State Key Laboratory of Crop Biology, Shandong Agricultural University, Tai'an 271018, Shandong, China.
BMC Plant Biol. 2012 Mar 20;12:40. doi: 10.1186/1471-2229-12-40.
It is known that excess reducing equivalents in the form of NADPH in chloroplasts can be transported via shuttle machineries, such as the malate-oxaloacetate (OAA) shuttle, into the mitochondria, where they are efficiently oxidised by the mitochondrial alternative oxidase (AOX) respiratory pathway. Therefore, it has been speculated that the AOX pathway may protect plants from photoinhibition, but the mechanism by which this protection occurs remains to be elucidated.
The observation that the malate-OAA shuttle activity and the AOX pathway capacity increased markedly after intense light treatment in Rumex K-1 leaves indicates that excess NADPH was transported from the chloroplasts and oxidised by the AOX pathway. The inhibition of the AOX pathway by salicylhydroxamic acid (SHAM) caused the over-reduction of the photosystem I (PSI) acceptor side, as indicated by the increases in the extent of reduction of P700+. Furthermore, the photosynthetic linear electron flow was restricted, which was indicated by the decreases in the PSII electron transport rate (ETR) and the photosynthetic O₂ evolution rate. The restriction of the photosynthetic linear electron flow, which generates the thylakoid ΔpH, inevitably decreased the de-epoxidation of the xanthophyll cycle (ΔPRI). Therefore, the induction of non-photochemical quenching (NPQ) was suppressed when the AOX pathway was inhibited. The effect of the inhibition of the AOX pathway on NPQ induction was less at 20 mM NaHCO₃ than at 1 mM NaHCO₃. The suppression of NPQ induction by the inhibition of the AOX pathway was also observed during the induction phase of photosynthesis. In addition, the inhibition of the AOX pathway increased the accumulation of hydrogen peroxide (H₂O₂), suggesting that the AOX pathway functions as an antioxidant mechanism.
The inhibition of the AOX pathway resulted in the rapid accumulation of NADPH in the chloroplasts, which caused the over-reduction of the PSI acceptor side. Furthermore, the restriction of the photosynthetic linear electron flow due to the inhibition of the AOX pathway limited the generation of the thylakoid ΔpH and suppressed the induction of NPQ. Therefore, the mitochondrial AOX pathway protected the photosynthetic apparatus against photodamage by alleviating the over-reduction of the PSI acceptor side and accelerating the induction of NPQ in Rumex K-1 leaves.
已知叶绿体中以 NADPH 形式存在的过量还原当量可以通过穿梭机制(如苹果酸-草酰乙酸(OAA)穿梭)运输到线粒体中,在那里它们被线粒体替代氧化酶(AOX)呼吸途径有效地氧化。因此,有人推测 AOX 途径可以保护植物免受光抑制,但这种保护作用的机制仍有待阐明。
在 Rumex K-1 叶片中强光处理后,观察到苹果酸-OAA 穿梭活性和 AOX 途径能力显著增加,表明过量的 NADPH 从叶绿体中运输并被 AOX 途径氧化。水杨羟肟酸(SHAM)抑制 AOX 途径导致 PSI 受体侧过度还原,如 P700+还原程度增加所示。此外,光合作用线性电子流受到限制,这表现为 PSII 电子传递率(ETR)和光合作用 O₂ 释放率降低。生成类囊体 ΔpH 的光合线性电子流的限制不可避免地降低了叶黄素循环(ΔPRI)的脱氧化作用。因此,当 AOX 途径被抑制时,非光化学猝灭(NPQ)的诱导受到抑制。在 20 mM NaHCO₃ 下,AOX 途径抑制对 NPQ 诱导的影响小于在 1 mM NaHCO₃ 下。在光合作用的诱导阶段,也观察到 AOX 途径抑制对 NPQ 诱导的抑制作用。此外,AOX 途径的抑制增加了过氧化氢(H₂O₂)的积累,表明 AOX 途径作为一种抗氧化机制发挥作用。
AOX 途径的抑制导致叶绿体中 NADPH 的快速积累,从而导致 PSI 受体侧的过度还原。此外,由于 AOX 途径的抑制,光合作用线性电子流的限制限制了类囊体 ΔpH 的产生,并抑制了 NPQ 的诱导。因此,线粒体 AOX 途径通过缓解 PSI 受体侧的过度还原和加速 NPQ 的诱导,保护光合器官免受光损伤。