Institute for Photobiology of Cells and Organelles, Brandeis University, 02154, Waltham, MA, USA.
Planta. 1979 Jan;146(2):119-27. doi: 10.1007/BF00388221.
When treated with blue light, intact cells of Euglena gracilis Klebs var. bacillaris Cori, bleached strain W3BUL, show a series of positive peaks at 384, 411, and 440 nm in the blue-light-minus-dark difference spectrum; bleached strain 1224-5/24 shows a series of positive peaks at 386, 417, and 448 nm under the same conditions. The same changes are observed in a 27,000xg supernatant from darkgrown W3. The absorption change appears to be a consequence of shifts in the absorption of carotenoids; it is not seen in cells of W3BUL grown on SAN 9789 (4-chloro-5-(methylamino)-2-(α,α, α-trifluoro-m-tolyl)-3(2H)pyridazinone) to deplete the carotenoids or in cells of W10BSmL, a mutant lacking carotenoids. Inhibitors of flavin-mediated reactions, reductants and valinomycin had no effect on the activity of the system. The activity in the 27,000xg supernatant was associated with material of a molecular weight more than 2.5×10(6) and was insensitive to heating for 2 min at 100° C but was reduced or eliminated on longer heat treatment or addition of Triton X-100, indicating a possible association with membrane material. Photoactivity is enriched in the lower density fractions of a flotation gradient, and correlates with the ζ-carotene content in all fractions. Similar spectral changes can be obtained by comparing the iodine catalyzed cis-to-trans isomerization of ζ-carotene in a CS2-CHCl3 solvent. The action spectrum for the absorbance change shows effectiveness peaks in the 370-390 and 420-448-nm regions, with no marked effectiveness past 500 nm. Thus the photosensitizer may not be a carotenoid (at least not a normally-occurring C40 carotenoid). These blue-lightinduced absorption changes and their action spectra are discussed in relation to such blue-light-mediated responses as carotenogenesis, chloroplast development and phototaxis.
当用蓝光处理完整的衣藻(Euglena gracilis Klebs var. bacillaris Cori),漂白菌株 W3BUL 在蓝光减去暗差光谱中显示一系列正峰,分别在 384、411 和 440nm;在相同条件下,漂白菌株 1224-5/24 在 386、417 和 448nm 处显示一系列正峰。在暗培养的 W3 的 27000xg 上清液中也观察到相同的变化。吸收变化似乎是类胡萝卜素吸收的变化的结果;在 W3BUL 细胞中未观察到,W3BUL 细胞在 SAN 9789(4-氯-5-(甲氨基)-2-(α,α,α-三氟-间甲苯基)-3(2H)哒嗪酮)上生长以耗尽类胡萝卜素,或在缺乏类胡萝卜素的 W10BSmL 突变体中也未观察到。黄素介导的反应抑制剂、还原剂和缬氨霉素对该系统的活性没有影响。27000xg 上清液中的活性与分子量大于 2.5×10(6)的物质有关,并且对在 100°C 加热 2 分钟不敏感,但在较长时间的热处理或添加 Triton X-100 时减少或消除,表明可能与膜材料有关。光活性在浮选梯度的较低密度部分富集,并且与所有部分的 ζ-胡萝卜素含量相关。在 CS2-CHCl3 溶剂中比较 ζ-胡萝卜素的碘催化顺式-反式异构化,可以获得类似的光谱变化。吸收变化的作用光谱在 370-390nm 和 420-448nm 区域显示出有效性峰,在 500nm 后没有明显的有效性。因此,光敏剂可能不是类胡萝卜素(至少不是通常存在的 C40 类胡萝卜素)。这些蓝光诱导的吸收变化及其作用光谱与类胡萝卜素生成、叶绿体发育和趋光性等蓝光介导的反应有关。