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Antifouling potential of Nature-inspired sulfated compounds

Natural products with a sulfated scaffold have emerged as antifouling agents with low or nontoxic effects to the environment. In this study 13 sulfated polyphenols were synthesized and tested for antifouling potential using the anti-settlement activity of mussel (Mytilus galloprovincialis) plantigra...

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Autores principales: Almeida, Joana R., Correia-da-Silva, Marta, Sousa, Emília, Antunes, Jorge, Pinto, Madalena, Vasconcelos, Vitor, Cunha, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5304334/
https://www.ncbi.nlm.nih.gov/pubmed/28205590
http://dx.doi.org/10.1038/srep42424
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author Almeida, Joana R.
Correia-da-Silva, Marta
Sousa, Emília
Antunes, Jorge
Pinto, Madalena
Vasconcelos, Vitor
Cunha, Isabel
author_facet Almeida, Joana R.
Correia-da-Silva, Marta
Sousa, Emília
Antunes, Jorge
Pinto, Madalena
Vasconcelos, Vitor
Cunha, Isabel
author_sort Almeida, Joana R.
collection PubMed
description Natural products with a sulfated scaffold have emerged as antifouling agents with low or nontoxic effects to the environment. In this study 13 sulfated polyphenols were synthesized and tested for antifouling potential using the anti-settlement activity of mussel (Mytilus galloprovincialis) plantigrade post-larvae and bacterial growth inhibition towards four biofilm-forming bacterial strains. Results show that some of these Nature-inspired compounds were bioactive, particularly rutin persulfate (2), 3,6-bis(β-D-glucopyranosyl) xanthone persulfate (6), and gallic acid persulfate (12) against the settlement of plantigrades. The chemical precursors of sulfated compounds 2 and 12 were also tested for anti-settlement activity and it was possible to conclude that bioactivity is associated with sulfation. While compound 12 showed the most promising anti-settlement activity (EC(50) = 8.95 μg.mL(−1)), compound 2 also caused the higher level of growth inhibition in bacteria Vibrio harveyi (EC(20) = 12.5 μg.mL(−1)). All the three bioactive compounds 2, 6, and 12 were also found to be nontoxic to the non target species Artemia salina (<10% mortality at 250 μM) and Vibrio fischeri (LC(50) > 1000 μg.mL(−1)). This study put forward the relevance of synthesizing non-natural sulfated small molecules to generate new nontoxic antifouling agents.
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spelling pubmed-53043342017-03-14 Antifouling potential of Nature-inspired sulfated compounds Almeida, Joana R. Correia-da-Silva, Marta Sousa, Emília Antunes, Jorge Pinto, Madalena Vasconcelos, Vitor Cunha, Isabel Sci Rep Article Natural products with a sulfated scaffold have emerged as antifouling agents with low or nontoxic effects to the environment. In this study 13 sulfated polyphenols were synthesized and tested for antifouling potential using the anti-settlement activity of mussel (Mytilus galloprovincialis) plantigrade post-larvae and bacterial growth inhibition towards four biofilm-forming bacterial strains. Results show that some of these Nature-inspired compounds were bioactive, particularly rutin persulfate (2), 3,6-bis(β-D-glucopyranosyl) xanthone persulfate (6), and gallic acid persulfate (12) against the settlement of plantigrades. The chemical precursors of sulfated compounds 2 and 12 were also tested for anti-settlement activity and it was possible to conclude that bioactivity is associated with sulfation. While compound 12 showed the most promising anti-settlement activity (EC(50) = 8.95 μg.mL(−1)), compound 2 also caused the higher level of growth inhibition in bacteria Vibrio harveyi (EC(20) = 12.5 μg.mL(−1)). All the three bioactive compounds 2, 6, and 12 were also found to be nontoxic to the non target species Artemia salina (<10% mortality at 250 μM) and Vibrio fischeri (LC(50) > 1000 μg.mL(−1)). This study put forward the relevance of synthesizing non-natural sulfated small molecules to generate new nontoxic antifouling agents. Nature Publishing Group 2017-02-13 /pmc/articles/PMC5304334/ /pubmed/28205590 http://dx.doi.org/10.1038/srep42424 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Almeida, Joana R.
Correia-da-Silva, Marta
Sousa, Emília
Antunes, Jorge
Pinto, Madalena
Vasconcelos, Vitor
Cunha, Isabel
Antifouling potential of Nature-inspired sulfated compounds
title Antifouling potential of Nature-inspired sulfated compounds
title_full Antifouling potential of Nature-inspired sulfated compounds
title_fullStr Antifouling potential of Nature-inspired sulfated compounds
title_full_unstemmed Antifouling potential of Nature-inspired sulfated compounds
title_short Antifouling potential of Nature-inspired sulfated compounds
title_sort antifouling potential of nature-inspired sulfated compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5304334/
https://www.ncbi.nlm.nih.gov/pubmed/28205590
http://dx.doi.org/10.1038/srep42424
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