Jia Husen, Oguchi Riichi, Hope Alexander B, Barber James, Chow Wah Soon
Photobioenergetics Group, Research School of Biological Sciences, The Australian National University, Canberra, ACT 0200, Australia.
Planta. 2008 Oct;228(5):803-12. doi: 10.1007/s00425-008-0783-4. Epub 2008 Jul 18.
Linear and cyclic electron fluxes through Photosystem I in 1% CO(2) were quantified in spinach leaf tissue under severe water stress. Using actinic light with a peak at 697 nm for preferential light absorption by Photosystem I while also stimulating Photosystem II to improve redox poising, the cyclic electron flux after 60 s of illumination was a substantial proportion (33-44%) of the total electron flux through PSI at irradiances up to ~1,070 micromol photons m(-2) s(-1). At the maximum irradiance, the cyclic electron flux changed little with the progressive water loss from leaf tissue up to ~60%; by contrast, the linear electron flux was approximately halved. A reason for this differential effect of water stress on the capacity for cyclic and linear electron flow could be the increased crowding of soluble proteins in the stroma due to chloroplast shrinkage. Indeed the confinement of soluble proteins to a smaller chloroplast volume was indicated by cryo-scanning electron microscopy. It is known that the diffusion coefficient of large proteins is decreased when the background concentration of small proteins is raised; by contrast, the diffusion coefficient of small proteins is not affected by increasing the concentration of a large protein (Muramatsu and Minton in Proc Natl Acad Sci USA 85:2984-2988, 1988). Therefore, we suggest that linear electron flow, being coupled to the Calvin-Benson cycle, is limited by the diffusion of large macromolecules, especially the ribulose 1, 5-bisphosphate carboxylase/oxygenase complex. By contrast, cyclic electron flow, involving relatively small macromolecules such as ferredoxin, is less susceptible to inhibition by crowding in the stroma.
在严重水分胁迫下,对菠菜叶片组织中通过光系统I的线性和循环电子通量进行了量化,该过程是在1%二氧化碳浓度下进行的。使用峰值波长为697nm的光化光,以便光系统I优先吸收光,同时也刺激光系统II来改善氧化还原平衡。在高达1,070微摩尔光子·米⁻²·秒⁻¹的辐照度下,光照60秒后的循环电子通量占通过光系统I的总电子通量的相当大比例(33 - 44%)。在最大辐照度下,随着叶片组织水分逐渐流失至60%,循环电子通量变化不大;相比之下,线性电子通量大约减半。水分胁迫对循环和线性电子流动能力产生这种差异效应的一个原因可能是叶绿体收缩导致基质中可溶性蛋白质拥挤程度增加。实际上,低温扫描电子显微镜显示可溶性蛋白质被限制在较小的叶绿体体积中。众所周知,当小蛋白质的背景浓度升高时,大蛋白质的扩散系数会降低;相反,增加大蛋白质的浓度不会影响小蛋白质的扩散系数(村松和明顿,《美国国家科学院院刊》85:2984 - 2988, 1988)。因此,我们认为与卡尔文 - 本森循环相关的线性电子流受到大分子尤其是核酮糖1,5 - 二磷酸羧化酶/加氧酶复合物扩散的限制。相比之下,涉及诸如铁氧化还原蛋白等相对较小大分子的循环电子流,受基质中拥挤效应的抑制较小。