Il'ina M D, Borisov A Iu
Biokhimiia. 1982 Dec;47(12):1954-62.
A number of membrane fragments and pigment-protein complexes of photosystem 1 was obtained from pea chloroplasts, using ionic and non-ionic detergents (SDS, digitonin, Triton X-100, lauryldimethylamine-N-oxide). The ratio of chlorophyll (Chl) a to P700 varied from 220 to 30. For non-dialyzed preparations the quantum yield of P700 photooxidation (phi e) measured by the initial rate of photobleaching at 696-698 nm with excitation at the Soret band of Chla was equal to 40-60%. When the P700 photooxidation was measured at 432 nm, the phi e value showed a further decrease to 20-40% during red light excitation over the range of 660-680 nm but rose to 70-90% at the exciting light wavelengths of greater than or equal to 695 nm. On the basis of the observed dependences the red absorption band was approximated by a sum of two spectra: the spectrum of Chla photoactive in P700 photooxidation and that of photoinactive Chla. Both spectra had maxima near the absorption peak of the object. The photoinactive fraction was additionally enriched by the long-wavelength absorption forms of Chla with an absorption maximum over the range of 684-690 nm. The amount of the bulk Chla in the photoinactive fraction was no less than 40%. The phi e value for freshly dialyzed preparation at a Chla/P700 ratio of 30 was equal to 50-60% independent of the exciting light wavelength. An addition of 0.05% Triton X-100 to this preparation caused: i) a blue shift of the absorption and fluorescence maxima; ii) a decrease of the long-wavelength absorption forms content of Chla and, iii) a considerable increase in fluorescence lifetime and quantum yield due to deaggregation of Chla and its solubilization by detergent micelles. The same phenomenon seems to be responsible for the formation of photoinactive fraction of a pigment, since after addition of a detergent the above-mentioned spectral dependence of phi e appeared, i.e. phi e showed a 3-fold decrease (down to 18%) within the region of 660-680 nm and a 1,6-fold increase (up to 90%) at 705-730 nm. These results suggest that the detergents destroy the intact construction of a light-harvesting antenna rather than that of the photosystem 1 reaction center.
使用离子型和非离子型去污剂(十二烷基硫酸钠、洋地黄皂苷、聚山梨醇酯80、月桂基二甲基氧化胺),从豌豆叶绿体中获得了一些光系统I的膜片段和色素-蛋白质复合物。叶绿素(Chl)a与P700的比例在220至30之间变化。对于未透析的制剂,通过在叶绿素a的Soret带激发下,在696 - 698nm处光漂白的初始速率测量的P700光氧化量子产率(φe)等于40 - 60%。当在432nm处测量P700光氧化时,在660 - 680nm范围内的红光激发期间,φe值进一步降至20 - 40%,但在大于或等于695nm的激发光波长下升至70 - 90%。基于观察到的依赖性,红色吸收带由两个光谱的总和近似:在P700光氧化中具有光活性的叶绿素a光谱和无光活性的叶绿素a光谱。两个光谱在目标吸收峰附近都有最大值。无光活性部分通过叶绿素a的长波长吸收形式进一步富集,其吸收最大值在684 - 690nm范围内。无光活性部分中大量叶绿素a的含量不少于40%。对于新鲜透析的制剂,在叶绿素a/P700比例为30时,φe值等于50 - 60%,与激发光波长无关加入0 . 05%的聚山梨醇酯80到该制剂中会导致:i)吸收和荧光最大值的蓝移;ii)叶绿素a的长波长吸收形式含量的降低;iii)由于叶绿素a的解聚及其被去污剂胶束溶解,荧光寿命和量子产率显著增加。相同的现象似乎是色素无光活性部分形成的原因,因为加入去污剂后出现了上述φe的光谱依赖性,即在660 - 680nm区域内φe下降3倍(降至18%),在705 - 730nm处增加1.6倍(高达90%)。这些结果表明,去污剂破坏了光捕获天线的完整结构,而不是光系统I反应中心的结构。