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首页> 外文期刊>Applied and Environmental Microbiology >Microbial transformation of deoxynivalenol (vomitoxin).
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Microbial transformation of deoxynivalenol (vomitoxin).

机译:脱氧雪腐酚(呕吐毒素)的微生物转化。

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Microbial inocula from rumen fluid, soil, and contents of the large intestines of chickens (CLIC) and of swine (SLIC) were tested for their ability to transform deoxynivalenol (vomitoxin) in vitro. Microorganisms in (CLIC) completely transformed pure vomitoxin, and this activity was retained through six serial subcultures. No alteration of the toxin by incubation with SLIC was detected, whereas 35% of the vomitoxin was metabolized in the original culture of rumen fluid and 50% was metabolized by the soil sample, though metabolism was decreased in subsequent subcultures of either sample. A single metabolite was isolated and identified as deepoxy vomitoxin. The increase in concentration of deepoxy vomitoxin in the culture medium corresponded with the decrease in vomitoxin concentration. The vomitoxin transformation rate was not affected by either the ratio of CLIC to vomitoxin (5 to 0.2 g of CLIC per mg of vomitoxin) or the initial concentration of vomitoxin (14 to 1,400 ppm) in the medium. Biotransformation of vomitoxin was completely inhibited when the pH in the medium was lowered to 5.20. Sodium azide at a 0.1% (wt/vol) concentration in the medium blocked the transformation of vomitoxin, suggesting that the deepoxidation of vomitoxin is an energy-dependent process. About 50% of the vomitoxin in moldy corn in culture medium was transformed by microorganisms from CLIC. The vomitoxin transformation rate in moldy corn was not affected when the concentration of CLIC changed from 0.2 to 0.8 g/ml of medium. Vomitoxin in the moldy corn was not transformed when CLIC were added to corn without culture medium.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:测试了瘤胃液,土壤和鸡(CLIC)和猪(SLIC)大肠内容物中的微生物接种物在体外转化脱氧雪腐烯醇(呕吐毒素)的能力。 (CLIC)中的微生物完全转化了纯毒素,并且通过六次连续亚培养保留了这种活性。未检测到通过与SLIC孵育而产生的毒素变化,而35%的呕吐毒素在瘤胃液的原始培养物中被代谢,而50%被土壤样品代谢,尽管随后在两个样品的继代培养中代谢均降低。分离出一种代谢产物,鉴定为深氧呕吐毒素。培养基中深氧呕吐毒素浓度的增加与呕吐毒素浓度的减少相对应。呕吐毒素的转化率不受培养基中CLIC与呕吐毒素的比例(每mg呕吐毒素5至0.2 g CLIC)或呕吐毒素的初始浓度(14至1,400 ppm)的影响。当培养基中的pH降低至5.20时,呕吐毒素的生物转化被完全抑制。介质中浓度为0.1%(wt / vol)的叠氮化钠会阻止沃莫毒素的转化,这表明沃莫毒素的深度氧化是能量依赖的过程。培养基中发霉的玉米中约50%的呕吐毒素被CLIC的微生物转化。当CLIC的浓度从0.2更改为0.8 g / ml培养基时,发霉玉米中的呕吐毒素转化率不受影响。当在没有培养基的情况下将CLIC添加到玉米中时,发霉的玉米中的呕吐毒素未转化。(摘要截短为250字)

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