Institut de Biologie Physico-Chimique, UMR 7141, CNRS et Université Pierre et Marie Curie (Paris VI), Paris, France.
Photosynth Res. 2009 Oct;102(1):85-93. doi: 10.1007/s11120-009-9487-2. Epub 2009 Aug 21.
Here, we describe a new imaging setup able to assess in vivo photosynthetic activity. The system specifically measures time-resolved chlorophyll fluorescence in response to light. It is composed of a fast digital camera equipped with a wide-angle lens for the analysis of samples up to 10 x 10 cm, i.e. entire plants or petri dishes. In the choice of CCD, we have opted for a 12-bits high frame rate [150 fps (frames per second)] at the expense of definition (640 x 480 pixels). Although the choice of digital camera is always a compromise between these two related features, we have designed a flexible system allowing the fast sampling of images (down to 100 micros) with a maximum spatial resolution. This image readout system, synchronized with actinic light and saturating pulses, allows a precise determination of F(0) and F(M), which is required to monitor PSII activity. This new imaging system, together with image processing techniques, is useful to investigate the heterogeneity of photosynthetic activity within leaves or to screen large numbers of unicellular algal mutant colonies to identify those with subtle changes in photosynthetic electron flow.
在这里,我们描述了一种新的成像设置,能够评估体内光合作用活性。该系统专门测量对光响应的时间分辨叶绿素荧光。它由一个快速的数码相机组成,配备广角镜头,可分析最大 10 x 10 厘米的样品,即整个植物或培养皿。在 CCD 的选择上,我们选择了 12 位高帧率[150 fps(每秒帧数)],牺牲了分辨率(640 x 480 像素)。尽管数码相机的选择总是这两个相关特性之间的折衷,但我们设计了一个灵活的系统,允许以最大的空间分辨率快速采集图像(低至 100 微秒)。该图像读出系统与光激活和饱和脉冲同步,允许精确确定 F(0)和 F(M),这是监测 PSII 活性所必需的。这种新的成像系统与图像处理技术一起,可用于研究叶片内光合作用活性的异质性,或筛选大量单细胞藻类突变体菌落,以鉴定那些光合作用电子流有细微变化的突变体。