Identification and Quantitative Determination of Glucosinolates in Brassica napus cv. Hanakkori

  • Kim, Sun-Ju (Crop Functionality and Utilization Research Subteam, Upland Farming Research Station, National Agriculture Research Center for Hokkaido Region) ;
  • Fujii, Kouei (Department of Crop Breeding, Yamaguchi Prefecture Agricultural Research Institute) ;
  • Mohamed, Zaidul Islam Sarker (Department of Food Science, Faculty of Food Science and Technology, Universiti Putra Malaysia) ;
  • Kim, Hyun-Woong (Life and Environmental Sciences Design, Faculty of Engineering, Chiba Institute of Technology) ;
  • Yamauchi, Hiroaki (Crop Functionality and Utilization Research Subteam, Upland Farming Research Station, National Agriculture Research Center for Hokkaido Region) ;
  • Ishii, Gensho (Local Crop Breeding Research Team, National Agricultural Research Center for Hokkaido Region)
  • 발행 : 2008.10.31

초록

The objective of this study was to identify and quantify glucosinolates (GSLs) in Brassica napus cv. Hanakkori and its parents and to evaluate its potential bitter taste. 'Hanakkori' materials were cultivated with commercial chemical nutrients (20 kg/ha, N-P-K: 16-10-10) at the field. GSLs were isolated by means of extraction with 70%(v/v) boiling methanol (MeOH) followed by desulfation from those plants by reversed-phase high performance liquid chromatography (HPLC) and identified by electronic spray ionization-mass spectrometry (ESI-MS) analysis. In 'Hanakkori', 11 GSLs were identified as progoitrin, glucoraphanin, glucoalyssin, gluconapoleiferin, gluconapin, 1-methylpropyl, glucobrassicanapin, glucobrassicin, 4-methoxyglucobrassicin, gluconasturtiin, and neoglucobrassicin. The total GSL contents were 109 and 36.1 mmol/kg dry weights (d.w.) for the seeds and edible parts, respectively. The major GSLs (>5 mmol/kg d.w.) in the seeds were progoitrin (78.8), gluconapin (10.7), and glucobrassicanapin (7.81), whereas they in the edible parts were progoitrin (16.1) and glucobrassicanapin (8.58). In addition, the bitter taste in the edible parts was presumably related with the presence of progoitrin (>45% to the total GSL).

키워드

참고문헌

  1. Matsumoto O, Okafuji Y, Kaneko K, Katakawa S. Breeding of new vegetable 'Hanakkori' by ovule culture. Bull. Yamaguchi Agric. Expt. Sta. 48: 21-24 (1997)
  2. Tompson KF. Breeding winter oilseed rape, Brassica napus. Adv. Appl. Biol. 7: 1-104 (1983)
  3. Yamamoto Y, Kaneko K, Okafuji Y. Plant regeneration from in vitro cultured plotoplasts and anthers of 'Hanaccori' (Brassica rapa L. x B. oleracea L.) and chracters in the progency lines derived from regenerated plants (in Japanese with English summary). Bull. Yamaguchi Agric. Expt. Sta. 53: 35-40 (2002)
  4. Fahey JW, Zalcmann AT, Talalay P. The chemical diversity and distribution of glucosinolates and isothiocyanates among plants. Phytochemistry 56: 5-51 (2001) https://doi.org/10.1016/S0031-9422(00)00316-2
  5. Sones K, Heaney RK, Fenwick GR. An estimate of the mean daily intake of glucosinolates from cruciferous vegetables in the UK. J. Sci. Food Agr. 35: 712-720 (1984) https://doi.org/10.1002/jsfa.2740350619
  6. Katakawa S. The characterization and cultivation of a new Brassica vegetable 'Hanakkori'. pp. 70-75. Agriculture of This Month: The Chemical Daily, Tokyo, Japan (1997)
  7. Fenwick GR, Griffiths NM, Hanley AB. Bitterness in Brussels sprouts (Brassica oleracea L. var. gemmifera): The role of glucosinolates and their breakdown products. J. Sci. Food Agr. 34: 73-80 (1983) https://doi.org/10.1002/jsfa.2740340111
  8. Fenwick GR, Heaney RK, Mullin WJ. Glucosinolates and their breakdown products in food and food plants. Crit. Rev. Food Sci. 18: 123-201 (1983) https://doi.org/10.1080/10408398209527361
  9. Gland A, Robbelen G, Thies W. Variation of alkenyl glucosinolates in seeds of Brassica species. Z. Pflanzenzuchtg. 87: 96-110 (1981)
  10. Parkin I, Magrath R, Keith D, Sharpe A, Mithen R, Lydiate D. Genetics of aliphatic glucosinolates. II. Hydroxylation of alkenyl glucosinolates in Brassica napus. Heredity 72: 594-598 (1994) https://doi.org/10.1038/hdy.1994.82
  11. Reichelt M, Brown PD, Schneider B, Oldham NJ, Stauber E, Tokuhisa J, Kliebenstein DJ, Mitchell-Olds T, Gershenzon J. Benzoic acid glucosinolate esters and other glucosinolates from Arabidopsis thaliana. Phytochemistry 59: 663-671 (2002) https://doi.org/10.1016/S0031-9422(02)00014-6
  12. Chen S, Petersen BL, Olsen CE, Schulz A, Halkier BN. Longdistance phloem transport of glucosinolates in arabidopsis. Plant Physiol. 127: 194-201 (2001) https://doi.org/10.1104/pp.127.1.194
  13. Kim S-J, Kawaharada C, Jin S, Hashimoto M, Ishii G, Yamauchi H. Structural elucidation of 4-(cystein-S-yl)butyl glucosinolate from the leaves of Eruca sativa. Biosci. Biotech. Bioch. 71: 114-121 (2007) https://doi.org/10.1271/bbb.60400
  14. ISO 9167-1 2, 1-9. Rapeseed-determination of glucosinolates content. The International Organization for Standardization, Geneva, Switzwerland (1992)
  15. Kim S-J, Ishii G. Effect of storage temperature and duration on glucosinolate, total vitamin C, and nitrate contents in rocket salad (Eruca sativa Mill.). J. Sci. Food Agr. 87: 966-973 (2007) https://doi.org/10.1002/jsfa.2787
  16. Sang JP, Minchinton IR, Johnstone PK, Truscott RJW. Glucosinolate profiles in the seed, root, and leaf tissue of cabbage, mustard, rapeseed, radish, and swede. Can. J. Plant Sci. 64: 77-93 (1984) https://doi.org/10.4141/cjps84-011
  17. Kim S-J, Kawaguchi S, Watanabe Y. Glucosinolate in vegetative tissues and seeds of twelve cultivars of vegetable turnip rape (Brassica rapa L.). Soil Sci. Plant Nutr. 49: 337-346 (2003) https://doi.org/10.1080/00380768.2003.10410018
  18. Kim S-J, Ishii G. Glucosinolate profiles in the seeds, leaves, and roots of rocket salad (Eruca sativa Mill.) and antioxidative activities of intact plant powder and purified 4-methoxyglucobrassicin. Soil Sci. Plant Nutr. 52: 394-400 (2006) https://doi.org/10.1111/j.1747-0765.2006.00049.x
  19. European Committee. Commission Regulation (EC) 2316/1999 of 22 October 1999 laying down detailedrules for the application of Council Regulation (EC) No 1251/1999 establishing asupport system for producers of certain arable crops. OJ L 280, 30.10.1999, pp. 43-65. Available from: http://europa.eu.int/smartapi/cgi/sga_doc?smartapi!celexapi!prod!CELEXnumdoc&lg=EN&numdoc=31999R2316&model=guichett. Accessed May 7, 2007
  20. Tookey HL, Daxenbichler ME, VanEtten CH. Cabbage glucosinolates: Correspondence of patterns in seeds and leafy heads. J. Am. Soc. Hortic. Sci. 105: 714-717 (1980)
  21. Fenwick GR, Griffiths NM. The identification of the goitrongen, (-) 5-vinyloxazolidine-2-thione (goitrin), as a bitter principle of cooked Brussels sprouts (Brassica oleracea L. var. gemmifera). Z. Lebensm. Unters. For. 172: 90-92 (1981) https://doi.org/10.1007/BF01042410
  22. Van Doorn HE, van der Kruk GC, van Holst G-J, Raaijmakers-Ruijs NCME, Postma E, Groeneweg B, Jongen WHF. The glucosinolates sinigrin and progoitrin are important determinants for taste preference and bitterness of Brussels sprouts. J. Sci. Food Agr. 78: 30-38 (1998) https://doi.org/10.1002/(SICI)1097-0010(199809)78:1<30::AID-JSFA79>3.0.CO;2-N
  23. Bell JM. Nutrients and toxicants in rapeseed meal: A review. J. Anim. Sci. 58: 996-1010 (1984) https://doi.org/10.2527/jas1984.584996x
  24. Chisholm MD, Wetter LR. The biosynthesis of some isothiocyanates and oxazolidinethiones in rape (Brassica campestris L.). Plant Physiol. 42: 1726-1730 (1967) https://doi.org/10.1104/pp.42.12.1726
  25. Halkier BA, Du L. The biosynthesis of glucosinolates: Reviews. Trends Plant Sci. 2: 425-431 (1997) https://doi.org/10.1016/S1360-1385(97)90026-1
  26. Magrath R, Bano F, Morgner M, Parkin I, Sharpe A, Lister C, Dean C, Turner J, Lydiate D, Mithen R. Genetics of aliphatic glucosinolates (I). Side chain elongation in Brassica napus and Arabidopsis thaliana. Heredity 72: 290-299 (1994) https://doi.org/10.1038/hdy.1994.39
  27. Carlson DG, Daxenbichler ME, Tookey HL. Glucosinolates in turnip tops and roots: Cultivars grown for greens and/or roots. J. Am. Soc. Hortic. Sci. 112: 179-183 (1987)