EPR Spin-Trapping for Monitoring Temporal Dynamics of Singlet Oxygen during Photoprotection in Photosynthesis.

A central goal of photoprotective energy dissipation processes is the regulation of singlet oxygen ( 1 O 2 *) and reactive oxygen species in the photosynthetic apparatus. Despite the involvement of 1 O 2 * in photodamage and cell signaling, few studies directly correlate 1 O 2 * formation to nonphotochemical quenching (NPQ) or lack thereof. Here, we combine spin-trapping electron paramagnetic resonance (EPR) and time-resolved fluorescence spectroscopies to track in real time the involvement of 1 O 2 * during photoprotection in plant thylakoid membranes. The EPR spin-trapping method for detection of 1 O 2 * was first optimized for photosensitization in dye-based chemical systems and then used to establish methods for monitoring the temporal dynamics of 1 O 2 * in chlorophyll-containing photosynthetic membranes. We find that the apparent 1 O 2 * concentration in membranes changes throughout a 1 h period of continuous illumination. During an initial response to high light intensity, the concentration of 1 O 2 * decreased in parallel with a decrease in the chlorophyll fluorescence lifetime via NPQ. Treatment of membranes with nigericin, an uncoupler of the transmembrane proton gradient, delayed the activation of NPQ and the associated quenching of 1 O 2 * during high light. Upon saturation of NPQ, the concentration of 1 O 2 * increased in both untreated and nigericin-treated membranes, reflecting the utility of excess energy dissipation in mitigating photooxidative stress in the short term (i.e., the initial ∼10 min of high light).