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Comparative Studies on Microbial and Chemical Modifications of Trichothecene Mycotoxins

机译:天花粉真菌毒素的微生物和化学修饰的比较研究

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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 4β-acetoxy-3α,7α,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one (fusarenon) into 3α,4β,7α,15-tetrahydroxy-12,13-epoxy-trichothec-9-en-8-one (nivalenol), whereas 3α,4β,7α,15-tetraacetoxy-12,13-epoxytrichothec-9-en-8-one (tetraacetylnivalenol) was deacetylated to yield 3α-hydroxy-4β,7α,15-triacetoxy-12,13-epoxytrichothec-9-en-8-one (4,7,15-triacetylnivalenol), which was resistant to further deacetylation. T-2 toxin was transformed into HT-2 toxin, and 8α-(3-methylbutyryloxy)-3α,4β,-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. 3α,-7α,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 7α,15 - diacetoxy - 3α - 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.
机译:研究了镰孢镰刀菌和茄形镰刀菌的产生上孢菌素的菌株对几种上孢菌素霉菌毒素的微生物修饰作用。将这些结果与相应的化学修饰进行了比较。镰刀菌的菌丝体生长。没有将4β-乙酰氧基-3α,7α,15-三羟基-12,13-环氧三茂9-en-8-one(fusarenon)转化为3α,4β,7α,15-四羟基-12,13-环氧三茂- 9-en-8-one(nivalenol),而3α,4β,7α,15-tetraacetoxy-12,13-epoxytrichothec-9-en-8-one(tetraacetylnivalenol)脱乙酰化,得到3α-羟基-4β,7α, 15-三乙酰氧基-12,13-环氧trichothec-9-en-8-one(4,7,15-三乙酰基新戊烯醇),可抵抗进一步的脱乙酰作用。将T-2毒素转化为HT-2毒素,然后将8α-(3-甲基丁酰氧基)-3α,4β,-15-三乙酰氧基-12,13-环氧三苯甲基-9-en-8-one(T-2乙酸酯)通过T-2毒素转化为HT-2毒素。用氢氧化铵进行化学改性,通过4,7,15-三乙酰基新戊烯醇将四乙酰基新戊烯醇转化为富沙隆。 3α,-7α,15-三乙酰氧基-12,13-环氧trichothec-9-en-8-one(三乙酰基脱氧雪茄烯醇)除7α,15外还提供了缺少C-7或C-15乙酰基的脱乙酰基产物-二乙酰氧基-3α-羟基-12,13-环氧三苯甲基-9-烯基-8-一(7,15-二乙酰基脱氧雪茄烯醇)。这些结果证明了在微生物修饰单端孢菌烯中的区域选择性。基于结果和关于毛霉菌素转化的可用知识,推测了这些霉菌毒素的生物学修饰机理。

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