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Antifouling activity of portimine, select semisynthetic analogues, and other microalga-derived spirocyclic imines

Brooke, Darby G. (author)
Cawthron Institute, New Zealand
Cervin, Gunnar, 1967 (author)
Gothenburg University,Göteborgs universitet,Institutionen för marina vetenskaper,Department of marine sciences,University of Gothenburg, Sweden
Champeau, Olivier (author)
Cawthron Institute, New Zealand
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Harwood, D. Tim (author)
Cawthron Institute, New Zealand
Pavia, Henrik, 1964 (author)
Gothenburg University,Göteborgs universitet,Institutionen för marina vetenskaper,Department of marine sciences,University of Gothenburg, Sweden
Selwood, Andrew I. (author)
Cawthron Institute, New Zealand
Svenson, Johan (author)
RISE,Kemi och material
Tremblay, Louis A. (author)
Cawthron Institute, New Zealand; University of Auckland, New Zealand
Cahill, Patrick L. (author)
Cawthron Institute, New Zealand
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 (creator_code:org_t)
2018-12-12
2018
English.
In: Biofouling. - : Informa UK Limited. - 0892-7014 .- 1029-2454. ; 34:8, s. 950-961
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group. A range of natural products from marine invertebrates, bacteria and fungi have been assessed as leads for nature-inspired antifouling (AF) biocides, but little attention has been paid to microalgal-derived compounds. This study assessed the AF activity of the spirocyclic imine portimine (1), which is produced by the benthic mat-forming dinoflagellate Vulcanodinium rugosum. Portimine displayed potent AF activity in a panel of four macrofouling bioassays (EC 50 0.06–62.5 ng ml −1 ), and this activity was distinct from that of the related compounds gymnodimine-A (2), 13-desmethyl spirolide C (3), and pinnatoxin-F (4). The proposed mechanism of action for portimine is induction of apoptosis, based on the observation that portimine inhibited macrofouling organisms at developmental stages known to involve apoptotic processes. Semisynthetic modification of select portions of the portimine molecule was subsequently undertaken. Observed changes in bioactivity of the resulting semisynthetic analogues of portimine were consistent with portimine’s unprecedented 5-membered imine ring structure playing a central role in its AF activity.

Subject headings

NATURVETENSKAP  -- Biologi -- Ekologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Ecology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Kemiteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Chemical Engineering (hsv//eng)

Keyword

Bioassay
biofouling
microalgae
natural product
portimine
Bioassay

Publication and Content Type

ref (subject category)
art (subject category)

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