Re-examining the iron paradox: the influence of growth medium on regulation and functionality of the tropodithietic acid (TDA) biosynthetic pathway in <i>Phaeobacter piscinae</i>

Tropodithietic acid (TDA) is a secondary metabolite with antimicrobial and iron-binding properties, produced by several marine Roseobacter group bacteria. Although classified as a siderophore, TDA is also produced under iron-replete conditions. To address this paradox, we fused the tdaCDE promoter region of Phaeobacter piscinae S26 with a promoter-less gfp reporter gene to monitor the transcription of TDA biosynthetic genes under different conditions and validated its accuracy using RT-qPCR. In both complex (½YTIO) and low-complexity (IOCGH) marine media, iron supplementation repressed tdaCDE transcription and reduced iron-chelation activity. However, TDA production responded differently depending on medium composition: iron suppressed TDA production in IOCGH but increased it in ½YTIO. Antimicrobial activity of culture supernatants declined in late-stage iron-limited ½YTIO-based cultures, even though tdaCDE transcription and iron-chelating activity increased. Acidification restored antimicrobial activity and increased detectable TDA levels, while several non-antimicrobial structural analogues - detected by LC-MS in non-acidified samples - diminished upon acidification, suggesting pH-driven interconversion. These findings reveal that TDA biosynthesis is regulated by iron availability but that the antimicrobial output of the producer depends on medium composition and pH-driven chemical transformations between TDA and its related structural analogues.

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Journal
FEMS Microbiology Ecology
Published
2026-07-17
DOI
https://doi.org/10.1093/femsec/fiag080
Primary Topic
Microbial Community Ecology and Physiology
Type
article
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article

Re-examining the iron paradox: the influence of growth medium on regulation and functionality of the tropodithietic acid (TDA) biosynthetic pathway in Phaeobacter piscinae

Sheng‐Da Zhang, Aaron J.C. Andersen, Michael S. Cowled, Morten Dencker Schostag et al.
FEMS Microbiology Ecology
Microbial Community Ecology and Physiology
article

Re-examining the iron paradox: the influence of growth medium on regulation and functionality of the tropodithietic acid (TDA) biosynthetic pathway in Phaeobacter piscinae

Sheng‐Da Zhang, Aaron J.C. Andersen, Michael S. Cowled, Morten Dencker Schostag, Morgane Mauduit, Lone Gram, Lauge Alfastsen, Nikoletta Angela Vig, Frederik Valdemar Holck Reimert, Robert Friis-Møller
article en

Abstract

Tropodithietic acid (TDA) is a secondary metabolite with antimicrobial and iron-binding properties, produced by several marine Roseobacter group bacteria. Although classified as a siderophore, TDA is also produced under iron-replete conditions. To address this paradox, we fused the tdaCDE promoter region of Phaeobacter piscinae S26 with a promoter-less gfp reporter gene to monitor the transcription of TDA biosynthetic genes under different conditions and validated its accuracy using RT-qPCR. In both complex (½YTIO) and low-complexity (IOCGH) marine media, iron supplementation repressed tdaCDE transcription and reduced iron-chelation activity. However, TDA production responded differently depending on medium composition: iron suppressed TDA production in IOCGH but increased it in ½YTIO. Antimicrobial activity of culture supernatants declined in late-stage iron-limited ½YTIO-based cultures, even though tdaCDE transcription and iron-chelating activity increased. Acidification restored antimicrobial activity and increased detectable TDA levels, while several non-antimicrobial structural analogues - detected by LC-MS in non-acidified samples - diminished upon acidification, suggesting pH-driven interconversion. These findings reveal that TDA biosynthesis is regulated by iron availability but that the antimicrobial output of the producer depends on medium composition and pH-driven chemical transformations between TDA and its related structural analogues.

FEMS Microbiology Ecology
The University of Melbourne (AU), National University of Misiones (AR), Technical University of Denmark (DK)
Life below water
Openalex Percentile: Top 9%
Microbial Community Ecology and Physiology
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