DOI QR코드

DOI QR Code

Purification and Characterization of an Anticoagulant from Corn Silk

옥발에서 항응고물질의 정제와 특성

  • Choi, Sang-Kyu (Dept. of Biological Sciences and Innunonodulation Research Center, University of Ulsan) ;
  • Choi, Hye-Seon (Dept. of Biological Sciences and Innunonodulation Research Center, University of Ulsan)
  • Published : 2004.10.01

Abstract

An anticoagulant was purified from corn silk which has been used in Oriental Medicine. The anticoagulant from corn silk has a molecular mass of 135 kDa, and purified by 24 folds with a recovery of 11%. It was not sensitive to heat and protease treatment. However, periodate oxidation of the anticoagulant resulted in loss of activity significantly, implying that a carbohydrate was responsible for an anticoagulant activity. Galactose, glucose, mannose, fucose, glucosamine, and galactosamine were detected after acid hydrolysis by thin layer chromatography (TLC) and Bio-LC. It was confirmed that anticoagulant had OH and NH bonds by IR, supporting that the anticoagulant is composed of neutrosugar and aminosugar. Its anticoagulating activity was measured by delay in thrombin time (TT) and prothrombin time (PT) without affecting clotting by snake venom and delay in activated partial thromboplastin time (APTT). TT was more sensitive than PT, and was delayed two and three times at the concentration of 60 and 88 nM, respectively. The anticoagulating activity was reduced in the thrombin-induced clotting assay using purified fibrinogen according to the increase of fibrinogen concentration with the apparent Ki value of 23 nM.

한약재의 재료로 사용되는 옥발에서 항응고물질(anticoagulant)을 추출하여 정제하였다. 정제된 항응고물질의 분자량은 135 kDa으로 측정되었고 옥발로부터 정제된 항응고물질의 회수율은 11%이고, 24배 농축되었다. 옥발의 항응고물질은 열에 안정하고 비특이적 단백질 가수분해 효소 처리 후에도 활성을 유지하였으나, periodate 산화 처리시 현저하게 활성이 소실되어 항응고물질의 성분은 당류인 것으로 추정된다. 옥발의 항응고물질을 thin layer chromatography(TLC)와 Bio-LC로 구성당을 분석한 결과 galactose, glucose, mannose, glucosamine, galactosamine, fucose로 구성되어있고, IR을 통하여 확인된 OH, N-H bond가 확인되어 항응고물질이 중성당과 아미노당으로 구성된 것을 뒷받침해주고 있다. 옥발의 항응고물질은 thrombin time(TT)에 가장 민감하고, TT에서 항응고 활성을 2배, 3배 지연시키는 농도는 60 nM와 88 nM이었다. Prothrombin time(PT)에도 민감하였지만, snake venom activity와 activated partial thromboplastin time(APTT)의 clotting activity에는 상대적으로 별 영향을 끼치지 않았다. 옥발의 항응고물질을 정제된 fibrinogen을 이용하여 thrombin과의 반응 시 fibrinogen의 농도가 증가함에 따라 응고 저해 정도가 감소하여 thrombin에 대해fibrinogen과 결합자리를 경쟁하고, 이 때 Ki 값은 23 nM이다.

Keywords

References

  1. Sherry S. 1987. Recombinant tissue plasminogen activator (rt-PA): is it the thrombolytic agent of choice for an evolving acute myocardial infarction? Am J Cardiol 59: 984-989 https://doi.org/10.1016/0002-9149(87)91139-8
  2. Duval-Jobe C, Parmely MJ. 1994. Regulation of plasminogen activation by human U937 promyelocytic cells. J Biol Chem 269: 21353-21357
  3. Stringer HA, Pannekoek H. 1995. The significance of fibrin binding by plasminogen activaotor inhibitor 1 for the mechanism of tissue-type plasminogen activator-mediated fibrinolysis. J Biol Chem 270: 11205-11208 https://doi.org/10.1074/jbc.270.19.11205
  4. Jakubowski JA, Maraganore JM. 1990. Inhibition of coagulation and thrombin-induced platelet activities by a synthetic dodecapeptide modeled on the carboxy-terminus of hirudin. Blood 75: 399-406
  5. Tsiang M, Lentz SR, Dittman WA, Scarpati EM, Sadler JE. 1990. Equilibrium binding of thrombin to recombinant human thrombomodulin: Effects of hirudin, fibrinogen, factor Va, and peptide analogues. Biochemistry 29: 10602- 10612 https://doi.org/10.1021/bi00499a005
  6. Olson ST, Bjo I, Sheffer R, Craig PA, Shore JD, Choay J. 1992. Role of the antithrombin-binding pentasaccharides in heparin accerleration of antithrombin-proteinase reactions. J Biol Chem 267: 12528-12538
  7. Strube KH, Kroger B, Bialojan S, Otte M, Dodt J. 1993. Isolation, sequence anlysis, and cloning of haemadin. J Biol Chem 268: 8590-8595
  8. Friedrich T, Kroger B, Bialojan S, Lemaire HG, Hoffken HW, Reuschenbach P, Otte M, Dodt J. 1993. A kazal-type inhibitor with thrombin specificity from Rhodnius prolixus. J Biol Chem 268: 16216-16222
  9. Holsat J, Lindblad B, Bergqvist D. 1994. Antithrombotic effect of recombinant truncated tissue factor pathway inhibitor (TFPI1-161) in experimental venous thrombosis-a comparison with low molecular weight heparin. Thromb Haemost 71: 214-219
  10. Rezaie AR, Cooper ST, Church FC, Esmon CT. 1995. Protein C inhibitor is a potent inhibitor of the thrombin-thrombomodulin complex. J Biol Chem 270: 25336-25339 https://doi.org/10.1074/jbc.270.43.25336
  11. Noeske-Jungblut C, Haendler B, Donner P, Alagon A, Possani L, Schleuning WD. 1995. Triabin, a highly potent exosite inhibitor of thrombin. J Biol Chem 270: 28629-28634 https://doi.org/10.1074/jbc.270.48.28629
  12. Dahlback B, Stenflo J. 1993. A natural anticoagulant pathway: biochemistry and physiology of protein C, S, C4b- binding protein and thrombomodulin. In Haemostasis and thrombosis. 3rd ed. Bloom AL, Forbes CD, Thomas DP, eds. Churchill livingstone, London. p 671-698
  13. Herbert JM, Herault JP, Bernat A, van Amsterdam RGM, Lormeau JC, Petitou M, van Boeckel C, Hoffmann P, Meuleman DG. 1998. Biochemical and pharmacological properties of Sanorg 34006, a potent and long-acting synthetic pentasaccharide. Blood 91: 4197-4205
  14. Kim W, Choi K, Kim Y, Park H, Choi J, Lee Y, Oh H, Kwon I, Lee S. 1996. Purification and characterization of a fibrinolytic enzyme produced from Bacillus sp. strain CK 11-4 screened from chungkook-jang. Appl Environ Microbiol 62: 2482-2488
  15. Sumi H, Hamada H, Tsushima H, Mihara H, Muraki H. 1987. A novel fibrinolytic enzyme in the vegetable cheese Natto: a typical and popular soybean food in the Japanese diet. Experimentia 43: 1110-1111 https://doi.org/10.1007/BF01956052
  16. Sumi H, Hamada H, Nakanishi K, Hiratani H. 1990. Enhancement of the fibrinolytic activity in plasma by oral administration of NK. Acta Haematol 84: 139-143 https://doi.org/10.1159/000205051
  17. Naski MC, Fenton II JW, Maraganore JM, Olson ST, Shafer JA. 1990. The COOH-terminal domain of hirudin. J Biol Chem 265: 13484-13489
  18. Choi HS, Shin HH. 1998. Purification and characterization of a fibrinolytic protease in Pleurotus ostreatus. Mycologia 90: 674-679 https://doi.org/10.2307/3761226
  19. Shin HH, Choi HS. 1999. Purification and partial characterization of a metalloprotease in Flammulina velutipes. J Microbiol 36: 20-25
  20. Choi HS, Sa YS. 2000. Fibrinolytic and antithrombotic protease from Ganoderma lucidum Mycologia 92: 545-552 https://doi.org/10.2307/3761514
  21. Choi HS, Sa YS. 2001. Fibrinolytic and antithrombotic protease from Spirodela polyrhiza. Biosci Biotechnol Biochem 65: 781-786 https://doi.org/10.1271/bbb.65.781
  22. 전국한의과대학교수공편. 1991. 본초학. 영림사, 서울. p 217-419
  23. 고경식, 김윤식. 1989. 한국원색식물도감. 도서출판 아카데미서적, 서울. p 264
  24. 과학백과사전출판사 엮음. 1991. 약초의 성분과 이용. 일월서각, 서울. p 187-189, 519, 651-652
  25. Sa YS, Kim KA, Choi HS. 2003. Purification and characterization of anti-coagulant activity from persimmon stem. J Korean Soc Foods Sci Nutr 32: 1323-1327 https://doi.org/10.3746/jkfn.2003.32.8.1323
  26. Yun SI, Cho HR, Choi HS. 2002. Anticoagulant from Taraxacum platycarpum. Biosci Biotechnol Biochem 66: 1859-1864 https://doi.org/10.1271/bbb.66.1859
  27. Cho HR, Choi HS. 2003. Effects of anticoagulant from Spirodela polyrhiza in rats. Biosci Biotechnol Biochem 67: 881-883 https://doi.org/10.1271/bbb.67.881

Cited by

  1. Acute toxicity and anti-fatigue activity of polysaccharide-rich extract from corn silk vol.90, 2017, https://doi.org/10.1016/j.biopha.2017.04.045
  2. Corn Silk Induced Cyclooxygenase-2 in Murine Macrophages vol.69, pp.10, 2005, https://doi.org/10.1271/bbb.69.1848
  3. Effects of Onion Peel Extracts on Blood Circulation in Male Smokers vol.39, pp.12, 2010, https://doi.org/10.3746/jkfn.2010.39.12.1790
  4. Anti-inflammatory Effect of Ethanol Extract from Sargassum fulvellum on Lipopolysaccharide Induced Inflammatory Responses in RAW 264.7 Cells and Mice Ears vol.43, pp.8, 2014, https://doi.org/10.3746/jkfn.2014.43.8.1158
  5. Antioxidant Activity and Safety Evaluation of Juice Containing Protaetia brevitarsis vol.41, pp.1, 2012, https://doi.org/10.3746/jkfn.2012.41.1.041
  6. Ameliorative effects of corn silk extract on acetaminophen-induced renal toxicity in rats vol.28, pp.2, 2004, https://doi.org/10.1007/s11356-020-10588-4