Departments of Biology and Chemistry, Washington University in St. Louis, MO 63130, USA.
Photosynth Res. 2010 Jun;104(2-3):283-92. doi: 10.1007/s11120-010-9554-8. Epub 2010 May 12.
In what appears to be a common theme for all phototrophs, heliobacteria exhibit complex modulations of fluorescence yield when illuminated with actinic light and probed on a time scale of micros to minutes. The fluorescence yield from cells of Heliobacterium modesticaldum remained nearly constant for the first 10-100 ms of illumination and then rose to a maximum level with one or two inflections over the course of many seconds. Fluorescence then declined to a steady-state value within about one minute. In this analysis, the origins of the fluorescence induction in whole cells of heliobacteria are investigated by treating cells with a combination of electron accepters, donors, and inhibitors of the photosynthetic electron transport, as well as varying the temperature. We conclude that fluorescence modulation in H. modesticaldum results from acceptor-side limitation in the reaction center (RC), possibly due to charge recombination between P(800) (+) and A(0) (-).
在所有光养生物中,似乎都存在一个共同的主题,即在光致发光时,当用微秒到分钟的时间尺度探测时,产氢菌会表现出荧光产率的复杂调制。温和产氢菌(Heliobacterium modesticaldum)细胞的荧光产率在照明的最初 10-100 毫秒内几乎保持不变,然后在几秒钟内上升到最大值,并出现一个或两个拐点。然后,荧光在大约一分钟内下降到稳定状态。在这项分析中,通过用电子受体、供体和光合作用电子传递抑制剂的组合处理细胞,以及改变温度,来研究产氢菌整个细胞中荧光诱导的起源。我们的结论是,温和产氢菌(H. modesticaldum)的荧光调制是由于反应中心(RC)的受体侧限制,可能是由于 P(800)(+)和 A(0)(-)之间的电荷复合。