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지충이 에탄올 추출물의 α-amylase 저해활성

Inhibitory Effects of Sargassum thunbergii Ethanol Extract against α-amylase

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참고문헌

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주제분류수산학

초록

This study was performed to investigate the inhibitory activity of Sargassum thunbergii (ST) against α-amylase and elucidate the availability of ST extract as a functional food agent. To test the inhibitory activity of ST against α-amylase, porcine pancreatic α-amylase and potato starch were used as substrates. It was revealed that ST crude ethanol extracts have high α-amylase inhibitory activity. Subsequently, ST crude ethanol extract was separated into five partition layers by solvent extraction: n-hexane, chloroform, ethyl acetate, butanol, and water. Chloroform and n-hexane fractions showed higher inhibitory activities than did acarbose (positive control). To confirm the changes in enzyme inhibitory activity by physical treatments, ST crude ethanol extract was subjected to heat, pH, and γ-irradiation treatments. In all heat treatments with the exception of one (121℃, 15 min), the inhibitory activity was increased compared with the untreated group. With regard to pH stability, ST extract showed no significant changes at pH 4–6, but somewhat decreased inhibitory activity was revealed at pH 2, 8, and 10. On the other hand, ST ethanol extract was stable under γ-irradiation under all conditions (3–20 kGy). In summary, ST ethanol extract can be used in the food industry as a natural α-amylase inhibitor.

Abstract

This study was performed to investigate the inhibitory activity of Sargassum thunbergii (ST) against α-amylase and elucidate the availability of ST extract as a functional food agent. To test the inhibitory activity of ST against α-amylase, porcine pancreatic α-amylase and potato starch were used as substrates. It was revealed that ST crude ethanol extracts have high α-amylase inhibitory activity. Subsequently, ST crude ethanol extract was separated into five partition layers by solvent extraction: n-hexane, chloroform, ethyl acetate, butanol, and water. Chloroform and n-hexane fractions showed higher inhibitory activities than did acarbose (positive control). To confirm the changes in enzyme inhibitory activity by physical treatments, ST crude ethanol extract was subjected to heat, pH, and γ-irradiation treatments. In all heat treatments with the exception of one (121℃, 15 min), the inhibitory activity was increased compared with the untreated group. With regard to pH stability, ST extract showed no significant changes at pH 4–6, but somewhat decreased inhibitory activity was revealed at pH 2, 8, and 10. On the other hand, ST ethanol extract was stable under γ-irradiation under all conditions (3–20 kGy). In summary, ST ethanol extract can be used in the food industry as a natural α-amylase inhibitor.

참고문헌 (36)

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