Antimycin A induces light hypersensitivity of photosystem II in the presence of quinone QB-site binding herbicides

Abstract

Photosynthetic electron transport consists of linear electron flow and two cyclic electron flow (CEF) pathways around photosystem I (PSI) (CEF-PSI). PROTON GRADIENT REGULATION 5 (PGR5)-dependent CEF-PSI is thought to be the major CEF-PSI pathway and an important regulator of photosynthetic electron transfer. Antimycin A (AA) is commonly recognized as an inhibitor of PGR5-dependent CEF-PSI in photosynthesis. Although previous findings imply that AA may also affect photosystem II (PSII), which does not participate in CEF-PSI, these “secondary effects” tend to be neglected, and AA is often used for inhibition of PGR5-dependent CEF-PSI as if it were a specific inhibitor. Here, we investigated the direct effects of AA on PSII using isolated spinach (Spinacia oleracea) PSII membranes, and thylakoid membranes isolated from spinach, Arabidopsis thaliana (wild-type Columbia-0 and PGR5-deficient mutant pgr5hope1), and Chlamydomonas reinhardtii. Measurements of quinone QA− reoxidation kinetics showed that AA directly affects the acceptor side of PSII and inhibits electron transport within PSII. Furthermore, repetitive Fv/Fm measurements revealed that, in the presence of quinone QB-site binding inhibitors, AA treatment results in severe photodamage even from a single-turnover flash. The direct effects of AA on PSII are non-negligible and caution is required when using AA as an inhibitor of PGR5-dependent CEF-PSI. Meanwhile, we found that the commercially available compound AA3, which is a component of the AA complex, inhibits PGR5-dependent CEF-PSI without having notable effects on PSII. Thus, we propose that AA3 should be used instead of AA for physiological studies of the PGR5-dependent CEF-PSI.