Biophysical evaluation of physiological effects of gilthead sea bream (Sparus aurata) farming using FTIR spectroscopy

•The level of glycogen and triglycerides and cholesterol esters increased and the in the aquacultured samples.•The level of unsaturation indicated elevated lipid peroxidation in the aquacultured samples.•Structural/organisational changes were observed in the nucleic acids in the aquacultured samples...

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Published inFood chemistry Vol. 145; pp. 1055 - 1060
Main Authors Ceylan, Cagatay, Tanrikul, Tansel, Özgener, Hüseyin
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 15.02.2014
Elsevier
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Summary:•The level of glycogen and triglycerides and cholesterol esters increased and the in the aquacultured samples.•The level of unsaturation indicated elevated lipid peroxidation in the aquacultured samples.•Structural/organisational changes were observed in the nucleic acids in the aquacultured samples. Sparus aurata is one of the two most important cultured fish species in the Mediterranean region. The present work investigates the effects of culturing in S. aurata liver tissue at the molecular level using Fourier Transform Infrared (FTIR) spectroscopy. FTIR spectroscopy revealed dramatic differences between the wild and aquacultured fish liver cells, which mainly indicated that the level of glycogen increased in the aquacultured samples and the protein/lipid ratio decreased by 42.29% indicating that triglycerides and cholesterol esters increased and the protein content decreased in the aquacultured samples. The 15.99% increase in the level of unsaturation indicated elevated lipid peroxidation. Structural/organisational changes in the nucleic acids along with increased transcriptional status of the liver tissue cells were observed in the cultured fish tissue. All these results indicated that culturing induces significant changes in fish physiology. In addition FTIR spectroscopy is a promising method to monitor the physiological changes in fish physiology.
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ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2013.08.111