Department of Biochemistry and Microbiology, Cook College, Rutgers University, 08903, New Brunswick, NJ, USA.
Photosynth Res. 1986 Jan;10(1-2):7-35. doi: 10.1007/BF00024183.
Phycobilisomes are aggregates of light-harvesting proteins attached to the stroma side of the thylakoid membranes of the cyanobacteria (blue-green algae) and red algae. The water-soluble phycobiliproteins, of which there are three major groups, tetrapyrrole chromophores covalently bound to apoprotein. Several additional protiens are found within the phycobilisome and serve to link the phycobiliproteins to each other in an ordered fashion and also to attach the phycobilisome to the thylakoid membrane. Excitation energy absorbed by phycoerythrin is transferred through phycocyanin to allophycocyanin with an efficiency approximating 100%. This pathway of excitation energy transfer, directly confirmed by time-resolved spectroscopic measurements, has been incorporated into models describing the ultrastructure of the phycobilisome. The model for the most typical type of phycobilisome describes an allophycocyanin-containing core composed of three cylinders arranged so that their longitudinal axes are parallel and their ends form a triangle. Attached to this core are six rod structures which contain phycocyanin proximal to the core and phycoerythrin distal to the core. The axes of these rods are perpendicular to the longitudinal axis of the core. This arrangement ensures a very efficient transfer of energy. The association of phycoerythrin and phycocyanin within the rods and the attachment of the rods to the core and the core to the thylakoid require the presence of several 'linker' polypeptides. It is recently possible to assemble functionally and structurally intact phycobilisomes in vitro from separated components as well as to reassociate phycobilisomes with stripped thylakoids. Understanding of the biosynthesis and in vivo assembly of phycobilisomes will be greatly aided by the current advances in molecular genetics, as exemplified by recent identification of several genes encoding phycobilisome components.Combined ultrastructural, biochemical and biophysical approaches to the study of cyanobacterial and red algal cells and isolated phycobilisome-thylakoid fractions are leading to a clearer understanding of the phycobilisome-thylakoid structural interactions, energy transfer to the reaction centers and regulation of excitation energy distribution. However, compared to our current knowledge concerning the structural and functional organization of the isolated phycobilisome, this research area is relatively unexplored.
藻胆体是由连接在蓝藻(蓝绿藻)和红藻类的类囊体膜基质侧的光捕获蛋白组成的聚集体。有三种主要的水溶性藻胆蛋白,它们的卟啉发色团与脱辅基蛋白共价结合。藻胆体中还发现了几种额外的蛋白质,它们的作用是将藻胆蛋白以有序的方式相互连接,并将藻胆体连接到类囊体膜上。藻红蛋白吸收的激发能通过藻蓝蛋白传递到别藻蓝蛋白,效率接近 100%。这种激发能传递途径已通过时间分辨光谱测量直接证实,并已纳入描述藻胆体超微结构的模型中。最典型的藻胆体模型描述了一个包含别藻蓝蛋白的核心,由三个平行排列的圆柱体组成,其末端形成一个三角形。连接在这个核心上的是六个棒状结构,它们含有靠近核心的藻蓝蛋白和远离核心的藻红蛋白。这些棒的轴垂直于核心的纵轴。这种排列确保了能量的高效传递。棒状结构内藻红蛋白和藻蓝蛋白的结合以及棒状结构与核心的结合、核心与类囊体膜的结合需要几种“连接”多肽的存在。最近,人们可以从分离的成分中体外组装功能和结构完整的藻胆体,也可以重新将藻胆体与剥离的类囊体结合。随着分子遗传学的最新进展,藻胆体的生物合成和体内组装的理解将得到极大的帮助,例如最近鉴定了几个编码藻胆体成分的基因。通过对蓝藻和红藻细胞以及分离的藻胆体-类囊体片段进行超微结构、生化和生物物理综合研究,人们对藻胆体-类囊体结构相互作用、能量向反应中心的转移以及激发能分布的调节有了更清晰的认识。然而,与我们目前对分离的藻胆体结构和功能组织的了解相比,这个研究领域相对没有得到充分探索。