首页> 外文期刊>Mycotoxin Research >Large-scale production of selected type A trichothecenes: the use of HT-2 toxin and T-2 triol as precursors for the synthesis of d 3-T-2 and d 3-HT-2 toxin
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Large-scale production of selected type A trichothecenes: the use of HT-2 toxin and T-2 triol as precursors for the synthesis of d 3-T-2 and d 3-HT-2 toxin

机译:大规模生产选定的A型毛发霉菌:以HT-2毒素和T-2三醇为前体合成d 3 -T-2和d 3 -HT-2毒素

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摘要

The type A trichothecenes T-2 and HT-2 toxins are toxic secondary metabolites produced by fungi of the Fusarium genus. Their occurrence in cereals, especially in oats, implies health risks for the consumer. Therefore, it is an important task to develop selective and sensitive methods for the analysis of T-2 and HT-2 toxins, and to undertake further studies on their stability and toxicity. Although most toxins are commercially available, their high prices are the limiting factor on the realization of these experiments. Thus, we developed a method for large-scale production of T-2 and HT-2 toxin as well as T-2 triol and T-2 tetraol. T-2 toxin was obtained in gram quantities by biosynthetic production with cultures of F. sporotrichioides. As HT-2 toxin was only formed as a by-product, and T-2 triol and T-2 tetraol were not generated, these compounds were produced by alkaline hydrolysis of T-2 toxin. Separation and isolation of crude toxins was achieved by fast centrifugal partition chromatography (FCPC), which is an efficient tool for the large-scale purification of natural products. Using this fast and yield effective technique, several hundred milligrams of HT-2 toxin, T-2 triol, and T-2 tetraol were obtained. Subsequent, HT-2 toxin and T-2 triol were used for the large-scale synthesis of isotope-labeled T-2 and HT-2 toxin, respectively. Using these standards, an isotope dilution-(ID)-HPLC-MS/MS method for the quantification of T-2 and HT-2 toxin in different matrices was developed.
机译:A型毛发霉菌T-2和HT-2毒素是镰刀菌属真菌产生的有毒次级代谢产物。它们在谷物中的存在,特别是在燕麦中,对消费者的健康构成隐患。因此,开发选择性和灵敏的方法来分析T-2和HT-2毒素,并对它们的稳定性和毒性进行进一步的研究是一项重要的任务。尽管大多数毒素是可商购的,但其高昂的价格是实现这些实验的限制因素。因此,我们开发了一种大规模生产T-2和HT-2毒素以及T-2三醇和T-2四醇的方法。 T-2毒素通过克孢孢菌的生物合成生产以克为单位获得。由于仅作为副产物形成HT-2毒素,并且不产生T-2三醇和T-2四醇,因此这些化合物是通过T-2毒素的碱水解而产生的。粗毒素的分离和分离是通过快速离心分配色谱(FCPC)实现的,它是大规模纯化天然产物的有效工具。使用这种快速且有效的高产技术,可获得数百毫克的HT-2毒素,T-2三醇和T-2四醇。随后,HT-2毒素和T-2三醇分别用于同位素标记的T-2和HT-2毒素的大规模合成。使用这些标准品,开发了一种同位素稀释-(ID)-HPLC-MS / MS方法,用于定量不同基质中的T-2和HT-2毒素。

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