In this study, the antimicrobial, antioxidant activities and α-glucosidase inhibitory activities of Amphidinium carterae ethanol extract (AE) was evaluated for using as a functional food ingredient. Chlorella ethanol extract (CE) was used to the comparison as a control. Anticancer activities of the AE and CE were analyzed by HepG2 and HT-29 human cancer cell. The AE showed antimicrobial activities for all tested bacterial strains. Whereas, CE showed antimicrobial activities for several tested bacterial strains only. The CE showed higher total phenolics contents, DPPH and ABTS radical-scavenging activities (47.36 mg/g, 22.42% and 28.58%, respectively) than those of AE (8.88 mg/g, 20.16% and 17.69%, respectively). AE showed anti-diabetic effect on α-glucosidase inhibitory activity with dose-dependantly manner. The cell viability of AE (125 μg/mL) on HepG2 and HT-29 human cancer cells were 38.12% and 11.27%, respectively. It was demonstrated that ethanol was efficient solvent for extracting functional components from A. carterae. These results indicated that AE can be described as a good candidate for using as a functional food ingredient.

The effect of UV on the mortality rate of toxic dinoflagellate Amphidinium carterae causing a red tide in the coastal area of south Korea was investigated in the batch and continuous-scale reactor equipped with ultraviolet irradiation-apparatus. Degussa P25 titanium oxide, a photocatalyst proved to be effective for the mortality of Amphidinium carterae supplied with photocatalyst and UV radiation were greater than 95% in 2 minutes of UV radiation and the rate were higher than that by UV-radiation without titanium dioxide in the batch and continuous-flow scale reactor. The mortality time of Amphidinium carterae increased with the cell density under UV-illumination in the batch scale reactor. The mortality rate in the density of 5.0×104 cells/mL at the same experimental condition was more than 90% in 4 minutes in the continuous flow scale reactor. The percentage of 99.9±0.1% of Amphidinium carterae in the density of 5.0×104 cells/mL was died in 20 minutes when the phytoplankton was illuminated with UV-radiation without photocatalyst.