Minimized dark consumption of Calvin cycle intermediates facilitates the initiation of photosynthesis in Synechocystis sp. PCC 6803.

IF 3.9 2区 生物学 Q2 CELL BIOLOGY Plant and Cell Physiology Pub Date : 2024-09-06 DOI:10.1093/pcp/pcae102
Kenya Tanaka, Akihiko Kondo, Tomohisa Hasunuma
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Abstract

Cyanobacteria intricately regulate their metabolic pathways during the diurnal cycle to ensure survival and growth. Under dark conditions, the breakdown of glycogen, an energy reserve, in these organisms replenishes Calvin cycle intermediates, especially downstream glycolytic metabolites, which are necessary for photosynthesis initiation upon light irradiation. However, it remains unclear how the accumulation of these intermediates is maintained in the dark despite limited glycogen availability. Therefore, in this study, we investigated the regulation of downstream glycolytic metabolites of the Calvin cycle under dark and light treatment using Synechocystis sp. PCC 6803. Our results showed that during the dark period, low pyruvate kinase (Pyk) activity ensured metabolite accumulation, while endogenous Pyk overexpression significantly lowered the accumulation of glycolytic intermediates. Remarkably, wild type Synechocystis maintained oxygen evolution ability throughout dark treatment for over 2 d, while Pyk overexpression resulted in decreased oxygen evolution after 16 h of dark treatment. These results indicated that limiting Pyk activity via darkness treatment facilitates photosynthetic initiation by maintaining glycolytic intermediates. Similarly, phosphoenolpyruvate carboxylase (PepC) overexpression decreased oxygen evolution under dark treatment; however, its effect was lower than that of Pyk. Further, we noted that as PepC overexpression decreased the levels of glycolytic intermediates in the dark, sugar phosphates in the Calvin-Benson-Bassham (CBB) cycle showed high accumulation, suggesting that sugar phosphates play important roles in supporting photosynthesis initiation. Therefore, our study highlights the importance of controlling the metabolic pathways through which glycolytic and CBB cycle intermediates are consumed (defined as cataplerosis of CBB cycle) to ensure stable photosynthesis.

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将卡尔文循环中间产物的暗消耗减至最低可促进 Synechocystis sp. PCC 6803 开始光合作用。
蓝藻在昼夜周期中复杂地调节其代谢途径,以确保生存和生长。在黑暗条件下,这些生物体内能量储备糖原的分解会补充卡尔文循环的中间产物,尤其是下游的糖酵解代谢产物,它们是在光照下启动光合作用所必需的。然而,尽管糖原的可用性有限,这些中间产物的积累在黑暗中是如何维持的仍不清楚。因此,在本研究中,我们使用 Synechocystis sp. PCC 6803 对卡尔文循环下游糖酵解代谢产物在黑暗和光照处理下的调控进行了研究。结果表明,在黑暗时期,低丙酮酸激酶(Pyk)活性确保了代谢物的积累,而内源 Pyk 的过表达则显著降低了糖酵解中间产物的积累。值得注意的是,野生型 Synechocystis 在超过 2 天的黑暗处理过程中都能保持氧进化能力,而 Pyk 过表达则会在黑暗处理 16 小时后导致氧进化能力下降。这些结果表明,通过黑暗处理限制 Pyk 活性可维持糖酵解中间产物,从而促进光合作用的启动。同样,过表达磷酸烯醇丙酮酸羧化酶(PepC)也会降低黑暗处理下的氧进化;但其影响低于 Pyk。此外,我们还注意到,由于 PepC 过表达降低了暗处糖酵解中间产物的水平,卡尔文-本森-巴塞尔姆(CBB)循环中的糖磷酸盐出现了高积累,这表明糖磷酸盐在支持光合作用启动方面发挥着重要作用。因此,我们的研究强调了控制糖酵解和 CBB 循环中间产物消耗的代谢途径(定义为 CBB 循环的催化)以确保光合作用稳定的重要性。
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来源期刊
Plant and Cell Physiology
Plant and Cell Physiology 生物-细胞生物学
CiteScore
8.40
自引率
4.10%
发文量
166
审稿时长
1.7 months
期刊介绍: Plant & Cell Physiology (PCP) was established in 1959 and is the official journal of the Japanese Society of Plant Physiologists (JSPP). The title reflects the journal''s original interest and scope to encompass research not just at the whole-organism level but also at the cellular and subcellular levels. Amongst the broad range of topics covered by this international journal, readers will find the very best original research on plant physiology, biochemistry, cell biology, molecular genetics, epigenetics, biotechnology, bioinformatics and –omics; as well as how plants respond to and interact with their environment (abiotic and biotic factors), and the biology of photosynthetic microorganisms.
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