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不同的样品处理方法用于分析基于燕麦的培养基中的 T-2 和 HT-2 毒素。

Different sample treatment approaches for the analysis of T-2 and HT-2 toxins from oats-based media.

机构信息

Applied Mycology Group, Cranfield Health, Vincent Building, Cranfield University, College Road, Cranfield, Bedfordshire, MK43 0AL, UK.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Aug 1;878(23):2145-9. doi: 10.1016/j.jchromb.2010.05.043. Epub 2010 Jun 8.

Abstract

A LC-DAD method is proposed for the determination of the T-2 and HT-2 toxins in cultures of Fusarium langsethiae in oat-based and other in vitro media. Test media consisted of freshly prepared milled oats to which T-2 and HT-2 toxin stock solutions were added. Different mixtures of extraction solvent (acetonitrile:water and methanol:water), extraction times (30', 60' or 90') and drying methods were investigated. Results showed that extraction with methanol:water (80:20, v/v) for 90 min, drying with N(2) and subsequent analysis by LC-DAD was the fastest and most user friendly method for detecting HT-2 and T-2 toxins production by F. langsethiae strains grown on oat-based media at levels of 0.459 and 0.508 mg of toxin/kg of agar, respectively. The proposed method was used to investigate toxin production of 6 F. langsethiae strains from northern Europe and provided clear chromatograms with no interfering peaks in media with and without glycerol as water activity modifier.

摘要

提出了一种 LC-DAD 方法,用于测定燕麦基和其他体外培养基中黄萎镰孢菌培养物中的 T-2 和 HT-2 毒素。测试培养基由新鲜制备的磨碎燕麦组成,向其中添加 T-2 和 HT-2 毒素储备溶液。研究了不同的提取溶剂(乙腈:水和甲醇:水)、提取时间(30'、60'或 90')和干燥方法的混合物。结果表明,用甲醇:水(80:20,v/v)提取 90 分钟,用 N(2)干燥,然后用 LC-DAD 分析,是检测燕麦基培养基上生长的黄萎镰孢菌菌株产生 HT-2 和 T-2 毒素的最快、最用户友好的方法,水平分别为 0.459 和 0.508 mg 毒素/kg 琼脂。该方法用于研究来自北欧的 6 株黄萎镰孢菌菌株的毒素产生情况,在有和没有甘油作为水活度调节剂的培养基中均提供了清晰的色谱图,没有干扰峰。

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