Regulation of Safracin Biosynthesis and Transport in Pseudomonas poae PMA22

<i>Pseudomonas poae</i> PMA22 produces safracins, a family of compounds with potent broad-spectrum anti-bacterial and anti-tumor activities. The safracins' biosynthetic gene cluster (BGC sac) consists of 11 ORFs organized in two divergent operons (<i>sacABCDEFGHK</i> and <i>sacIJ</i>) that are controlled by <i>P<sub>a</sub></i> and <i>P<sub>i</sub></i> promoters. Contiguous to the BGC sac, we have located a gene that encodes a putative global regulator of the LysR family annotated as MexT that was originally described as a transcriptional activator of the MexEF-OprN multidrug efflux pump in <i>Pseudomonas</i>. Through both in vitro and in vivo experiments, we have demonstrated the involvement of the dual regulatory system MexT-MexS on the BGC sac expression acting as an activator and a repressor, respectively. The MexEF-OprN transport system of PMA22, also controlled by MexT, was shown to play a fundamental role in the metabolism of safracin. The overexpression of <i>mexEF-oprN</i> in PMA22 resulted in fourfold higher production levels of safracin. These results illustrate how a pleiotropic regulatory system can be critical to optimizing the production of tailored secondary metabolites, not only through direct interaction with the BGC promoters, but also by controlling their transport.

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Journal
Marine Drugs
Published
2024-09-13
DOI
https://doi.org/10.3390/md22090418
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Regulation of Safracin Biosynthesis and Transport in Pseudomonas poae PMA22

Fernando de la Calle, Beatriz Galán, Miguel G. Acedos, José L. Garcı́a et al.
Marine Drugs
Microbial Natural Products and Biosynthesis
article

Regulation of Safracin Biosynthesis and Transport in Pseudomonas poae PMA22

Fernando de la Calle, Beatriz Galán, Miguel G. Acedos, José L. Garcı́a, Pilar Rodríguez, J. Gerardo Hernández Delgado
article en

Abstract

<i>Pseudomonas poae</i> PMA22 produces safracins, a family of compounds with potent broad-spectrum anti-bacterial and anti-tumor activities. The safracins' biosynthetic gene cluster (BGC sac) consists of 11 ORFs organized in two divergent operons (<i>sacABCDEFGHK</i> and <i>sacIJ</i>) that are controlled by <i>P<sub>a</sub></i> and <i>P<sub>i</sub></i> promoters. Contiguous to the BGC sac, we have located a gene that encodes a putative global regulator of the LysR family annotated as MexT that was originally described as a transcriptional activator of the MexEF-OprN multidrug efflux pump in <i>Pseudomonas</i>. Through both in vitro and in vivo experiments, we have demonstrated the involvement of the dual regulatory system MexT-MexS on the BGC sac expression acting as an activator and a repressor, respectively. The MexEF-OprN transport system of PMA22, also controlled by MexT, was shown to play a fundamental role in the metabolism of safracin. The overexpression of <i>mexEF-oprN</i> in PMA22 resulted in fourfold higher production levels of safracin. These results illustrate how a pleiotropic regulatory system can be critical to optimizing the production of tailored secondary metabolites, not only through direct interaction with the BGC promoters, but also by controlling their transport.

Marine DrugsVol. 22(9)
Consejo Superior de Investigaciones Científicas (ES), PharmaMar (Spain) (ES), Centro de Investigaciones Biológicas Margarita Salas (ES)
Ministerio de Economía y Competitividad
Openalex Percentile: Top 85%
Microbial Natural Products and Biosynthesis
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