• Media type: E-Article
  • Title: Carboxythiazole is a key microbial nutrient currency and critical component of thiamin biosynthesis
  • Contributor: Paerl, Ryan W.; Bertrand, Erin M.; Rowland, Elden; Schatt, Phillippe; Mehiri, Mohamed; Niehaus, Thomas D.; Hanson, Andrew D.; Riemann, Lasse; Bouget, Francois-Yves
  • imprint: Springer Science and Business Media LLC, 2018
  • Published in: Scientific Reports
  • Language: English
  • DOI: 10.1038/s41598-018-24321-2
  • ISSN: 2045-2322
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>Almost all cells require thiamin, vitamin B1 (B1), which is synthesized via the coupling of thiazole and pyrimidine precursors. Here we demonstrate that 5-(2-hydroxyethyl)-4-methyl-1,3-thiazole-2-carboxylic acid (cHET) is a useful <jats:italic>in vivo</jats:italic> B1 precursor for representatives of ubiquitous marine picoeukaryotic phytoplankton and <jats:italic>Escherichia coli</jats:italic> – drawing attention to cHET as a valuable exogenous micronutrient for microorganisms with ecological, industrial, and biomedical value. Comparative utilization experiments with the terrestrial plant <jats:italic>Arabidopsis thaliana</jats:italic> revealed that it can also use exogenous cHET, but notably, picoeukaryotic marine phytoplankton and <jats:italic>E. coli</jats:italic> were adapted to grow on low (picomolar) concentrations of exogenous cHET. Our results call for the modification of the conventional B1 biosynthesis model to incorporate cHET as a key precursor for B1 biosynthesis in two domains of life, and for consideration of cHET as a microbial micronutrient currency modulating marine primary productivity and community interactions in human gut-hosted microbiomes.</jats:p>
  • Access State: Open Access