藻类在稳态光合作用中荧光能力的变化

Michael Kamrin
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引用次数: 2

摘要

小球藻悬浮液的光照时间足够长,使诱导期完成,从而达到稳态光合作用。然后用狭缝器将激发的光以每秒4次的速度切割,然后在黑暗时期用低强度测量光束跟踪藻类发出荧光的能力。荧光容量的衰减近似为指数,在室温下的时间常数约为20毫秒。该时间常数的温度依赖性符合活化能为0.34 eV的Arrhenius方程。我们从这些结果中得出结论,荧光提供了稳态光合作用过程中光合能量迁移的直接测量,并且这种能量迁移的动力学限制步骤涉及电子传递链酶。
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Changes in the capacity of algae to fluoresce during steady-state photosynthesis

A suspension of Chlorella was illuminated long enough for the induction period to be complete and thus for stead-state photosynthesis to be achieved. Then the exciting light was chopped by a slotter about 4 times per sec and the capacity of the algae to fluoresce was followed by means of a low-intensity measuring beam during the dark period. The decay of the fluorescence capacity was approximately exponential and was characterized by a time constant of about 20 msec at room temperature. The temperature dependence of this time constant fits an Arrhenius equation with an activation energy of 0.34 eV. We concluded from these results that fluorescence provides a direct measure of photosynthetic energy migration during steady-state photosynthesis and also that the kinetically limiting step in this energy migration involves the electron transport chain enzymes.

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