4.7 Article

iTRAQ-based proteomic analysis of Bacillus subtilis strain NCD-2 regulated by PhoPR two-component system: A comparative analysis with transcriptomics revealed the regulation for fengycin production by branched chain amino acids

Journal

MICROBIOLOGICAL RESEARCH
Volume 260, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.micres.2022.127024

Keywords

ITRAQ; Proteomics; Bacillus subtilis; Two-component system; Fengycin

Categories

Funding

  1. Natural Science Foundation of Hebei Province [C2021301030]
  2. National Natural Science Foundation of China [32172487]
  3. Earmarked Fund for the China Agriculture Research System [CARS-15-19]
  4. Key Research and Development Program of Hebei Province [19226510D]

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This study characterizes the regulatory mechanism of the PhoPR two-component system (TCS) in Bacillus subtilis, showing its role in the regulation of fengycin production through the biosynthesis of branched chain amino acids (BCAAs). These findings provide insights into the signaling pathway involved in the phosphate starvation response and the production of antibiotics in bacteria.
The PhoPR two-component system (TCS) is a signal transduction pathway to regulate the phosphate starvation response in Bacillus subtilis and regulated fengycin production in strain NCD-2 under low phosphate condition. The purpose of this study was to characterize the proteome level responses in the phoP-null mutant (MP) and the phoR-null mutant (MR), and to integrate the proteomics with the transcriptomic data obtained previously. The metabolic pathway for fengycin was predicted based on omics analysis as well as molecular genetics assay. Results showed the proteins and genes associated with biosynthesis of branched chain amino acids (BCAAs) were regulated by PhoPR TCS, and liquid chromatography mass spectrometry (LC-MS) analysis also confirmed that the production of BCAAs was down-regulated in the MP and MR mutants, when compared to wild-type strain NCD-2. Protein network analysis showed that the BCAA metabolism was linked to the biosynthesis of lipopeptides. The MP and MR strains decreased the fengycin production when cultured in modified Landy medium supplied with 0.42 mM phosphate, however, the fengycin production could be restored when the glutamic acid was replaced with BCAAs that were added to modified Landy medium. The lpdV gene, which is responsible for the BCAA degradation process, was deleted in strain NCD-2. Compared with the wild-type strain, the lpdV mutant produced significantly less fengycin in the medium supplied with BCAAs. Considered together, the results of this study indicate that the PhoPR TCS regulates fengycin production by affecting BCAA biosynthesis.

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