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Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins
Phlorotannins are a group of complex polymers of phloroglucinol (1,3,5-trihydroxybenzene) unique to macroalgae. These phenolic compounds are integral structural components of the cell wall in brown algae, but also play many secondary ecological roles such as protection from UV radiation and defense...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306949/ https://www.ncbi.nlm.nih.gov/pubmed/25603345 http://dx.doi.org/10.3390/md13010509 |
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author | Heffernan, Natalie Brunton, Nigel P. FitzGerald, Richard J. Smyth, Thomas J. |
author_facet | Heffernan, Natalie Brunton, Nigel P. FitzGerald, Richard J. Smyth, Thomas J. |
author_sort | Heffernan, Natalie |
collection | PubMed |
description | Phlorotannins are a group of complex polymers of phloroglucinol (1,3,5-trihydroxybenzene) unique to macroalgae. These phenolic compounds are integral structural components of the cell wall in brown algae, but also play many secondary ecological roles such as protection from UV radiation and defense against grazing. This study employed Ultra Performance Liquid Chromatography (UPLC) with tandem mass spectrometry to investigate isomeric complexity and observed differences in phlorotannins derived from macroalgae harvested off the Irish coast (Fucus serratus, Fucus vesiculosus, Himanthalia elongata and Cystoseira nodicaulis). Antioxidant activity and total phenolic content assays were used as an index for producing phlorotannin fractions, enriched using molecular weight cut-off dialysis with subsequent flash chromatography to profile phlorotannin isomers in these macroalgae. These fractions were profiled using UPLC-MS with multiple reaction monitoring (MRM) and the level of isomerization for specific molecular weight phlorotannins between 3 and 16 monomers were determined. The majority of the low molecular weight (LMW) phlorotannins were found to have a molecular weight range equivalent to 4–12 monomers of phloroglucinol. The level of isomerization within the individual macroalgal species differed, resulting in substantially different numbers of phlorotannin isomers for particular molecular weights. F. vesiculosus had the highest number of isomers of 61 at one specific molecular mass, corresponding to 12 phloroglucinol units (PGUs). These results highlight the complex nature of these extracts and emphasize the challenges involved in structural elucidation of these compounds. |
format | Online Article Text |
id | pubmed-4306949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43069492015-02-02 Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins Heffernan, Natalie Brunton, Nigel P. FitzGerald, Richard J. Smyth, Thomas J. Mar Drugs Article Phlorotannins are a group of complex polymers of phloroglucinol (1,3,5-trihydroxybenzene) unique to macroalgae. These phenolic compounds are integral structural components of the cell wall in brown algae, but also play many secondary ecological roles such as protection from UV radiation and defense against grazing. This study employed Ultra Performance Liquid Chromatography (UPLC) with tandem mass spectrometry to investigate isomeric complexity and observed differences in phlorotannins derived from macroalgae harvested off the Irish coast (Fucus serratus, Fucus vesiculosus, Himanthalia elongata and Cystoseira nodicaulis). Antioxidant activity and total phenolic content assays were used as an index for producing phlorotannin fractions, enriched using molecular weight cut-off dialysis with subsequent flash chromatography to profile phlorotannin isomers in these macroalgae. These fractions were profiled using UPLC-MS with multiple reaction monitoring (MRM) and the level of isomerization for specific molecular weight phlorotannins between 3 and 16 monomers were determined. The majority of the low molecular weight (LMW) phlorotannins were found to have a molecular weight range equivalent to 4–12 monomers of phloroglucinol. The level of isomerization within the individual macroalgal species differed, resulting in substantially different numbers of phlorotannin isomers for particular molecular weights. F. vesiculosus had the highest number of isomers of 61 at one specific molecular mass, corresponding to 12 phloroglucinol units (PGUs). These results highlight the complex nature of these extracts and emphasize the challenges involved in structural elucidation of these compounds. MDPI 2015-01-16 /pmc/articles/PMC4306949/ /pubmed/25603345 http://dx.doi.org/10.3390/md13010509 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Heffernan, Natalie Brunton, Nigel P. FitzGerald, Richard J. Smyth, Thomas J. Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins |
title | Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins |
title_full | Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins |
title_fullStr | Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins |
title_full_unstemmed | Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins |
title_short | Profiling of the Molecular Weight and Structural Isomer Abundance of Macroalgae-Derived Phlorotannins |
title_sort | profiling of the molecular weight and structural isomer abundance of macroalgae-derived phlorotannins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306949/ https://www.ncbi.nlm.nih.gov/pubmed/25603345 http://dx.doi.org/10.3390/md13010509 |
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