DOI QR코드

DOI QR Code

Icaritin Preparation from Icariin by a Special Epimedium Flavonoid-Glycosidase from Aspergillus sp.y848 Strain

  • Wang, Zhenghao (College of Biotechnology, Dalian Polytechnic University) ;
  • Liu, Chunying (School of Life Science and Biotechnology, Liaoning Marine Microbial Engineering and Technology Center, Dalian University) ;
  • Yu, Hongshan (College of Biotechnology, Dalian Polytechnic University) ;
  • Wu, Bo (College of Biotechnology, Dalian Polytechnic University) ;
  • Huai, Baoyu (College of Biotechnology, Dalian Polytechnic University) ;
  • Zhuang, Ziyu (Dalian Center for Certification and Food and Drug) ;
  • Sun, Changkai (Research & Educational Center for the Control Engineering of Translational Precision Medicine, Dalian University of Technology) ;
  • Xu, Longquan (College of Biotechnology, Dalian Polytechnic University) ;
  • Jin, Fengxie (College of Biotechnology, Dalian Polytechnic University)
  • Received : 2021.12.20
  • Accepted : 2022.02.09
  • Published : 2022.04.28

Abstract

In this study, to obtain icaritin with high pharmacological activities from icariin, which has a content ratio of over 58% in the total flavonoids of Epimedium herb, a special Epimedium flavonoid-glycosidase was produced, purified and characterized from Aspergillus sp.y848 strain. The optimal enzyme production was gained in a medium containing 5% (w/v) wheat bran extract and 0.7% (w/v) Epimedium leaf powder as the enzyme inducer, and strain culture at 30℃ for 6-7 days. The molecular weight of the enzyme was approximately 73.2 kDa; the optimal pH and temperature were 5.0 and 40℃. The enzyme Km and Vmax values for icariin were 15.63 mM and 55.56 mM/h. Moreover, the enzyme hydrolyzed the 7-O-glucosides of icariin into icariside II, and finally hydrolyzed 3-Orhamnoside of icariside II into icaritin. The enzyme also hydrolyzed 7-O-glucosides of epimedin B to sagittatoside B, and then further hydrolyzed terminal 3-O-xyloside of sagittatoside B to icarisiede II, before finally hydrolyzing 3-O-rhamnoside of icarisiede II into icaritin. The enzyme only hydrolyzed 7-O-glucoside of epimedin A or epimedin C into sagittatoside A or sagittatoside C. It is possible to prepare icaritin from the high-content icariin in Epimedium herb using this enzyme. When 2.5% icariin was reacted at 40℃ for 18-20 h by the low-cost crude enzyme, 5.04 g icaritin with 98% purity was obtained from 10 g icariin. Also, the icaritin molar yield was 92.5%. Our results showed icaritin was successfully produced via cost-effective and relatively simple methods from icariin by crude enzyme. Our results should be very useful for the development of medicines from Epimedium herb.

Keywords

Acknowledgement

This work was supported by the National Key Research and Development Program of China, No. 2018AAA0100300 and 2012ZX09503001-003, and the National High-end Foreign Expert Project of China, No. GDT20152100019. The NMR experiment was performed and analyzed by senior engineer Yijie Wu from the Changchun Institute of Applied Chemistry Chinese Academy of Sciences, People's Republic of China.

References

  1. Jin FX. (Ed.). 2009. Biotransformation of natural products, chemical industry press, Beijin, 2009, pp. 258-272. [Tianran-chanwu Shengwu-zhuanhua in Chinese].
  2. Xu YQ, Jiang Y, Huang H, Li RQ, Li FQ. Liu Y, et al. 2020.Taxonomic study of Epimedium L.: Status, issues and prospect. Guihaia 40: 601-617.
  3. The pharmacopoeia of the People's Republic of China (I), 2020 ed., pp. 340-342. Chinese Medical Science and Technology Press, Beijing, 2020.
  4. Guo BL, Xiao PG. 2003. Comment on main species of herba Epimedii. China J. Chin. Materia Medica 28: 303-307. https://doi.org/10.3321/j.issn:1001-5302.2003.04.005
  5. Wu B, Liu CY, Guo MJ, Li H, Yu HS. Jin FX. 2017. Separation of epimedium flavonoids in several epimedium extracts. J. Dalian Polytechnic University 36: 89-91.
  6. Li C.C, Peng P, Zhao YQ, Zhu LH, Liu SA, Li J.S. 2020. Research progress on pharmacological activity of Yinyanghuo (Epimedium). Acta. Chin. Medicine35: 781-785.
  7. Zhang P, Shi J, Liu L, Yang YY. Zhang RX. 2016. Study on antioxidant activity of icariin and its derivatives. Chin. Food Addtives 2: 85-88.
  8. Angeloni C, Barbalace MC, Hrelia S. 2019. Icariin and its derivatives as potential protective phytochemcals agaist Alzheir's disease. Front. Pharm. Published online Mar. 19, 2019.
  9. Liu TH, Wang Y, Wang BX, Wu LJ. 2000. Studies on the metabolism of icariin by intestinal baeteria part 1?The transformation of icariin by intestinal flora, Chin. Trad. Herbal Drugs 31: 834-837. https://doi.org/10.3321/j.issn:0253-2670.2000.11.018
  10. Qiu F, Chen YJ, Kano Yao Y XS. 1999. Metabolism of orally administered icariin in rats. Acta Pharm. Sinica. 34: 222-226. https://doi.org/10.3321/j.issn:0513-4870.1999.03.016
  11. Chen R, Jia XB, Tan XB, Fan CY, Hu M. 2009. Absorption and metabolism of flavonoids in Herba Epimedii via rat intestinal perfusion model. China J. Chinese Materia Medica 34: 2928-2931.
  12. Liu S, Liu CM, Lai LJ, Li LD. 2017. Research progress in pharmacological effects of icaritin. J. Gannan Medical University. 37: 631-635. DOI: 10.3969/j.issn. 1001-5779.2017.04.044.
  13. Nan M, Li SK, Zhao YW, Na L, He Y, Huang JZ, et al. 2015. Preparation method and pharmacological activity of anhydroicaritin. Chin. J. Exp. Trad. Med. Formula 21: 227-231.
  14. Hu JM, Jiang HW. 2018. Research progress on anti-tumor mechanisms of icaritin and its related derivatives. Shanghai J. TCM. 52: 107-112.
  15. Yu SY, Liu JH, Zhang XY, Xu ZW. Xie GX, Wu HB. et al. 2020. Molecular mechanism of icariin effects on articular chondrocytes, subchondral bone and synovium in the treatment of osteoarthritis. Chin. J. Tissue Engineering Res. 24: 2243-2249.
  16. Zhou ML, Wang XW, Huang LL, Zheng XH, Fu HM, Chen WF. 2019. Effect of icaritin on lipopoly saccharide-induced inflammatory response in the hippocampus of mice with Alzheimer's disease. J. Precis. Med. 34: 237-239.
  17. Zhou JY, Li XL. 2010. Study on acid hydrolysis condition of icariin glycoside. Studies of Trace Elements and Health. 27: 49-51.
  18. Mu GM, Pu WC, Zhou M, Yan L, Yang HJ, Wang C. 2013. Synthesis of Icaritin. Chin. J. Org. Chem. 33: 1293-1303.
  19. Yang Y, Han B, Jin FX, Yu HS. 2009. Purification of Icariin-glycosidase and its enzymatic characteristics. Food Ferment. Ind. 35: 31-34.
  20. Gao X, Liu X, Chen Y, Wang Y, Jia XB. 2013. Analysis on biotransformation of Epimedium brevicornu flavonoids. Chin J. Chinese Materia Medica 38: 4079-4083.
  21. Fu YX, Liu CY, Guo MJ, Zhao Y, Jin FX, Yu HS. 2017. Bioconversion utilization of waste-residue from icarrin extraction. Sci. Tech. Food Indus. 8: 167-171,177.
  22. Li HL, Chen HJ, Lin YC, Ye DX, Zhou JL. 2020. Study on the preparation of icaritin by enzyme. Bio Chem. Eng. 6: 62-64, 68.
  23. Xie JC, Zhang SS, Tong XY, Wu T, Pei JJ, Zhao LG. 2020. Biochemical characterization of a novel hyperthermophilic α-L-rhamnosidase from Thermotoga petrophila and its application in production of icaritin from epimedin C with a thermostable β-glucosidase. Process Biochem. 93: 115-124. https://doi.org/10.1016/j.procbio.2020.03.019
  24. Zhang SS, Lou JH, Dong YR, Wang ZZ, Xiao W, Zhao LG. 2021. Biotransformation of the total flavonoid extract of epimedium into icaritin by two thermostable glycosidases from Dictyoglomus thermophilum DSM3960. Process Biochem. 105: 8-18. https://doi.org/10.1016/j.procbio.2021.03.002
  25. Yu HS, Liu QM, Zhang CZ, Lu MC, Fu YY, Im WT, et al. 2009. A new ginsenosidase from Aspergillus strain hydrolyzing 20-O-multiglycoside of PPD ginsenoside. Process Biochem. 44: 772-775. https://doi.org/10.1016/j.procbio.2009.02.005
  26. Liu CY, Zhou RX, Sun CK, Jin YH, Yu HS, Zhang TY, et al. 2015. Preparation of minor ginsenoside C-Mc, C-Y, F2 and C-K from American ginseng PPD ginsenoside using special ginsenosidase type-I from Aspegillus niger g.848. J. Ginseng Res. 39: 221-229. https://doi.org/10.1016/j.jgr.2014.12.003
  27. Yu HS, Han YT, Liu CY, Wu XB, Sun CK, Xu LQ, et al. 2020. Preparation of baicalein from baicalin using a baicalin-β-D-glucuronidase from Aspergillus niger b.48 strain, Process Biochem. 97: 168-175. https://doi.org/10.1016/j.procbio.2020.05.030
  28. Yue HL, Liu CY, Han YT, Zhuang ZY, Yu HS, Wang ZW, et al. 2021. Preparation of minor ginsenosides C-K and C-Mx from protopanaxadiol ginsenosides of American ginseng leaves by a enzyme from Aspergillus sp. agl-84 strain. Process Biochem. 103: 50-59. https://doi.org/10.1016/j.procbio.2021.02.006
  29. Li JW (Ed). 1997. Methods for Biochemistry [Shengwu-huaxue Shiyan-yuanli he Fangfa], pp. 189-196. University Press, Beijing, 1997, (in Chinese).
  30. Weber K, Pringle JR, Osborn M. 1971. Measurement of molecular weights by electrophoresis on SDS-acrylamide gel method. Enzymology 26: 3-27. https://doi.org/10.1016/S0076-6879(72)26003-7
  31. Lineweaver H, Burk D. 1934. The determination of enzyme dissociation constants. J. Am. Chem. Soc. 56: 658-666. https://doi.org/10.1021/ja01318a036
  32. The pharmacopoeia of the People's Republic of China (I), 2010 ed., pp36-37. Chinese Medical Science and Technology Press, Beijing, 2010, appendix.
  33. Jin X, Zhang ZH, Sun E, Li SL, Jia XB. 2912. Statistically designed enzymatic hydrolysis of an icariin/β-cyclodextrin inclusion complex optimized for production of icaritin. Acta Pharm. Sinica B 2: 83-89. https://doi.org/10.1016/j.apsb.2011.12.004