STUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT

In a field test for antifouling activity the raw extract and the organic fraction obtained from the marine sponge Cliona delitrix, collected at the San Andrés Islas (Colombia, Caribbean Sea), showed activity. The organic fraction was separated by column chromatography to obtain enriched fractions of...

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Autores principales: Leonardo CASTELLANOS H., Humberto MAYORGA W., Carmenza DUQUE B.
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Publicado: Universidad de Antioquia 2010
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Acceso en línea:https://doaj.org/article/51f6d6fe039d44beaa3198a9645c0847
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spelling oai:doaj.org-article:51f6d6fe039d44beaa3198a9645c08472021-11-19T04:14:21ZSTUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT0121-40042145-2660https://doaj.org/article/51f6d6fe039d44beaa3198a9645c08472010-07-01T00:00:00Zhttps://revistas.udea.edu.co/index.php/vitae/article/view/6346https://doaj.org/toc/0121-4004https://doaj.org/toc/2145-2660In a field test for antifouling activity the raw extract and the organic fraction obtained from the marine sponge Cliona delitrix, collected at the San Andrés Islas (Colombia, Caribbean Sea), showed activity. The organic fraction was separated by column chromatography to obtain enriched fractions of glycerides, glycolipids, phospholipids, free fatty acids, fatty acids methyl esters (FAMEs) and monohydroxysterols identified by TLC and dereplication techniques (NMR). The glyceride, glycolipid, and phospholipid fractions were hydrolyzed, and the fatty acids methyl esters obtained, together with the initial fatty acids fraction were converted into their methyl esters and analyzed by HRGC-MS. In order to locate unsaturations and alkyl branches in fatty acids, their methyl esters derivates were transformed to the corresponding pyrrolidides and subsequently analyzed by HRGC-MS. The identification of the marifatty acids was carried out using their ECL value as methyl esters, and particularly the study of their pyrrolidide spectra was used to locate unsaturations and alkyl branch positions. The analysis allowed the identification of 89 fatty acids. The main acids include the new 7,10,12,14-icosatetraenoic acid, as well as 5,9-hexacosadienoic acid and hexadecanoic acid. Additionally, 19 monohydroxysterols were identified by HRGC-MS and NMR 1H. Cholestanol and clionasterol were the most abundant compounds and the stanols presence (near to 30%) was not previously reported for this genus.Leonardo CASTELLANOS H.Humberto MAYORGA W.Carmenza DUQUE B.Universidad de AntioquiaarticleCliona delitrixlipidsfatty acidssterolsantifoulingFood processing and manufactureTP368-456Pharmaceutical industryHD9665-9675ENVitae, Vol 17, Iss 2 (2010)
institution DOAJ
collection DOAJ
language EN
topic Cliona delitrix
lipids
fatty acids
sterols
antifouling
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
spellingShingle Cliona delitrix
lipids
fatty acids
sterols
antifouling
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
Leonardo CASTELLANOS H.
Humberto MAYORGA W.
Carmenza DUQUE B.
STUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT
description In a field test for antifouling activity the raw extract and the organic fraction obtained from the marine sponge Cliona delitrix, collected at the San Andrés Islas (Colombia, Caribbean Sea), showed activity. The organic fraction was separated by column chromatography to obtain enriched fractions of glycerides, glycolipids, phospholipids, free fatty acids, fatty acids methyl esters (FAMEs) and monohydroxysterols identified by TLC and dereplication techniques (NMR). The glyceride, glycolipid, and phospholipid fractions were hydrolyzed, and the fatty acids methyl esters obtained, together with the initial fatty acids fraction were converted into their methyl esters and analyzed by HRGC-MS. In order to locate unsaturations and alkyl branches in fatty acids, their methyl esters derivates were transformed to the corresponding pyrrolidides and subsequently analyzed by HRGC-MS. The identification of the marifatty acids was carried out using their ECL value as methyl esters, and particularly the study of their pyrrolidide spectra was used to locate unsaturations and alkyl branch positions. The analysis allowed the identification of 89 fatty acids. The main acids include the new 7,10,12,14-icosatetraenoic acid, as well as 5,9-hexacosadienoic acid and hexadecanoic acid. Additionally, 19 monohydroxysterols were identified by HRGC-MS and NMR 1H. Cholestanol and clionasterol were the most abundant compounds and the stanols presence (near to 30%) was not previously reported for this genus.
format article
author Leonardo CASTELLANOS H.
Humberto MAYORGA W.
Carmenza DUQUE B.
author_facet Leonardo CASTELLANOS H.
Humberto MAYORGA W.
Carmenza DUQUE B.
author_sort Leonardo CASTELLANOS H.
title STUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT
title_short STUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT
title_full STUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT
title_fullStr STUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT
title_full_unstemmed STUDY OF THE CHEMICAL COMPOSITION AND <i>ANTIFOULING</i> ACTIVITY OF THE MARINE SPONGE <i>Cliona delitrix</i> EXTRACT
title_sort study of the chemical composition and <i>antifouling</i> activity of the marine sponge <i>cliona delitrix</i> extract
publisher Universidad de Antioquia
publishDate 2010
url https://doaj.org/article/51f6d6fe039d44beaa3198a9645c0847
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