Table 1.
Excitation wavelength, nm | Fluence, μJ/cm2 per pulse | Absorption probability per pulse | kA→B, s−1 | kB→A, s−1 |
515 | 26.9 | 0.32 | 0.94 | 0.50 |
11.4 | 0.14 | 0.077 | 0.33 | |
4.1 | 0.049 | 0.011 | 0.31 | |
840 | 18.4 | 0.41 | 0.086 | 0.26 |
8.1 | 0.18 | 0.11 | 0.27 | |
2.4 | 0.054 | 0.016 | 0.098 | |
1.3 | 0.029 | 0.0079 | 0.26 | |
0.51 | 0.011 | 0.0068 | 0.11 |
The switching rates kA→B and kB→A were determined for carotenoid and B850 excitation. The rates (ki→j) are calculated by dividing the number of events (i→j) by the total time in state i. The orders-of-magnitude increase in kA→B upon orders-of-magnitude increase in excitation fluence suggests this process is photoactivated. In contrast, kB→A remains the same order of magnitude, suggesting a thermal process. The linear dependence on excitation fluence, as well as the per pulse absorption probabilities for a single LH2 complex (23, 39), shows that the dynamics of states A and B are not a result of nonlinear effects.