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首页> 外文期刊>Journal of Pure & Applied Microbiology >Genetic variability of aflatoxigenic and non-aflatoxigenic A. flavus isolates by using aflatoxin biosynthesis genes.
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Genetic variability of aflatoxigenic and non-aflatoxigenic A. flavus isolates by using aflatoxin biosynthesis genes.

机译:通过使用黄曲霉毒素生物合成基因,黄曲霉毒素和非黄曲霉毒素黄曲霉菌株的遗传变异性。

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摘要

The five aflatoxin (AF) biosynthetic pathway genes included regulatory genes aflR and aflS and the structural genes aflD, aflM, aflP were evaluated in 81 Aspergillus flavus isolates isolated from wheat, corn, barley and sorghum. The amounts of aflatoxin B1 (B1) produced by 81 isolates varied from 0.3 to 1.2 ppb. The isolates were placed into seven groups based on their DNA banding pattern and B1 production. Only one group their isolates were able to produce B1 and six groups their isolates were unable to produce aflatoxin B1. All aflatoxinogenic isolates showed in group I, representing more than (17%), amplification DNA fragments that correspond to the complete set of genes. Non-aflatoxigenic isolates showed six groups, group I constituted by twenty eight isolates (34.6%) correspond to the complete set of genes. Group II constituted by sixteen isolates (19.8%) showed four DNA banding pattern clustered in three profiles: aflD, aflM, aflP and aflS was the most frequent profile (11.1%) followed by aflD, aflM, aflR and aflS (6.2%) and aflD, aflR and aflS (2.5%). Group III constituted by twelve isolates (13.5%) yielded three DNA banding pattern grouped in two characteristic profiles: aflD, aflP and aflS (7.4%) and aflD, aflM and aflR (6.1%). Group IV seven isolates (8.6%) showed two DNA banding pattern clustered in two profiles. Group V constituted by three strains (3.7%) gave one profile with one DNA fragment specific for aflD gene. Finally, a group VI constituted by two isolates (2.5%) gave no DNA bands were found. Our data show a non genetic variability in aflatoxigenic A. flavus isolates, whereas a high level of genetic variability in non-aflatoxigenic A. flavus isolates.
机译:在从小麦,玉米,大麦和高粱中分离出的81种黄曲霉分离物中评估了5个黄曲霉毒素(AF)生物合成途径基因,包括调节基因aflR和aflS,并评估了结构基因aflD,aflM,aflP。由81个分离株产生的黄曲霉毒素B1(B1)的量在0.3到1.2 ppb之间变化。根据分离物的DNA谱带模式和B1产生将其分为七个组。他们的分离株中只有一组能够产生B1,而其分离株中只有六组不能产生黄曲霉毒素B1。所有黄曲霉毒素分离株均显示在I组中,代表超过(17%)个扩增DNA片段,与完整的基因相对应。非黄曲霉毒素分离株显示六个组,第一组由二十八个分离株构成(34.6%),对应完整的基因组。由16个分离株(19.8%)构成的第二组显示四个DNA条带模式,聚集在三个分布图中:aflD,aflM,aflP和aflS是最常见的分布(11.1%),其次是aflD,aflM,aflR和aflS(6.2%)和aflD,aflR和aflS(2.5%)。由十二个分离株(13.5%)组成的第三组产生了三个DNA谱带,分为两个特征谱:aflD,aflP和aflS(7.4%)和aflD,aflM和aflR(6.1%)。第四组的七个分离株(8.6%)显示出两个DNA谱带模式聚集在两个谱中。由三株(3.7%)组成的V组给出了一个带有一个针对aflD基因的DNA片段的图谱。最后,由两个分离物(2.5%)组成的VI组没有发现DNA条带。我们的数据显示在黄曲霉毒素黄曲霉分离株中非遗传变异性,而在非黄曲霉毒素黄曲霉分离株中高遗传变异性。

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