posted on 2013-09-20, 00:00authored byAshley M. Sidebottom, Andrew
R. Johnson, Jonathan A. Karty, Darci J. Trader, Erin E. Carlson
Natural
products exhibit a broad range of biological properties and have been
a crucial source of therapeutic agents and novel scaffolds. Although
bacterial secondary metabolomes are widely explored, they remain incompletely
cataloged by current isolation and characterization strategies. To
identify metabolites residing in unexplored chemical space, we have
developed an integrated discovery approach that combines bacterial
growth perturbation, accurate mass spectrometry, comparative mass
spectra data analysis, and fragmentation spectra clustering for the
identification of low-abundant, novel compounds from complex biological
matrices. In this investigation, we analyzed the secreted metabolome
of the extensively studied Actinomycete, Streptomyces coelicolor M145, and discovered a low-abundant suite of 15 trihydroxamate,
amphiphilic siderophores. Compounds in this class have primarily been
observed in marine microorganisms making their detection in the soil-dwelling S. coelicolor M145 significant. At least 10 of these ferrioxamine-based
molecules are not known to be produced by any organism, and none have
previously been detected from S. coelicolor M145.
In addition, we confirmed the production of ferrioxamine D1, a relatively hydrophilic family member that has not been shown
to be biosynthesized by this organism. The identified molecules are
part of only a small list of secondary metabolites that have been
discovered since sequencing of S. coelicolor M145
revealed that it possessed numerous putative secondary metabolite-producing
gene clusters with no known metabolites. Thus, the identified siderophores
represent the unexplored metabolic potential of both well-studied
and new organisms that could be uncovered with our sensitive and robust
approach.