Cyanobacterial antimetabolite 7-deoxy-sedoheptulose blocks the shikimate pathway to inhibit the growth of prototrophic organisms.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
01 02 2019
Historique:
received: 10 07 2018
accepted: 09 01 2019
entrez: 3 2 2019
pubmed: 3 2 2019
medline: 2 4 2019
Statut: epublish

Résumé

Antimetabolites are small molecules that inhibit enzymes by mimicking physiological substrates. We report the discovery and structural elucidation of the antimetabolite 7-deoxy-sedoheptulose (7dSh). This unusual sugar inhibits the growth of various prototrophic organisms, including species of cyanobacteria, Saccharomyces, and Arabidopsis. We isolate bioactive 7dSh from culture supernatants of the cyanobacterium Synechococcus elongatus. A chemoenzymatic synthesis of 7dSh using S. elongatus transketolase as catalyst and 5-deoxy-D-ribose as substrate allows antimicrobial and herbicidal bioprofiling. Organisms treated with 7dSh accumulate 3-deoxy-D-arabino-heptulosonate 7-phosphate, which indicates that the molecular target is 3-dehydroquinate synthase, a key enzyme of the shikimate pathway, which is absent in humans and animals. The herbicidal activity of 7dSh is in the low micromolar range. No cytotoxic effects on mammalian cells have been observed. We propose that the in vivo inhibition of the shikimate pathway makes 7dSh a natural antimicrobial and herbicidal agent.

Identifiants

pubmed: 30710081
doi: 10.1038/s41467-019-08476-8
pii: 10.1038/s41467-019-08476-8
pmc: PMC6358636
doi:

Substances chimiques

Antifungal Agents 0
Antimetabolites 0
Heptoses 0
Herbicides 0
Shikimic Acid 29MS2WI2NU
sedoheptulose 3019-74-7
3-dehydroquinate synthetase EC 4.2.3.4
Phosphorus-Oxygen Lyases EC 4.6.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

545

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Auteurs

Klaus Brilisauer (K)

Institute of Organic Chemistry, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076, Tübingen, Germany.
Microbiology, Organismic Interactions, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 28, 72076, Tübingen, Germany.

Johanna Rapp (J)

Microbiology, Organismic Interactions, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 28, 72076, Tübingen, Germany.

Pascal Rath (P)

Institute of Organic Chemistry, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076, Tübingen, Germany.

Anna Schöllhorn (A)

Microbiology, Organismic Interactions, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 28, 72076, Tübingen, Germany.

Lisa Bleul (L)

Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), Eberhard Karls Universität Tübingen, Eugenstraße 6, 72076, Tübingen, Germany.

Elisabeth Weiß (E)

Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), Eberhard Karls Universität Tübingen, Eugenstraße 6, 72076, Tübingen, Germany.

Mark Stahl (M)

Center for Plant Molecular Biology, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 32, 72076, Tübingen, Germany.

Stephanie Grond (S)

Institute of Organic Chemistry, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076, Tübingen, Germany. biomolchemie@orgchem.uni-tuebingen.de.

Karl Forchhammer (K)

Microbiology, Organismic Interactions, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 28, 72076, Tübingen, Germany. biomolchemie@orgchem.uni-tuebingen.de.

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Classifications MeSH