1. Molecular bases of an alternative dual-enzyme system for light color acclimation of marine Synechococcus cyanobacteria.
- Author
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Grébert T, Nguyen AA, Pokhrel S, Joseph KL, Ratin M, Dufour L, Chen B, Haney AM, Karty JA, Trinidad JC, Garczarek L, Schluchter WM, Kehoe DM, and Partensky F
- Subjects
- Acclimatization, Aquatic Organisms, Bacterial Proteins genetics, Cloning, Molecular, Escherichia coli genetics, Escherichia coli metabolism, Gene Expression Regulation, Bacterial, Genetic Complementation Test, Genetic Vectors chemistry, Genetic Vectors metabolism, Genomic Islands, Light, Light-Harvesting Protein Complexes genetics, Lyases genetics, Phycobilins biosynthesis, Phycobilins genetics, Phycocyanin genetics, Phycoerythrin genetics, Phylogeny, Pigments, Biological genetics, Protein Subunits genetics, Protein Subunits metabolism, Recombinant Proteins genetics, Recombinant Proteins metabolism, Synechococcus classification, Synechococcus genetics, Synechococcus radiation effects, Urobilin analogs & derivatives, Urobilin biosynthesis, Urobilin genetics, Bacterial Proteins metabolism, Light-Harvesting Protein Complexes metabolism, Lyases metabolism, Phycocyanin biosynthesis, Phycoerythrin biosynthesis, Pigments, Biological biosynthesis, Synechococcus metabolism
- Abstract
Marine Synechococcus cyanobacteria owe their ubiquity in part to the wide pigment diversity of their light-harvesting complexes. In open ocean waters, cells predominantly possess sophisticated antennae with rods composed of phycocyanin and two types of phycoerythrins (PEI and PEII). Some strains are specialized for harvesting either green or blue light, while others can dynamically modify their light absorption spectrum to match the dominant ambient color. This process, called type IV chromatic acclimation (CA4), has been linked to the presence of a small genomic island occurring in two configurations (CA4-A and CA4-B). While the CA4-A process has been partially characterized, the CA4-B process has remained an enigma. Here we characterize the function of two members of the phycobilin lyase E/F clan, MpeW and MpeQ, in Synechococcus sp. strain A15-62 and demonstrate their critical role in CA4-B. While MpeW, encoded in the CA4-B island and up-regulated in green light, attaches the green light-absorbing chromophore phycoerythrobilin to cysteine-83 of the PEII α-subunit in green light, MpeQ binds phycoerythrobilin and isomerizes it into the blue light-absorbing phycourobilin at the same site in blue light, reversing the relationship of MpeZ and MpeY in the CA4-A strain RS9916. Our data thus reveal key molecular differences between the two types of chromatic acclimaters, both highly abundant but occupying distinct complementary ecological niches in the ocean. They also support an evolutionary scenario whereby CA4-B island acquisition allowed former blue light specialists to become chromatic acclimaters, while former green light specialists would have acquired this capacity by gaining a CA4-A island., Competing Interests: The authors declare no competing interest.
- Published
- 2021
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