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bioRxiv · 10.1101/2020.08.22.262592

Cytochrome b6f complex inhibition by antimycin-A requires Stt7 kinase activation but not PGR5.

Buchert, F.·Hippler, M.
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Abstract

Ferredoxin-plastoquinone reductase (FQR) activity during cyclic electron flow (CEF) was first ascribed to the cytochrome b6f complex (b6f). However, this was later dismissed since b6f inhibition by antimycin-A (AA) could not be reproduced. AA presumably fails to ligate with haem bh, at variance with cytochrome bc1 complex, owing to a specific Qi-site occupation in b6f. Currently, PROTON GRADIENT REGULATION5 (PGR5) and the associated PGR5-Like1 are considered as FQR in the AA-sensitive CEF pathway. Here, we show that the b6f is conditionally inhibited by AA in a PGR5-independent manner when CEF is promoted. AA inhibition, demonstrated by single b6f turnover and electron transfer measurements, coincided with an altered Qi-site function which required Stt7 kinase activation by a strongly reduced plastoquinone pool. Thus, PGR5 and Stt7 were necessary for b6f activity and AA-sensitive electron transfer in CEF-favouring conditions. Extending previous findings, a new FQR activity model of the b6f is discussed.

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Buchert, F., Hippler, M.. 2020-08-24. Cytochrome b6f complex inhibition by antimycin-A requires Stt7 kinase activation but not PGR5.. https://doi.org/10.1101/2020.08.22.262592

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