Localization of photophosphorylation and proton transport activities in various regions of the chloroplast lamellae
Identifieur interne : 000222 ( Istex/Corpus ); précédent : 000221; suivant : 000223Localization of photophosphorylation and proton transport activities in various regions of the chloroplast lamellae
Auteurs : C. J. Arntzen ; R. A. Dilley ; J. NeumannSource :
- BBA - Bioenergetics [ 0005-2728 ] ; 1971.
English descriptors
Abstract
Membrane fragments released by French pressure cell treatment of whole chloroplasts and isolated by differential centrifugation have been characterized structurally and with respect to phosophorylating and proton transport activities. In agreement with results of other workers, the heavy fraction released by pressure treatment was found by electron microscopy studies to be made up of mostly intact grana stacks while the light fraction was comprised of vesicles derived from the stromal lamellae. Both fractions were found to carry out rapid rates of cyclic photophosphorylation catalyzed by phenazine methosulfate (PMS). However, only the grana membranes demonstrated active proton accumulation in the presence of PMS. No light induced H+ uptake could be detected in the stromal lamellae fraction; and as expected, proton gradient dissipating agents such as NH4Cl, nigericin in the presence of K+, and gramicidin were only slightly inhibitory to phosphorylation at concentrations which were very inhibitory in the grana membrane fraction.Further evidence that stromal lamellae do not have active proton transport in the intact chloroplast was obtained by comparing various chloroplasts having different amounts of stromal and grana membranes. Comparative studies on young and old chloroplasts from lettuce, mesophyll and bundle sheath cell plastids from sorghum, and greening plastids from etiolated corn seedlings revealed a direct correlation between the extent of grana formation and the amount of proton transport activity. Samples which had larger amounts of stromal lamellae had high rates of ATP formation but a reduced capacity for H+ accumulation.
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DOI: 10.1016/0005-2728(71)90159-9
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In agreement with results of other workers, the heavy fraction released by pressure treatment was found by electron microscopy studies to be made up of mostly intact grana stacks while the light fraction was comprised of vesicles derived from the stromal lamellae. Both fractions were found to carry out rapid rates of cyclic photophosphorylation catalyzed by phenazine methosulfate (PMS). However, only the grana membranes demonstrated active proton accumulation in the presence of PMS. No light induced H+ uptake could be detected in the stromal lamellae fraction; and as expected, proton gradient dissipating agents such as NH4Cl, nigericin in the presence of K+, and gramicidin were only slightly inhibitory to phosphorylation at concentrations which were very inhibitory in the grana membrane fraction.Further evidence that stromal lamellae do not have active proton transport in the intact chloroplast was obtained by comparing various chloroplasts having different amounts of stromal and grana membranes. Comparative studies on young and old chloroplasts from lettuce, mesophyll and bundle sheath cell plastids from sorghum, and greening plastids from etiolated corn seedlings revealed a direct correlation between the extent of grana formation and the amount of proton transport activity. Samples which had larger amounts of stromal lamellae had high rates of ATP formation but a reduced capacity for H+ accumulation.</div></front></TEI><istex><corpusName>elsevier</corpusName><author><json:item><name>C.J. Arntzen</name><affiliations><json:string>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</json:string></affiliations></json:item><json:item><name>R.A. Dilley</name><affiliations><json:string>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</json:string></affiliations></json:item><json:item><name>J. Neumann</name><affiliations><json:string>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>DCIP : 2,6-dichlorophenolindophenol</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>CCCP : m-chlorocyanocarbonyl phenylhydrazone</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>PMS : phenazine methosulfate</value></json:item></subject><articleId><json:string>71901599</json:string></articleId><language><json:string>eng</json:string></language><abstract>Membrane fragments released by French pressure cell treatment of whole chloroplasts and isolated by differential centrifugation have been characterized structurally and with respect to phosophorylating and proton transport activities. In agreement with results of other workers, the heavy fraction released by pressure treatment was found by electron microscopy studies to be made up of mostly intact grana stacks while the light fraction was comprised of vesicles derived from the stromal lamellae. Both fractions were found to carry out rapid rates of cyclic photophosphorylation catalyzed by phenazine methosulfate (PMS). However, only the grana membranes demonstrated active proton accumulation in the presence of PMS. No light induced H+ uptake could be detected in the stromal lamellae fraction; and as expected, proton gradient dissipating agents such as NH4Cl, nigericin in the presence of K+, and gramicidin were only slightly inhibitory to phosphorylation at concentrations which were very inhibitory in the grana membrane fraction.Further evidence that stromal lamellae do not have active proton transport in the intact chloroplast was obtained by comparing various chloroplasts having different amounts of stromal and grana membranes. Comparative studies on young and old chloroplasts from lettuce, mesophyll and bundle sheath cell plastids from sorghum, and greening plastids from etiolated corn seedlings revealed a direct correlation between the extent of grana formation and the amount of proton transport activity. 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F. Kettering Research Laboratory.</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Localization of photophosphorylation and proton transport activities in various regions of the chloroplast lamellae</title><author><persName><forename type="first">C.J.</forename><surname>Arntzen</surname></persName><note type="biography">Present address: Department of Botany, University of Illinois, Urbana, Ill., U.S.A.</note><affiliation>Present address: Department of Botany, University of Illinois, Urbana, Ill., U.S.A.</affiliation><affiliation>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</affiliation></author><author><persName><forename type="first">R.A.</forename><surname>Dilley</surname></persName><affiliation>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</affiliation></author><author><persName><forename type="first">J.</forename><surname>Neumann</surname></persName><note type="biography">Present address: Department of Botany, University of Tel-Aviv, Tel-Aviv, Israel.</note><affiliation>Present address: Department of Botany, University of Tel-Aviv, Tel-Aviv, Israel.</affiliation><affiliation>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</affiliation></author></analytic><monogr><title level="j">BBA - Bioenergetics</title><title level="j" type="abbrev">BBABIO</title><idno type="pISSN">0005-2728</idno><idno type="PII">S0005-2728(00)X0155-7</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1971"></date><biblScope unit="volume">245</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="409">409</biblScope><biblScope unit="page" to="424">424</biblScope></imprint></monogr><idno type="istex">A0893BA5FC98B631B6CEF0C7DF8E5A3CB817F5CA</idno><idno type="DOI">10.1016/0005-2728(71)90159-9</idno><idno type="PII">0005-2728(71)90159-9</idno><idno type="ArticleID">71901599</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1971</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Membrane fragments released by French pressure cell treatment of whole chloroplasts and isolated by differential centrifugation have been characterized structurally and with respect to phosophorylating and proton transport activities. In agreement with results of other workers, the heavy fraction released by pressure treatment was found by electron microscopy studies to be made up of mostly intact grana stacks while the light fraction was comprised of vesicles derived from the stromal lamellae. Both fractions were found to carry out rapid rates of cyclic photophosphorylation catalyzed by phenazine methosulfate (PMS). However, only the grana membranes demonstrated active proton accumulation in the presence of PMS. No light induced H+ uptake could be detected in the stromal lamellae fraction; and as expected, proton gradient dissipating agents such as NH4Cl, nigericin in the presence of K+, and gramicidin were only slightly inhibitory to phosphorylation at concentrations which were very inhibitory in the grana membrane fraction.Further evidence that stromal lamellae do not have active proton transport in the intact chloroplast was obtained by comparing various chloroplasts having different amounts of stromal and grana membranes. Comparative studies on young and old chloroplasts from lettuce, mesophyll and bundle sheath cell plastids from sorghum, and greening plastids from etiolated corn seedlings revealed a direct correlation between the extent of grana formation and the amount of proton transport activity. Samples which had larger amounts of stromal lamellae had high rates of ATP formation but a reduced capacity for H+ accumulation.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Abbreviations</head><item><term>DCIP</term><term>2,6-dichlorophenolindophenol</term></item><item><term>CCCP</term><term>m-chlorocyanocarbonyl phenylhydrazone</term></item><item><term>PMS</term><term>phenazine methosulfate</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1971-02-26">Received</change><change when="1971">Published</change></revisionDesc></teiHeader></istex:fulltextTEI></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="UTF-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla" xml:lang="en"><item-info><jid>BBABIO</jid><aid>71901599</aid><ce:pii>0005-2728(71)90159-9</ce:pii><ce:doi>10.1016/0005-2728(71)90159-9</ce:doi><ce:copyright type="unknown" year="1971"></ce:copyright></item-info><head><ce:article-footnote><ce:label>☆</ce:label><ce:note-para>Contribution No. 440 from the C. F. Kettering Research Laboratory.</ce:note-para></ce:article-footnote><ce:title>Localization of photophosphorylation and proton transport activities in various regions of the chloroplast lamellae</ce:title><ce:author-group><ce:author><ce:given-name>C.J.</ce:given-name><ce:surname>Arntzen</ce:surname><ce:cross-ref refid="FN1"><ce:sup loc="post">∗∗</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>R.A.</ce:given-name><ce:surname>Dilley</ce:surname></ce:author><ce:author><ce:given-name>J.</ce:given-name><ce:surname>Neumann</ce:surname><ce:cross-ref refid="FN2"><ce:sup loc="post">∗∗∗</ce:sup></ce:cross-ref></ce:author><ce:affiliation><ce:textfn>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</ce:textfn></ce:affiliation><ce:footnote id="FN1"><ce:label>∗∗</ce:label><ce:note-para>Present address: Department of Botany, University of Illinois, Urbana, Ill., U.S.A.</ce:note-para></ce:footnote><ce:footnote id="FN2"><ce:label>∗∗∗</ce:label><ce:note-para>Present address: Department of Botany, University of Tel-Aviv, Tel-Aviv, Israel.</ce:note-para></ce:footnote></ce:author-group><ce:date-received day="26" month="2" year="1971"></ce:date-received><ce:abstract class="author"><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para view="all" id="simple-para.0010">Membrane fragments released by French pressure cell treatment of whole chloroplasts and isolated by differential centrifugation have been characterized structurally and with respect to phosophorylating and proton transport activities. In agreement with results of other workers, the heavy fraction released by pressure treatment was found by electron microscopy studies to be made up of mostly intact grana stacks while the light fraction was comprised of vesicles derived from the stromal lamellae. Both fractions were found to carry out rapid rates of cyclic photophosphorylation catalyzed by phenazine methosulfate (PMS). However, only the grana membranes demonstrated active proton accumulation in the presence of PMS. No light induced H<ce:sup loc="post">+</ce:sup> uptake could be detected in the stromal lamellae fraction; and as expected, proton gradient dissipating agents such as NH<ce:inf loc="post">4</ce:inf>Cl, nigericin in the presence of K<ce:sup loc="post">+</ce:sup>, and gramicidin were only slightly inhibitory to phosphorylation at concentrations which were very inhibitory in the grana membrane fraction.</ce:simple-para><ce:simple-para view="all" id="simple-para.0015">Further evidence that stromal lamellae do not have active proton transport in the intact chloroplast was obtained by comparing various chloroplasts having different amounts of stromal and grana membranes. Comparative studies on young and old chloroplasts from lettuce, mesophyll and bundle sheath cell plastids from sorghum, and greening plastids from etiolated corn seedlings revealed a direct correlation between the extent of grana formation and the amount of proton transport activity. Samples which had larger amounts of stromal lamellae had high rates of ATP formation but a reduced capacity for H<ce:sup loc="post">+</ce:sup> accumulation.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:keywords class="abr"><ce:section-title>Abbreviations</ce:section-title><ce:keyword><ce:text>DCIP</ce:text><ce:keyword><ce:text>2,6-dichlorophenolindophenol</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>CCCP</ce:text><ce:keyword><ce:text><ce:italic>m</ce:italic>-chlorocyanocarbonyl phenylhydrazone</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>PMS</ce:text><ce:keyword><ce:text>phenazine methosulfate</ce:text></ce:keyword></ce:keyword></ce:keywords></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Localization of photophosphorylation and proton transport activities in various regions of the chloroplast lamellae</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>Localization of photophosphorylation and proton transport activities in various regions of the chloroplast lamellae</title></titleInfo><name type="personal"><namePart type="given">C.J.</namePart><namePart type="family">Arntzen</namePart><affiliation>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</affiliation><description>Present address: Department of Botany, University of Illinois, Urbana, Ill., U.S.A.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R.A.</namePart><namePart type="family">Dilley</namePart><affiliation>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J.</namePart><namePart type="family">Neumann</namePart><affiliation>C. F. Kettering Research Laboratory, Yellow Springs, Ohio 45387 U.S.A.</affiliation><description>Present address: Department of Botany, University of Tel-Aviv, Tel-Aviv, Israel.</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article"></genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1971</dateIssued><dateCaptured encoding="w3cdtf">1971-02-26</dateCaptured><copyrightDate encoding="w3cdtf">1971</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Membrane fragments released by French pressure cell treatment of whole chloroplasts and isolated by differential centrifugation have been characterized structurally and with respect to phosophorylating and proton transport activities. In agreement with results of other workers, the heavy fraction released by pressure treatment was found by electron microscopy studies to be made up of mostly intact grana stacks while the light fraction was comprised of vesicles derived from the stromal lamellae. Both fractions were found to carry out rapid rates of cyclic photophosphorylation catalyzed by phenazine methosulfate (PMS). However, only the grana membranes demonstrated active proton accumulation in the presence of PMS. No light induced H+ uptake could be detected in the stromal lamellae fraction; and as expected, proton gradient dissipating agents such as NH4Cl, nigericin in the presence of K+, and gramicidin were only slightly inhibitory to phosphorylation at concentrations which were very inhibitory in the grana membrane fraction.Further evidence that stromal lamellae do not have active proton transport in the intact chloroplast was obtained by comparing various chloroplasts having different amounts of stromal and grana membranes. Comparative studies on young and old chloroplasts from lettuce, mesophyll and bundle sheath cell plastids from sorghum, and greening plastids from etiolated corn seedlings revealed a direct correlation between the extent of grana formation and the amount of proton transport activity. Samples which had larger amounts of stromal lamellae had high rates of ATP formation but a reduced capacity for H+ accumulation.</abstract><note>Contribution No. 440 from the C. F. Kettering Research Laboratory.</note><subject lang="en"><genre>Abbreviations</genre><topic>DCIP : 2,6-dichlorophenolindophenol</topic><topic>CCCP : m-chlorocyanocarbonyl phenylhydrazone</topic><topic>PMS : phenazine methosulfate</topic></subject><relatedItem type="host"><titleInfo><title>BBA - Bioenergetics</title></titleInfo><titleInfo type="abbreviated"><title>BBABIO</title></titleInfo><genre type="Journal">journal</genre><originInfo><dateIssued encoding="w3cdtf">19710907</dateIssued></originInfo><identifier type="ISSN">0005-2728</identifier><identifier type="PII">S0005-2728(00)X0155-7</identifier><part><date>19710907</date><detail type="volume"><number>245</number><caption>vol.</caption></detail><detail type="issue"><number>2</number><caption>no.</caption></detail><extent unit="issue pages"><start>263</start><end>516</end></extent><extent unit="pages"><start>409</start><end>424</end></extent></part></relatedItem><identifier type="istex">A0893BA5FC98B631B6CEF0C7DF8E5A3CB817F5CA</identifier><identifier type="DOI">10.1016/0005-2728(71)90159-9</identifier><identifier type="PII">0005-2728(71)90159-9</identifier><identifier type="ArticleID">71901599</identifier><recordInfo><recordContentSource>ELSEVIER</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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