Molecular basis for coordinating secondary metabolite production by bacterial and plant signaling molecules

• Published in: The Journal of biological chemistry 2022-06, Vol.298 (6), p.102027-102027, Article 102027
• Main Authors: Zhang, Nannan, Wu, Jin, Zhang, Siping, Yuan, Maoran, Xu, Hang, Li, Jie, Zhang, Pingping, Wang, Mingzhu, Kempher, Megan L., Tao, Xuanyu, Zhang, Li-Qun, Ge, Honghua, He, Yong-Xing
• Format: Article
• Language: English
• Subjects: 2,4-diacetylphloroglucinol; allosteric switching mechanism; bacterial metabolic coregulation; secondary metabolite; TetR-family transcriptional regulator
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2022.102027

The production of secondary metabolites is a major mechanism used by beneficial rhizobacteria to antagonize plant pathogens. These bacteria have evolved to coordinate the production of different secondary metabolites due to the heavy metabolic burden imposed by secondary metabolism. However, for most secondary metabolites produced by bacteria, it is not known how their biosynthesis is coordinated. Here, we showed that PhlH from the rhizobacterium Pseudomonas fluorescens is a TetR-family regulator coordinating the expression of enzymes related to the biosynthesis of several secondary metabolites, including 2,4-diacetylphloroglucinol (2,4-DAPG), mupirocin, and pyoverdine. We present structures of PhlH in both its apo form and 2,4-DAPG-bound form and elucidate its ligand-recognizing and allosteric switching mechanisms. Moreover, we found that dissociation of 2,4-DAPG from the ligand-binding domain of PhlH was sufficient to allosterically trigger a pendulum-like movement of the DNA-binding domains within the PhlH dimer, leading to a closed-to-open conformational transition. Finally, molecular dynamics simulations confirmed that two distinct conformational states were stabilized by specific hydrogen bonding interactions and that disruption of these hydrogen bonds had profound effects on the conformational transition. Our findings not only reveal a well-conserved route of allosteric signal transduction in TetR-family regulators but also provide novel mechanistic insights into bacterial metabolic coregulation.