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Purification and quantification of nivalenol

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Abstract

A mean of 2.7 g fusarenon-X (FUS-X)/L was produced in cultures ofFusarium sp Fn-2B on SSA, a synthetic medium containing sucrose and asparagine. When culturing Fn-2B on several other media, or using otherFusarium strains, much lower concentrations of FUS-X or nivalenol (NIV) were obtained. The SSA-incubations with Fn-2B in an optimal volume of 100 mL were stopped just before reaching maximal FUS-X concentration and the start of conversion to NIV. FUS-X was extracted from the 22 days old cultures and partially purified on a silica gel column. It was then hydrolysed to NIV, which was rechromatographed on silica and crystallized.

The purity and the chemical and physical properties of the NIV produced were investigated. Potential sources of error when quantifying NIV were also studied.

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References

  1. Scott PM (1989) The natural occurrence of trichothecenes. In: Trichothecene mycotoxicosis: pathophysiologic effects. Volume I. Beasley VR (Ed) CRC Press, Boca Raton, pp 1–26.

    Google Scholar 

  2. Hedman R, Pettersson H, Engström B, Elwinger K and Fossum O (1995) Effects of feeding nivalenol-contaminated diets to male broiler chickens. Poultry Sci. 74:620–625.

    CAS  Google Scholar 

  3. Hedman R, Pettersson H and Lindberg JE (1996) Absorption and metabolism of nivalenol in pigs. Arch. Anim. Nutr. In press.

  4. Tatsuno T, Saito M, Enomoto M and Tsunoda H (1968) Nivalenol, a toxic principle of Fusarium nivale. Chem. Pharm. Bull. 16: 2519–2520.

    CAS  PubMed  Google Scholar 

  5. Morozumi S, Wauke T, Hitokoto H and Kudoh Y (1988) Synthetic medium for production of trichothecene mycotoxins by Fusarium species (In Japanese). Japan. J. Food Microbiol. 5: 131–136.

    Google Scholar 

  6. Mulé G, Logrieco A and Bottalico A (1995)Fusarium sp. FN-2B: a controversial strain genetically close toFusarium poae. Mycotoxin Res. 11: 53–58.

    Google Scholar 

  7. Nirenberg HI (1981) A simplified method for identifyingFusarium spp. occurring on wheat. Can. J. Bot. 59: 1599–1609.

    Google Scholar 

  8. Lauren DR, di Menna ME, Greenhalgh R, Miller JD, Neish GA and Burgess LW (1988) Toxin-producing potential of someFusarium species from a New Zealand pasture. New Zealand J. Agric. Res. 31: 219–225.

    CAS  Google Scholar 

  9. Cappellini RA and Peterson JL (1965) Macroconidium formation in submerged cultures by a nonsporulating strain ofGibberella zeae. Mycologia 57: 962–966.

    Article  Google Scholar 

  10. Tanaka T, Hasegawa A, Yamamoto S, Matsuki Y, Ishii K and Ueno Y (1986) Producibility ofFusarium sp. Fn 2B for nivalenol and fusarenon-X on cereal substrates. Proc. Japan Assoc. Mycotoxicology No 24: 60–62.

    Google Scholar 

  11. Morooka N and Tatsuno T. (1970) Toxic substances (Fusarenon and nivalenol) produced byFusarium nivale. In: Proc. First U.S.-Japan Conference on Toxic Micro-organisms. Herzberg M (Ed) US, New York, pp 114–119.

  12. Lee YW and Mirocha CJ (1984) Production of nivalenol and fusarenoneÄX byFusariumtricinctum Fn-2B on a rice substrate. Appl. Environ. Microbiol. 48: 857–858.

    CAS  PubMed  Google Scholar 

  13. Ueno Y, Ueno I, Tatsuno T, Ohokubo K and Tsunoda H (1969) Fusarenon-X, a toxic principle ofFusarium nivale-culture filtrate. Experientia 25: 1062.

    Article  CAS  PubMed  Google Scholar 

  14. Ueno Y, Ueno I, Amakai K, Ishikawa Y, Tsunoda H, Okubo K, Saito M and Enomoto M (1971) Toxikological approaches to the metabolites ofFusaria. II. Isolation of fusarenon-x from culture filtrate ofFusarium nivale Fn 2B. Japan J. Exp. Med. 41: 507–519.

    CAS  Google Scholar 

  15. Grove JF (1970) Phytotoxic compounds produced by Fusarium equiseti. Part V. Transformation products of 4ß, 15-Diacetoxy-3, 7-dihydroxy-12, 13-epoxy-trichothec-9-en-8-one and the structures of nivalenol and fusarenone. J. Chem. Soc. C. pp. 375–378.

  16. Jarvis BB, Mazzocchi DB, Ammon HL, Mazzola EP, Flippen-Anderson JL, Gilardi RD and George CF (1990) Conformational effects in trichothecenes: structures of 15-hydroxy C4 and C8 ketones. J. Org. Chem. 55: 3660–3662.

    Article  CAS  Google Scholar 

  17. Fujimoto Y, Morita Y and Tatsuno T (1972) Recherches toxicologiques sur substances toxiques deFusarium nivale: Etude chimique des toxinns principales, nivalenol, fusarenon-X et nivalenol-4,15-di-O-acetate. Chem. Pharm. Bull. 20:1194–1203.

    CAS  PubMed  Google Scholar 

  18. Tatsuno T, Fujimoto Y and Morita Y (1969) Toxicological research on substances fromFusarium nivale III. The structure of nivalenol and its monoacetate. Tetrahedron Lett. 33: 2823–2826.

    Article  CAS  PubMed  Google Scholar 

  19. Bennett GA and Shotwell OL (1990) Criteria for determining purity ofFusarium mycotoxins. J. Assoc. Off. Anal. Chem. 73: 270–275.

    CAS  PubMed  Google Scholar 

  20. Kanhere SR and Scott PM (1990) Heptafluorobutyrylation of trichothecenes using a solid-phase catalyst. J. Chromatogr. 511: 384–389.

    Article  CAS  Google Scholar 

  21. Kientz CE and Verweij A (1986) Trimethylsilylation and trifluoroacetylation of a number of trichothecenes followed by gas chromatographic analysis on fused-silica capillary columns. J. Chromatogr. 355: 229–240.

    Article  CAS  Google Scholar 

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Hedman, R., Pettersson, H. Purification and quantification of nivalenol. Mycotox Res 12, 79–90 (1996). https://doi.org/10.1007/BF03192266

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  • DOI: https://doi.org/10.1007/BF03192266

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