Comparison of the structure of the extrinsic 33 kDa protein from different organisms
The psbO gene encoding the extrinsic 33 kDa protein of oxygen-evolving photosystem 2 (PS2) complex was cloned and sequenced from a red alga, Cyanidium caldarium. The gene encodes a polypeptide of 333 residues, of which the first 76 residues served as transit peptides for transfer across the chloropl...
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description | The psbO gene encoding the extrinsic 33 kDa protein of oxygen-evolving photosystem 2 (PS2) complex was cloned and sequenced from a red alga, Cyanidium caldarium. The gene encodes a polypeptide of 333 residues, of which the first 76 residues served as transit peptides for transfer across the chloroplast envelope and thylakoid membrane. The mature protein consists of 257 amino acids with a calculated molecular mass of 28,290 Da. The sequence homology of the mature 33 kDa protein was 42.9-50.8% between the red alga and cyanobacteria, and 44.7-48.6% between the red alga and higher plants. The cloned gene was expressed in Escherichia coli, and the recombinant protein was purified, subjected to protease-treatments. The cleavage sites of the 33 kDa protein by chymotrypsin or V8 protease were determined and compared among a cyanobacterium (Synechococcus elongatus), a euglena (Euglena gracilis), a green alga (Chlamydomonas reinhardtii) and two higher plants (Spinacia oleracea and Oryza sativa). The cleavage sites by chymotrypsin were at 156F and 190F for the cyanobacterium, 159M, 160F and 192L for red alga, 11Y and 151F for euglena, 10Yand 150F for green alga, and 16Y for spinach, respectively. The cleavage sites by V8 protease were at 181E (cyanobacterium), 182E and 195E (red alga), 13E, 67E, 69E, 153D and 181E (euglena), 176E and 180E (green alga), and 18E or 19E (higher plants). Since most of the residues at these cleavage sites were conserved among the six organisms, the results indicate that the structure of the 33 kDa protein, at least the structure based on the accessibility by proteases, is different among these organisms. In terms of the cleavage sites, the structure of the 33 kDa protein can be divided into three major groups: cyanobacterial and red algal-type has cleavage sites at residues around 156-195, higher plant-type at residues 16-19, and euglena and green algal-type at residues of both cyanobacterial and higher plant-types. |
doi_str_mv | 10.1093/pcp/pcf053 |
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(Science Univ. of Tokyo (Japan). Faculty of Science) ; Suzuki, T ; Okuyama, S ; Kamino, K ; Motoki, A ; Hirano, M ; Ohta, H ; Shen, J.R ; Yamamoto, Y ; Enami, I</creator><creatorcontrib>Tohri, A. (Science Univ. of Tokyo (Japan). Faculty of Science) ; Suzuki, T ; Okuyama, S ; Kamino, K ; Motoki, A ; Hirano, M ; Ohta, H ; Shen, J.R ; Yamamoto, Y ; Enami, I</creatorcontrib><description>The psbO gene encoding the extrinsic 33 kDa protein of oxygen-evolving photosystem 2 (PS2) complex was cloned and sequenced from a red alga, Cyanidium caldarium. The gene encodes a polypeptide of 333 residues, of which the first 76 residues served as transit peptides for transfer across the chloroplast envelope and thylakoid membrane. The mature protein consists of 257 amino acids with a calculated molecular mass of 28,290 Da. The sequence homology of the mature 33 kDa protein was 42.9-50.8% between the red alga and cyanobacteria, and 44.7-48.6% between the red alga and higher plants. The cloned gene was expressed in Escherichia coli, and the recombinant protein was purified, subjected to protease-treatments. The cleavage sites of the 33 kDa protein by chymotrypsin or V8 protease were determined and compared among a cyanobacterium (Synechococcus elongatus), a euglena (Euglena gracilis), a green alga (Chlamydomonas reinhardtii) and two higher plants (Spinacia oleracea and Oryza sativa). The cleavage sites by chymotrypsin were at 156F and 190F for the cyanobacterium, 159M, 160F and 192L for red alga, 11Y and 151F for euglena, 10Yand 150F for green alga, and 16Y for spinach, respectively. The cleavage sites by V8 protease were at 181E (cyanobacterium), 182E and 195E (red alga), 13E, 67E, 69E, 153D and 181E (euglena), 176E and 180E (green alga), and 18E or 19E (higher plants). Since most of the residues at these cleavage sites were conserved among the six organisms, the results indicate that the structure of the 33 kDa protein, at least the structure based on the accessibility by proteases, is different among these organisms. In terms of the cleavage sites, the structure of the 33 kDa protein can be divided into three major groups: cyanobacterial and red algal-type has cleavage sites at residues around 156-195, higher plant-type at residues 16-19, and euglena and green algal-type at residues of both cyanobacterial and higher plant-types.</description><identifier>ISSN: 0032-0781</identifier><identifier>EISSN: 1471-9053</identifier><identifier>DOI: 10.1093/pcp/pcf053</identifier><identifier>PMID: 11978871</identifier><language>eng</language><publisher>Japan: Oxford University Press</publisher><subject>Abbreviation: CP ; Amino Acid Sequence ; Animals ; Base Sequence ; BINDING PROTEINS ; CELL STRUCTURE ; Chlamydomonas reinhardtii - genetics ; Chlamydomonas reinhardtii - metabolism ; chlorophyll-binding protein ; Cloning, Molecular ; Cyanobacteria - genetics ; Cyanobacteria - metabolism ; Euglena - genetics ; Euglena - metabolism ; GENE EXPRESSION ; Key words: Evolution — Extrinsic 33 kDa protein — Limited proteolysis — psbO gene — Red alga ; LIC ; ligation independent cloning ; MALDI-TOF ; matrix-assisted laser desorption/ionization ; MICROORGANISMS ; Molecular Sequence Data ; Oxygen - metabolism ; Photosynthetic Reaction Center Complex Proteins - genetics ; Photosynthetic Reaction Center Complex Proteins - metabolism ; Photosystem II Protein Complex ; PHOTOSYSTEMS ; PLANTS ; Plants - genetics ; Plants - metabolism ; PROTEASES ; RHODOPHYCEAE ; Rhodophyta - genetics ; Rhodophyta - metabolism ; Sequence Homology, Amino Acid ; TFA ; time of flight ; trifluoroacetic acid</subject><ispartof>Plant and cell physiology, 2002-04, Vol.43 (4), p.429-439</ispartof><rights>Copyright Oxford University Press(England) Apr 15, 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-2cfbfe12fa4555090d76a5c36cfee4ee8f42162b4744ff7ae30a0edaf1a967a43</citedby><cites>FETCH-LOGICAL-c431t-2cfbfe12fa4555090d76a5c36cfee4ee8f42162b4744ff7ae30a0edaf1a967a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11978871$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tohri, A. (Science Univ. of Tokyo (Japan). Faculty of Science)</creatorcontrib><creatorcontrib>Suzuki, T</creatorcontrib><creatorcontrib>Okuyama, S</creatorcontrib><creatorcontrib>Kamino, K</creatorcontrib><creatorcontrib>Motoki, A</creatorcontrib><creatorcontrib>Hirano, M</creatorcontrib><creatorcontrib>Ohta, H</creatorcontrib><creatorcontrib>Shen, J.R</creatorcontrib><creatorcontrib>Yamamoto, Y</creatorcontrib><creatorcontrib>Enami, I</creatorcontrib><title>Comparison of the structure of the extrinsic 33 kDa protein from different organisms</title><title>Plant and cell physiology</title><addtitle>Plant Cell Physiol</addtitle><description>The psbO gene encoding the extrinsic 33 kDa protein of oxygen-evolving photosystem 2 (PS2) complex was cloned and sequenced from a red alga, Cyanidium caldarium. The gene encodes a polypeptide of 333 residues, of which the first 76 residues served as transit peptides for transfer across the chloroplast envelope and thylakoid membrane. The mature protein consists of 257 amino acids with a calculated molecular mass of 28,290 Da. The sequence homology of the mature 33 kDa protein was 42.9-50.8% between the red alga and cyanobacteria, and 44.7-48.6% between the red alga and higher plants. The cloned gene was expressed in Escherichia coli, and the recombinant protein was purified, subjected to protease-treatments. The cleavage sites of the 33 kDa protein by chymotrypsin or V8 protease were determined and compared among a cyanobacterium (Synechococcus elongatus), a euglena (Euglena gracilis), a green alga (Chlamydomonas reinhardtii) and two higher plants (Spinacia oleracea and Oryza sativa). The cleavage sites by chymotrypsin were at 156F and 190F for the cyanobacterium, 159M, 160F and 192L for red alga, 11Y and 151F for euglena, 10Yand 150F for green alga, and 16Y for spinach, respectively. The cleavage sites by V8 protease were at 181E (cyanobacterium), 182E and 195E (red alga), 13E, 67E, 69E, 153D and 181E (euglena), 176E and 180E (green alga), and 18E or 19E (higher plants). Since most of the residues at these cleavage sites were conserved among the six organisms, the results indicate that the structure of the 33 kDa protein, at least the structure based on the accessibility by proteases, is different among these organisms. In terms of the cleavage sites, the structure of the 33 kDa protein can be divided into three major groups: cyanobacterial and red algal-type has cleavage sites at residues around 156-195, higher plant-type at residues 16-19, and euglena and green algal-type at residues of both cyanobacterial and higher plant-types.</description><subject>Abbreviation: CP</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>BINDING PROTEINS</subject><subject>CELL STRUCTURE</subject><subject>Chlamydomonas reinhardtii - genetics</subject><subject>Chlamydomonas reinhardtii - metabolism</subject><subject>chlorophyll-binding protein</subject><subject>Cloning, Molecular</subject><subject>Cyanobacteria - genetics</subject><subject>Cyanobacteria - metabolism</subject><subject>Euglena - genetics</subject><subject>Euglena - metabolism</subject><subject>GENE EXPRESSION</subject><subject>Key words: Evolution — Extrinsic 33 kDa protein — Limited proteolysis — psbO gene — Red alga</subject><subject>LIC</subject><subject>ligation independent cloning</subject><subject>MALDI-TOF</subject><subject>matrix-assisted laser desorption/ionization</subject><subject>MICROORGANISMS</subject><subject>Molecular Sequence Data</subject><subject>Oxygen - metabolism</subject><subject>Photosynthetic Reaction Center Complex Proteins - genetics</subject><subject>Photosynthetic Reaction Center Complex Proteins - metabolism</subject><subject>Photosystem II Protein Complex</subject><subject>PHOTOSYSTEMS</subject><subject>PLANTS</subject><subject>Plants - genetics</subject><subject>Plants - metabolism</subject><subject>PROTEASES</subject><subject>RHODOPHYCEAE</subject><subject>Rhodophyta - genetics</subject><subject>Rhodophyta - metabolism</subject><subject>Sequence Homology, Amino Acid</subject><subject>TFA</subject><subject>time of flight</subject><subject>trifluoroacetic acid</subject><issn>0032-0781</issn><issn>1471-9053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0c9rFDEUB_BQFLutXrwrwUMPhdGXSSaZOZbtj1Xa2kOF4iVksy817c5kTDJQ__tGZlUQEvJIPjwe3xDylsFHBh3_NNqxbAcN3yMLJhSrulK_IAsAXlegWrZPDlJ6ACg1h1dkn7FOta1iC3K7DP1ook9hoMHR_ANpynGyeYr45wKfcvRD8pZyTh9PDR1jyOgH6mLo6cY7hxGHTEO8N4NPfXpNXjqzTfhmdx6Sb-dnt8tVdfn14vPy5LKygrNc1datHbLaGdE0DXSwUdI0lkvrEAVi60TNZL0WSgjnlEEOBnBjHDOdVEbwQ3I09y0D_ZwwZd37ZHG7NQOGKWnFJAepugI__AcfwhSHMpuugTVcSCELOp6RjSGliE6P0fcm_tIM9O-gdQlaz0EX_H7XcVr3uPlHd8kWUM3Ap4xPf99NfNRScdXo1d13fXW9XF237FTfFP9u9s4Ebe7Lj-gvNzVAWZK1NX8GX3iSFw</recordid><startdate>20020401</startdate><enddate>20020401</enddate><creator>Tohri, A. (Science Univ. of Tokyo (Japan). Faculty of Science)</creator><creator>Suzuki, T</creator><creator>Okuyama, S</creator><creator>Kamino, K</creator><creator>Motoki, A</creator><creator>Hirano, M</creator><creator>Ohta, H</creator><creator>Shen, J.R</creator><creator>Yamamoto, Y</creator><creator>Enami, I</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>20020401</creationdate><title>Comparison of the structure of the extrinsic 33 kDa protein from different organisms</title><author>Tohri, A. (Science Univ. of Tokyo (Japan). Faculty of Science) ; Suzuki, T ; Okuyama, S ; Kamino, K ; Motoki, A ; Hirano, M ; Ohta, H ; Shen, J.R ; Yamamoto, Y ; Enami, I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-2cfbfe12fa4555090d76a5c36cfee4ee8f42162b4744ff7ae30a0edaf1a967a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Abbreviation: CP</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>BINDING PROTEINS</topic><topic>CELL STRUCTURE</topic><topic>Chlamydomonas reinhardtii - genetics</topic><topic>Chlamydomonas reinhardtii - metabolism</topic><topic>chlorophyll-binding protein</topic><topic>Cloning, Molecular</topic><topic>Cyanobacteria - genetics</topic><topic>Cyanobacteria - metabolism</topic><topic>Euglena - genetics</topic><topic>Euglena - metabolism</topic><topic>GENE EXPRESSION</topic><topic>Key words: Evolution — Extrinsic 33 kDa protein — Limited proteolysis — psbO gene — Red alga</topic><topic>LIC</topic><topic>ligation independent cloning</topic><topic>MALDI-TOF</topic><topic>matrix-assisted laser desorption/ionization</topic><topic>MICROORGANISMS</topic><topic>Molecular Sequence Data</topic><topic>Oxygen - metabolism</topic><topic>Photosynthetic Reaction Center Complex Proteins - genetics</topic><topic>Photosynthetic Reaction Center Complex Proteins - metabolism</topic><topic>Photosystem II Protein Complex</topic><topic>PHOTOSYSTEMS</topic><topic>PLANTS</topic><topic>Plants - genetics</topic><topic>Plants - metabolism</topic><topic>PROTEASES</topic><topic>RHODOPHYCEAE</topic><topic>Rhodophyta - genetics</topic><topic>Rhodophyta - metabolism</topic><topic>Sequence Homology, Amino Acid</topic><topic>TFA</topic><topic>time of flight</topic><topic>trifluoroacetic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tohri, A. (Science Univ. of Tokyo (Japan). Faculty of Science)</creatorcontrib><creatorcontrib>Suzuki, T</creatorcontrib><creatorcontrib>Okuyama, S</creatorcontrib><creatorcontrib>Kamino, K</creatorcontrib><creatorcontrib>Motoki, A</creatorcontrib><creatorcontrib>Hirano, M</creatorcontrib><creatorcontrib>Ohta, H</creatorcontrib><creatorcontrib>Shen, J.R</creatorcontrib><creatorcontrib>Yamamoto, Y</creatorcontrib><creatorcontrib>Enami, I</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 & 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 & 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>Tohri, A. (Science Univ. of Tokyo (Japan). Faculty of Science)</au><au>Suzuki, T</au><au>Okuyama, S</au><au>Kamino, K</au><au>Motoki, A</au><au>Hirano, M</au><au>Ohta, H</au><au>Shen, J.R</au><au>Yamamoto, Y</au><au>Enami, I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the structure of the extrinsic 33 kDa protein from different organisms</atitle><jtitle>Plant and cell physiology</jtitle><addtitle>Plant Cell Physiol</addtitle><date>2002-04-01</date><risdate>2002</risdate><volume>43</volume><issue>4</issue><spage>429</spage><epage>439</epage><pages>429-439</pages><issn>0032-0781</issn><eissn>1471-9053</eissn><abstract>The psbO gene encoding the extrinsic 33 kDa protein of oxygen-evolving photosystem 2 (PS2) complex was cloned and sequenced from a red alga, Cyanidium caldarium. The gene encodes a polypeptide of 333 residues, of which the first 76 residues served as transit peptides for transfer across the chloroplast envelope and thylakoid membrane. The mature protein consists of 257 amino acids with a calculated molecular mass of 28,290 Da. The sequence homology of the mature 33 kDa protein was 42.9-50.8% between the red alga and cyanobacteria, and 44.7-48.6% between the red alga and higher plants. The cloned gene was expressed in Escherichia coli, and the recombinant protein was purified, subjected to protease-treatments. The cleavage sites of the 33 kDa protein by chymotrypsin or V8 protease were determined and compared among a cyanobacterium (Synechococcus elongatus), a euglena (Euglena gracilis), a green alga (Chlamydomonas reinhardtii) and two higher plants (Spinacia oleracea and Oryza sativa). The cleavage sites by chymotrypsin were at 156F and 190F for the cyanobacterium, 159M, 160F and 192L for red alga, 11Y and 151F for euglena, 10Yand 150F for green alga, and 16Y for spinach, respectively. The cleavage sites by V8 protease were at 181E (cyanobacterium), 182E and 195E (red alga), 13E, 67E, 69E, 153D and 181E (euglena), 176E and 180E (green alga), and 18E or 19E (higher plants). Since most of the residues at these cleavage sites were conserved among the six organisms, the results indicate that the structure of the 33 kDa protein, at least the structure based on the accessibility by proteases, is different among these organisms. In terms of the cleavage sites, the structure of the 33 kDa protein can be divided into three major groups: cyanobacterial and red algal-type has cleavage sites at residues around 156-195, higher plant-type at residues 16-19, and euglena and green algal-type at residues of both cyanobacterial and higher plant-types.</abstract><cop>Japan</cop><pub>Oxford University Press</pub><pmid>11978871</pmid><doi>10.1093/pcp/pcf053</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abbreviation: CP Amino Acid Sequence Animals Base Sequence BINDING PROTEINS CELL STRUCTURE Chlamydomonas reinhardtii - genetics Chlamydomonas reinhardtii - metabolism chlorophyll-binding protein Cloning, Molecular Cyanobacteria - genetics Cyanobacteria - metabolism Euglena - genetics Euglena - metabolism GENE EXPRESSION Key words: Evolution — Extrinsic 33 kDa protein — Limited proteolysis — psbO gene — Red alga LIC ligation independent cloning MALDI-TOF matrix-assisted laser desorption/ionization MICROORGANISMS Molecular Sequence Data Oxygen - metabolism Photosynthetic Reaction Center Complex Proteins - genetics Photosynthetic Reaction Center Complex Proteins - metabolism Photosystem II Protein Complex PHOTOSYSTEMS PLANTS Plants - genetics Plants - metabolism PROTEASES RHODOPHYCEAE Rhodophyta - genetics Rhodophyta - metabolism Sequence Homology, Amino Acid TFA time of flight trifluoroacetic acid |
title | Comparison of the structure of the extrinsic 33 kDa protein from different organisms |
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