Time-resolved targeted metabolomics shows an abrupt switch from Calvin-Benson-Bassham cycle to tricarboxylic acid cycle when the light is turned off.

IF 3.7 3区 生物学 Q2 PLANT SCIENCES
Yuan Xu, Stephanie C Schmiege, Thomas D Sharkey
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引用次数: 0

Abstract

In leaves, major CO₂ fluxes alternate between fixation by the Calvin-Benson-Bassham (CBB) cycle during light and release by the tricarboxylic acid (TCA) cycle in darkness. The speed at which leaf metabolism transitions between these pathways likely influences plant tolerance to fluctuating light conditions. To investigate these rapid metabolic shifts, we exposed leaves to ¹³CO₂ for 20 min to establish a quasi-steady state before abruptly turning off the light while maintaining ¹³CO₂ feeding. Within 10 s of dark transition, 3-phosphoglycerate levels rose significantly while most other CBB cycle intermediates decreased by more than 90%. Simultaneously, carbon accumulated in alanine, likely via pyruvate. Over the subsequent 10 min, six- and five-carbon TCA cycle intermediates steadily increased. In contrast, four-carbon TCA intermediates peaked at one minute, declined at three minutes, and rose again at 10 min, a pattern mirrored by most measured amino acids. These results reveal an exceptionally rapid metabolic reconfiguration from CO₂ fixation by the CBB cycle in light to TCA cycle activation for energy production in darkness, accompanied by substantial changes in amino acid metabolism.

时间分辨目标代谢组学显示,当光线关闭时,从卡尔文-本森-巴萨姆循环突然切换到三羧酸循环。
在叶片中,主要的CO₂通量在光照下由Calvin-Benson-Bassham (CBB)循环固定和黑暗中由三羧酸(TCA)循环释放之间交替进行。叶片代谢在这些途径之间转换的速度可能影响植物对波动光条件的耐受性。为了研究这些快速的代谢变化,我们将叶片暴露在¹³CO₂中20分钟以建立准稳定状态,然后在保持¹³CO₂摄食的情况下突然关灯。在暗转10 s内,3-磷酸甘油酸水平显著上升,而大多数其他CBB循环中间体水平下降90%以上。同时,碳可能通过丙酮酸在丙氨酸中积累。在随后的10分钟内,六碳和五碳TCA循环中间体稳步增加。相比之下,四碳TCA中间体在1分钟达到峰值,在3分钟下降,在10分钟再次上升,大多数测量的氨基酸都反映了这一模式。这些结果揭示了一个异常快速的代谢重构,从光下CBB循环固定CO 2到暗下TCA循环激活产生能量,伴随着氨基酸代谢的实质性变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Photosynthesis Research
Photosynthesis Research 生物-植物科学
CiteScore
6.90
自引率
8.10%
发文量
91
审稿时长
4.5 months
期刊介绍: Photosynthesis Research is an international journal open to papers of merit dealing with both basic and applied aspects of photosynthesis. It covers all aspects of photosynthesis research, including, but not limited to, light absorption and emission, excitation energy transfer, primary photochemistry, model systems, membrane components, protein complexes, electron transport, photophosphorylation, carbon assimilation, regulatory phenomena, molecular biology, environmental and ecological aspects, photorespiration, and bacterial and algal photosynthesis.
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