Structure Revision of a Widespread Marine Sulfonolipid Class Based on Isolation and Total Synthesis

Author:

Roman Dávid12ORCID,Meisinger Philippe13,Guillonneau Richard4,Peng Chia‐Chi12,Peltner Lukas K.5,Jordan Paul M.5ORCID,Haensch Veit3,Götze Sebastian2ORCID,Werz Oliver5ORCID,Hertweck Christian36ORCID,Chen Yin7ORCID,Beemelmanns Christine128ORCID

Affiliation:

1. Chemical Biology of Microbe-Host Interactions Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (HKI) Beutenbergstrasse 11 A 07745 Jena Germany

2. Anti-Infectives from Microbiota Helmholtz Institute for Pharmaceutical Research Saarland (HIPS) Helmholtz Centre for Infection Research (HZI) Campus E8.1 66123 Saarbrücken Germany

3. Biomolecular Chemistry Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (HKI) Beutenbergstrasse 11 A 07745 Jena Germany

4. Nantes Université CNRS, US2B, UMR 6286 F-44000 Nantes France

5. Department of Pharmaceutical/Medicinal Chemistry Institute of Pharmacy— Friedrich-Schiller-University Jena Philosophenweg 14 07743 Jena Germany

6. Institute of Microbiology— Friedrich-Schiller-University Jena 07743 Jena Germany

7. School of Biosciences University of Birmingham Edgbaston B15 2TT United Kingdom

8. Saarland University Campus E8.1 66123 Saarbrücken Germany

Abstract

AbstractThe cosmopolitan marine Roseobacter clade is of global biogeochemical importance. Members of this clade produce sulfur‐containing amino lipids (SALs) involved in biofilm formation and marine surface colonization processes. Despite their physiological relevance and abundance, SALs have only been explored through genomic mining approaches and lipidomic studies based on mass spectrometry, which left the relative and absolute structures of SALs unresolved, hindering progress in biochemical and functional investigations. Herein, we report the structural revision of a new group of SALs, which we named cysteinolides, using a combination of analytical techniques, isolation and degradation experiments and total synthetic efforts. Contrary to the previously proposed homotaurine‐based structures, cysteinolides are composed of an N,O‐acylated cysteinolic acid‐containing head group carrying various different (α‐hydroxy)carboxylic acids. We also performed the first validated targeted‐network based analysis, which allowed us to map the distribution and structural diversity of cysteinolides across bacterial lineages. Beyond offering structural insight, our research provides SAL standards and validated analytical data. This information holds significance for forthcoming investigations into bacterial sulfonolipid metabolism and biogeochemical nutrient cycling within marine environments.

Funder

Deutsche Forschungsgemeinschaft

Studienstiftung des Deutschen Volkes

HORIZON EUROPE European Research Council

Publisher

Wiley

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