Volume 55, Issue 43 pp. 13611-13614
Communication

Discovery of a Mosaic-Like Biosynthetic Assembly Line with a Decarboxylative Off-Loading Mechanism through a Combination of Genome Mining and Imaging

Dr. Mahsa Mir Mohseni

Dr. Mahsa Mir Mohseni

Institut für Pharmazeutische Biologie, Universität Bonn, 53115 Bonn, Germany

These authors contributed equally

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Dr. Thomas Höver

Dr. Thomas Höver

Institut für Pharmazeutische Biologie, Universität Bonn, 53115 Bonn, Germany

These authors contributed equally

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Lena Barra

Lena Barra

Kekulé-Institut für Organische Chemie und Biochemie, Universität Bonn, 53121 Bonn, Germany

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Marcel Kaiser

Marcel Kaiser

Schweizerisches Tropen- und Public-Health-Institut (Swiss TPH), Basel, CH-4002 Switzerland

Universität Basel, CH-4003 Basel, Switzerland

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Prof. Pieter C. Dorrestein

Prof. Pieter C. Dorrestein

Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, La Jolla, CA, USA

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Prof. Jeroen S. Dickschat

Prof. Jeroen S. Dickschat

Kekulé-Institut für Organische Chemie und Biochemie, Universität Bonn, 53121 Bonn, Germany

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Dr. Till F. Schäberle

Corresponding Author

Dr. Till F. Schäberle

Institut für Pharmazeutische Biologie, Universität Bonn, 53115 Bonn, Germany

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First published: 26 September 2016
Citations: 12

Graphical Abstract

A mine of information: The biosynthetic gene cluster for the antiplasmodial natural product siphonazole from gliding bacteria of the genus Herpetosiphon was identified through a combination of genome mining, imaging, and expression studies. Product release proceeds through decarboxylation and dehydration.

Abstract

The biosynthetic gene cluster for the antiplasmodial natural product siphonazole was identified by using a combination of genome mining, imaging, and expression studies in the natural producer Herpetosiphon sp. B060. The siphonazole backbone is assembled from an unusual starter unit from the shikimate pathway that is extended by the action of polyketide synthases and non-ribosomal peptide synthetases with unusual domain structures, including several split modules and a large number of duplicated domains and domains predicted to be inactive. Product release proceeds through decarboxylation and dehydration independent of the thioesterase SphJ and yields the diene terminus of siphonazole. High variation in terms of codon-usage within the gene cluster, together with the dislocated domain organization, suggest a recent emergence in evolutionary terms.

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