Faculty of Animal Science, Animal Breeding and Animal Hygiene Research Group of the Hungarian Academy of Sciences, University of Kaposvár, Guba S. 40, H-7400, Kaposvár, Hungary,
Mycotoxin Res. 2006 Dec;22(4):211-6. doi: 10.1007/BF02946744.
Studies were performed to develop an efficient method for fumonisin toxin production in sufficient quantities for animal toxicological experiments, on the basis of three earlier published fumonisin toxin production methods.Three absolutely necessary factors were taken into account and tested in a serial experiment. TheFusarium verticillioides strain MRC 826 was directly inoculated onto soaked, autoclaved, whole maize kernels (50 g/1.71 jar). The inoculation was performed by standard spore suspension (l×l0(6)/ml), a 5/2 surface/volume culture was prepared and incubated at 25 °C for 5 weeks. To maintain the optimal aw of approximately 1.00, the evaporated water was re-filled weekly. A final concentration of 4454±1060.9 ppm fumonisin B1 was reached, with good repeatability. In the laboratory practice, consistent production of constant amounts of FB1 can be obtained by applying the above settings.
研究旨在开发一种有效的方法,以足够的数量生产伏马菌素毒素,用于动物毒理学实验,该方法基于之前发表的三种伏马菌素毒素生产方法。在一系列实验中,考虑并测试了三个绝对必要的因素。将尖孢镰刀菌 MRC 826 菌株直接接种到浸泡、高压灭菌的整粒玉米(50 g/1.71 罐)上。接种采用标准孢子悬浮液(1×10(6)/ml)进行,制备 5/2 表面/体积培养物,并在 25°C 下孵育 5 周。为了保持约 1.00 的最佳 aw,每周重新填充蒸发的水。最终达到 4454±1060.9 ppm 的伏马菌素 B1 浓度,重复性好。在实验室实践中,通过应用上述设置,可以获得恒定数量的 FB1 的一致生产。