Distribution of the extrinsic proteins as a potential marker for the evolution of photosynthetic oxygen‐evolving photosystem II
Distribution of photosystem II (PSII) extrinsic proteins was examined using antibodies raised against various extrinsic proteins from different sources. The results showed that a glaucophyte (Cyanophora paradoxa) having the most primitive plastids contained the cyanobacterial‐type extrinsic proteins...
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description | Distribution of photosystem II (PSII) extrinsic proteins was examined using antibodies raised against various extrinsic proteins from different sources. The results showed that a glaucophyte (Cyanophora paradoxa) having the most primitive plastids contained the cyanobacterial‐type extrinsic proteins (PsbO, PsbV, PsbU), and the primitive red algae (Cyanidium caldarium) contained the red algal‐type extrinsic proteins (PsO, PsbQ′, PsbV, PsbU), whereas a prasinophyte (Pyraminonas parkeae), which is one of the most primitive green algae, contained the green algal‐type ones (PsbO, PsbP, PsbQ). These suggest that the extrinsic proteins had been diverged into cyanobacterial‐, red algal‐ and green algal‐types during early phases of evolution after a primary endosymbiosis. This study also showed that a haptophyte, diatoms and brown algae, which resulted from red algal secondary endosymbiosis, contained the red algal‐type, whereas Euglena gracilis resulted from green algal secondary endosymbiosis contained the green algal‐type extrinsic proteins, suggesting that the red algal‐ and green algal‐type extrinsic proteins have been retained unchanged in the different lines of organisms following the secondary endosymbiosis. Based on these immunological analyses, together with the current genome data, the evolution of photosynthetic oxygen‐evolving PSII was discussed from a view of distribution of the extrinsic proteins, and a new model for the evolution of the PSII extrinsic proteins was proposed. |
doi_str_mv | 10.1111/j.1742-4658.2005.04912.x |
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The results showed that a glaucophyte (Cyanophora paradoxa) having the most primitive plastids contained the cyanobacterial‐type extrinsic proteins (PsbO, PsbV, PsbU), and the primitive red algae (Cyanidium caldarium) contained the red algal‐type extrinsic proteins (PsO, PsbQ′, PsbV, PsbU), whereas a prasinophyte (Pyraminonas parkeae), which is one of the most primitive green algae, contained the green algal‐type ones (PsbO, PsbP, PsbQ). These suggest that the extrinsic proteins had been diverged into cyanobacterial‐, red algal‐ and green algal‐types during early phases of evolution after a primary endosymbiosis. This study also showed that a haptophyte, diatoms and brown algae, which resulted from red algal secondary endosymbiosis, contained the red algal‐type, whereas Euglena gracilis resulted from green algal secondary endosymbiosis contained the green algal‐type extrinsic proteins, suggesting that the red algal‐ and green algal‐type extrinsic proteins have been retained unchanged in the different lines of organisms following the secondary endosymbiosis. Based on these immunological analyses, together with the current genome data, the evolution of photosynthetic oxygen‐evolving PSII was discussed from a view of distribution of the extrinsic proteins, and a new model for the evolution of the PSII extrinsic proteins was proposed.</description><identifier>ISSN: 1742-464X</identifier><identifier>EISSN: 1742-4658</identifier><identifier>DOI: 10.1111/j.1742-4658.2005.04912.x</identifier><identifier>PMID: 16176274</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Algae ; Antibodies - immunology ; Bacillariophyceae ; Biological Evolution ; Biomarkers ; Cyanidium caldarium ; Cyanophora - metabolism ; Cyanophora paradoxa ; Euglena gracilis ; evolution ; Evolutionary biology ; immunological assay ; Immunology ; Oxygen ; Oxygen - metabolism ; oxygen evolution ; Photosynthesis ; photosystem II ; Photosystem II Protein Complex - metabolism ; Proteins ; PSII extrinsic proteins ; Rhodophyta - metabolism ; Spinacia oleracea - metabolism</subject><ispartof>The FEBS journal, 2005-10, Vol.272 (19), p.5020-5030</ispartof><rights>2005 FEBS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5422-b367c248b222d912c49b431b8439a0e33ef6e56ee26816326c8cbb36b8b443193</citedby><cites>FETCH-LOGICAL-c5422-b367c248b222d912c49b431b8439a0e33ef6e56ee26816326c8cbb36b8b443193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1742-4658.2005.04912.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1742-4658.2005.04912.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16176274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Enami, Isao</creatorcontrib><creatorcontrib>Suzuki, Takehiro</creatorcontrib><creatorcontrib>Tada, Osamu</creatorcontrib><creatorcontrib>Nakada, Yoshiko</creatorcontrib><creatorcontrib>Nakamura, Kumi</creatorcontrib><creatorcontrib>Tohri, Akihiko</creatorcontrib><creatorcontrib>Ohta, Hisataka</creatorcontrib><creatorcontrib>Inoue, Isao</creatorcontrib><creatorcontrib>Shen, Jian‐Ren</creatorcontrib><title>Distribution of the extrinsic proteins as a potential marker for the evolution of photosynthetic oxygen‐evolving photosystem II</title><title>The FEBS journal</title><addtitle>FEBS J</addtitle><description>Distribution of photosystem II (PSII) extrinsic proteins was examined using antibodies raised against various extrinsic proteins from different sources. The results showed that a glaucophyte (Cyanophora paradoxa) having the most primitive plastids contained the cyanobacterial‐type extrinsic proteins (PsbO, PsbV, PsbU), and the primitive red algae (Cyanidium caldarium) contained the red algal‐type extrinsic proteins (PsO, PsbQ′, PsbV, PsbU), whereas a prasinophyte (Pyraminonas parkeae), which is one of the most primitive green algae, contained the green algal‐type ones (PsbO, PsbP, PsbQ). These suggest that the extrinsic proteins had been diverged into cyanobacterial‐, red algal‐ and green algal‐types during early phases of evolution after a primary endosymbiosis. This study also showed that a haptophyte, diatoms and brown algae, which resulted from red algal secondary endosymbiosis, contained the red algal‐type, whereas Euglena gracilis resulted from green algal secondary endosymbiosis contained the green algal‐type extrinsic proteins, suggesting that the red algal‐ and green algal‐type extrinsic proteins have been retained unchanged in the different lines of organisms following the secondary endosymbiosis. Based on these immunological analyses, together with the current genome data, the evolution of photosynthetic oxygen‐evolving PSII was discussed from a view of distribution of the extrinsic proteins, and a new model for the evolution of the PSII extrinsic proteins was proposed.</description><subject>Algae</subject><subject>Antibodies - immunology</subject><subject>Bacillariophyceae</subject><subject>Biological Evolution</subject><subject>Biomarkers</subject><subject>Cyanidium caldarium</subject><subject>Cyanophora - metabolism</subject><subject>Cyanophora paradoxa</subject><subject>Euglena gracilis</subject><subject>evolution</subject><subject>Evolutionary biology</subject><subject>immunological assay</subject><subject>Immunology</subject><subject>Oxygen</subject><subject>Oxygen - metabolism</subject><subject>oxygen evolution</subject><subject>Photosynthesis</subject><subject>photosystem II</subject><subject>Photosystem II Protein Complex - metabolism</subject><subject>Proteins</subject><subject>PSII extrinsic proteins</subject><subject>Rhodophyta - metabolism</subject><subject>Spinacia oleracea - metabolism</subject><issn>1742-464X</issn><issn>1742-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS1ERUvhFZDFgt0E_8VxNkhQWjpSpS4AiZ0Vpzeth0w82E6Z2dE36DPyJL1hhkFiA5YlX9vfOdK9hxDKWcFxvV4UvFJipnRpCsFYWTBVc1GsH5Gj_cfjfa2-HJKnKS0Yk6Wq6yfkkGteaVGpI3L33qccvRuzDwMNHc03QGGNT0PyLV3FkAFL2uCmK7wM2Tc9XTbxK0TahbgV3IZ-77C6CTmkzYAfGS3CenMNw88f9xN064fr30DKsKTz-TNy0DV9gue785h8Pjv9dHI-u7j8MD95ezFrSyXEzEldtUIZJ4S4wmZbVTsluTNK1g0DKaHTUGoAoQ3XUujWtA5FzjiFXC2PyautL_b0bYSU7dKnFvq-GSCMyWqjWa2M-CeIU1W8VhLBl3-BizDGAZuwginOKsEnN7OF2hhSitDZVfQ4vo3lzE5h2sXkKOyUmZ3CtL_CtGuUvtj5j24JV3-Eu_QQeLMFvvseNv9tbM9O332cSvkAdEiwdQ</recordid><startdate>200510</startdate><enddate>200510</enddate><creator>Enami, Isao</creator><creator>Suzuki, Takehiro</creator><creator>Tada, Osamu</creator><creator>Nakada, Yoshiko</creator><creator>Nakamura, Kumi</creator><creator>Tohri, Akihiko</creator><creator>Ohta, Hisataka</creator><creator>Inoue, Isao</creator><creator>Shen, Jian‐Ren</creator><general>Blackwell Science Ltd</general><general>Blackwell Publishing Ltd</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>200510</creationdate><title>Distribution of the extrinsic proteins as a potential marker for the evolution of photosynthetic oxygen‐evolving photosystem II</title><author>Enami, Isao ; Suzuki, Takehiro ; Tada, Osamu ; Nakada, Yoshiko ; Nakamura, Kumi ; Tohri, Akihiko ; Ohta, Hisataka ; Inoue, Isao ; Shen, Jian‐Ren</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5422-b367c248b222d912c49b431b8439a0e33ef6e56ee26816326c8cbb36b8b443193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Algae</topic><topic>Antibodies - immunology</topic><topic>Bacillariophyceae</topic><topic>Biological Evolution</topic><topic>Biomarkers</topic><topic>Cyanidium caldarium</topic><topic>Cyanophora - metabolism</topic><topic>Cyanophora paradoxa</topic><topic>Euglena gracilis</topic><topic>evolution</topic><topic>Evolutionary biology</topic><topic>immunological assay</topic><topic>Immunology</topic><topic>Oxygen</topic><topic>Oxygen - metabolism</topic><topic>oxygen evolution</topic><topic>Photosynthesis</topic><topic>photosystem II</topic><topic>Photosystem II Protein Complex - metabolism</topic><topic>Proteins</topic><topic>PSII extrinsic proteins</topic><topic>Rhodophyta - metabolism</topic><topic>Spinacia oleracea - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Enami, Isao</creatorcontrib><creatorcontrib>Suzuki, Takehiro</creatorcontrib><creatorcontrib>Tada, Osamu</creatorcontrib><creatorcontrib>Nakada, Yoshiko</creatorcontrib><creatorcontrib>Nakamura, Kumi</creatorcontrib><creatorcontrib>Tohri, Akihiko</creatorcontrib><creatorcontrib>Ohta, Hisataka</creatorcontrib><creatorcontrib>Inoue, Isao</creatorcontrib><creatorcontrib>Shen, Jian‐Ren</creatorcontrib><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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>The FEBS journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Enami, Isao</au><au>Suzuki, Takehiro</au><au>Tada, Osamu</au><au>Nakada, Yoshiko</au><au>Nakamura, Kumi</au><au>Tohri, Akihiko</au><au>Ohta, Hisataka</au><au>Inoue, Isao</au><au>Shen, Jian‐Ren</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution of the extrinsic proteins as a potential marker for the evolution of photosynthetic oxygen‐evolving photosystem II</atitle><jtitle>The FEBS journal</jtitle><addtitle>FEBS J</addtitle><date>2005-10</date><risdate>2005</risdate><volume>272</volume><issue>19</issue><spage>5020</spage><epage>5030</epage><pages>5020-5030</pages><issn>1742-464X</issn><eissn>1742-4658</eissn><abstract>Distribution of photosystem II (PSII) extrinsic proteins was examined using antibodies raised against various extrinsic proteins from different sources. The results showed that a glaucophyte (Cyanophora paradoxa) having the most primitive plastids contained the cyanobacterial‐type extrinsic proteins (PsbO, PsbV, PsbU), and the primitive red algae (Cyanidium caldarium) contained the red algal‐type extrinsic proteins (PsO, PsbQ′, PsbV, PsbU), whereas a prasinophyte (Pyraminonas parkeae), which is one of the most primitive green algae, contained the green algal‐type ones (PsbO, PsbP, PsbQ). These suggest that the extrinsic proteins had been diverged into cyanobacterial‐, red algal‐ and green algal‐types during early phases of evolution after a primary endosymbiosis. This study also showed that a haptophyte, diatoms and brown algae, which resulted from red algal secondary endosymbiosis, contained the red algal‐type, whereas Euglena gracilis resulted from green algal secondary endosymbiosis contained the green algal‐type extrinsic proteins, suggesting that the red algal‐ and green algal‐type extrinsic proteins have been retained unchanged in the different lines of organisms following the secondary endosymbiosis. Based on these immunological analyses, together with the current genome data, the evolution of photosynthetic oxygen‐evolving PSII was discussed from a view of distribution of the extrinsic proteins, and a new model for the evolution of the PSII extrinsic proteins was proposed.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>16176274</pmid><doi>10.1111/j.1742-4658.2005.04912.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Algae Antibodies - immunology Bacillariophyceae Biological Evolution Biomarkers Cyanidium caldarium Cyanophora - metabolism Cyanophora paradoxa Euglena gracilis evolution Evolutionary biology immunological assay Immunology Oxygen Oxygen - metabolism oxygen evolution Photosynthesis photosystem II Photosystem II Protein Complex - metabolism Proteins PSII extrinsic proteins Rhodophyta - metabolism Spinacia oleracea - metabolism |
title | Distribution of the extrinsic proteins as a potential marker for the evolution of photosynthetic oxygen‐evolving photosystem II |
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