Accumulation of the D2 protein is a key regulatory step for assembly of the photosystem II reaction center complex in Synechocystis PCC 6803
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15347679
DOI
10.1074/jbc.m405725200
PII: S0021-9258(19)32244-6
Knihovny.cz E-zdroje
- MeSH
- 2D gelová elektroforéza MeSH
- autoradiografie MeSH
- biologické modely MeSH
- chlorofyl chemie MeSH
- delece genu MeSH
- elektroforéza v polyakrylamidovém gelu MeSH
- fotosyntetické reakční centrum - proteinové komplexy chemie MeSH
- fotosystém II - proteinový komplex chemie metabolismus MeSH
- mutace MeSH
- sinice metabolismus MeSH
- světlosběrné proteinové komplexy chemie MeSH
- Synechocystis fyziologie MeSH
- tylakoidy metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chlorofyl MeSH
- fotosyntetické reakční centrum - proteinové komplexy MeSH
- fotosystém II - proteinový komplex MeSH
- photosystem II, chlorophyll binding protein, CP-43 MeSH Prohlížeč
- photosystem II, chlorophyll-binding protein, CP-47 MeSH Prohlížeč
- světlosběrné proteinové komplexy MeSH
Accumulation of monomer and dimer photosystem (PS) II reaction center core complexes has been analyzed by two-dimensional Blue-native/SDS-PAGE in Synechocystis PCC 6803 wild type and in mutant strains lacking genes psbA, psbB, psbC, psbDIC/DII, or the psbEFLJ operon. In vivo pulse-chase radiolabeling experiments revealed that mutant cells assembled PSII precomplexes only. In DeltapsbC and DeltapsbB, assembly of reaction center cores lacking CP43 and reaction center complexes was detected, respectively. In DeltapsbA, protein subunits CP43, CP47, D2, and cytochrome b559 were synthesized, but proteins did not assemble. Similarly, in DeltapsbD/C lacking D2, and CP43, the de novo synthesized proteins D1, CP47, and cytochrome b559 did not form any mutual complexes, indicating that assembly of the reaction center complex is a prerequisite for assembly with core subunits CP47 and CP43. Finally, although CP43 and CP47 accumulated in DeltapsbEFLJ, D2 was neither expressed nor accumulated. We, furthermore, show that the amount of D2 is high in the strain lacking D1, whereas the amount of D1 is low in the strain lacking D2. We conclude that expression of the psbEFLJ operon is a prerequisite for D2 accumulation that is the key regulatory step for D1 accumulation and consecutive assembly of the PSII reaction center complex.
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