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Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy

The Eastern oyster (Crassostrea virginica) is a useful, robust model marine organism for tissue metabolism studies. Its relatively few organs are easily delineated and there is sufficient understanding of their functions based on classical assays to support interpretation of advanced spectroscopic a...

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Autores principales: Tikunov, Andrey P., Johnson, Christopher B., Lee, Haakil, Stoskopf, Michael K., Macdonald, Jeffrey M.
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992993/
https://www.ncbi.nlm.nih.gov/pubmed/21116407
http://dx.doi.org/10.3390/md8102578
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author Tikunov, Andrey P.
Johnson, Christopher B.
Lee, Haakil
Stoskopf, Michael K.
Macdonald, Jeffrey M.
author_facet Tikunov, Andrey P.
Johnson, Christopher B.
Lee, Haakil
Stoskopf, Michael K.
Macdonald, Jeffrey M.
author_sort Tikunov, Andrey P.
collection PubMed
description The Eastern oyster (Crassostrea virginica) is a useful, robust model marine organism for tissue metabolism studies. Its relatively few organs are easily delineated and there is sufficient understanding of their functions based on classical assays to support interpretation of advanced spectroscopic approaches. Here we apply high-resolution proton nuclear magnetic resonance ((1)H NMR)-based metabolomic analysis to C. virginica to investigate the differences in the metabolic profile of different organ groups, and magnetic resonance imaging (MRI) to non-invasively identify the well separated organs. Metabolites were identified in perchloric acid extracts of three portions of the oyster containing: (1) adductor muscle, (2) stomach and digestive gland, and (3) mantle and gills. Osmolytes dominated the metabolome in all three organ blocks with decreasing concentration as follows: betaine > taurine > proline > glycine > ß-alanine > hypotaurine. Mitochondrial metabolism appeared most pronounced in the adductor muscle with elevated levels of carnitine facilitating ß-oxidation, and ATP, and phosphoarginine synthesis, while glycogen was elevated in the mantle/gills and stomach/digestive gland. A biochemical schematic is presented that relates metabolites to biochemical pathways correlated with physiological organ functions. This study identifies metabolites and corresponding (1)H NMR peak assignments for future NMR-based metabolomic studies in oysters.
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spelling pubmed-29929932010-11-29 Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy Tikunov, Andrey P. Johnson, Christopher B. Lee, Haakil Stoskopf, Michael K. Macdonald, Jeffrey M. Mar Drugs Article The Eastern oyster (Crassostrea virginica) is a useful, robust model marine organism for tissue metabolism studies. Its relatively few organs are easily delineated and there is sufficient understanding of their functions based on classical assays to support interpretation of advanced spectroscopic approaches. Here we apply high-resolution proton nuclear magnetic resonance ((1)H NMR)-based metabolomic analysis to C. virginica to investigate the differences in the metabolic profile of different organ groups, and magnetic resonance imaging (MRI) to non-invasively identify the well separated organs. Metabolites were identified in perchloric acid extracts of three portions of the oyster containing: (1) adductor muscle, (2) stomach and digestive gland, and (3) mantle and gills. Osmolytes dominated the metabolome in all three organ blocks with decreasing concentration as follows: betaine > taurine > proline > glycine > ß-alanine > hypotaurine. Mitochondrial metabolism appeared most pronounced in the adductor muscle with elevated levels of carnitine facilitating ß-oxidation, and ATP, and phosphoarginine synthesis, while glycogen was elevated in the mantle/gills and stomach/digestive gland. A biochemical schematic is presented that relates metabolites to biochemical pathways correlated with physiological organ functions. This study identifies metabolites and corresponding (1)H NMR peak assignments for future NMR-based metabolomic studies in oysters. Molecular Diversity Preservation International 2010-10-08 /pmc/articles/PMC2992993/ /pubmed/21116407 http://dx.doi.org/10.3390/md8102578 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Tikunov, Andrey P.
Johnson, Christopher B.
Lee, Haakil
Stoskopf, Michael K.
Macdonald, Jeffrey M.
Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy
title Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy
title_full Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy
title_fullStr Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy
title_full_unstemmed Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy
title_short Metabolomic Investigations of American Oysters Using (1)H-NMR Spectroscopy
title_sort metabolomic investigations of american oysters using (1)h-nmr spectroscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992993/
https://www.ncbi.nlm.nih.gov/pubmed/21116407
http://dx.doi.org/10.3390/md8102578
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