Miyatake Tomohiro, Shitasue Kyouhei, Omori Yushi, Nakagawa Kazuya, Fujiwara Manabu, Matsushita Takayuki, Tamiaki Hitoshi
Department of Materials Chemistry, Faculty of Science and Technology, Ryukoku University, Otsu, Shiga, 520-2194, Japan.
Photosynth Res. 2005 Nov;86(1-2):131-6. doi: 10.1007/s11120-005-2441-z.
The self-aggregation process of 3(1)-epimerically pure and mixed zinc methyl bacteriopheophorbides-d (ZMBPhes-d) was examined by stopped-flow technique. A 33(v/v)% tetrahydrofuran (THF) - water solution of ZMBPhe-d was rapidly mixed with a 7(v/v)% THF - water solution to form a chlorosome-type aggregate with a red-shifted Qy band around 700 nm. We observed a rapid autocatalytic aggregation in a subsecond time scale. Aggregates of the 3(1)R epimer increased with a change in the Qy absorption maximum from 698 to 705 nm, suggesting that small aggregates formed as intermediate species. In addition, the rate of aggregation was dependent on the stereochemistry at the 3(1)-position of ZMBPhe-d; the 3(1)R epimer self-aggregated more rapidly than the 3(1)S epimer.
采用停流技术研究了3(1)-差向异构体纯的和混合的甲基锌细菌脱镁叶绿酸-d(ZMBPhes-d)的自聚集过程。将ZMBPhe-d的33(体积/体积)%四氢呋喃(THF)-水溶液与7(体积/体积)%THF-水溶液快速混合,形成具有红移至700nm左右的Qy带的叶绿体样聚集体。我们观察到在亚秒时间尺度上的快速自催化聚集。3(1)R差向异构体的聚集体随着Qy吸收最大值从698nm变为705nm而增加,这表明小聚集体作为中间物种形成。此外,聚集速率取决于ZMBPhe-d 3(1)位的立体化学;3(1)R差向异构体比3(1)S差向异构体自聚集得更快。