date><risdate>1996</risdate><volume>198</volume><issue>2</issue><spage>202</spage><epage>210</epage><pages>202-210</pages><issn>0032-0935</issn><eissn>1432-2048</eissn><coden>PLANAB</coden><abstract>The generation of non-photochemical fluorescence quenching under photoinhibitory illumination and its relaxation under subsequent low light illumination in leaves from intermittent-light-grown pea (Pisum sativum L.) plants (IML-plants) has been investigated. In parallel, we studied (i) the activity of the xanthophyll cycle with emphasis on zeaxanthin formation and reconversion to violaxanthin and (ii) the degradation rate of D1 protein. In comparison to control plants grown in continuous light, IML-plants were much more susceptible to photoinhibition as determined from the increase of slowly (halftimes > 20 min) relaxing quenching (qI) of variable chlorophyll fluorescence. The relaxation (recovery) kinetics of qI (under weak light) in both types of plant depended on the photon flux density, temperature and duration of pre-illumination. The recovery time generally increased with an increasing degree of qI. In IML-plants, relaxation of qI was kinetically closely related to the epoxidation of zeaxanthin. At high degrees of photosystem II inhibition the kinetics resembled those of D1 degradation. The results are discussed in terms of the mechanisms of photosystem II inactivation in vivo.</abstract><cop>Berlin</cop><pub>Springer-Verlag</pub><doi>10.1007/BF00206245</doi><tpages>9</tpages></addata></record> |
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subjects | Biological and medical sciences chlorophyll chlorophyll a/b binding protein Chlorophylls D1 protein Epoxidation Fluorescence Fundamental and applied biological sciences. Psychology Kinetics Leaves light light intensity lutein Metabolism Photoinhibition photoperiod Photosynthesis, respiration. Anabolism, catabolism photosystem II Pigments Pisum sativum Plant physiology and development Plants Xanthophylls |
title | Kinetic correlation of recovery from photoinhibition and zeaxanthin epoxidation |
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