Radiation Biology & Health Sciences Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400 085, India.
Ministry of Environment, Forest & Climate Change, Indira Paryavaran Bhawan, New Delhi, 110003, India.
Sci Rep. 2019 Jul 8;9(1):9863. doi: 10.1038/s41598-019-46288-4.
The distinct sequence feature and spectral blue-shift (~10 nm) of phycocyanin, isolated from Nostoc sp. R76DM (N-PC), were investigated by phylogenetic and crystallographic analyses. Twelve conserved substitutions in N-PC sequence were found distributed unequally among α- and β-subunit (3 in α- and 9 in β-subunit). The phylogenetic analysis suggested that molecular evolution of α- and β-subunit of Nostoc-phycocyanin is faster than evolution of Nostoc-species. The divergence events seem to have occurred more frequently in β-subunit, compared to α-subunit (relative divergence, 7.38 for α-subunit and 9.66 for β-subunit). Crystal structure of N-PC was solved at 2.35 Å resolution to reasonable R-factors (R/R = 0.199/0.248). Substitutions congregate near interface of two αβ-monomer in N-PC trimer and are of compensatory nature. Six of the substitutions in β-subunit may be involved in maintaining topology of β-subunit, one in inter-monomer interaction and one in interaction with linker-protein. The β153Cys-attached chromophore adopts high-energy conformational state resulting due to reduced coplanarity of B- and C-pyrrole rings. Distortion in chromophore conformation can result in blue-shift in N-PC spectral properties. N-PC showed significant in-vitro and in-vivo antioxidant activity comparable with other phycocyanin. Since Nostoc-species constitute a distinct phylogenetic clade, the present structure would provide a better template to build a model for phycocyanins of these species.
从 Nostoc sp. R76DM(N-PC)中分离得到的藻蓝蛋白具有独特的序列特征和光谱蓝移(~10nm),通过系统发育和晶体学分析进行了研究。在 N-PC 序列中发现了 12 个保守取代,分布在α-和β-亚基不均匀(3 个在α-亚基和 9 个在β-亚基)。系统发育分析表明,Nostoc-藻蓝蛋白的α-和β-亚基的分子进化速度快于 Nostoc 物种的进化。与α-亚基相比,β-亚基似乎发生了更多的分歧事件(相对分歧,α-亚基为 7.38,β-亚基为 9.66)。N-PC 的晶体结构在 2.35Å分辨率下得到解决,得到了合理的 R 因子(R/R=0.199/0.248)。取代集中在 N-PC 三聚体的两个αβ-单体界面附近,具有补偿性质。β-亚基中的 6 个取代可能参与维持β-亚基的拓扑结构,1 个参与单体间相互作用,1 个参与与连接蛋白的相互作用。β153Cys 连接的发色团采用高能构象状态,由于 B-和 C-吡咯环的共面性降低。发色团构象的扭曲会导致 N-PC 光谱性质的蓝移。N-PC 表现出显著的体外和体内抗氧化活性,可与其他藻蓝蛋白相媲美。由于 Nostoc 物种构成了一个独特的系统发育分支,本结构将为这些物种的藻蓝蛋白提供更好的模板来构建模型。