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首页> 外文期刊>Photosynthesis Research: An International Journal >Snapshot transient absorption spectroscopy: toward in vivo investigations of nonphotochemical quenching mechanisms
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Snapshot transient absorption spectroscopy: toward in vivo investigations of nonphotochemical quenching mechanisms

机译:快照瞬态吸收光谱:朝向体内研究的非平淡细胞淬火机制

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摘要

Although the importance of nonphotochemical quenching (NPQ) on photosynthetic biomass production and crop yields is well established, the in vivo operation of the individual mechanisms contributing to overall NPQ is still a matter of controversy. In order to investigate the timescale and activation dynamics of specific quenching mechanisms, we have developed a technique called snapshot transient absorption (TA) spectroscopy, which can monitor molecular species involved in the quenching response with a time resolution of 30 s. Using intact thylakoid membrane samples, we show how conventional TA kinetic and spectral analyses enable the determination of the appropriate wavelength and time delay for snapshot TA experiments. As an example, we show how the chlorophyll-carotenoid charge transfer and excitation energy transfer mechanisms can be monitored based on signals corresponding to the carotenoid (Car) radical cation and Car S-1 excited state absorption, respectively. The use of snapshot TA spectroscopy together with the previously reported fluorescence lifetime snapshot technique (Sylak-Glassman et al. in Photosynth Res 127:69-76, 2016) provides valuable information such as the concurrent appearance of specific quenching species and overall quenching of excited Chl. Furthermore, we show that the snapshot TA technique can be successfully applied to completely intact photosynthetic organisms such as live cells of Nannochloropsis. This demonstrates that the snapshot TA technique is a valuable method for tracking the dynamics of intact samples that evolve over time, such as the photosynthetic system in response to high-light exposure.
机译:虽然非平淡细胞淬火(NPQ)对光合生物量产生和作物产量的重要性成立,但为整体NPQ提供的各个机制的体内运作仍然是一个争议的问题。为了研究特定猝灭机制的时间尺度和激活动态,我们开发了一种称为快照瞬态吸收(TA)光谱的技术,其可以通过30 s的时间分辨率监测猝灭响应中涉及的分子种类。使用完整的囊体膜样品,我们展示了常规的TA动力学和光谱分析如何确定快照TA实验的适当波长和时间延迟。作为一个例子,我们展示了如何基于对应于类胡萝卜素(汽车)自由基阳离子和汽车S-1激发状态吸收的信号来监测叶绿素类电荷转移和激发能量转移机制。使用快照TA光谱与先前报告的荧光寿命快照技术(Sylak-Glassman等人。在Photosynth Res 127:69-76,2016中)提供了有价值的信息,例如特定淬火物种的并发外观和兴奋的整体淬火chl。此外,我们表明快照TA技术可以成功应用于完全完整的光合生物,例如Nannchloropsis的活细胞。这表明快照TA技术是跟踪随时间发展的完整样本的动态的有价值方法,例如响应于高光曝光的光合系统。

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