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Characterization of antibiofilm compound from marine sponge Stylissa carteri
The fouling phenomenon grabbed global attention and caused huge economic losses specifically in marine-related industries. Sessile behavior exposed the sponge to the risk of fouling. However, their bodies remained free from foulers, which were attributed to the chemical defense system. The objective...
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Published in: | Environmental science and pollution research international 2024-05, Vol.31 (25), p.37552-37563 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | The fouling phenomenon grabbed global attention and caused huge economic losses specifically in marine-related industries. Sessile behavior exposed the sponge to the risk of fouling. However, their bodies remained free from foulers, which were attributed to the chemical defense system. The objectives of this study were to determine the antibiofilm activity of the marine sponge,
Stylissa carteri
, and to characterize the isolated compound involved. The antibiofilm activity of
S. carteri
methanolic crude extract (MCE) and fractions was tested against biofilm-producing bacteria,
Pseudomonas aeruginosa
, using two different modes of crystal violet biofilm assays: preventive and detachment. Besides that, the disc-diffusion test was conducted to screen the antibacterial activity against
gram
-positive and
gram
-negative bacteria while a cytotoxicity assay was conducted on the HepG2 cell line. Bioassay-guided fractionation was carried out using vacuum liquid chromatography (VLC) and solid phase extraction using a C18 Sep-Pak Cartridge. The crystal compound was isolated and characterized through thin-layer chromatography (TLC), Fourier transform infrared (FTIR) spectroscopy, liquid chromatography-mass spectrometry (LCMS), and nuclear magnetic resonance (NMR) spectroscopy. The
S. carteri
MCE showed a promising result with a half-maximal inhibitory concentration (IC
50
) of 20.22 μg/mL in the preventive assay, while no IC
50
was determined in the detachment assay since all inhibitions |
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ISSN: | 1614-7499 0944-1344 1614-7499 |
DOI: | 10.1007/s11356-024-33704-0 |