Department of Plant and Environmental Sciences, Institute of Life Sciences, The Hebrew University of Jerusalem, Israel.
FEBS J. 2023 Jan;290(2):400-411. doi: 10.1111/febs.16597. Epub 2022 Aug 29.
The light environment in a mixing water column is arguably the most erratic condition under which photosynthesis functions. Shifts in light intensity, by an order of magnitude, can occur over the time scale of hours. In marine Synechococcus, light is harvested by massive, membrane attached, phycobilisome chromophore-protein complexes (PBS). We examined the ability of a phycobilisome-containing marine Synechococcus strain (WH8102) to acclimate to illumination perturbations on this scale. Although changes in pigment composition occurred gradually over the course of days, we did observe significant and reversible changes in the pigment's fluorescence emission spectra on a time scale of hours. Upon transition to ten-fold higher intensities, we observed a decrease in the energy transferred to Photosystem II. At the same time, the spectral composition of PBS fluorescence emission shifted. Unlike fluorescence quenching mechanisms, this phenomenon resulted in increased fluorescence intensities. These data suggest a mechanism by which marine Synechococcus WH8102 detaches hexamers from the phycobilisome structure. The fluorescence yield of these uncoupled hexamers is high. The detachment process does not require protein synthesis as opposed to reattachment. Hence, the most likely process would be the degradation and resynthesis of labile PBS linker proteins. Experiments with additional species yielded similar results, suggesting that this novel mechanism might be broadly used among PBS-containing organisms.
混合水柱中的光照环境可以说是光合作用功能最不稳定的条件之一。光强度的变化可以在小时的时间尺度上发生数量级的变化。在海洋聚球藻中,光由大量的、膜附着的、藻胆体发色团-蛋白复合物(PBS)来收集。我们研究了含有藻胆体的海洋聚球藻菌株(WH8102)在这种规模的光照扰动下适应的能力。尽管色素组成的变化在几天的时间里逐渐发生,但我们确实观察到在小时的时间尺度上,色素的荧光发射光谱发生了显著的、可逆的变化。当光强增加到十倍时,我们观察到能量向光系统 II 的转移减少。同时,PBS 荧光发射的光谱组成也发生了变化。与荧光猝灭机制不同,这种现象导致荧光强度增加。这些数据表明了一种机制,即海洋聚球藻 WH8102 从藻胆体结构中分离出六聚体。这些分离的六聚体的荧光产率很高。与重新附着相反,该分离过程不需要蛋白质合成。因此,最有可能的过程是不稳定的 PBS 连接蛋白的降解和重新合成。对其他物种的实验也得到了类似的结果,这表明这种新的机制可能在含有 PBS 的生物中广泛使用。