Oxborough K, Baker N R
Department of Biological Sciences, University of Essex, Colchester, UK.
Philos Trans R Soc Lond B Biol Sci. 2000 Oct 29;355(1402):1489-98. doi: 10.1098/rstb.2000.0709.
Photoinactivation of photosystem II (PS II) is a light-dependent process that frequently leads to break-down and replacement of the D1 polypeptide. Photoinhibition occurs when the rate of photoinactivation is greater than the rate at which D1 is replaced and results in a decrease in the maximum efficiency of PS II photochemistry. Downregulation, which increases non-radiative decay within PS II, also decreases the maximum efficiency of PS II photochemistry and plays an important role in protecting against photoinhibition by reducing the yield of photoinactivation. The yield of photoinactivation has been shown to be relatively insensitive to photosynthetically active photon flux density (PPFD). Formation of the P680 radical (P680+), through charge separation at PS II, generation of triplet-state P680 (3P680*), through intersystem crossing and charge recombination, and double reduction of the primary stable electron acceptor of PS II (the plastoquinone, Q(A)) are all potentially critical steps in the triggering of photoinactivation. In this paper, these processes are assessed using fluorescence data from attached leaves of higher plant species, in the context of a Stern-Volmer model for downregulation and the reversible radical pair equilibrium model. It is shown that the yield of P680+ is very sensitive to PPFD and that downregulation has very little effect on its production. Consequently, it is unlikely to be the trigger for photoinactivation. The yields of 3P680* generated through charge recombination or intersystem crossing are both less sensitive to PPFD than the yield of P680+ and are both decreased by down regulation. The yield of doubly reduced Q(A) increases with incident photon flux density at low levels, but is relatively insensitive at moderate to high levels, and is greatly decreased by downregulation. Consequently, 3P680* and doubly reduced Q(A) are both viable as triggers of photoinactivation.
光系统II(PS II)的光失活是一个依赖光的过程,常常导致D1多肽的分解和替换。当光失活速率大于D1被替换的速率时,就会发生光抑制,导致PS II光化学的最大效率降低。下调通过增加PS II内的非辐射衰变,也会降低PS II光化学的最大效率,并通过降低光失活产率在防止光抑制方面发挥重要作用。已表明光失活产率对光合有效光子通量密度(PPFD)相对不敏感。通过PS II处的电荷分离形成P680自由基(P680+),通过系间窜越和电荷复合产生三线态P680(3P680*),以及PS II的初级稳定电子受体(质体醌,Q(A))的双还原,都是触发光失活的潜在关键步骤。在本文中,在下调的Stern-Volmer模型和可逆自由基对平衡模型的背景下,使用来自高等植物附着叶片的荧光数据评估了这些过程。结果表明,P680+的产率对PPFD非常敏感,而下调对其产生的影响很小。因此,它不太可能是光失活的触发因素。通过电荷复合或系间窜越产生的3P680的产率对PPFD的敏感性均低于P680+的产率,且均因下调而降低。双还原Q(A)的产率在低水平时随入射光子通量密度增加,但在中高水平时相对不敏感,且因下调而大大降低。因此,3P680和双还原Q(A)都有可能作为光失活的触发因素。