Comparative studies on microbial and chemical modifications of trichothecene mycotoxins
- PMID: 1147618
- PMCID: PMC187110
- DOI: 10.1128/am.30.1.38-43.1975
Comparative studies on microbial and chemical modifications of trichothecene mycotoxins
Abstract
The microbial modification of several trichothecene mycotoxins by trichothecene-producing strains of Fusarium nivale and F. solani was studied. These results were compared with the corresponding chemical modifications. The growing mycelia of Fusarium spp. did not convert 4beta-acetoxy-3alpha,7alpha, 15-trihydroxy-12, 13-epoxytrichothec-9-en-8-one (fusarenon) into 3alpha,4beta, 7alpha,15-tetrahydroxy-12,13-epoxy-trichothec-9-en-8-one (nivalenol), whereas 3alpha,4beta,7alpha,15-tetracetoxy-12,13-epoxytrichothec-9-en-8-one (tetraacetylnivalenol) was deacetylated to yield 3alpha-hydroxy-4beta,7alpha,15-triacetoxy-12,13-epoxytrichothec-9-en-8-one (4,7,15-triae-tylnivalenol), which was resistant to further deacetylation. T-2 toxin was transformed intoHT-2 toxin, and 8alpha-(3-methylbutyryloxy)-3alpha,4beta,-15-triacetoxy-12,13-epoxytrichothec-9-en-8-one (T-2 acetate) was transformed into HT-2 toxin via T-2 toxin. Chemical modification with ammonium hydroxide converted tetraacetylnivalenol into fusarenon via 4,7,15-triacetylnivalenol. 3alpha-7alpha,15-Triacetoxy-12,13-epoxytrichothec-9-en-8-one (triacetyldeoxynivalenol) gave deacetylation products lacking the C-7 or c-15 acetyl group in addition to 7alpha,15- diacetoxy-3alpha-hydroxy-12, 13-epoxytrichothec-9-en-8-one (7,15-diacetyldeoxynivalenol). These results demonstrate the regio-selectivity in microbial modification of trichothecenes. Based on the results and available knowledge concerning the transformation of trichothecenes, mechanisms for biological modifications of these mycotoxins are postulated.
Similar articles
-
Microbial acetyl conjugation of T-2 toxin and its derivatives.Appl Environ Microbiol. 1980 May;39(5):962-6. doi: 10.1128/aem.39.5.962-966.1980. Appl Environ Microbiol. 1980. PMID: 7396487 Free PMC article.
-
Biological modification of trichothecene mycotoxins: acetylation and deacetylation of deoxynivalenols by Fusarium spp.Appl Microbiol. 1975 Jan;29(1):54-8. doi: 10.1128/am.29.1.54-58.1975. Appl Microbiol. 1975. PMID: 234156 Free PMC article.
-
The isolation and identification of several trichothecene mycotoxins from Fusarium heterosporum.J Nat Prod. 1981 May-Jun;44(3):324-30. doi: 10.1021/np50015a015. J Nat Prod. 1981. PMID: 7264681
-
Metabolic pathways of trichothecenes.Drug Metab Rev. 2010 May;42(2):250-67. doi: 10.1080/03602530903125807. Drug Metab Rev. 2010. PMID: 19678805 Review.
-
Microbial Inhibition of Fusarium Pathogens and Biological Modification of Trichothecenes in Cereal Grains.Toxins (Basel). 2017 Dec 20;9(12):408. doi: 10.3390/toxins9120408. Toxins (Basel). 2017. PMID: 29261142 Free PMC article. Review.
Cited by
-
Adjustment of the conditions required for complete decontamination of T-2 toxin residues with alkaline sodium hypochlorite.Bull Environ Contam Toxicol. 1994 Jan;52(1):102-8. doi: 10.1007/BF00197364. Bull Environ Contam Toxicol. 1994. PMID: 8130404 No abstract available.
-
Accumulation kinetics of three scirpentriol-based toxins in oats inoculated in Vitro with isolates of Fusarium sporotrichioides and Fusarium poae.Toxins (Basel). 2011 May;3(5):442-52. doi: 10.3390/toxins3050442. Epub 2011 May 9. Toxins (Basel). 2011. PMID: 22069718 Free PMC article.
-
Microbial and chemical transformations of some 12,13-epoxytrichothec-9,10-enes.Appl Environ Microbiol. 1978 Jul;36(1):63-7. doi: 10.1128/aem.36.1.63-67.1978. Appl Environ Microbiol. 1978. PMID: 100053 Free PMC article.
-
Microbial acetyl conjugation of T-2 toxin and its derivatives.Appl Environ Microbiol. 1980 May;39(5):962-6. doi: 10.1128/aem.39.5.962-966.1980. Appl Environ Microbiol. 1980. PMID: 7396487 Free PMC article.
-
Metabolism of T-2 toxin in Curtobacterium sp. strain 114-2.Appl Environ Microbiol. 1983 Jul;46(1):120-7. doi: 10.1128/aem.46.1.120-127.1983. Appl Environ Microbiol. 1983. PMID: 6614901 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous