Balevičius Vytautas, Duffy Christopher D P
School of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London, E1 4NS, UK.
Photosynth Res. 2020 Jun;144(3):301-315. doi: 10.1007/s11120-020-00737-8. Epub 2020 Apr 8.
Plants possess an essential ability to rapidly down-regulate light-harvesting in response to high light. This photoprotective process involves the formation of energy-quenching interactions between the chlorophyll and carotenoid pigments within the antenna of Photosystem II (PSII). The nature of these interactions is currently debated, with, among others, 'incoherent' or 'coherent' quenching models (or a combination of the two) suggested by a range of time-resolved spectroscopic measurements. In 'incoherent quenching', energy is transferred from a chlorophyll to a carotenoid and is dissipated due to the intrinsically short excitation lifetime of the latter. 'Coherent quenching' would arise from the quantum mechanical mixing of chlorophyll and carotenoid excited state properties, leading to a reduction in chlorophyll excitation lifetime. The key parameters are the energy gap, [Formula: see text] and the resonance coupling, J, between the two excited states. Coherent quenching will be the dominant process when [Formula: see text] i.e., when the two molecules are resonant, while the quenching will be largely incoherent when [Formula: see text] One would expect quenching to be energetically unfavorable for [Formula: see text] The actual dynamics of quenching lie somewhere between these limiting regimes and have non-trivial dependencies of both J and [Formula: see text] Using the Hierarchical Equation of Motion (HEOM) formalism we present a detailed theoretical examination of these excitation dynamics and their dependence on slow variations in J and [Formula: see text] We first consider an isolated chlorophyll-carotenoid dimer before embedding it within a PSII antenna sub-unit (LHCII). We show that neither energy transfer, nor the mixing of excited state lifetimes represent unique or necessary pathways for quenching and in fact discussing them as distinct quenching mechanisms is misleading. However, we do show that quenching cannot be switched 'on' and 'off' by fine tuning of [Formula: see text] around the resonance point, [Formula: see text] Due to the large reorganization energy of the carotenoid excited state, we find that the presence (or absence) of coherent interactions have almost no impact of the dynamics of quenching. Counter-intuitively significant quenching is present even when the carotenoid excited state lies above that of the chlorophyll. We also show that, above a rather small threshold value of [Formula: see text]quenching becomes less and less sensitive to J (since in the window [Formula: see text] the overall lifetime is independent of it). The requirement for quenching appear to be only that [Formula: see text] Although the coherent/incoherent character of the quenching can vary, the overall kinetics are likely robust with respect to fluctuations in J and [Formula: see text] This may be the basis for previous observations of NPQ with both coherent and incoherent features.
植物具有一项基本能力,即能在高光条件下迅速下调光捕获。这种光保护过程涉及到在光系统II(PSII)天线内叶绿素和类胡萝卜素色素之间形成能量猝灭相互作用。目前,这些相互作用的本质存在争议,一系列时间分辨光谱测量结果提出了“非相干”或“相干”猝灭模型(或两者的组合)等观点。在“非相干猝灭”中,能量从叶绿素转移到类胡萝卜素,并由于后者固有的短激发寿命而耗散。“相干猝灭”则源于叶绿素和类胡萝卜素激发态性质的量子力学混合,导致叶绿素激发寿命缩短。关键参数是两个激发态之间的能隙,[公式:见原文]以及共振耦合J。当[公式:见原文]时,即两个分子共振时,相干猝灭将是主导过程,而当[公式:见原文]时,猝灭在很大程度上是非相干的。对于[公式:见原文],人们会预期猝灭在能量上是不利的。猝灭的实际动力学介于这些极限情况之间,并且对J和[公式:见原文]都有复杂的依赖性。我们使用运动方程分层(HEOM)形式体系,对这些激发动力学及其对J和[公式:见原文]缓慢变化的依赖性进行了详细的理论研究。我们首先考虑一个孤立的叶绿素 - 类胡萝卜素二聚体,然后将其嵌入PSII天线亚基(LHCII)中。我们表明,能量转移以及激发态寿命的混合都不代表猝灭的独特或必要途径,实际上将它们作为不同的猝灭机制来讨论是具有误导性的。然而,我们确实表明,围绕共振点[公式:见原文]微调[公式:见原文]并不能使猝灭“开启”和“关闭”。由于类胡萝卜素激发态的大重组能,我们发现相干相互作用的存在(或不存在)对猝灭动力学几乎没有影响。与直觉相反,即使类胡萝卜素激发态高于叶绿素激发态,也存在显著的猝灭。我们还表明,在[公式:见原文]的一个相当小的阈值以上,猝灭对J的敏感性越来越低(因为在[公式:见原文]的窗口内,总体寿命与之无关)。猝灭的条件似乎仅仅是[公式:见原文]。尽管猝灭的相干/非相干特性可能会有所不同,但总体动力学可能对J和[公式:见原文]的波动具有鲁棒性。这可能是先前观察到的具有相干和非相干特征的非光化学猝灭的基础。