The transcription factor RppA regulates chlorophyll and carotenoid biosynthesis to improve photoprotection in cyanobacteria

Plant Physiol. 2024 Dec 23;197(1):kiae502. doi: 10.1093/plphys/kiae502.

Abstract

Chlorophyll is an essential photosynthetic pigment but also a strong photosensitizer. Excessive free chlorophyll and its precursors can cause oxidative damage to photosynthetic organisms. Cyanobacteria are the oldest oxygenic photosynthetic organisms and the ancestors of the chloroplast. Owing to their complex habitats, cyanobacteria require precise regulation of chlorophyll synthesis to respond to environmental factors, especially changes in light. Chlorophyll synthase, encoded by chlG, is the enzyme catalyzing the final step of chlorophyll biosynthesis, which is closely related to photosynthesis biogenesis. However, the transcriptional regulation on chlG remains unclear. Here, the transcription factor, regulator of photosynthesis and photopigment-related gene expression A (RppA), was identified to bind to the chlG promoter by screening a yeast 1-hybrid library in the cyanobacterium Synechocystis sp. PCC 6803. The rppA knockout mutant showed a phenotype of slow growth and severe oxidative damage under dark-light transition conditions. The upregulated transcriptional expression of chlG was significantly higher and more chlorophyll and its precursors accumulated in the rppA knockout mutant than those in the wild-type strain during the transition from darkness to light, indicating that RppA represses the expression of chlG in Synechocystis. Meanwhile, RppA could synchronously promote the transcription of carotenoids biosynthesis-related genes to enhance carotenoids synthesis during the dark-light transition. These results reveal synergistic regulation of chlorophyll and carotenoids biosynthesis in cyanobacteria in response to frequent dark-light transitions, which slows down chlorophyll biosynthesis while promoting carotenoids biosynthesis to avoid oxidative damage caused by excessive reactive oxygen species accumulation.

MeSH terms

  • Bacterial Proteins* / genetics
  • Bacterial Proteins* / metabolism
  • Carotenoids* / metabolism
  • Chlorophyll* / metabolism
  • Gene Expression Regulation, Bacterial
  • Light*
  • Oxidative Stress
  • Photosynthesis
  • Promoter Regions, Genetic / genetics
  • Synechocystis* / genetics
  • Synechocystis* / metabolism
  • Synechocystis* / radiation effects
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism

Substances

  • Chlorophyll
  • Carotenoids
  • Transcription Factors
  • Bacterial Proteins