Regulation of central carbon metabolism and storage polymers by PTSNtr in Rhizobium leguminosarum.

IF 4.2 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2026-10-21 Epub Date: 2026-09-30 DOI:10.1128/aem.01073-26
Olivia Tjahjono, Jingkai Wang, Evan Turner, Jürgen Prell, Wei E Huang, Philip S Poole, Carmen Sánchez-Cañizares
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引用次数: 0

Abstract

The coordination of intracellular carbon and nitrogen levels is essential for optimal bacterial growth and, in rhizobia, for survival in the soil, root colonization, and symbiotic interactions with their host plants. Here, we show that the phosphotransferase system PTSNtr, 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 Rhizobium leguminosarum. The unphosphorylated form of the effector protein ManX is sufficient for the full activation of the TCA cycle dehydrogenase enzymes. Accordingly, loss of manX 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 R. leguminosarum is also tightly regulated by the HPr kinase (HprK) protein. In an hprK mutant, loss of NPr Ser48 phosphorylation favors phosphotransfer through the histidyl arm and is predicted to increase phosphorylation of downstream PTSNtr components. When grown on glucose, the hprK 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 PTSNtr, influencing central metabolism while repressing exopolysaccharide production, likely by promoting the unphosphorylated state of PtsN.IMPORTANCEBacteria 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 PTSNtr 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 Rhizobium leguminosarum, we show that disruption of PTSNtr 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.

PTSNtr对豆科根瘤菌中心碳代谢和储存聚合物的调控。
细胞内碳氮水平的协调对细菌生长和根瘤菌在土壤中的生存、根定植以及与寄主植物的共生相互作用至关重要。本研究表明,作为碳氮代谢的全球性调节因子,磷酸转移酶系统PTSNtr调节豆科根瘤菌三羧酸(TCA)循环活性和三种主要储碳聚合物(糖原、聚羟基丁酸酯和胞外多糖)的积累。效应蛋白ManX的未磷酸化形式足以充分激活TCA循环脱氢酶。因此,manX的损失降低了脱氢酶的活性,并将溢出的碳重新定向到存储聚合物中,在氮饥饿下生长的表型复制野生型细胞。我们进一步证明豆科植物的碳代谢也受到HPr激酶(HprK)蛋白的严格调控。在hprK突变体中,NPr Ser48磷酸化的缺失有利于通过组氨酸臂进行磷转移,预计会增加下游PTSNtr成分的磷酸化。当生长在葡萄糖上时,hprK突变体积累了升高的细胞内嘧啶水平,并表现出增加的苹果酸脱氢酶和TCA循环活性,这与糖异生的错误调节相一致。该突变体也过量产生外多糖,这一效应可能是由磷酸化的PtsN和ChvI/ChvG双组分调控系统之间的串扰介导的。总之,这些数据表明HprK对PTSNtr调控的过程施加多向性控制,影响中枢代谢,同时抑制胞外多糖的产生,可能是通过促进PtsN的非磷酸化状态。细菌必须不断平衡生长、营养供应和储存,以确保在波动的环境中适应和生存。然而,调控网络如何整合中枢代谢与碳储存仍然知之甚少。这项研究强化了PTSNtr系统作为碳路径和聚合物积累的中心协调者的作用。通过揭示ManX和hprk依赖性磷酸化如何影响豆科根瘤菌的中心代谢和主要碳储存聚合物的产生,我们发现PTSNtr信号的破坏可以重编程碳分配,使生长与碳储存分离,甚至在氮充满的条件下也能模拟氮饥饿。这些发现强调了碳氮信号和细菌储存策略之间的调节联系,对细胞存活和植物共生具有重要意义。更广泛地说,我们的工作阐明了全球代谢调节因子如何塑造细菌的生理状态,为支持微生物在复杂环境中的适应机制提供了新的见解。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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