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在叶内对光系统 I/光系统 II 叶绿素比值进行成像。

Imaging the Photosystem I/Photosystem II chlorophyll ratio inside the leaf.

机构信息

Laboratory of Biophysics, Wageningen University, P.O. Box 8128, 6700 ET Wageningen, The Netherlands.

Laboratory of Biophysics, Wageningen University, P.O. Box 8128, 6700 ET Wageningen, The Netherlands.

出版信息

Biochim Biophys Acta Bioenerg. 2017 Mar;1858(3):259-265. doi: 10.1016/j.bbabio.2017.01.008. Epub 2017 Jan 15.

Abstract

Oxygenic photosynthesis is driven by photosystems I (PSI) and II (PSII). In plants the number of chlorophylls of PSI versus PSII is adjusted to the light irradiance spectrum. On a timescale of days, this is regulated at the level of protein concentration. Instead, on a timescale of minutes, it is regulated by the dynamic association of light-harvesting complex II with either PSI or PSII. Thus far very diverse values have been reported for the PSI/PSII chlorophyll ratio, ranging from 0.54 to 1.4. The methods used require the isolation of chloroplasts and are time consuming. We present a fluorescence lifetime imaging approach that quantifies the PSI/PSII Chl ratio of chloroplasts directly in their natural leaf environment. In wild type Arabidopsis thaliana plants, grown under white light, the PSI/PSII chlorophyll ratio appeared to be 0.99±0.09 at the adaxial side and 0.83±0.05 at the abaxial side of the leaf. When these plants were acclimated to far red light for several days the PSI/PSII chlorophyll ratio decreased by more than a factor of 3 to compensate for the ineffective far red light absorption of PSII. This shows how plants optimize their light-harvesting capacity to the specific light conditions they encounter. Zooming in on single chloroplasts inside the leaf allowed to study the grana/stroma membrane network and their PSI/PSII chlorophyll ratios. The developed method will be useful to study dynamic processes in chloroplasts in intact leaves which involve changes in the grana and the stroma membranes such as state transitions.

摘要

放氧光合作用由光系统 I(PSI)和 II(PSII)驱动。在植物中,PSI 与 PSII 的叶绿素数量根据光辐照度谱进行调整。在数天的时间尺度上,这是通过蛋白质浓度水平进行调节的。相反,在数分钟的时间尺度上,它是通过光捕获复合物 II 与 PSI 或 PSII 的动态关联来调节的。到目前为止,PSI/PSII 叶绿素比的报告值差异很大,范围从 0.54 到 1.4。所使用的方法需要分离叶绿体,并且耗时。我们提出了一种荧光寿命成像方法,可直接在其天然叶片环境中定量测量叶绿体的 PSI/PSII Chl 比。在生长在白光下的野生型拟南芥植物中,PSI/PSII 叶绿素比在叶片的腹侧表面似乎为 0.99±0.09,在背侧表面为 0.83±0.05。当这些植物适应远红光数天时,PSI/PSII 叶绿素比下降了三倍以上,以补偿 PSII 对远红光的无效吸收。这表明植物如何根据它们遇到的特定光照条件优化其光捕获能力。在叶片内放大单个叶绿体,可以研究基粒/基质膜网络及其 PSI/PSII 叶绿素比。所开发的方法将有助于研究完整叶片中涉及基粒和基质膜变化(如状态转换)的叶绿体中的动态过程。

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