Plant Molecular Sciences Group, Department of Botany, University of Glasgow, G12 8QQ, Glasgow, Scotland, UK.
Photosynth Res. 1994 Apr;40(1):107-17. doi: 10.1007/BF00019049.
A profile of high light to intense self-shading conditions was constructed using a white light source and cultures of the cyanobacterium Synechococcus 6301; this profile approximates to a natural self-shading gradient of decreasing light intensity and PS II/PS I excitation ratio. Samples of S.6301 were placed along this profile and allowed to state adapt. To separate the effects of light intensity and wavelength on state adaptation, samples were also placed in a shade profile produced by a white light source and neutral density filters. After adaptation, samples were fixed in their resulting state by the addition of glutaraldehyde, and fluorescence measurements were made at 35° C or -160 °C. It is concluded: 1. Under conditions of deep shade (<5 μmol m(-2)s(-1) PAR) and weak shade (>200 μmol m(-2)s(-1) PAR), cells adapt to a low PS II fluorescence state (state 2); in moderate shade (20-60 μmol m(-2)s(-1)PAR) cells adapt to a high PS II fluorescence state (state 1). We suggest these findings provide evidence for the operation of different factors on the control of state adaptations in cyanobacteria; one set operates at low light and another at high light intensities. 2. Under conditions of self-shading, there is little evidence to support the contention that state adaptations in cyanobacteria are produced by wavelength-dependent changes in the PS II/PS I excitation ratio, instead, it appaers they are produced by changes in the intensity of incident irradiation. 3. The observed fluorescence changes do not appear to involve major changes in the phycobilisome sensitisation of PS II and PS I. Instead, it appears that these changes are effected by alterations in Φ(F) of PS II (i.e. changes in PS II excitation density caused by alterations in the rate constants controlling spillover to PS I, photochemistry, fluorescence emission or thermal deactivation.
构建了一个高光强到强自遮光条件的轮廓,使用白光光源和蓝藻聚球藻 6301 的培养物;该轮廓近似于光强度和 PS II/PS I 激发比逐渐降低的自然自遮光梯度。将 S.6301 的样品放置在该轮廓上,并允许其适应。为了分离光强度和波长对状态适应的影响,还将样品放置在白光光源和中性密度滤光片产生的遮光轮廓中。适应后,通过添加戊二醛将样品固定在其最终状态,并在 35°C 或-160°C 下进行荧光测量。得出结论:1. 在深遮光(<5 μmol m(-2)s(-1)PAR)和弱遮光(>200 μmol m(-2)s(-1)PAR)条件下,细胞适应于低 PS II 荧光状态(状态 2);在中度遮光(20-60 μmol m(-2)s(-1)PAR)下,细胞适应于高 PS II 荧光状态(状态 1)。我们认为这些发现为蓝藻中状态适应的控制存在不同因素提供了证据;一组在低光下运作,另一组在高光强下运作。2. 在自遮光条件下,几乎没有证据支持蓝藻中的状态适应是由 PS II/PS I 激发比的波长依赖性变化产生的论点,相反,它们似乎是由入射辐射强度的变化产生的。3. 观察到的荧光变化似乎不涉及藻胆体对 PS II 和 PS I 的敏化的重大变化。相反,似乎这些变化是通过 PS II 的 Φ(F)的改变来实现的(即通过控制溢至 PS I、光化学、荧光发射或热失活的速率常数的改变来改变 PS II 的激发密度。