用高效液相色谱法分析半镰刀菌中两种抗真菌α -吡啶酮和脱氧吡啶酮。

A Evidente, C Amalfitano, R Pengue, C Altomare
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引用次数: 13

摘要

建立了一种简便、灵敏、快速的高效液相色谱(HPLC)方法,用于同时定量分析稻瘟病菌(Fusarium semitectum)粗提物中3-取代-4-羟基-6-烷基-2-吡酮(fusapyrone, FP)和脱氧fusapyrone (DFP)。该方法在C-18反相色谱柱上进行优化,以分离的代谢物为标准物,以甲醇-氢氧(2)O混合物为线性洗脱步骤,使用固定在285 nm的紫外检测器,两种α -吡咯酮均具有最大的特征吸收。采用该方法定量测定了两株半乳梭菌有机粗提物的生物活性代谢物。FP和DFP的回收率测量了从一个差代谢物生产者半乳F.菌株的粗提取物。FP的回收率为84% ~ 99%,DFP的回收率为99% ~ 101%,表明该方法接近定量回收率。建立了一种高效的中压柱层析和薄层色谱相结合的分离纯化真菌培养提取物中FP和DFP的方法。
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High performance liquid chromatography for the analysis of fusapyrone and deoxyfusapyrone, two antifungal alpha-pyrones from Fusarium semitectum.

A simple, very sensitive and rapid HPLC method was developed for the simultaneous quantitative analysis of both fusapyrone (FP) and deoxyfusapyrone (DFP), the two antifungal 3-substituted-4-hydroxy-6-alkyl-2-pyrones isolated from rice culture of Fusarium semitectum, in crude extracts. Such method was optimized on C-18 reverse phase column, using the isolated metabolites as standards, with a sequence of linear elution steps with a MeOH-H(2)O mixture and using an ultraviolet detector fixed at 285 nm, where both alpha-pyrones showed a characteristic absorption maximum. This method was used to quantify the bioactive metabolites in crude organic extracts from two F. semitectum strains. The recovery of FP and DFP was measured in a crude extract from a poor metabolite producer F. semitectum strain. The recovery values ranged from 84% to 99% for FP and from 99% to 101% for DFP, indicating that the method was close to quantitative recovery. Furthermore, an efficient medium pressure column chromatography and TLC combined method was developed for the isolation and purification of FP and DFP from fungal culture extracts.

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Erratum: Alfonso D, Johnson HA, Colman-Saizarbitoria T, Presley CP, McCabe GP, McLaughlin JL (1996): SARs of annonaceous acetogenins in rat liver mitochondria. Nat Toxins 4:181-188. Advances in detection methods for fungal and algal toxins. HPLC/MS analysis of fusarium mycotoxins, fumonisins and deoxynivalenol. Neuronal binding of tetanus toxin compared to its ganglioside binding fragment (H(c)). A new type sandwich immunoassay for microcystin: production of monoclonal antibodies specific to the immune complex formed by microcystin and an anti-microcystin monoclonal antibody.
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