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Herpetopanone, a diterpene from Herpetosiphon aurantiacus discovered by isotope labeling.


ABSTRACT: The genome of the predatory bacterium Herpetosiphon aurantiacus 114-95T harbors a number of biosynthesis genes, including four terpene cyclase genes. To identify the terpenes biosynthesized from H. aurantiacus 114-95T, we fed the strain with 13C-labeled glucose and, subsequently, searched for characteristic mass shifts in its metabolome. This approach led to the discovery of a new natural product, of which the isotope pattern is indicative for a diterpene originating from the methylerythritol phosphate pathway. After large-scale fermentation of H. aurantiacus 114-95T, the putative diterpene was isolated in sufficient quantity to enable NMR-based structure elucidation. The compound, for which the name herpetopanone is proposed, features a rare octahydro-1H-indenyl skeleton. Herpetopanone bears resemblance to cadinane-type sesquiterpenes from plants, but is structurally entirely unprecedented in bacteria. Based on its molecular architecture, a possible biosynthetic pathway is postulated.

SUBMITTER: Pan X 

PROVIDER: S-EPMC5704754 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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Herpetopanone, a diterpene from <i>Herpetosiphon aurantiacus</i> discovered by isotope labeling.

Pan Xinli X   Domin Nicole N   Schieferdecker Sebastian S   Kage Hirokazu H   Roth Martin M   Nett Markus M  

Beilstein journal of organic chemistry 20171117


The genome of the predatory bacterium <i>Herpetosiphon aurantiacus</i> 114-95<sup>T</sup> harbors a number of biosynthesis genes, including four terpene cyclase genes. To identify the terpenes biosynthesized from <i>H. aurantiacus</i> 114-95<sup>T</sup>, we fed the strain with <sup>13</sup>C-labeled glucose and, subsequently, searched for characteristic mass shifts in its metabolome. This approach led to the discovery of a new natural product, of which the isotope pattern is indicative for a dit  ...[more]

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