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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Veröffentlicht in:Plant and cell physiology 2002-04, Vol.43 (4), p.429-439
Hauptverfasser: 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
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container_issue 4
container_start_page 429
container_title Plant and cell physiology
container_volume 43
creator 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
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.
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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. 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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. 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(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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