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Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism

[Image: see text] 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 secon...

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Autores principales: Puri, Aaron W., Mevers, Emily, Ramadhar, Timothy R., Petras, Daniel, Liu, Darren, Piel, Jörn, Dorrestein, Pieter C., Greenberg, E. Peter, Lidstrom, Mary E., Clardy, Jon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817624/
https://www.ncbi.nlm.nih.gov/pubmed/29361220
http://dx.doi.org/10.1021/jacs.7b12240
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author Puri, Aaron W.
Mevers, Emily
Ramadhar, Timothy R.
Petras, Daniel
Liu, Darren
Piel, Jörn
Dorrestein, Pieter C.
Greenberg, E. Peter
Lidstrom, Mary E.
Clardy, Jon
author_facet Puri, Aaron W.
Mevers, Emily
Ramadhar, Timothy R.
Petras, Daniel
Liu, Darren
Piel, Jörn
Dorrestein, Pieter C.
Greenberg, E. Peter
Lidstrom, Mary E.
Clardy, Jon
author_sort Puri, Aaron W.
collection PubMed
description [Image: see text] 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.
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spelling pubmed-58176242018-02-20 Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism Puri, Aaron W. Mevers, Emily Ramadhar, Timothy R. Petras, Daniel Liu, Darren Piel, Jörn Dorrestein, Pieter C. Greenberg, E. Peter Lidstrom, Mary E. Clardy, Jon J Am Chem Soc [Image: see text] 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. American Chemical Society 2018-01-23 2018-02-14 /pmc/articles/PMC5817624/ /pubmed/29361220 http://dx.doi.org/10.1021/jacs.7b12240 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Puri, Aaron W.
Mevers, Emily
Ramadhar, Timothy R.
Petras, Daniel
Liu, Darren
Piel, Jörn
Dorrestein, Pieter C.
Greenberg, E. Peter
Lidstrom, Mary E.
Clardy, Jon
Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism
title Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism
title_full Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism
title_fullStr Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism
title_full_unstemmed Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism
title_short Tundrenone: An Atypical Secondary Metabolite from Bacteria with Highly Restricted Primary Metabolism
title_sort tundrenone: an atypical secondary metabolite from bacteria with highly restricted primary metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817624/
https://www.ncbi.nlm.nih.gov/pubmed/29361220
http://dx.doi.org/10.1021/jacs.7b12240
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