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Systems Analysis of the Response of Photosynthesis, Metabolism, and Growth to an Increase in Irradiance in the Photosynthetic Model Organism Chlamydomonas reinhardtii

机译:光合作用模型生物莱茵衣藻光合作用,代谢和生长对辐照度增加的响应的系统分析

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We investigated the systems response of metabolism and growth after an increase in irradiance in the nonsaturating range in the algal model Chlamydomonas reinhardtii. In a three-step process, photosynthesis and the levels of metabolites increased immediately, growth increased after 10 to 15 min, and transcript and protein abundance responded by 40 and 120 to 240 min, respectively. In the first phase, starch and metabolites provided a transient buffer for carbon until growth increased. This uncouples photosynthesis from growth in a fluctuating light environment. In the first and second phases, rising metabolite levels and increased polysome loading drove an increase in fluxes. Most Calvin-Benson cycle (CBC) enzymes were substrate-limited in vivo, and strikingly, many were present at higher concentrations than their substrates, explaining how rising metabolite levels stimulate CBC flux. Rubisco, fructose-1,6-biosphosphatase, and seduheptulose-1,7-bisphosphatase were close to substrate saturation in vivo, and flux was increased by posttranslational activation. In the third phase, changes in abundance of particular proteins, including increases in plastidial ATP synthase and some CBC enzymes, relieved potential bottlenecks and readjusted protein allocation between different processes. Despite reasonable overall agreement between changes in transcript and protein abundance (R-2 = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance.
机译:我们研究了藻类模型莱茵衣藻非饱和范围内辐照度增加后新陈代谢和生长的系统响应。在三步过程中,光合作用和代谢物水平立即增加,在10至15分钟后生长增加,并且转录本和蛋白质丰度分别在40和120至240分钟时响应。在第一阶段,淀粉和代谢产物为碳提供了暂时的缓冲,直到生长增加。这使光合作用与波动的光照环境中的生长脱钩。在第一和第二阶段,代谢物水平的提高和多核糖体负荷的增加推动了通量的增加。大多数Calvin-Benson循环(CBC)酶在体内受底物限制,而且引人注目的是,许多酶的浓度都高于其底物,这说明了代谢物水平的提高如何刺激CBC通量。 Rubisco,1,6-果糖生物磷酸酶和seduheptulose-1,7-双磷酸酶在体内接近底物饱和度,并且通量通过翻译后激活而增加。在第三阶段,特定蛋白质的丰度变化,包括质体ATP合酶和某些CBC酶的增加,缓解了潜在的瓶颈,并重新调整了不同过程之间的蛋白质分配。尽管转录本变化和蛋白质丰度之间存在合理的总体一致(R-2 = 0.24),但许多蛋白质(包括光合作用中的蛋白质)的变化与转录本丰度无关。

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