4.5 Article

IN VITRO ANTIOXIDANT ACTIVITIES OF THE FERMENTED MARINE MICROALGA PAVLOVA LUTHERI (HAPTOPHYTA) WITH THE YEAST HANSENULA POLYMORPHA

Journal

JOURNAL OF PHYCOLOGY
Volume 48, Issue 2, Pages 475-482

Publisher

WILEY
DOI: 10.1111/j.1529-8817.2012.01117.x

Keywords

antioxidant activities; fermented; Hansenula polymorpha; marine microalgae; Pavlova lutheri

Funding

  1. New and Renewable Energy of the Korea Institute of Energy Technology Evaluation and Planning (KETEP)
  2. Korea government Ministry of Knowledge Economy [20103020090020]
  3. Ministry for Food, Agriculture, Forestry and Fisheries, Republic of Korea
  4. Korea Ocean Research and Development Institute [PE98472]
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [20103020090020] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Council of Science & Technology (NST), Republic of Korea [pe98472, PE98472] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Microalgae are major primary producers of organic matter in aquatic environments through their photosynthetic activities. Fermented microalga (Pavlova lutheri Butcher) preparation (FMP) is the product of yeast fermentation by Hansenula polymorpha. It was tested for the antioxidant activities including lipid peroxidation inhibitory activity, free-radical-scavenging activity, inhibition of reactive oxygen species (ROS) on mouse macrophages (RAW264.7 cell), and inhibited myeloperoxidase (MPO) activity in human myeloid cells (HL60). FMP exhibited the highest antioxidant activity on free-radical scavenging, inhibitory intracellular ROS, and inhibited MPO activity. MTT [3-(4,5-dimethyl-2-yl)-2,5-diphenyltetrazolium bromide] assay showed no cytotoxicity in mouse macrophages (RAW264.7 cell), human myeloid cells (HL60), and human fetal lung fibroblast cell line (MRC-5). Furthermore, the antioxidative mechanism of FMP was evaluated by protein expression levels of antioxidant enzyme (superoxide dismutase [SOD] and glutathione [GSH]) using Western blot. The results obtained in the present study indicated that FMP is a potential source of natural antioxidant.

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