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| Main Authors: | , , , , , , , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
Marine drugs
2024
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| Subjects: | |
| Online Access: | https://pubmed.ncbi.nlm.nih.gov/39728146/ |
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Table of Contents:
- Identification and Characterization of Two Aryl Sulfotransferases from Deep-Sea Marine Fungi and Their Implications in the Sulfation of Secondary Metabolites. Graziano, Nicolas Arce-López, Beatriz Barbeyron, Tristan Delage, Ludovic Gerometta, Elise Roullier, Catherine Burgaud, Gaëtan Poirier, Elisabeth Martinelli, Laure Jany, Jean-Luc Hymery, Nolwenn Meslet-Cladiere, Laurence Sulfotransferases Phylogeny Aquatic Organisms Secondary Metabolism Fungi Ascomycota Aspergillus Sulfates Substrate Specificity Animals Sulfation plays a critical role in the biosynthesis of small molecules, regulatory mechanisms such as hormone signaling, and detoxification processes (phase II enzymes). The sulfation reaction is catalyzed by a broad family of enzymes known as sulfotransferases (SULTs), which have been extensively studied in animals due to their medical importance, but also in plant key processes. Despite the identification of some sulfated metabolites in fungi, the mechanisms underlying fungal sulfation remain largely unknown. To address this knowledge gap, we conducted a comprehensive search of available genomes, resulting in the identification of 174 putative SULT genes in the Ascomycota phylum. Phylogenetic analysis and structural modeling revealed that these SULTs belong to the aryl sulfotransferase family, and they are divided into two potential distinct clusters of PAPS-dependent SULTs within the fungal kingdom. SULT genes from two marine fungi isolated from deep-sea hydrothermal vents, UBOCC-A-208029 (SULT) and UBOCC-A-108050 SULT (SULT), were selected as representatives of each cluster. Recombinant proteins were expressed in and biochemically characterized. SULT demonstrated high and versatile activity, while SULT appeared more substrate-specific. Here, SULT was used to sulfate the mycotoxin zearalenone, enhancing its cytotoxicity toward healthy feline intestinal cells.