Proctor Michael C F, Ligrone Roberto, Duckett Jeffrey G
School of Biological Sciences, University of Exeter, Geoffrey Pope Building, Stocker Road, Exeter EX4 4QD, UK.
Ann Bot. 2007 Jun;99(6):1243. doi: 10.1093/aob/mcm098.
This study explores basic physiological features and time relations of recovery of photosynthetic activity and CO2 uptake following rehydration of a desiccation-tolerant moss in relation to the full temporal sequence of cytological changes associated with recovery to the normal hydrated state. It seeks reconciliation of the apparently conflicting published physiological and cytological evidence on recovery from desiccation in bryophytes.
Observations were made of water-stress responses and recovery using infrared gas analysis and modulated chlorophyll fluorescence, and of structural and ultrastructural changes by light and transmission electron microscopy.
Net CO2 uptake fell to zero at approx. 40 % RWC, paralleling the fluorescence parameter PhiPSII at 200 micromol m(-2) s(-1) PPFD. On re-wetting the moss after 9-18 d desiccation, the initially negative net CO2 uptake became positive 10-30 min after re-wetting, restoring a net carbon balance after approx. 0.3-1 h. The parameter Fv/Fm reached approx. 80 % of its pre-desiccation value within approx. 10 min of re-wetting. In the presence of the protein-synthesis inhibitors chloramphenicol and cycloheximide, recovery of Fv/Fm (and CO2 exchange) proceeded normally in the dark, but declined rapidly in the light. Though initial recovery was rapid, both net CO2 uptake and Fv/Fm required approx. 24 h to recover completely to pre-desiccation values. The fixation protocols produced neither swelling of tissues nor plasmolysis. Thylakoids, grana and mitochondrial cristae remained intact throughout the drying-re-wetting cycle, but there were striking changes in the form of the organelles, especially the chloroplasts, which had prominent lobes and lamellar extensions in the normally hydrated state, but rounded off when desiccated, returning slowly to their normal state within approx. 24 h of re-wetting. Sub-cellular events during desiccation and re-wetting were generally similar to those seen in published data from the pteridophyte Selaginella lepidophylla.
Initial recovery of respiration and photosynthesis (as of protein synthesis) is very rapid, and independent of protein synthesis, suggesting physical reactivation of systems conserved intact through desiccation and rehydration, but full recovery takes approx. 24 h. This is consistent with the cytological evidence, which shows the thylakoids and cristae remaining intact through the whole course of dehydration and rehydration. Substantial and co-ordinated changes in other cell components, which must affect spatial relationships of organelles and metabolic systems, return to normal on a time span similar to full recovery of photosynthesis. Comparison of the present data with recently published results suggests a significant role for the cytoskeleton in desiccation responses.
本研究探讨了耐旱苔藓复水后光合活性恢复和二氧化碳吸收的基本生理特征及时间关系,以及与恢复到正常水合状态相关的细胞学变化的完整时间序列。本研究旨在调和已发表的关于苔藓植物从脱水状态恢复的生理和细胞学证据之间明显矛盾的情况。
利用红外气体分析和调制叶绿素荧光观察水分胁迫响应和恢复情况,通过光学显微镜和透射电子显微镜观察结构和超微结构变化。
净二氧化碳吸收在相对含水量约40%时降至零,与200 μmol m⁻² s⁻¹光合有效辐射下的荧光参数光化学猝灭系数(PhiPSII)平行。在脱水9 - 18天后对苔藓进行复水,最初负的净二氧化碳吸收在复水后10 - 30分钟变为正值,约0.3 - 1小时后恢复净碳平衡。光系统II最大光化学效率(Fv/Fm)参数在复水约10分钟内达到脱水前值的约80%。在存在蛋白质合成抑制剂氯霉素和放线菌酮的情况下,Fv/Fm(以及二氧化碳交换)的恢复在黑暗中正常进行,但在光照下迅速下降。尽管初始恢复迅速,但净二氧化碳吸收和Fv/Fm都需要约24小时才能完全恢复到脱水前的值。固定方案既未导致组织肿胀也未导致质壁分离。类囊体、基粒和线粒体嵴在整个干燥 - 复水周期中保持完整,但细胞器的形态有显著变化,尤其是叶绿体,在正常水合状态下有突出的叶和片层延伸,但脱水时变圆,复水约24小时内缓慢恢复到正常状态。脱水和复水过程中的亚细胞事件通常与已发表的来自蕨类植物卷柏的数据中观察到的相似。
呼吸作用和光合作用(以及蛋白质合成)的初始恢复非常迅速,且与蛋白质合成无关,这表明通过脱水和复水保持完整的系统发生了物理性再激活,但完全恢复需要约24小时。这与细胞学证据一致,该证据表明类囊体和嵴在脱水和复水的整个过程中保持完整。其他细胞成分发生的大量且协调的变化,必然会影响细胞器和代谢系统的空间关系,在与光合作用完全恢复相似的时间跨度内恢复正常。将本研究数据与最近发表的结果进行比较表明,细胞骨架在脱水响应中起重要作用。