posted on 2018-01-23, 00:00authored byAaron
W. Puri, Emily Mevers, Timothy R. Ramadhar, Daniel Petras, Darren Liu, Jörn Piel, Pieter C. Dorrestein, E. Peter Greenberg, Mary E. Lidstrom, Jon Clardy
Methane-oxidizing bacteria, aerobes
that utilize methane as their
sole carbon and energy source, are being increasingly studied for
their environmentally significant ability to remove methane from the
atmosphere. Their genomes indicate that they also have a robust and
unusual secondary metabolism. Bioinformatic analysis of the Methylobacter tundripaludum genome identified biosynthetic
gene clusters for several intriguing metabolites, and this report
discloses the structural and genetic characterization of tundrenone,
one of these metabolites. Tundrenone is a highly oxidized metabolite
that incorporates both a modified bicyclic chorismate-derived fragment
and a modified lipid tail bearing a β,γ-unsaturated α-hydroxy
ketone. Tundrenone has been genetically linked to its biosynthetic
gene cluster, and quorum sensing activates its production. M. tundripaludum’s genome and tundrenone’s
discovery support the idea that additional studies of methane-oxidizing
bacteria will reveal new naturally occurring molecular scaffolds and
the biosynthetic pathways that produce them.