Structure Elucidation of the First Sex‐Inducing Pheromone of a Diatom

GND
1314924648
ORCID
0000-0003-0868-8172
Zugehörigkeit
Institute for Inorganic and Analytical Chemistry Bioorganic Analytics Friedrich Schiller University Jena Lessingstrasse 8 07743 Jena Germany
Klapper, Franziska A.;
GND
1179717465
Zugehörigkeit
Institute for Inorganic and Analytical Chemistry Bioorganic Analytics Friedrich Schiller University Jena Lessingstrasse 8 07743 Jena Germany
Kiel, Christine;
GND
1051819113
Zugehörigkeit
Institute of Organic and Macromolecular Chemistry Friedrich Schiller University Jena Humboldtstraße 10 07743 Jena Germany
Bellstedt, Peter;
Zugehörigkeit
Laboratory of Protistology and Aquatic Ecology Department of Biology Ghent University Krijgslaan 281 S8 9000 Ghent Belgium
Vyverman, Wim;
GND
1131364872
ORCID
0000-0003-2351-6336
Zugehörigkeit
Institute for Inorganic and Analytical Chemistry Bioorganic Analytics Friedrich Schiller University Jena Lessingstrasse 8 07743 Jena Germany
Pohnert, Georg

Abstract Diatoms are abundant unicellular microalgae, responsible for ≈20 % of global photosynthetic CO 2 fixation. Nevertheless, we know little about fundamental aspects of their biology, such as their sexual reproduction. Pheromone‐mediated chemical communication is crucial for successful mating. An attraction pheromone was identified in the diatom Seminavis robusta , but metabolites priming cells for sex and synchronizing search and mating behavior remained elusive. These sex‐inducing pheromones (SIP) induce cell cycle arrest and trigger the production of the attraction pheromone. Here we describe the challenging structure elucidation of an S. robusta SIP. Guided by metabolomics, a candidate metabolite was identified and elucidated by labeling experiments, NMR, ESI MS n analyses, and chemical transformations. The use of negative ion mode MS was essential to decipher the unprecedented hydroxyproline and β‐sulfated aspartate‐containing cyclic heptapeptide that acts in femtomolar concentrations.

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