Abstract
Inorganic polyphosphate (poly P), in chains of tens to hundreds of phosphate residues, linked by high-energy bonds, is environmentally ubiquitous and abundant. In prebiotic evolution it could have provided a flexible, polyanionic scaffold to assemble macromolecules. It has been conserved in every cell in nature. In prokaryotes, a major poly P synthetic enzyme is poly P kinase 1 (PPK1), which is found in 100 bacterial genomes, including numerous pathogens. Null mutants of PPK1, with low poly P levels, are defective in survival: namely, they show defective responses to physical/chemical stresses and predation. Pathogens with a PPK1 deletion are defective in biofilm formation, quorum sensing, general stress and stringent responses, motility, and other virulence properties. With the exception of Dictyostelium, PPK1 is absent in eukaryotes and provides a novel target for chemotherapy that would affect both virulence and susceptibility to antibacterial compounds. Remarkably, another PPK in Dictyostelium discoideum (PPK2) is an actin-related protein (Arp) complex that is polymerized into an actin-like filament, concurrent with its reversible synthesis of a poly P chain from ATP.
MeSH Terms
Adenosine Triphosphate/metabolism
Animals
Bacteria/enzymology,genetics
Biological Evolution
Dictyostelium/enzymology,genetics
Origin of Life
Phosphotransferases (Phosphate Group Acceptor)/genetics,metabolism
Polyphosphates/metabolism
Chemicals
Polyphosphates
Adenosine Triphosphate
Phosphotransferases (Phosphate Group Acceptor)
polyphosphate kinase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Brown Michael R W
Department of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305-5307, USA.
Kornberg Arthur
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