DOI QR코드

DOI QR Code

Optimal Fermentation Conditions of Hyaluronidase Inhibition Activity on Asparagus cochinchinensis Merrill by Weissella cibaria

  • Kim, Minji (Department of Food Science and Nutrition, College of Human Ecology, Pusan National University) ;
  • Kim, Won-Baek (Department of Food Science and Nutrition, College of Human Ecology, Pusan National University) ;
  • Koo, Kyoung Yoon (Department of Food Science and Nutrition, College of Human Ecology, Pusan National University) ;
  • Kim, Bo Ram (Department of Food Science and Nutrition, College of Human Ecology, Pusan National University) ;
  • Kim, Doohyun (Department of Food Science and Nutrition, College of Human Ecology, Pusan National University) ;
  • Lee, Seoyoun (Department of Food Science and Nutrition, College of Human Ecology, Pusan National University) ;
  • Son, Hong Joo (Department of Life Science and Environment Biochemistry, College of Natural Resource and Life Sciences, Pusan National University) ;
  • Hwang, Dae Youn (Department of Biomaterials Science, College of Natural Resource and Life Sciences, Pusan National University) ;
  • Kim, Dong Seob (Department of Food Science and Technology, College of Natural Resource and Life Sciences, Pusan National University) ;
  • Lee, Chung Yeoul (Gangrim Organics) ;
  • Lee, Heeseob (Department of Food Science and Nutrition, College of Human Ecology, Pusan National University)
  • Received : 2016.11.18
  • Accepted : 2017.02.09
  • Published : 2017.04.28

Abstract

This study was conducted to evaluate the hyaluronidase (HAase) inhibition activity of Asparagus cochinchinesis (AC) extracts following fermentation by Weissella cibaria through response surface methodology. To optimize the HAase inhibition activity, a central composite design was introduced based on four variables: the concentration of AC extract ($X_1$: 1-5%), amount of starter culture ($X_2$: 1-5%), pH ($X_3$: 4-8), and fermentation time ($X_4$: 0-10 days). The experimental data were fitted to quadratic regression equations, the accuracy of the equations was analyzed by ANOVA, and the regression coefficients for the surface quadratic model of HAase inhibition activity in the fermented AC extract were estimated by the F test and the corresponding p values. The HAase inhibition activity indicated that fermentation time was most significant among the parameters within the conditions tested. To validate the model, two different conditions among those generated by the Design Expert program were selected. Under both conditions, predicted and experimental data agreed well. Moreover, the content of protodioscin (a well-known compound related to anti-inflammation activity) was elevated after fermentation of the AC extract at the optimized fermentation condition.

Keywords

References

  1. Huang KC. 1993. The Pharmacology of Chinese Herbs. CRC Press, Boca Raton, FL, USA.
  2. Lee DY, Choo BK, Yoon TS, Cheon MS, Lee HW, Lee AY, Kim HK. 2009. Anti-inflammatory effects of Asparagus cochinchinensis extract in acute and chronic cutaneous inflammation. J. Ethnopharmacol. 121: 28-34. https://doi.org/10.1016/j.jep.2008.07.006
  3. Xiong D, Yu LX, Yan X, Guo C, Xiong Y. 2011. Effects of root and stem extracts of Asparagus cochinchinensis on biochemical indicators related to aging in the brain and liver of mice. Am. J. Chin. Med. 39: 719-726. https://doi.org/10.1142/S0192415X11009159
  4. Lee JH, Lim HJ, Lee CW, Son KH, Son JK, Lee SK, Kim HP. 2015. Methyl protodioscin from the roots of Asparagus cochinchinensis attenuates airway inflammation by inhibiting cytokine production. Evid. Based Complement. Alternat. Med. 2015: 640846.
  5. Samad NB, Debnath T, Hasnat A, Pervin M, Km DH, Jo JE, et al. 2014. Phenolic contents, antioxidant and anti-inflammatory activities of Asparagus cochinchinensis Merrill. J. Food Biochem. 38: 83-91. https://doi.org/10.1111/jfbc.12028
  6. Choo DY, Choo BK, Yoon TS, Cheon MS, Lee HW, Lee AY, Kim HK. 2009. Anti-inflammatory effects of Asparagus cochinchinensis extract in acute and chronic cutaneous inflammation. J. Ethnopharmacol. 121: 28-34. https://doi.org/10.1016/j.jep.2008.07.006
  7. Shen Y, Xu CL, Xuan WD, Li HL, Liu RH, Xu XK, Chen HS. 2011. A new furostanol saponin from Asparagus cohinchinensis. Arch. Pharm Res. 34: 1587-1591. https://doi.org/10.1007/s12272-011-1001-7
  8. Zhang HJ, Sydara K, Tan GT, Ma C, Southavong B, Soejarto DD, et al. 2004. Bioactive constituents from Asparagus cochinchinensis. J. Nat. Prod. 67: 194-200. https://doi.org/10.1021/np030370b
  9. Jung HG, Lee CW, Lee JH, Kim SJ, Kwon SJ, Kwon YS, et al. 2016. The new phytoformula containing Morus alba, Schizandra sinensis and Asparagus cochinchinensis inhibits lung inflammation in vitro and in vivo. Nat. Prod. Sci. 22: 70-75. https://doi.org/10.20307/nps.2016.22.1.70
  10. Lee HJ, Park JS, Yoon YP, Shin YJ, Lee SK, Kim YS, et al. 2015. Dioscin and methylprotodioscin isolated from the root of Asparagus cochinchinensis suppressed the gene expression and production of airway MUC5AC mucin induced by phorbol ester and growth factor. Phytomedicine 22: 568-572. https://doi.org/10.1016/j.phymed.2015.03.009
  11. Wang M, Tadmor Y, Wu QL, Chin CK, Garrison SA, Simon JE. 2003. Quantification of protodioscin and rutin in asparagus shoots by LC/MS and HPLC methods. J. Agric. Food Chem. 51: 6132-6136. https://doi.org/10.1021/jf0344587
  12. Jang HJ, Kang MS, Yi SH, Hong JY, Hong SP. 2016. Comparative study on the characteristics of Weissella cibaria CMU and probiotic strains for oral care. Molecules 21: 1752. https://doi.org/10.3390/molecules21121752
  13. Kang MS, Na HS, Oh JS. 2005. Coaggregation ability of Weissella cibaria isolates with Fusobacterium nucleatum and their adhesiveness to epithelial cells. FEMS Microbiol. Lett. 253: 323-329. https://doi.org/10.1016/j.femsle.2005.10.002
  14. Lee KW, Park JY, Chun JY, Han NS, Kim JH. 2010. Importance of Weissella species during kimchi fermentation and future works. Korean J. Microbiol. Biotechnol. 38: 341-348.
  15. Fusco V, Quero GM, Cho GS, Kabisch J, Meske D, Neve H, et al. 2015. The genus Weissella: taxonomy, ecology and biotechnological potential. Front. Microbiol. 6: 155.
  16. Cameron E, Pauling L, Leibovitz B. 1979. Ascorbic acid and cancer: a review. Cancer Res. 39: 663-681.
  17. Girish KS, Kemparaju K. 2007. The magic glue hyaluronan and its eraser hyaluronidase: a biological overview. Life Sci. 80: 1921-1943. https://doi.org/10.1016/j.lfs.2007.02.037
  18. Guo X, Liu F, Zhu X, Su Y, Ling P. 2009. Expression of a novel hyaluronidase from Streptococcus zooepidemicus in Escherichia coli and its application for the preparation of HA oligosaccharides. Carbohydr. Polym. 77: 254-260. https://doi.org/10.1016/j.carbpol.2008.12.036
  19. Kakegawa H, Matsumoto H, Satoh T. 1999. Inhibitory effects of some natural products on the activation of hyaluronidase and their antiallergic action. Chem. Pharm. Bull. 40: 1439-1442.
  20. Meyer K. 1947. The biological significance of hyaluronic acid hyaluronidase. Physiol. Rev. 27: 335-359. https://doi.org/10.1152/physrev.1947.27.3.335
  21. Vincent JC, Lenormand H. 2009. How hyaluronan-protein complexes modulate the hyaluronidase activity: the model. Biophys. Chem. 145: 126-134. https://doi.org/10.1016/j.bpc.2009.09.010
  22. Elson LA, Morgan WTJ. 1933. A colorimetric method for the determination of glucosamine and chondrosamine. Biochem. J. 27: 1824-1828. https://doi.org/10.1042/bj0271824
  23. Kaegawa H, Matsumoto H, Endo K, Satoh T, Nonaka GI, Noshioka I. 1985. Inhibitory effects of tannins on hyaluronidase activation and on the degranulation from rat mesentery mast cells. Chem. Pharm. Bull. 33: 5079-5082. https://doi.org/10.1248/cpb.33.5079
  24. Lee KK, Kim JH, Cho JJ, Choi JD. 1999. Inhibitory effects of 150 plant extracts on elastase activity, and their anti-inflammatory effects. Int. J. Cosmet. Sci. 21: 71-82. https://doi.org/10.1046/j.1467-2494.1999.181638.x
  25. Haaland PD, Lust JC, Liddle FR, Curry JW. 1990. Dexter: a guide to selecting the best design for an industrial screening experiment. Ann. Math. Artif. Intell. 2: 179-196.
  26. Liu JZ, Weng LP, Zhang QL. 2003. Optimization of glucose oxidase production by Aspergillus niger in benchtop bioreactor using response surface methodology. World J. Microbiol. Biotechnol. 19: 317-323. https://doi.org/10.1023/A:1023622925933
  27. Zhang ZF, Lv GY, Jiang X, Cheng JH, Fan LF. 2015. Extraction optimization and biological properties of a polysaccharide isolated from Gleoestereum incarnatum. Carbohydr. Polym. 117: 185-191. https://doi.org/10.1016/j.carbpol.2014.09.059
  28. Zhang YJ, Li Q, Zhang YX, Wang D, Xing JM. 2012. Optimization of succinic acid fermentation with Actinobacillus succinogenes by response surface methodology (RSM). J. Zhejiang Univ. Sci. B Biomed. Biotechnol. 13: 103-110.
  29. Yoon CH, Bok HS, Choi DK, Row KH. 2012. Optimization condition of astaxanthin extract from shrimp waste using response surface methodology. Korean Chem. Eng. Res. 50: 545-550. https://doi.org/10.9713/kcer.2012.50.3.545
  30. Ghosh D, Hallenbeck PC. 2010. Response surface methodology for process parameter optimization of hydrogen yield by the metabolically engineered strain Escherichia coli DJT135. Bioresour. Technol. 101: 1820-1825. https://doi.org/10.1016/j.biortech.2009.10.020
  31. Zhu T, Heo HJ, Row KH. 2010. Optimization of crude polysaccharides extraction from Hizikia fusiformis using response surface methodology. Carbohydr. Polym. 82: 106-110. https://doi.org/10.1016/j.carbpol.2010.04.029

Cited by

  1. 천문동 뿌리의 자연발효에 관여하는 미생물 및 발효 후 효능 변화 vol.18, pp.2, 2017, https://doi.org/10.15429/jkomor.2018.18.2.96
  2. Effects of silencing epididymal vascular endothelial growth factor (VEGF) expression on hyaluronidase (HYD) activity in arsenic poisoning rats through downregulating VEGF receptor 2 (VEGFR2) vol.12, pp.1, 2017, https://doi.org/10.1080/21655979.2021.1915726