engleski

Bacterial single-stranded DNA-binding proteins are phosphorylated on tyrosine

Single-stranded DNA-binding proteins (SSBs) are required for repair, recombination and replication in all organisms. Eukaryotic SSBs are regulated by phosphorylation on serine and threonine residues. To our knowledge phosphorylation of SSBs in bacteria has not been reported. A systematic search for phosphotyrosine-containing proteins in Streptomyces griseus by immunoaffinity chromatography identified bacterial SSBs as a novel target of bacterial tyrosine kinases. Since genes encoding protein-tyrosine kinases have not been recognized in streptomycetes, and SSBs from Streptomyces coelicolor and Bacillus subtilis share 40% identity, we used a B. subtilis protein-tyrosine kinase YwqD to phosphorylate two cognate SSBs (Ssb and YwpH) in vitro. We demonstrate that in vivo phosphorylation of B. subtilis Ssb occurs on tyrosine residue 82, and this reaction is affected antagonistically by kinase YwqD and phosphatase YwqE. Phosphorylation of B. subtilis Ssb increased binding almost 200 fold to single-stranded DNA in vitro. Tyrosine phosphorylation of B. subtilis, S. coelicolor, and Escherichia coli SSBs occured while they were expressed in E. coli, indicating that tyrosine phosphorylation of SSBs is a conserved process of post-translational modification in taxonomically distant bacteria.

Bacterial tyrosine kinase; single-stranded DNA-binding protein; B. Subtilis; E. coli Streptomyces sp.

nije evidentirano