Literature DB >> 11978871

Comparison of the structure of the extrinsic 33 kDa protein from different organisms.

Akihiko Tohri1, Takehiro Suzuki, Satoshi Okuyama, Kei Kamino, Akihiro Motoki, Masahiko Hirano, Hisataka Ohta, Jian-Ren Shen, Yasushi Yamamoto, Isao Enami.   

Abstract

The psbO gene encoding the extrinsic 33 kDa protein of oxygen-evolving photosystem II (PSII) 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.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11978871     DOI: 10.1093/pcp/pcf053

Source DB:  PubMed          Journal:  Plant Cell Physiol        ISSN: 0032-0781            Impact factor:   4.927


  11 in total

1.  Structural studies of the manganese stabilizing subunit in photosystem II.

Authors:  Bengt Svensson; David M Tiede; David R Nelson; Bridgette A Barry
Journal:  Biophys J       Date:  2004-03       Impact factor: 4.033

2.  Treatment news bulletin.

Authors: 
Journal:  Curr Treat Options Neurol       Date:  2000-01       Impact factor: 3.598

3.  Amino acid sequences and solution structures of manganese stabilizing protein that affect reconstitution of Photosystem II activity.

Authors:  Hana Popelkova; Aaron Wyman; Charles Yocum
Journal:  Photosynth Res       Date:  2003       Impact factor: 3.573

4.  Analysis of the Structure of the PsbO Protein and its Implications.

Authors:  Javier De Las Rivas; James Barber
Journal:  Photosynth Res       Date:  2004       Impact factor: 3.573

Review 5.  Structures and functions of the extrinsic proteins of photosystem II from different species.

Authors:  Isao Enami; Akinori Okumura; Ryo Nagao; Takehiro Suzuki; Masako Iwai; Jian-Ren Shen
Journal:  Photosynth Res       Date:  2008-08-21       Impact factor: 3.573

Review 6.  Quality control of photosystem II: impact of light and heat stresses.

Authors:  Yasusi Yamamoto; Ryota Aminaka; Miho Yoshioka; Mahbuba Khatoon; Keisuke Komayama; Daichi Takenaka; Amu Yamashita; Nobuyoshi Nijo; Kayo Inagawa; Noriko Morita; Takayuki Sasaki; Yoko Yamamoto
Journal:  Photosynth Res       Date:  2008-10-21       Impact factor: 3.573

7.  Data-directed top-down Fourier-transform mass spectrometry of a large integral membrane protein complex: photosystem II from Galdieria sulphuraria.

Authors:  Balakumar Thangaraj; Christopher M Ryan; Puneet Souda; Kirsten Krause; Kym F Faull; Andreas P M Weber; Petra Fromme; Julian P Whitelegge
Journal:  Proteomics       Date:  2010-10       Impact factor: 3.984

Review 8.  Structural and functional aspects of the MSP (PsbO) and study of its differences in thermophilic versus mesophilic organisms.

Authors:  Adele K Williamson
Journal:  Photosynth Res       Date:  2008-09-09       Impact factor: 3.573

9.  The importance of protein-protein interactions for optimising oxygen activity in photosystem II: reconstitution with a recombinant thioredoxin--manganese stabilising protein.

Authors:  A K Williamson; J R Liggins; W Hillier; T Wydrzynski
Journal:  Photosynth Res       Date:  2007-05-05       Impact factor: 3.573

10.  Importance of a single disulfide bond for the PsbO protein of photosystem II: protein structure stability and soluble overexpression in Escherichia coli.

Authors:  Julia Nikitina; Tatiana Shutova; Bogdan Melnik; Sergey Chernyshov; Victor Marchenkov; Gennady Semisotnov; Vyacheslav Klimov; Göran Samuelsson
Journal:  Photosynth Res       Date:  2008-08-16       Impact factor: 3.573

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.