Antioxidant and Tyrosinase Inhibition Activity Promoting Effects of Perilla by the Light Emitting Plasma
2017
Yoo, J.H., Kangwon National University, Chuncheon, Republic of Korea | Choi, J.H., Kangwon National University, Chuncheon, Republic of Korea | Kang, B.J., Kangwon National University, Chuncheon, Republic of Korea | Jeon, M.R., Kangwon National University, Chuncheon, Republic of Korea | Lee, C.O., Kangwon National University, Chuncheon, Republic of Korea | Kim, C.H., Kangwon National University, Chuncheon, Republic of Korea | Seong, E.S., Suwon Women's University, Suwon, Republic of Korea | Heo, K., Kangwon National University, Chuncheon, Republic of Korea | Yu, C.Y., Kangwon National University, Chuncheon, Republic of Korea | Choi, S.K., Kangwon National University, Chuncheon, Republic of Korea
Background: The light emitting plasma (LEP) has recently attracted attention as a novel artificial light source for plant growth and functional component enhancement. We investigated the effects of LEP on whitening and antioxidant activities of the plant parts of perilla. Methods and Results: Previously germianted seeds of perilla were cultivated under different light conditions (fluoresce lamp, LED red, blue, white, green, and LEP) in a culture room for 2 months. Parts of perilla were harvested and extracted in 70% EtOH. The extracts were used to detect total phenolic contents, total flavonoid contents, 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2'-azino-bis3-ethylbenzothiazoline-6-sulfonic acid (ABTS), reducing power and tyrosinase inhibition activity as indicators of biological activity. Biological activity was highest in seedlings grown under LEP. The total phenolic content was highest in the stems and the total flavonoid content was highest in the roots of perilla exposed to LEP. The DPPH and ABTS radical activity in all the parts of perilla exposed to LEP were higher by approximately three-fold compared to that in the control (fluoresce lamp). The reducing power values of perilla significantly increased after treatment with LEP. In addition, all the extract of perilla plants exposed to LEP promoted the tyrosinase inhibitory activity. These results suggest that LEP can be an important artificial light source for enhancement of biological activity.
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