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1 oxygenic photosynthesis is generated by the cytochrome b6f complex.
2 ch requires diffusible intermediates and the cytochrome b6f complex.
3 electron transfer from plastoquinone to the cytochrome b6f complex.
4 on of electron transport is achieved via the cytochrome b6f complex.
5 he photosynthetic reaction center II and the cytochrome b6f complex.
6 s modified in a way reminiscent of that of a cytochrome b6f complex.
7 hat are defective in the accumulation of the cytochrome b6f complex.
8 of subunits of the PSII, photosystem I, and cytochrome b6f complexes.
10 owing that the M subunit is as essential for cytochrome b6f complex accumulation as the Rieske protei
11 m cytochrome c6, inhibiting reduction by the cytochrome b6f complex and facilitating establishment of
13 sis that CPLD38 impacts the stability of the cytochrome b6f complex and possibly plays a role in bala
14 ies of cytochrome f (cyt f), a member of the cytochrome b6f complex and reaction partner with plastoc
15 hotosystem II, showing the susceptibility of cytochrome b6f complexes (and proteins involved in the c
16 ochrome b6 and su IV subunits of chloroplast cytochrome b6f complexes, and together with the unmodifi
19 cytochrome bc1 complexes and the chloroplast cytochrome b6f complexes are direct consequences of spli
22 2 )], rhodopsin [Palczewski ( 24 )], and the cytochrome b6f complex [Cramer et al. ( 35 )] represents
23 The availability of the structures of the cytochrome b6f complex (cyt b6f), plastocyanin (PC), and
25 ent of the Rieske iron-sulfur protein of the cytochrome b6f complex from spinach chloroplasts was obt
27 nit of the photosynthetic electron transport cytochrome b6f complex in chloroplast and cyanobacterial
31 an FtsH-dependent loss of photosystem II and cytochrome b6f complexes in darkness upon sulfur depriva
35 energy transducing hetero-oligomeric dimeric cytochrome b6f complex of oxygenic photosynthesis from t
36 Oxidation of plastoquinol mediated by the cytochrome b6f complex on the electrochemically positive
39 that the selective depletion of Rubisco and cytochrome b6f complex that occurs when Chlamydomonas re
41 transcripts and polypeptide subunits of the cytochrome b6f complex were also significantly lower in
42 ts of photosystem I, photosystem II, and the cytochrome b6f complex were inferred to be pseudogenes.
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