scholarly journals PGR5 is required for efficient Q cycle in the cytochrome b6f complex during cyclic electron flow

2019 ◽  
Author(s):  
Felix Buchert ◽  
Laura Mosebach ◽  
Philipp Gäbelein ◽  
Michael Hippler

AbstractProton Gradient Regulation 5 (PGR5) is involved in the control of photosynthetic electron transfer but its mechanistic role is not yet clear. Several models have been proposed to explain phenotypes such as a diminished steady state proton motive force (pmf) and increased photodamage of photosystem I (PSI). Playing a regulatory role in cyclic electron flow (CEF) around PSI, PGR5 contributes indirectly to PSI protection by enhancing photosynthetic control, which is a pH-dependent downregulation of electron transfer at the cytochrome b6f complex (b6f). Here, we re-evaluated the role of PGR5 in the green alga Chlamydomonas reinhardtii and conclude that pgr5 possesses a dysfunctional b6f. Our data indicate that the b6f low-potential chain redox activity likely operated in two distinct modes – via the canonical Q cycle during linear electron flow and via an alternative Q cycle during CEF, attributing a ferredoxin-plastoquinone reductase activity to the b6f. The latter mode allowed efficient oxidation of the low-potential chain in the WT b6f. A switch between the two Q cycle modes was dependent of PGR5 and relied on unknown stromal electron carrier(s), which were a general requirement for b6f activity. In CEF-favouring conditions the electron transfer bottleneck in pgr5 was the b6f and insufficient flexibility in the low-potential chain redox tuning might account for the mutant pmf phenotype and the secondary consequences. Models of our findings are discussed.

2020 ◽  
Vol 477 (9) ◽  
pp. 1631-1650 ◽  
Author(s):  
Felix Buchert ◽  
Laura Mosebach ◽  
Philipp Gäbelein ◽  
Michael Hippler

Proton gradient regulation 5 (PGR5) is involved in the control of photosynthetic electron transfer, but its mechanistic role is not yet clear. Several models have been proposed to explain phenotypes such as a diminished steady-state proton motive force (pmf) and increased photodamage of photosystem I (PSI). Playing a regulatory role in cyclic electron flow (CEF) around PSI, PGR5 contributes indirectly to PSI protection by enhancing photosynthetic control, which is a pH-dependent down-regulation of electron transfer at the cytochrome b6f complex (b6f). Here, we re-evaluated the role of PGR5 in the green alga Chlamydomonas reinhardtii and conclude that pgr5 possesses a dysfunctional b6f. Our data indicate that the b6f low-potential chain redox activity likely operated in two distinct modes — via the canonical Q cycle during linear electron flow and via an alternative Q cycle during CEF, which allowed efficient oxidation of the low-potential chain in the WT b6f. A switch between the two Q cycle modes was dependent on PGR5 and relied on unknown stromal electron carrier(s), which were a general requirement for b6f activity. In CEF-favoring conditions, the electron transfer bottleneck in pgr5 was the b6f, in which insufficient low-potential chain redox tuning might account for the mutant pmf phenotype. By attributing a ferredoxin-plastoquinone reductase activity to the b6f and investigating a PGR5 cysteine mutant, a current model of CEF is challenged.


2012 ◽  
Vol 30 (1) ◽  
pp. 100
Author(s):  
Wei HUANG ◽  
Shi-Bao ZHANG ◽  
Kun-Fang CAO

1984 ◽  
Vol 11 (4) ◽  
pp. 267 ◽  
Author(s):  
AB Hope ◽  
DB Matthews

The deposition of protons in the inside spaces of pea class C chloroplasts was studied by means of the acidification of neutral red measured spectrophotometrically, with the outside space buffered. Careful kinetic analysis of such signals revealed three components, during non-cyclic electron flow induced by single-turnover flashes. These components included a 'slow' phase not emphasized in previous studies. The half-times of these phases were: 'Fast', < 1 ms (not resolved); 'Intermediate', 13-25 ms with added electron acceptor or 4 ms without; and 'Slow', 70-90 ms. Under conditions for cyclic electron flow only the I phase remained; it was the same magnitude as the I phase in non-cyclic flow, and its half-time was c. 3 ms. The F phase, which is usually attributed to protons from the oxidation of water, increased in average size with number of flashes (taken four flashes at a time) and was not fully patent until more than 20 flashes. The size of the I phase, which is usually attributed to protons from the oxidation of plastohydroquinone, when measured in a sequence of flashes to dark-adapted suspensions under non- cyclic conditions, had a binary oscillation in phase with the oscillation in proton uptake reported previously. It was concluded that protons leave PQH2 two at a time on alternate flashes. The S phase (average in 10 test flashes) was reduced by fast preflashes; an origin near photosystem II is suggested. The S phase may imply a small pool of proton-sequestering ability near the water oxidation site, or a number of other possibilities. In steady-state conditions, the ratio of the protons from PQH2 to those from water was 1.0 under all conditions examined except in the absence of added electron acceptor, when it was as high as 1.6. This was the only condition apparently indicating a Q-cycle, with infrequent single-turnover flashes.


2022 ◽  
Author(s):  
Felix Buchert ◽  
Martin Scholz ◽  
Michael Hippler

The cytochrome b6f complex (b6f) has been initially considered as the ferredoxin-plastoquinone reductase (FQR) during cyclic electron flow (CEF) with photosystem I that is inhibited by antimycin A (AA). The binding of AA to the b6f Qi-site is aggravated by heme-ci, which challenged the FQR function of b6f during CEF. Alternative models suggest that PROTON GRADIENT REGULATION5 (PGR5) is involved in a b6f-independent, AA-sensitive FQR. Here, we show in Chlamydomonas reinhardtii that the b6f is conditionally inhibited by AA in vivo and that the inhibition did not require PGR5. Instead, activation of the STT7 kinase upon anaerobic treatment induced the AA sensitivity of b6f which was absent in stt7-1. However, a lock in State 2 due to persisting phosphorylation in the phosphatase double mutant pph1;pbcp did not increase AA sensitivity of electron transfer. The latter required a redox poise, supporting the view that state transitions and CEF are not coercively coupled. This suggests that the b6f-interacting kinase is required for structure-function modulation of the Qi-site under CEF favoring conditions. We propose that PGR5 and STT7 independently sustain AA-sensitive FQR activity of the b6f. Accordingly, PGR5-mediated electron injection into an STT7-modulated Qi-site drives a Mitchellian Q cycle in CEF conditions.


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