Daftar Isi:
  • ABSTRACT Sponges produce distinct fatty acids (FAs) that (potentially) can be used as chemotaxonomic and ecological biomarkers to study endosymbiont-host interactions and the functional ecology of sponges. Here, we present FA profiles of five common habitat-building deep-sea sponges (class Demospongiae, order Tetractinellida), which are classified as high microbial abundance (HMA) species. Geodia hentscheli, G. parva, G. atlantica, G. barretti, and Stelletta rhaphidiophora were collected from boreal and Arctic sponge grounds in the North-Atlantic Ocean. Bacterial FAs dominated in all five species and particularly isomeric mixtures of mid-chain branched FAs (MBFAs, 8- and 9-Me-C16:0 and 10 and 11-Me-C18:0) were found in high abundance (together ≥ 20% of total FAs) aside more common bacterial markers. In addition, the sponges produced long-chain linear, mid- and a(i)-branched unsaturated FAs (LCFAs) with a chain length of 24‒28 C atoms and had predominantly the typical Δ5,9unsaturation, although also Δ9,19 and (yet undescribed) Δ11,21 unsaturations were identified. G. parva and S. rhaphidiophora each produced distinct LCFAs, while G. atlantica, G. barretti, and G. hentscheli produced similar LCFAs, but in different ratios. The different bacterial precursors varied in carbon isotopic composition (δ13C), with MBFAs being more enriched compared to other bacterial (linear and a(i)-branched) FAs. We propose biosynthetic pathways for different LCFAs from their bacterial precursors, that are consistent with small isotopic differences found in LCFAs. Indeed, FA profiles of deep-sea sponges can serve as chemotaxonomic markers and support the conception that sponges acquire building blocks from their endosymbiotic bacteria.
  • ACKNOWLEDGEMENTS We thank Antje Boetius for supporting and promoting this study and organizing the PS101. We thank the captain and crew of PS101 for excellent support at sea. We thank late Hans Tore Rapp (UiB) for organizing the G.O. Sars expeditions and excellent project coordination. We thank Desmond Eefting for analytical assistance. We thank master students Gydo Geijer, Sean Hoetjes, David Lenkes, Floor Wille, and Femke van Dam for their help in the lab and with analyses. We thank Eva de Rijke, Samira Absalah and Stefan Schouten for their help in protocol development. Irene Rijpstra and Volker Thiel are acknowledged for their help with FA identification. We thank Pieter van Rijswijk and Marco Houtekamer for sharing their analytical knowledge and identification libraries. Paco Cardenas is acknowledged for sharing his taxonomic knowledge.