Improved capacity for the repair of photosystem II via reinforcement of the translational and antioxidation systems in Synechocystis sp. PCC 6803

Abstract

SUMMARYIn the cyanobacterium Synechocystis sp. PCC 6803, translation factor EF‐Tu is inactivated by reactive oxygen species (ROS) via oxidation of Cys82 and the oxidation of EF‐Tu enhances the inhibition of the repair of photosystem II (PSII) by suppressing protein synthesis. In our present study, we generated transformants of Synechocystis that overexpressed a mutated form of EF‐Tu, designated EF‐Tu (C82S), in which Cys82 had been replaced by a Ser residue, and ROS‐scavenging enzymes individually or together. Expression of EF‐Tu (C82S) alone in Synechocystis enhanced the repair of PSII under strong light, with the resultant mitigation of PSII photoinhibition, but it stimulated the production of ROS. However, overexpression of superoxide dismutase and catalase, together with the expression of EF‐Tu (C82S), lowered intracellular levels of ROS and enhanced the repair of PSII more significantly under strong light, via facilitation of the synthesis de novo of the D1 protein. By contrast, the activity of photosystem I was hardly affected in wild‐type cells and in all the lines of transformed cells under the same strong‐light conditions. Furthermore, transformed cells that overexpressed EF‐Tu (C82S), superoxide dismutase, and catalase were able to survive longer under stronger light than wild‐type cells. Thus, the reinforced capacity for both protein synthesis and ROS scavenging allowed both photosynthesis and cell proliferation to tolerate strong light.