PhlG mediates the conversion of DAPG to MAPG in Pseudomonas fluorescens 2P24

• Published in: Scientific reports 2020-03, Vol.10 (1), p.4296-4296, Article 4296
• Main Authors: Zhao, Ming-Min, Lyu, Ning, Wang, Dong, Wu, Xiao-Gang, Zhao, Yuan-Zheng, Zhang, Li-Qun, Zhou, Hong-You
• Format: Article
• Language: English
• Subjects: 38/77; 42/44; 42/70; 631/326/22; 631/326/2522; Anti-Bacterial Agents - pharmacology; Antibiotics; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Biosynthesis; Clonal deletion; Deletion mutant; Gene deletion; Humanities and Social Sciences; multidisciplinary; Phloroglucinol - analogs & derivatives; Phloroglucinol - metabolism; Plant diseases; Plant Diseases - immunology; Plant Diseases - microbiology; Plant growth; Post-transcription; Pseudomonas fluorescens; Pseudomonas fluorescens - growth & development; Pseudomonas fluorescens - metabolism; Science; Science (multidisciplinary); Soil microorganisms; Triticum - drug effects; Triticum - growth & development; Triticum - microbiology
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-60555-9

The antibiotic 2,4-diacetylphoroglucinol (2,4-DAPG), produced by the Gram-negative rod-shaped bacterium Pseudomonas fluorescens 2P24, is active against various soil-borne bacterial and fungal pathogens that cause plant diseases. Biosynthesis of 2,4-DAPG is controlled by regulating expression of the phlACBD operon at the post-transcriptional level. The phlG gene is located between the phlF and phlH genes, upstream of the phlACBD biosynthetic operon. Herein, we cloned the phlG gene, generated a phlG deletion mutant, and investigated its regulatory role in 2,4-DAPG biosynthesis. The results showed that deletion of phlG had no effect on the biosynthesis of 2,4-DAPG, but it affected conversion of 2,4-DAPG to its precursor monoacetylphloroglucinol (MAPG). The global regulatory factor encoded by gacS positively regulated expression of phlG , while rsmE negatively regulated its expression. Deleting phlG did not alter the ability of the bacterium to colonise plants or promote plant growth. These results suggest that phlG collaborates with other factors to regulate production of the antibiotic 2,4-DAPG in P. fluorescens 2P24.