The cyanobacterial homologue of HCF136/YCF48 is a component of an early photosystem II assembly complex and is important for both the efficient assembly and repair of photosystem II in Synechocystis sp. PCC 6803
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
Biotechnology and Biological Sciences Research Council - United Kingdom
PubMed
18550538
DOI
10.1074/jbc.m801917200
PII: S0021-9258(20)74771-X
Knihovny.cz E-zdroje
- MeSH
- bakteriální proteiny genetika fyziologie MeSH
- cystein metabolismus MeSH
- cytochromy typu b genetika izolace a purifikace MeSH
- fotosystém II - proteinový komplex genetika izolace a purifikace fyziologie MeSH
- membránové proteiny genetika fyziologie MeSH
- methionin metabolismus MeSH
- polarografie MeSH
- polymerázová řetězová reakce MeSH
- radioizotopy síry MeSH
- sinice fyziologie MeSH
- Synechocystis fyziologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- bakteriální proteiny MeSH
- cystein MeSH
- cytochrome b559 MeSH Prohlížeč
- cytochromy typu b MeSH
- fotosystém II - proteinový komplex MeSH
- membránové proteiny MeSH
- methionin MeSH
- radioizotopy síry MeSH
The role of the slr2034 (ycf48) gene product in the assembly and repair of photosystem II (PSII) has been studied in the cyanobacterium Synechocystis PCC 6803. YCF48 (HCF136) is involved in the assembly of Arabidopsis thaliana PSII reaction center (RC) complexes but its mode of action is unclear. We show here that YCF48 is a component of two cyanobacterial PSII RC-like complexes in vivo and is absent in larger PSII core complexes. Interruption of ycf48 slowed the formation of PSII complexes in wild type, as judged from pulse-labeling experiments, and caused a decrease in the final level of PSII core complexes in wild type and a marked reduction in the levels of PSII assembly complexes in strains lacking either CP43 or CP47. Absence of YCF48 also led to a dramatic decrease in the levels of the COOH-terminal precursor (pD1) and the partially processed form, iD1, in a variety of PSII mutants and only low levels of unassembled mature D1 were observed. Yeast two-hybrid analyses using the split ubiquitin system showed an interaction of YCF48 with unassembled pD1 and, to a lesser extent, unassembled iD1, but not with unassembled mature D1 or D2. Overall our results indicate a role for YCF48 in the stabilization of newly synthesized pD1 and in its subsequent binding to a D2-cytochrome b559 pre-complex, also identified in this study. Besides a role in assembly, we show for the first time that YCF48 also functions in the selective replacement of photodamaged D1 during PSII repair.
Citace poskytuje Crossref.org
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