Systems Analysis of the Response of Photosynthesis, Metabolism, and Growth to an Increase in Irradiance in the Photosynthetic Model Organism Chlamydomonas reinhardtii
We investigated the systems response of metabolism and growth after an increase in irradiance in the nonsaturating range in the algal model Chlamydomonas reinhardtii. In a three-step process, photosynthesis and the levels of metabolites increased immediately, growth increased after 10 to 15 min, and...
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creator | Mettler, Tabea Mühlhaus, Timo Hemme, Dorothea Schöttler, Mark-Aurel Rupprecht, Jens Idoine, Adam Veyel, Daniel Pal, Sunil Kumar Yaneva-Roder, Liliya Winck, Flavia Vischi Sommer, Frederik Vosloh, Daniel Seiwert, Bettina Erban, Alexander Burgos, Asdrubal Arvidsson, Samuel Schönfelder, Stephanie Arnold, Anne Günther, Manuela Krause, Ursula Lohse, Marc Kopka, Joachim Nikoloski, Zoran Mueller-Roeber, Bernd Willmitzer, Lothar Bock, Ralph Schroda, Michael Stitt, Mark |
description | We investigated the systems response of metabolism and growth after an increase in irradiance in the nonsaturating range in the algal model Chlamydomonas reinhardtii. In a three-step process, photosynthesis and the levels of metabolites increased immediately, growth increased after 10 to 15 min, and transcript and protein abundance responded by 40 and 120 to 240 min, respectively. In the first phase, starch and metabolites provided a transient buffer for carbon until growth increased. This uncouples photosynthesis from growth in a fluctuating light environment. In the first and second phases, rising metabolite levels and increased polysome loading drove an increase in fluxes. Most Calvin-Benson cycle (CBC) enzymes were substrate-limited in vivo, and strikingly, many were present at higher concentrations than their substrates, explaining how rising metabolite levels stimulate CBC flux. Rubisco, fructose-1,6-biosphosphatase, and seduheptulose-1,7-bisphosphatase were close to substrate saturation in vivo, and flux was increased by posttranslational activation. In the third phase, changes in abundance of particular proteins, including increases in plastidial ATP synthase and some CBC enzymes, relieved potential bottlenecks and readjusted protein allocation between different processes. Despite reasonable overall agreement between changes in transcript and protein abundance (R² = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance. |
doi_str_mv | 10.1105/tpc.114.124537 |
format | Article |
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In a three-step process, photosynthesis and the levels of metabolites increased immediately, growth increased after 10 to 15 min, and transcript and protein abundance responded by 40 and 120 to 240 min, respectively. In the first phase, starch and metabolites provided a transient buffer for carbon until growth increased. This uncouples photosynthesis from growth in a fluctuating light environment. In the first and second phases, rising metabolite levels and increased polysome loading drove an increase in fluxes. Most Calvin-Benson cycle (CBC) enzymes were substrate-limited in vivo, and strikingly, many were present at higher concentrations than their substrates, explaining how rising metabolite levels stimulate CBC flux. Rubisco, fructose-1,6-biosphosphatase, and seduheptulose-1,7-bisphosphatase were close to substrate saturation in vivo, and flux was increased by posttranslational activation. In the third phase, changes in abundance of particular proteins, including increases in plastidial ATP synthase and some CBC enzymes, relieved potential bottlenecks and readjusted protein allocation between different processes. Despite reasonable overall agreement between changes in transcript and protein abundance (R² = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance.</description><identifier>ISSN: 1040-4651</identifier><identifier>EISSN: 1532-298X</identifier><identifier>DOI: 10.1105/tpc.114.124537</identifier><identifier>PMID: 24894045</identifier><language>eng</language><publisher>England: American Society of Plant Biologists</publisher><subject>Bioreactors ; carbon dioxide fixation ; Chlamydomonas reinhardtii ; Enzyme substrates ; Enzymes ; Large-Scale Biology ; LARGE-SCALE BIOLOGY ARTICLE ; light intensity ; Luminous intensity ; metabolites ; Photons ; Photosynthesis ; Plant cells ; Plants ; Protein metabolism ; Starches ; systems analysis</subject><ispartof>The Plant cell, 2014-06, Vol.26 (6), p.2310-2350</ispartof><rights>2014 American Society of Plant Biologists</rights><rights>2014 American Society of Plant Biologists. All rights reserved.</rights><rights>2014 American Society of Plant Biologists. All rights reserved. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-303a5cfd8ea582ed9a6e5b5d1713562dc4960df02f91b077f743c0f009b81e993</citedby><cites>FETCH-LOGICAL-c405t-303a5cfd8ea582ed9a6e5b5d1713562dc4960df02f91b077f743c0f009b81e993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43190684$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43190684$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24894045$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mettler, Tabea</creatorcontrib><creatorcontrib>Mühlhaus, Timo</creatorcontrib><creatorcontrib>Hemme, Dorothea</creatorcontrib><creatorcontrib>Schöttler, Mark-Aurel</creatorcontrib><creatorcontrib>Rupprecht, Jens</creatorcontrib><creatorcontrib>Idoine, Adam</creatorcontrib><creatorcontrib>Veyel, Daniel</creatorcontrib><creatorcontrib>Pal, Sunil Kumar</creatorcontrib><creatorcontrib>Yaneva-Roder, Liliya</creatorcontrib><creatorcontrib>Winck, Flavia Vischi</creatorcontrib><creatorcontrib>Sommer, Frederik</creatorcontrib><creatorcontrib>Vosloh, Daniel</creatorcontrib><creatorcontrib>Seiwert, Bettina</creatorcontrib><creatorcontrib>Erban, Alexander</creatorcontrib><creatorcontrib>Burgos, Asdrubal</creatorcontrib><creatorcontrib>Arvidsson, Samuel</creatorcontrib><creatorcontrib>Schönfelder, Stephanie</creatorcontrib><creatorcontrib>Arnold, Anne</creatorcontrib><creatorcontrib>Günther, Manuela</creatorcontrib><creatorcontrib>Krause, Ursula</creatorcontrib><creatorcontrib>Lohse, Marc</creatorcontrib><creatorcontrib>Kopka, Joachim</creatorcontrib><creatorcontrib>Nikoloski, Zoran</creatorcontrib><creatorcontrib>Mueller-Roeber, Bernd</creatorcontrib><creatorcontrib>Willmitzer, Lothar</creatorcontrib><creatorcontrib>Bock, Ralph</creatorcontrib><creatorcontrib>Schroda, Michael</creatorcontrib><creatorcontrib>Stitt, Mark</creatorcontrib><title>Systems Analysis of the Response of Photosynthesis, Metabolism, and Growth to an Increase in Irradiance in the Photosynthetic Model Organism Chlamydomonas reinhardtii</title><title>The Plant cell</title><addtitle>Plant Cell</addtitle><description>We investigated the systems response of metabolism and growth after an increase in irradiance in the nonsaturating range in the algal model Chlamydomonas reinhardtii. 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In the third phase, changes in abundance of particular proteins, including increases in plastidial ATP synthase and some CBC enzymes, relieved potential bottlenecks and readjusted protein allocation between different processes. Despite reasonable overall agreement between changes in transcript and protein abundance (R² = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance.</description><subject>Bioreactors</subject><subject>carbon dioxide fixation</subject><subject>Chlamydomonas reinhardtii</subject><subject>Enzyme substrates</subject><subject>Enzymes</subject><subject>Large-Scale Biology</subject><subject>LARGE-SCALE BIOLOGY ARTICLE</subject><subject>light intensity</subject><subject>Luminous intensity</subject><subject>metabolites</subject><subject>Photons</subject><subject>Photosynthesis</subject><subject>Plant cells</subject><subject>Plants</subject><subject>Protein metabolism</subject><subject>Starches</subject><subject>systems analysis</subject><issn>1040-4651</issn><issn>1532-298X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFUk1v1DAQjRCIlsKVG8hHDs3izyS-IFUrKJVaFfEhcbO89qRxldhb2wvKH-J34rBlVU6c_Mbz5mlG71XVS4JXhGDxNm9NAXxFKBesfVQdE8FoTWX3_XHBmOOaN4IcVc9SusUYk5bIp9UR5Z3kmIvj6teXOWWYEjrzepyTSyj0KA-APkPaBp9gqT8NIYc0-_JfGKfoCrLehNGl6RRpb9F5DD_zgHIoFbrwJoIug67gGLV12ps_1SL7QCo7g66ChRFdxxvtixpaD6OeZhum4HVCEZwfdLTZuefVk16PCV7cvyfVtw_vv64_1pfX5xfrs8vacCxyzTDTwvS2Ay06ClbqBsRG2HI2Ew21hssG2x7TXpINbtu-5czgHmO56QhIyU6qd3vd7W4zgTXgc9Sj2kY36TiroJ36t-PdoG7CD8WLCZK1ReDNvUAMdztIWU0uGRhH7SHskqKLCV1xi_6XSjraCMkpXdZa7akmhpQi9IeNCFZLDlTJQQFc7XNQBl4_vONA_2t8IbzaE25TDvHQ54xI3HSc_QZnobxL</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Mettler, Tabea</creator><creator>Mühlhaus, Timo</creator><creator>Hemme, Dorothea</creator><creator>Schöttler, Mark-Aurel</creator><creator>Rupprecht, Jens</creator><creator>Idoine, Adam</creator><creator>Veyel, Daniel</creator><creator>Pal, Sunil Kumar</creator><creator>Yaneva-Roder, Liliya</creator><creator>Winck, Flavia Vischi</creator><creator>Sommer, Frederik</creator><creator>Vosloh, Daniel</creator><creator>Seiwert, Bettina</creator><creator>Erban, Alexander</creator><creator>Burgos, Asdrubal</creator><creator>Arvidsson, Samuel</creator><creator>Schönfelder, Stephanie</creator><creator>Arnold, Anne</creator><creator>Günther, Manuela</creator><creator>Krause, Ursula</creator><creator>Lohse, Marc</creator><creator>Kopka, Joachim</creator><creator>Nikoloski, Zoran</creator><creator>Mueller-Roeber, Bernd</creator><creator>Willmitzer, Lothar</creator><creator>Bock, Ralph</creator><creator>Schroda, Michael</creator><creator>Stitt, Mark</creator><general>American Society of Plant Biologists</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20140601</creationdate><title>Systems Analysis of the Response of Photosynthesis, Metabolism, and Growth to an Increase in Irradiance in the Photosynthetic Model Organism Chlamydomonas reinhardtii</title><author>Mettler, Tabea ; 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In a three-step process, photosynthesis and the levels of metabolites increased immediately, growth increased after 10 to 15 min, and transcript and protein abundance responded by 40 and 120 to 240 min, respectively. In the first phase, starch and metabolites provided a transient buffer for carbon until growth increased. This uncouples photosynthesis from growth in a fluctuating light environment. In the first and second phases, rising metabolite levels and increased polysome loading drove an increase in fluxes. Most Calvin-Benson cycle (CBC) enzymes were substrate-limited in vivo, and strikingly, many were present at higher concentrations than their substrates, explaining how rising metabolite levels stimulate CBC flux. Rubisco, fructose-1,6-biosphosphatase, and seduheptulose-1,7-bisphosphatase were close to substrate saturation in vivo, and flux was increased by posttranslational activation. In the third phase, changes in abundance of particular proteins, including increases in plastidial ATP synthase and some CBC enzymes, relieved potential bottlenecks and readjusted protein allocation between different processes. Despite reasonable overall agreement between changes in transcript and protein abundance (R² = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance.</abstract><cop>England</cop><pub>American Society of Plant Biologists</pub><pmid>24894045</pmid><doi>10.1105/tpc.114.124537</doi><tpages>41</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bioreactors carbon dioxide fixation Chlamydomonas reinhardtii Enzyme substrates Enzymes Large-Scale Biology LARGE-SCALE BIOLOGY ARTICLE light intensity Luminous intensity metabolites Photons Photosynthesis Plant cells Plants Protein metabolism Starches systems analysis |
title | Systems Analysis of the Response of Photosynthesis, Metabolism, and Growth to an Increase in Irradiance in the Photosynthetic Model Organism Chlamydomonas reinhardtii |
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