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The reversible reduction of GSSR substrates usually requires only the first active-site cysteinyl residue and is therefore catalyzed by a monothiol mechanism with ping-pong bi-bi kinetic patterns (Fig
Physiological assessments indicated early reductions in stomatal conductance and photochemical efficiency, partially compensated by increased non-photochemical quenching and preserved PSII integrity
In a complementary manner, an activating phosphomimetic mutation was engineered to permanently mimic the phosphates bulky negative charge by replacing the serine with an aspartic acid (S114D)
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