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Here, we show that the phosphotransferase system PTS\n                      <jats:sup>Ntr<\/jats:sup>\n                      , a global regulator of carbon and nitrogen metabolism, modulates the tricarboxylic acid (TCA) cycle activity and the accumulation of three major carbon storage polymers: glycogen, polyhydroxybutyrate, and exopolysaccharide in\n                      <jats:italic toggle=\"yes\">Rhizobium leguminosarum<\/jats:italic>\n                      . The unphosphorylated form of the effector protein ManX is sufficient for the full activation of the TCA cycle dehydrogenase enzymes. Accordingly, loss of\n                      <jats:italic toggle=\"yes\">manX<\/jats:italic>\n                      reduced dehydrogenase activity and redirected overflow carbon into storage polymers, phenocopying wild-type cells grown under nitrogen starvation. We further demonstrate that carbon metabolism in\n                      <jats:italic toggle=\"yes\">R. leguminosarum<\/jats:italic>\n                      is also tightly regulated by the HPr kinase (HprK) protein. In an\n                      <jats:italic toggle=\"yes\">hprK<\/jats:italic>\n                      mutant, loss of NPr Ser48 phosphorylation favors phosphotransfer through the histidyl arm and is predicted to increase phosphorylation of downstream PTS\n                      <jats:sup>Ntr<\/jats:sup>\n                      components. When grown on glucose, the\n                      <jats:italic toggle=\"yes\">hprK<\/jats:italic>\n                      mutant accumulates elevated intracellular pyrimidine levels and exhibits increased malate dehydrogenase and TCA cycle activity, consistent with a misregulated shift toward gluconeogenesis. This mutant also overproduces exopolysaccharide, an effect potentially mediated by crosstalk between phosphorylated PtsN and the ChvI\/ChvG two-component regulatory system. Together, these data suggest that HprK exerts pleiotropic control over processes regulated by PTS\n                      <jats:sup>Ntr<\/jats:sup>\n                      , influencing central metabolism while repressing exopolysaccharide production, likely by promoting the unphosphorylated state of PtsN.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        Bacteria must continuously balance growth, nutrient availability, and storage to ensure fitness and survival in fluctuating environments. However, how regulatory networks integrate central metabolism with carbon storage remains poorly understood. This study reinforces the role of the PTS\n                        <jats:sup>Ntr<\/jats:sup>\n                        system as a central coordinator of carbon routing and polymer accumulation. By revealing how ManX and HprK-dependent phosphorylation influence central metabolism and the production of major carbon storage polymers in\n                        <jats:italic toggle=\"yes\">Rhizobium leguminosarum<\/jats:italic>\n                        , we show that disruption of PTS\n                        <jats:sup>Ntr<\/jats:sup>\n                        signaling reprograms carbon allocation, uncoupling growth from carbon storage and mimicking nitrogen starvation even under nitrogen-replete conditions. These findings highlight a regulatory link between carbon-nitrogen signaling and bacterial storage strategies, with implications for cellular survival and plant symbiosis. More broadly, our work illustrates how global metabolic regulators shape bacterial physiological states, providing new insights into mechanisms that support microbial adaptation in complex environments.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/aem.01073-26","type":"journal-article","created":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T13:01:37Z","timestamp":1790773297000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Regulation of central carbon metabolism and storage polymers by PTS\n                    <sup>Ntr<\/sup>\n                    in\n                    <i>Rhizobium 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