Kotabová Eva, Kana Radek, Kyseláková Helena, Lípová Lenka, Novák Ondrej, Ilík Petr
Laboratory of Biophysics, Faculty of Science, Palacký University, Olomouc, Czech Republic.
J Plant Physiol. 2008 Oct 9;165(15):1563-71. doi: 10.1016/j.jplph.2008.01.005.
Light-induced deepoxidation of violaxanthin to antheraxanthin and zeaxanthin in plants is associated with the induction of pronounced xanthophyll-dependent non-photochemical quenching (NPQ). To date, a misbalance between a high amount of zeaxanthin in thylakoid membranes and low NPQ has been explained by an absence of lumen acidification (e.g. when NPQ is measured in the dark after high light stress). In this study, we report that this misbalance can also be observed under moderate light. We found this result (deepoxidation state, DEPS, above 55% and NPQ approximately 0.9) in barley leaves treated with 10 microM methyl viologen (MV) under white light (100 micromol photonsm(-2)s(-1), photosynthetically active radiation (PAR), growth irradiance). The addition of MV at this moderate light did not accelerate electron transport in thylakoid membranes, and induced only slight oxidative stress (no lipid peroxidation, almost unchanged maximum yield of photosystem II photochemistry, a decrease in activity of ascorbate peroxidase, and an increase in that of glutathion reductase). We suggest that, in leaves treated under the conditions used here, the lumen acidification induced by light-limited electron transport in thylakoid membranes was high enough to activate violaxanthin deepoxidase, but not sufficiently high to form the expected number of zeaxanthin-dependent quenching centers in photosystem II antennae.
植物中光诱导紫黄质深度氧化形成花药黄质和玉米黄质与显著的叶黄素依赖性非光化学猝灭(NPQ)的诱导有关。迄今为止,类囊体膜中大量玉米黄质与低NPQ之间的失衡已被解释为缺乏腔酸化(例如,在高光胁迫后于黑暗中测量NPQ时)。在本研究中,我们报告这种失衡在中等光照下也能观察到。我们在用10 microM甲基紫精(MV)处理的大麦叶片中发现了这一结果(深度氧化状态,DEPS,高于55%且NPQ约为0.9),处理条件为白光(100微摩尔光子·米⁻²·秒⁻¹,光合有效辐射(PAR),生长辐照度)。在这种中等光照下添加MV并未加速类囊体膜中的电子传递,且仅诱导了轻微的氧化应激(无脂质过氧化,光合系统II光化学的最大产量几乎不变,抗坏血酸过氧化物酶活性降低,谷胱甘肽还原酶活性增加)。我们认为,在此处所用条件下处理的叶片中,类囊体膜中光限制电子传递诱导的腔酸化足以激活紫黄质脱环氧化酶,但不足以在光合系统II天线中形成预期数量的玉米黄质依赖性猝灭中心。