Cyclic and pseudo-cyclic electron pathways play antagonistic roles during nitrogen deficiency in Chlamydomonas reinhardtii.

IF 6.5 1区 生物学 Q1 PLANT SCIENCES Plant Physiology Pub Date : 2024-11-19 DOI:10.1093/plphys/kiae617
Ousmane Dao, Adrien Burlacot, Felix Buchert, Marie Bertrand, Pascaline Auroy, Carolyne Stoffel, Sai Kiran Madireddi, Jacob Irby, Michael Hippler, Gilles Peltier, Yonghua Li-Beisson
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Abstract

Nitrogen (N) scarcity frequently constrains global biomass productivity. N deficiency halts cell division, downregulates photosynthetic electron transfer, and enhances carbon storage. However, the molecular mechanism downregulating photosynthesis during N deficiency and its relationship with carbon storage are not fully understood. Proton Gradient Regulator-like 1 (PGRL1) controlling cyclic electron flow (CEF) and Flavodiiron proteins (FLV) involved in pseudo-CEF (PCEF) are major players in the acclimation of photosynthesis. To determine the role of PGRL1 or FLV in photosynthesis under N deficiency, we measured photosynthetic electron transfer, oxygen gas exchange, and carbon storage in Chlamydomonas reinhardtii pgrl1 and flvB knockout mutants. Under N deficiency, pgrl1 maintained higher net photosynthesis and O2 photoreduction rates and higher levels of Cytochrome b6f and PSI compared to the control and flvB. The photosynthetic activity of flvB and pgrl1 flvB double mutants decreased in response to N deficiency, similar to the control strains. Furthermore, the preservation of photosynthetic activity in pgrl1 was accompanied by an increased accumulation of triacylglycerol in certain genetic backgrounds but not others, highlighting the importance of gene-environment interaction in determining traits such as oil content. Our results suggest that in the absence of PGRL1-controlled CEF, FLV-mediated PCEF maintains net photosynthesis at a high level and that CEF and PCEF play antagonistic roles during N deficiency. They further illustrate how a strain's nutrient status and genetic makeup can affect regulation of photosynthetic energy conversion in relation to carbon storage and provide additional strategies for improving lipid productivity in algae.

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环状电子途径和假环状电子途径在莱茵衣藻缺氮过程中发挥拮抗作用
氮(N)的缺乏经常制约全球生物量的生产。缺氮会导致细胞分裂停止、光合电子传递失调以及碳储存增加。然而,人们对缺氮时光合作用下调的分子机制及其与碳储存的关系还不完全清楚。控制循环电子流(CEF)的类质子梯度调节器 1(PGRL1)和参与假CEF(PCEF)的黄酮铁蛋白(FLV)是光合作用适应性的主要参与者。为了确定 PGRL1 或 FLV 在氮缺乏条件下光合作用中的作用,我们测量了莱茵衣藻 pgrl1 和 flvB 基因敲除突变体的光合电子传递、氧气体交换和碳储存。与对照和flvB相比,在氮缺乏条件下,pgrl1能维持较高的净光合作用和O2光还原率,以及较高的细胞色素b6f和PSI水平。flvB 和 pgrl1 flvB 双突变体的光合作用活性在氮缺乏时下降,与对照品系相似。此外,在某些遗传背景中,pgrl1光合作用活性的保持伴随着三酰甘油积累的增加,而在其他遗传背景中则没有,这凸显了基因与环境相互作用在决定含油量等性状方面的重要性。我们的研究结果表明,在缺乏 PGRL1 控制的 CEF 的情况下,FLV 介导的 PCEF 可将净光合作用维持在较高水平,而且在氮缺乏时,CEF 和 PCEF 起着拮抗作用。它们进一步说明了菌株的营养状况和基因组成如何影响光合作用能量转换与碳储存的关系,并为提高藻类的脂质生产力提供了新的策略。
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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
期刊最新文献
Histone modification H3K27me3 is essential during chilling-induced flowering in Litchi chinensis Packaging “vegetable oils”: Insights into plant lipid droplet proteins CELL DIVISION CYCLE 5 controls floral transition by regulating flowering gene transcription and splicing in Arabidopsis. Cyclic and pseudo-cyclic electron pathways play antagonistic roles during nitrogen deficiency in Chlamydomonas reinhardtii. The E3 ubiquitin ligase COP1 and transcription factors HY5 and RHD6 integrate light signaling and root hair development.
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