AI Article Synopsis

  • The study investigates antifouling properties of four compounds from the synoxazolidinone and pulmonarin families, discovered in a sub-Arctic ascidian from Norway.
  • Several tested compounds showed strong effectiveness against various marine species, particularly affecting microfouling and macrofouling processes with minimal toxicity.
  • Notably, synoxazolidinone C's antifouling activity was comparable to a commercial product, while the pulmonarins were effective against bacteria but less so against microalgae and barnacles.

Article Abstract

The current study describes the antifouling properties of four members belonging to the recently discovered synoxazolidinone and pulmonarin families, isolated from the sub-Arctic sessile ascidian Synoicum pulmonaria collected off the Norwegian coast. Four simplified synthetic analogues were also prepared and included in the study. Several of the studied compounds displayed MIC values in the micro-nanomolar range against 16 relevant marine species involved in both the micro- and macrofouling process. Settlement studies on Balanus improvisus cyprids indicated a deterrent effect and a low toxicity for selected compounds. The two synoxazolidinones displayed broad activity and are shown to be among the most active natural antifouling bromotyrosine derivatives described. Synoxazolidinone C displayed selected antifouling properties comparable to the commercial antifouling product Sea-Nine-211. The pulmonarins prevented the growth of several bacterial strains at nanomolar concentrations but displayed a lower activity toward microalgae and no effect on barnacles. The linear and cyclic synthetic peptidic mimics also displayed potent antifouling activities mainly directed against bacterial adhesion and growth.

Download full-text PDF

Source
http://dx.doi.org/10.1021/np5005032DOI Listing

Publication Analysis

Top Keywords

ascidian synoicum
8
synoicum pulmonaria
8
synthetic analogues
8
antifouling properties
8
antifouling
6
displayed
5
antifouling compounds
4
compounds sub-arctic
4
sub-arctic ascidian
4
pulmonaria synoxazolidinones
4

Similar Publications

We have synthesised short analogues of the marine antimicrobial peptide Turgencin A from the colonial Arctic ascidian In this study, we focused on a central, cationic 12-residue Cys-Cys loop region within the sequence. Modified (tryptophan- and arginine-enriched) linear peptides were compared with Cys-Cys cyclic derivatives, and both linear and Cys-cyclic peptides were N-terminally acylated with octanoic acid (C), decanoic acid (C) or dodecanoic acid (C). The highest antimicrobial potency was achieved by introducing dodecanoic acid to a cyclic Turgencin A analogue with low intrinsic hydrophobicity, and by introducing octanoic acid to a cyclic analogue displaying a higher intrinsic hydrophobicity.

View Article and Find Full Text PDF

Five new alkaloids have been isolated from the lipophilic extract of the Antarctic tunicate sp. Deep-sea specimens of sp. were collected during a 2011 cruise of the R/V to the southern Scotia Arc, Antarctica.

View Article and Find Full Text PDF

Seven new polyaromatic bis-spiroketal-containing butenolides, the prunolides D-I (-) and -prunolide C (), a new dibrominated β-carboline sulfamate named pityriacitrin C (), alongside the known prunolides A-C (-) were isolated from the Australian colonial ascidian . The prunolides D-G (-) represent the first asymmetrically brominated prunolides, while -prunolide C () is the first reported with a -configuration about the prunolide's bis-spiroketal core. The prunolides displayed binding activities with the Parkinson's disease-implicated amyloid protein α-synuclein in a mass spectrometry binding assay, while the prunolides (- and ) were found to significantly inhibit the aggregation (>89.

View Article and Find Full Text PDF

Complex interactions exist between microbiomes and their hosts. Increasingly, defensive metabolites that have been attributed to host biosynthetic capability are now being recognized as products of host-associated microbes. These unique metabolites often have bioactivity targets in human disease and can be purposed as pharmaceuticals.

View Article and Find Full Text PDF

The Antarctic marine ecosystem harbors a wealth of biological and chemical innovation that has risen in concert over millennia since the isolation of the continent and formation of the Antarctic circumpolar current. Scientific inquiry into the novelty of marine natural products produced by Antarctic benthic invertebrates led to the discovery of a bioactive macrolide, palmerolide A, that has specific activity against melanoma and holds considerable promise as an anticancer therapeutic. While this compound was isolated from the Antarctic ascidian Synoicum adareanum, its biosynthesis has since been hypothesized to be microbially mediated, given structural similarities to microbially produced hybrid nonribosomal peptide-polyketide macrolides.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!