Zhu Yanping, Zhang Hanlei, Pang Xiuhua
The State Key Laboratory of Microbial Technology, Shandong University, Qingdao, Shandong, China.
Suzhou Research Institute, Shandong University, Suzhou, Jiangsu, China.
Microbiol Spectr. 2025 Aug 5;13(8):e0009625. doi: 10.1128/spectrum.00096-25. Epub 2025 Jun 30.
The response regulator MtrA of regulates secondary metabolism as well as primary metabolism, including nitrogen metabolism and phosphate metabolism; however, it is not known whether MtrA is involved in the control of central carbon metabolism in . In this study, we revealed that the growth medium of the MtrA mutant strain (Δ) is acidic under multiple growth conditions and that this acidification is dependent on the type of medium used. We performed targeted metabolomic analysis to determine the types and levels of organic acids produced by the wild-type strain M145 and Δ, and the results revealed that production of multiple organic acids associated with the tricarboxylic acid cycle (TCA) and glycolysis pathway was changed significantly in Δ, compared with M145, indicating a broad impact of MtrA on carbon metabolism and suggesting the basis for the acidification of the growth media by Δ. Multiple potential MtrA sites were predicted in the sequences upstream of genes involved in the TCA cycle, including genes encoding citrate synthases, and we showed that MtrA bound these potential sites, suggesting that MtrA targets these carbon metabolism genes. Our transcriptional analysis showed that carbon metabolism genes with MtrA sites are differentially expressed in Δ, indicating regulation of these genes by MtrA. Overall, our study indicates that the response regulator MtrA has a broad impact on central carbon metabolism, adding new insight into our understanding of the regulation of carbon metabolism in .IMPORTANCECentral carbon metabolism is a key primary metabolic process, and its tight regulation is crucial for maintaining normal physiology in microbes. However, carbon metabolism is the least understood metabolic process in primary metabolism in . In this study, we demonstrated a broad impact of the response regulator MtrA on the production of metabolites associated with the tricarboxylic acid cycle and glycolysis pathway, thereby leading to the accumulation of organic acids and decreases in the pH values of the growth medium with an MtrA mutant strain. We further revealed MtrA sites upstream of genes involved in carbon metabolism and determined that MtrA bound to these sites, revealing MtrA as a regulator for carbon metabolism in . Our study enhances the understanding of the role of MtrA and helps to elucidate the regulatory mechanisms of a major metabolic process in .
应答调节因子MtrA不仅调控初级代谢,还调控次级代谢,包括氮代谢和磷代谢;然而,尚不清楚MtrA是否参与了[具体微生物名称]中中心碳代谢的调控。在本研究中,我们发现MtrA突变株(Δ)在多种生长条件下的生长培养基呈酸性,且这种酸化取决于所用培养基的类型。我们进行了靶向代谢组学分析,以确定野生型菌株M145和Δ产生的有机酸的类型和水平,结果显示,与M145相比,Δ中与三羧酸循环(TCA)和糖酵解途径相关的多种有机酸的产生发生了显著变化,这表明MtrA对碳代谢有广泛影响,并为Δ导致生长培养基酸化提供了依据。在参与TCA循环的基因上游序列中预测到多个潜在的MtrA结合位点,包括编码柠檬酸合酶的基因,并且我们证明MtrA与这些潜在位点结合,表明MtrA靶向这些碳代谢基因。我们的转录分析表明,具有MtrA结合位点的碳代谢基因在Δ中差异表达,表明这些基因受MtrA调控。总体而言,我们的研究表明应答调节因子MtrA对中心碳代谢有广泛影响,为我们理解[具体微生物名称]中碳代谢的调控增添了新的见解。
中心碳代谢是关键的初级代谢过程,其严格调控对于维持微生物的正常生理功能至关重要。然而,碳代谢是[具体微生物名称]初级代谢中了解最少的代谢过程。在本研究中,我们证明了应答调节因子MtrA对与三羧酸循环和糖酵解途径相关的代谢产物产生有广泛影响,从而导致有机酸积累以及MtrA突变株生长培养基pH值降低。我们进一步揭示了碳代谢相关基因上游的MtrA结合位点,并确定MtrA与这些位点结合,揭示了MtrA是[具体微生物名称]中碳代谢的调节因子。我们的研究增进了对MtrA作用的理解,并有助于阐明[具体微生物名称]中一个主要代谢过程的调控机制。