Komenda Josef, Krynická Vendula, Zakar Tomas
Centre Algatech, Institute of Microbiology, Academy of Sciences, Třeboň, Czech Republic.
Institute of Plant Biology, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Bio Protoc. 2019 Jan 5;9(1):e3126. doi: 10.21769/BioProtoc.3126.
Cyanobacteria represent a frequently used model organism for the study of oxygenic photosynthesis. They belong to prokaryotic microorganisms but their photosynthetic apparatus is quite similar to that found in algal and plant chloroplasts. The key players in light reactions of photosynthesis are Photosystem I and Photosystem II complexes (PSI and PSII, resp.), large membrane complexes of proteins, pigments and other cofactors embedded in specialized photosynthetic membranes named thylakoids. For the study of these complexes a mild method for the isolation of the thylakoids, their subsequent solubilization and analysis is essential. The presented protocol describes such a method which utilizes breaking the cyanobacterial cells using glass beads in an optimized buffer. This is followed by their solubilization using dodecyl-maltoside and analysis using optimized clear-native gel electrophoresis which preserves the native oligomerization state of both complexes and allows the estimation of their content.
蓝细菌是研究产氧光合作用常用的模式生物。它们属于原核微生物,但其光合装置与藻类和植物叶绿体中的光合装置非常相似。光合作用光反应的关键参与者是光系统I和光系统II复合物(分别为PSI和PSII),它们是嵌入称为类囊体的特殊光合膜中的由蛋白质、色素和其他辅因子组成的大型膜复合物。为了研究这些复合物,一种温和的类囊体分离方法、随后的增溶和分析方法至关重要。本文介绍的方案描述了一种利用在优化缓冲液中使用玻璃珠破碎蓝细菌细胞的方法。随后使用十二烷基麦芽糖苷对其进行增溶,并使用优化的非变性清晰凝胶电泳进行分析,该电泳可保留两种复合物的天然寡聚状态并允许估计其含量。