4.7 Article

Dynamic Changes in the Thylakoid Proteome of Cyanobacteria during Light-Regulated Thylakoid Membrane Development

Journal

PLANTS-BASEL
Volume 12, Issue 23, Pages -

Publisher

MDPI
DOI: 10.3390/plants12233967

Keywords

cyanobacteria; photosynthesis; acclimation; thylakoid membrane; membrane biogenesis; proteome

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This study provides an in-depth statistical analysis of protein components and functionally linked complexes during cyanobacterial thylakoid membrane biogenesis. The findings reveal significant variations in abundance of photosystems, light-harvesting antennae, ABC transporters, and oxidative stress response and protein folding pathway enzymes between high light and growth light conditions. The results and analytical methodologies developed in this study may be valuable for studying global responses of thylakoid membrane biogenesis in plants and algae.
Cyanobacteria were among the oldest organisms to undertake oxygenic photosynthesis and have an essential impact on the atmosphere and carbon/nitrogen cycles on the planet. The thylakoid membrane of cyanobacteria represents an intricate compartment that houses a variety of multi-component (pigment-)protein complexes, assembly factors, and regulators, as well as transporters involved in photosynthetic light reactions, and respiratory electron transport. How these protein components are incorporated into membranes during thylakoid formation and how individual complexes are regulated to construct the functional machinery remains elusive. Here, we carried out an in-depth statistical analysis of the thylakoid proteome data obtained during light-induced thylakoid membrane biogenesis in the model cyanobacterium Synechococcus elongatus PCC 7942. A total of 1581 proteins were experimentally quantified, among which 457 proteins demonstrated statistically significant variations in abundance at distinct thylakoid biogenesis stages. Gene Ontology and KEGG enrichment analysis revealed that predominantly photosystems, light-harvesting antennae, ABC transporters, and pathway enzymes involved in oxidative stress responses and protein folding exhibited notable alternations in abundance between high light and growth light. Moreover, through cluster analysis the 1581 proteins were categorized into six distinct clusters that have significantly different trajectories of the change in their abundance during thylakoid development. Our study provides insights into the physiological regulation for the membrane integration of protein components and functionally linked complexes during the cyanobacterial TM biogenesis process. The findings and analytical methodologies developed in this study may be valuable for studying the global responses of TM biogenesis and photosynthetic acclimation in plants and algae.

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