Enzymatic Preparation of Kaempferol from Green Tea Seed and Its Antioxidant Activity

Jun Seong Park,* Ho Sik Rho, Duck Hee Kim, and Ih Seop Chang
Skin Research Institute, AMOREPACIFIC R&D Center, 314-1, Bora-ri, Giheung-eup, Yongin-si, Gyeonggi-do, 449-729, Korea
J. Agric. Food Chem., 2006, 54 (8), pp 2951–2956
DOI: 10.1021/jf052900a
Publication Date (Web): March 24, 2006
Copyright © 2006 American Chemical Society
*

 To whom correspondence should be addressed. Tel:  82 31 280 5878. Fax:  82 31 281 8397. E-mail:  superbody@amorepacific.com.

Abstract

Among the flavonols in green tea, kaempferol has many biological activities but kaempferol of plant origin is too expensive to be used in commercial products. Recently, we confirmed that green tea seed (GTS) contained a reasonable amount of kaempferol glycoside. After conducting structure analysis, two kaempferol glycosides were identified, kaempferol-3-O-[2-O-β-d-galactopyranosyl-6-O-α-l-rhamnopyranosyl]-β-d-glucopyranoside (compound 1) and kaempferol-3-O-[2-O-β-d-xylopyranosyl-6-O-α-l-rhamnopyranosyl]-β-d-glucopyranoside (compound 2), respectively. Also, a commercially useful method for kaempferol preparation was suggested by enzymatic hydrolysis using these two flavonoids. After several enzyme reactions were performed for the complete bioconversion of compounds 1 and 2 to kaempferol, we found that the optimum enzyme combination was reaction with β-galactosidase and hesperidinase. Finally, we produced pure kaempferol with over 95% purity. We also compared the antioxidant effect of these two GTS flavonoids and its aglycone, kaempferol. Kaempferol is a more efficient scavenger of 1,1-diphenyl-2-picrylhydrazyl radicals and a better inhibitor of xanthine/xanthine oxidase than the two glycosides.

Keywords: Tea seed; enzymatic hydrolysis; antioxidant; kaempferol; kaempferol glycoside

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History

  • Published In Issue April 19, 2006
  • Received for review November 22, 2005. Revised manuscript received February 28, 2006. Accepted February 28, 2006.

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