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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.
9               In line with these phenotypes, cytochrome b6f complex accumulation and linear electron
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
12 photosynthetic electron transfer between the cytochrome b6f complex and photosystem I.
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
17        At the protein level, ferredoxin, the cytochrome-b6f complex, and Fe-containing enzymes of the
18 the Stt7 kinase and its interaction with the cytochrome b6f complex are unknown or unclear.
19 cytochrome bc1 complexes and the chloroplast cytochrome b6f complexes are direct consequences of spli
20  of +295-300 mV of the Rieske cluster in the cytochrome b6f complex at pH 6 and 7.
21                            The switch-off of cytochrome b6f complex biogenesis in mature leaves may r
22 odes core subunits of photosystem II and the cytochrome b6f complex, can lead to hybrid incompatibili
23 2 )], rhodopsin [Palczewski ( 24 )], and the cytochrome b6f complex [Cramer et al. ( 35 )] represents
24    The availability of the structures of the cytochrome b6f complex (cyt b6f), plastocyanin (PC), and
25                   Purified detergent-soluble cytochrome b6f complex from chloroplast thylakoid membra
26 ent of the Rieske iron-sulfur protein of the cytochrome b6f complex from spinach chloroplasts was obt
27 me bc1 complexes from purple bacteria and of cytochrome b6f complexes from chloroplasts.
28 nit of the photosynthetic electron transport cytochrome b6f complex in chloroplast and cyanobacterial
29 hat it could act as electron acceptor of the cytochrome b6f complex in chromorespiration.
30                 Furthermore, subunits of the cytochrome b6f complex in mutant cells turned over much
31                        The biogenesis of the cytochrome b6f complex in tobacco (Nicotiana tabacum) se
32 an FtsH-dependent loss of photosystem II and cytochrome b6f complexes in darkness upon sulfur depriva
33 bromo-3-methyl-6-isopropyl-p-benzoquinone, a cytochrome b6f complex inhibitor.
34             The mutant had less PSI and more cytochrome b6f complex, its thylakoids were organized ma
35 eaves, these data indicate a lifetime of the cytochrome b6f complex of at least 1 week.
36                                          The cytochrome b6f complex of oxygenic photosynthesis carrie
37 energy transducing hetero-oligomeric dimeric cytochrome b6f complex of oxygenic photosynthesis from t
38    Oxidation of plastoquinol mediated by the cytochrome b6f complex on the electrochemically positive
39                       The other strains show cytochrome b6f complex/photosystem I reaction center chl
40                                          The cytochrome b6f complex provides the electronic connectio
41 nstrated that the encoded protein, the small cytochrome b6f complex subunit PetL, crucially contribut
42  that the selective depletion of Rubisco and cytochrome b6f complex that occurs when Chlamydomonas re
43 tochrome c553 can shuttle electrons from the cytochrome b6f complex to cytochrome cM.
44  transcripts and polypeptide subunits of the cytochrome b6f complex were also significantly lower in
45 ts of photosystem I, photosystem II, and the cytochrome b6f complex were inferred to be pseudogenes.