4.7 Article

CP12 fine-tunes the Calvin-Benson cycle and carbohydrate metabolism in cyanobacteria

Journal

FRONTIERS IN PLANT SCIENCE
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2022.1028794

Keywords

diurnal cycle; fluorescence tagging; photomixotrophy; glyceraldehyde 3-phosphate dehydrogenase; phosphoribulokinase; redox regulation; Synechocystis 6803

Categories

Funding

  1. German Research Foundation [HA 2002/23-1, GU 1522/5-1, FOR2816]
  2. University of Rostock
  3. Max Planck Society
  4. University of Kassel

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The regulatory protein CP12 plays a crucial role in controlling the flux through the Calvin-Benson cycle (CBC) in photosynthetic organisms. Through studying a mutant cyanobacterium, researchers discovered that CP12 is essential for metabolic adjustment under conditions leading to redox changes.
The regulatory protein CP12 can bind glyceraldehyde 3-phosphate dehydrogenase (GapDH) and phosphoribulokinase (PRK) in oxygenic phototrophs, thereby switching on and off the flux through the Calvin-Benson cycle (CBC) under light and dark conditions, respectively. However, it can be assumed that CP12 is also regulating CBC flux under further conditions associated with redox changes. To prove this hypothesis, the mutant Delta cp12 of the model cyanobacterium Synechocystis sp. PCC 6803 was compared to wild type and different complementation strains. Fluorescence microscopy showed for the first time the in vivo kinetics of assembly and disassembly of the CP12-GapDH-PRK complex, which was absent in the mutant Delta cp12. Metabolome analysis revealed differences in the contents of ribulose 1,5-bisphosphate and dihydroxyacetone phosphate, the products of the CP12-regulated enzymes GapDH and PRK, between wild type and mutant Delta cp12 under changing CO2 conditions. Growth of Delta cp12 was not affected at constant light under different inorganic carbon conditions, however, the addition of glucose inhibited growth in darkness as well as under diurnal conditions. The growth defect in the presence of glucose is associated with the inability of Delta cp12 to utilize external glucose. These phenotypes could be complemented by ectopic expression of the native CP12 protein, however, expression of CP12 variants with missing redox-sensitive cysteine pairs only partly restored the growth with glucose. These experiments indicated that the loss of GapDH-inhibition via CP12 is more critical than PRK association. Measurements of the NAD(P)H oxidation revealed an impairment of light intensity-dependent redox state regulation in Delta cp12. Collectively, our results indicate that CP12-dependent regulation of the CBC is crucial for metabolic adjustment under conditions leading to redox changes such as diurnal conditions, glucose addition, and different CO2 conditions in cyanobacteria.

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