量子体的分子取向2。吸收光谱、山活性和荧光产率

Kenneth Sauer, Roderic B. Park
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引用次数: 20

摘要

比较了菠菜量子体与全叶绿体和完整叶片的吸收光谱。利用散射透射技术表明,在制备分离叶绿体或超声分离小量子体聚集体的过程中,菠菜叶片在678.5 μ处的最大吸收不会发生变化。几种有机化合物和表面活性剂对量子体的吸收光谱、叶绿素荧光和希尔反应活性的影响可分为两大类。添加的丙酮、甲醇、尿素或十二烷基硫酸钠在明显低于在678 μ m处产生显著荧光增加或最大吸收蓝移所需的浓度时,可引起希尔活性损失。另一方面,用Triton X-100处理的量子体在高浓度的非离子洗涤剂中保持希尔活性,而不是产生明显的吸收和荧光变化。得出的主要结论是:(1)叶绿素最大值在红色区域的位置不是衡量光合作用材料进行希尔反应能力的敏感指标;(2)从正常光化学途径转移的能量通常不会立即表现为增强的荧光;(3)与量子体聚集体的叶绿素浓度相当的洗涤剂浓度能够对物理性质产生深远的影响。
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Molecular orientation in quantasomes II. Absorption spectra, hill activity and fluorescence yields

The absorption spectrum of spinach quantasomes is compared with those of whole chloroplasts and intact leaves. Using the scattered-transmission technique, it is shown that the absorption maximum at 678.5 mμ in spinach leaves is not shifted in the preparation of isolated chloroplasts or by sonication and separation of small quantasome aggregates.

The effects of several organic compounds and surface-active agents on the absorption spectra, chlorophyll fluorescence and Hill-reaction activity of quantasomes fall into two general classes. Added acetone, methanol, urea or sodium dodecyl sulfate induce a loss in Hill activity at appreciably lower concentrations than are required to give a pronounced fluorescence increase or blue shift in the absorption maximum at 678 mμ. On the other hand, quantasomes treated with Triton X-100 retain Hill activity at higher concentrations of the non-ionic detergent than are necessary to produce pronounced absorption and fluorescence changes. The principal conclusions reached are: (1) the position of the chlorophyll maximum in the red is not a sensitive measure of the ability of photosynthetic materials to carry out the Hill reaction, (2) energy diverted from normal photochemical pathways does not in general immediately appear as enhanced fluorescence, and (3) detergent concentrations comparable to the chlorophyll concentrations of quantasome aggregates are capable of profound effects on physical properties.

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Subject index Author index Photoreduction of nicotinamide-adenine dinucleotide by a cell-free system from Chromatium Chlorophylls of photosynthetic bacteria Photodimerization of urocanic acid in vitro and in vivo
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