Department of Biochemistry/Molecular Plant Biology, University of Turku, Finland.
Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.
FEBS Lett. 2020 Jan;594(2):367-375. doi: 10.1002/1873-3468.13605. Epub 2019 Sep 27.
Here, we developed a method for measuring the in vivo redox state of the plastoquinone (PQ) pool in the cyanobacteria Synechocystis sp. PCC 6803. Cells were illuminated on a glass fiber filter, PQ was extracted with ethyl acetate and determined with HPLC. Control samples with fully oxidized and reduced photoactive PQ pool were prepared by far-red and high light treatments, respectively, or by blocking the photosynthetic electron transfer chemically before or after PQ in moderate light. The photoactive pool comprised 50% of total PQ. We find that the PQ pool of cyanobacteria behaves under light treatments qualitatively similarly as in plant chloroplasts, is less reduced during growth under high than under ambient CO and remains partly reduced in darkness.
在这里,我们开发了一种测量蓝藻 Synechocystis sp. PCC 6803 中质体醌 (PQ) 池体内氧化还原状态的方法。细胞在玻璃纤维滤光片上被照射,用乙酸乙酯提取 PQ,并通过 HPLC 进行测定。用远红光和高光处理、或在中光下用化学方法阻断光合电子传递来分别制备完全氧化和还原的光活性 PQ 池的对照样品。光活性池包含 50%的总 PQ。我们发现,蓝藻的 PQ 池在光处理下的行为与植物叶绿体中的类似,在高光下比在环境 CO 下生长时还原程度较低,在黑暗中仍部分还原。