Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, 16802, USA.
Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT, 59717, USA.
Photosynth Res. 2021 Jan;147(1):11-26. doi: 10.1007/s11120-020-00787-y. Epub 2020 Oct 14.
Phycobilisomes (PBS), the major light-harvesting antenna in cyanobacteria, are supramolecular complexes of colorless linkers and heterodimeric, pigment-binding phycobiliproteins. Phycocyanin and phycoerythrin commonly comprise peripheral rods, and a multi-cylindrical core is principally assembled from allophycocyanin (AP). Each AP subunit binds one phycocyanobilin (PCB) chromophore, a linear tetrapyrrole that predominantly absorbs in the orange-red region of the visible spectrum (600-700 nm). AP facilitates excitation energy transfer from PBS peripheral rods or from directly absorbed red light to accessory chlorophylls in the photosystems. Paralogous forms of AP that bind PCB and are capable of absorbing far-red light (FRL; 700-800 nm) have recently been identified in organisms performing two types of photoacclimation: FRL photoacclimation (FaRLiP) and low-light photoacclimation (LoLiP). The FRL-absorbing AP (FRL-AP) from the thermophilic LoLiP strain Synechococcus sp. A1463 was chosen as a platform for site-specific mutagenesis to probe the structural differences between APs that absorb in the visible region and FRL-APs and to identify residues essential for the FRL absorbance phenotype. Conversely, red light-absorbing allophycocyanin-B (AP-B; ~ 670 nm) from the same organism was used as a platform for creating a FRL-AP. We demonstrate that the protein environment immediately surrounding pyrrole ring A of PCB on the alpha subunit is mostly responsible for the FRL absorbance of FRL-APs. We also show that interactions between PCBs bound to alpha and beta subunits of adjacent protomers in trimeric AP complexes are responsible for a large bathochromic shift of about ~ 20 nm and notable sharpening of the long-wavelength absorbance band.
藻胆体(PBS)是蓝细菌中主要的光捕获天线,是无色连接体和异二聚体、色素结合藻胆蛋白的超分子复合物。藻蓝蛋白和藻红蛋白通常构成外围棒状结构,而多圆柱核心主要由别藻蓝蛋白(AP)组装而成。每个 AP 亚基结合一个藻胆素(PCB)发色团,这是一种线性四吡咯,主要在可见光光谱的橙红色区域(600-700nm)吸收。AP 有助于从 PBS 外围棒状结构或直接吸收的红光将激发能转移到光系统中的辅助叶绿素中。最近在进行两种光驯化的生物体中鉴定出与 PCB 结合并能够吸收远红光(FRL;700-800nm)的 AP 同工型:FRL 光驯化(FaRLiP)和低光光驯化(LoLiP)。来自嗜热 LoLiP 菌株 Synechococcus sp. A1463 的 FRL 吸收 AP(FRL-AP)被选为定点突变的平台,以探测在可见区域吸收的 AP 和 FRL-AP 之间的结构差异,并鉴定对 FRL 吸收表型至关重要的残基。相反,来自同一生物体的红光吸收别藻蓝蛋白-B(AP-B;670nm)被用作构建 FRL-AP 的平台。我们证明,PCB 吡咯环 A 上的 alpha 亚基周围的蛋白质环境主要负责 FRL-AP 的 FRL 吸收。我们还表明,在三聚体 AP 复合物中相邻原聚体的 alpha 和 beta 亚基结合的 PCB 之间的相互作用负责约20nm 的大红移和长波长吸收带的显著锐化。