昼夜节律引起c-二- amp信号级联蓝藻突变体的代谢危机

Michael Haffner, Oliver Mantovani, Philipp Spaet, Boris Macek, Martin Hagemann, Karl Forchhammer, Khaled A. Selim
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引用次数: 1

摘要

在自然界中,蓝藻的光自养生活方式必须应对连续的昼夜变化的光供应。白天的光线供应使光合作用和糖原生物合成成为可能,而夜间则需要切换到依赖糖原分解代谢的异养生活方式。我们之前强调了碳控制蛋白SbtB及其效应分子c-di-AMP的独特功能,通过调节糖原合成代谢来调节蓝藻的夜间生存。然而,c-di-AMP和SbtB在多大程度上影响昼夜生存能力的细胞代谢仍然是难以捉摸的。为了更好地了解SbtB或c-di-AMP调控的细胞过程,我们比较了模型菌株Synechocystis sp. PCC 6803 ΔsbtB和不含c-di-AMP (ΔdacA)突变体的代谢组学和蛋白质组学景观。虽然我们的研究结果表明SbtB的细胞作用仅限于碳/糖原代谢,但ΔdacA的昼夜致死率似乎是多种代谢过程失调的结果。这些过程包括光合作用和氧化还原调节,导致细胞内ROS和谷胱甘肽水平升高。此外,我们还展示了c-di-AMP对中心碳和氮代谢的影响。对氮代谢的影响与全球氮转录调节剂NtcA水平的降低有关,并与谷氨酰胺与谷氨酸比例的不平衡以及精氨酸途径代谢物水平的降低有关。我们进一步确定了HCO3-吸收系统,BicA和BCT1作为SbtB的新靶点,与其在调节碳稳态中的广泛作用一致。
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Diurnal rhythm causes metabolic crises in the cyanobacterial mutants of c-di-AMP signalling cascade
In nature, the photoautotrophic lifestyle of cyanobacteria has to cope with the successive diurnal changes in light supply. Light supply throughout the day enables photosynthesis and glycogen biosynthesis, while night phases require the switch to a heterotrophic-like lifestyle relying on glycogen catabolism. We previously highlighted a unique function of the carbon control protein, SbtB, and its effector molecule c-di-AMP, for the nighttime survival of cyanobacteria through the regulation of glycogen anabolism. However, the extent to which c-di-AMP and SbtB impact the cellular metabolism for day-night survivability remained elusive. To gain better understanding of cellular processes regulated by SbtB or c-di-AMP, we compared the metabolomic and proteomic landscapes of ΔsbtB and the c-di-AMP-free (ΔdacA) mutants of the model strain Synechocystis sp. PCC 6803. While our results indicate that the cellular role of SbtB is restricted to carbon/glycogen metabolism, the diurnal lethality of ΔdacA seems to be a sum of dysregulation of multiple metabolic processes. These processes include photosynthesis and redox regulation, which lead to elevated levels of intracellular ROS and glutathione. Further, we show an impact of c-di-AMP on central carbon as well as on nitrogen metabolism. Effects on nitrogen metabolism are linked to reduced levels of the global nitrogen transcription regulator NtcA and highlighted by an imbalance of the glutamine to glutamate ratio as well as reduced metabolite levels of the arginine pathway. We further identified the HCO3- uptake systems, BicA and BCT1 as novel SbtB targets, in agreement with its broader role in regulating carbon homeostasis.
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