Role of Polyphosphate in Thermophilic Synechococcus sp. from Microbial Mats

• Published in: Journal of Bacteriology 2013-08, Vol.195 (15), p.3309-3319
• Main Authors: Gomez-Garcia, Maria R, Fazeli, Fariba, Grote, Alexandra, Grossman, Arthur R, Bhaya, Devaki
• Format: Article
• Language: English
• Subjects: Bacteriology; Blotting, Western; Cell growth; Cyanobacteria; Enzymes; exopolysaccharides; Gene Deletion; Gene Expression Profiling; Genes; Microbiology; mutants; Mutation; national parks; phenotype; Phosphoprotein Phosphatases - genetics; Phosphoprotein Phosphatases - metabolism; Phosphorus; Phosphotransferases (Phosphate Group Acceptor) - genetics; Phosphotransferases (Phosphate Group Acceptor) - metabolism; Polyphosphates - metabolism; Prokaryotes; prokaryotic cells; regulon; starvation; Synechococcus; Synechococcus - enzymology; Synechococcus - genetics; Synechococcus - metabolism; transporters; Western blotting
• ISSN: 0021-9193; 1098-5530; 1067-8832
• DOI: 10.1128/JB.00207-13

Synechococcus OS-B′, a thermophilic unicellular cyanobacterium, recently isolated from the microbial mats in Octopus Spring (Yellowstone National Park), induces a suite of genes, including phosphatases and transporters, in response to phosphorus (P) starvation. Here we describe two different approaches to examine the ability of Synechococcus OS-B′ to synthesize and break down polyphosphate (poly P), a key storage compound in many prokaryotes. First, we developed a transformation protocol to create mutants in the polyphosphate kinase (ppk), the major enzyme responsible for the synthesis of poly P. The ppk mutant exhibited a pleiotropic phenotype with defects in poly P accumulation, aberrant levels of Pho regulon transcripts, growth defects, and changes in cell size and exopolysaccharide levels, among others. Second, we measured transcripts of ppk and ppx (encoding the polyphosphatase) directly from mat samples and found that the levels varied dramatically over a diel cycle. We also used Western blot analysis to quantify levels of PPK and PPX and found that these enzymes differentially accumulated during the diel cycle. Levels of polyphosphate kinase peaked at night, while polyphosphatase levels were highest during the early morning hours. We hypothesize that the opposing activities of these two enzymes allow cells to store and utilize poly P to optimize growth over a diel cycle.