Abstract

Objective: The objective of the study was to examine the nutritive value of Helix lucorum meat and to create awareness about fatty acid composition of phospholipid subclasses of the total body and cephalopedal tissues of the snail. Methods: Thin layer chromatography plates contained lipid samples placed in the chromatography tank containing: chloroform/ethanol/water/triethylamine. The phospholipid subclasses were dissolved in about 5 ml of methanol and 5 drop of sulfuric acid. The mixture was refluxed for 2 h to form fatty acid methyl esters at 85 °C. Fatty acids were detected by Gas chromatography. Results: The most noteworthy result was the high level of C20:2ω6 in PE (10.49%-11.35%) and PC (17.33%-12.96%). Appreciable quantity of essential fatty acid C18:2ω6 was determined in PC (20.85%-17.46%) and PE (16.88%-17.53%) from both tissues. Precursor of eicosanoids, C20:4ω6 was found apparently high in PI, PS and PE of the total body. The highest level of ΣPUFA was 63.90% in PE from total body whereas the highest level of ΣSFA was 60.79% in PI from the cephalopedal. ΣMUFA level was pretty low in PI, PS and PE. Conclusion: The study is a guide for biochemical and nutritional value of edible snails and can be useful for further investigation on physiological and systematic studies of other species.

Highlights

  • Molluscs constitute an excellent source of protein and lipid; demand for qualified food research is increasing day by day

  • Mollusc lipids are characterized by a great variety of fatty acids especially in major lipid classes, because of a large number of molecular species exist for each class [1]

  • The mixture was refluxed for 2 h to form fatty acid methyl esters (FAME) at 85°C

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Summary

Methods

Thin layer chromatography plates contained lipid samples placed in the chromatography tank containing: chloroform/ethanol/water/triethylamine. The phospholipid subclasses were dissolved in about 5 ml of methanol and 5 drop of sulfuric acid. The mixture was refluxed for 2 h to form fatty acid methyl esters at 85 °C. Fatty acids were detected by Gas chromatography

Results
Conclusion
Introduction
Material and Methods
Results and Discussion

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