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首页> 外文期刊>Biotropia: the Southeast Asian journal of tropical biology >Identification of Aspergillus flavus and Detection of Its Aflatoxin Genes Isolated from Peanut and Peanut Processed Products
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Identification of Aspergillus flavus and Detection of Its Aflatoxin Genes Isolated from Peanut and Peanut Processed Products

机译:从花生和花生加工产品中分离出黄曲霉的鉴定及其黄曲霉毒素基因的检测

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Aspergillus flavus is one of the main fungi that are able to produce aflatoxin. The presence of the fungi and its aflatoxin are become serious problem on food safety . This research was aimed to isolate and identify A. flavus from peanut and its processed products collected from some traditional markets in Bogor, Depok and Jakarta, and detection of their aflatoxin genes. Fungal isolation was using AFPA media. Fungal identification was carried out by combining morphological and molecular analysis used species specific primers FVAVIQ1/FLAQ2 and AFLA-F/AFLA-R, while detection of ? aflatoxin genes employed four specific primers of apa-2 ( aflR ), nor-1 ( aflD ), ver-1 ( aflM ) and omt-1 ( aflP ). From 36 samples, the A. flavus group was only found in peanut kernels samples with viable count of specific colonies in the range of 0.01 -5.52 x 10 -4 cfu/g. The total 18 isolates were identified as A. flavus based on species specific primers FVAVIQ1/FLAQ2 and AFLA-F/AFLA-R by producing amplicons about 100 and 413 bp respectively. Based on aflatoxin gene analysis showed that all 18 isolates successfully amplified by both apa-2 and nor-1 , 83.3 % by omt-1 and 72.2 % by ver-1 genes which taking part in aflatoxin production. The amplicons size of apa-2, nor-1, ver-1 and omt-1 ?? primer pairs were about 1032, 400, 895 and 1024 bp respectively. Normal 0 false false false IN X-NONE X-NONE /* Style Definitions */ table.MsoNormalTable{mso-style-name:"Table Normal";mso-tstyle-rowband-size:0;mso-tstyle-colband-size:0;mso-style-noshow:yes;mso-style-priority:99;mso-style-qformat:yes;mso-style-parent:"";mso-padding-alt:0cm 5.4pt 0cm 5.4pt;mso-para-margin:0cm;mso-para-margin-bottom:.0001pt;line-height:150%;mso-pagination:widow-orphan;font-size:11.0pt;font-family:"Calibri","sans-serif";mso-ascii-font-family:Calibri;mso-ascii-theme-font:minor-latin;mso-fareast-font-family:"Times New Roman";mso-fareast-theme-font:minor-fareast;mso-hansi-font-family:Calibri;mso-hansi-theme-font:minor-latin;mso-bidi-font-family:"Times New Roman";mso-bidi-theme-font:minor-bidi;}
机译:黄曲霉是能够产生黄曲霉毒素的主要真菌之一。真菌及其黄曲霉毒素的存在已成为食品安全的严重问题。这项研究旨在从花生及其从茂物,德波和雅加达的一些传统市场中收集的加工产品中分离和鉴定黄曲霉,并检测其黄曲霉毒素基因。使用AFPA培养基进行真菌分离。通过形态学和分子分析相结合,使用物种特异性引物FVAVIQ1 / FLAQ2和AFLA-F / AFLA-R进行真菌鉴定,同时检测λ。黄曲霉毒素基因使用了apa-2(aflR),nor-1(aflD),ver-1(aflM)和omt-1(aflP)的四种特异性引物。从36个样品中,仅在花生果粒样品中发现了黄曲霉菌群,其特定菌落的存活数在0.01 -5.52 x 10 -4 cfu / g的范围内。根据物种特异性引物FVAVIQ1 / FLAQ2和AFLA-F / AFLA-R,通过分别产生约100和413 bp的扩增子,将总共18种分离物鉴定为黄曲霉。基于黄曲霉毒素基因的分析表明,所有18个分离株均成功地被apa-2和nor-1扩增,omt-1的83.3%和ver-1基因的72.2%参与了黄曲霉毒素的生产。 apa-2,nor-1,ver-1和omt-1的扩增子大小?引物对分别为约1032、400、895和1024bp。正常0否否否IN X-NONE X-NONE / *样式定义* / table.MsoNormalTable {mso-style-name:“ Table Normal”; mso-tstyle-rowband-size:0; mso-tstyle-colband-size :0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:“”; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso -para-margin:0cm; mso-para-margin-bottom:.0001pt;行高:150%; mso-pagination:寡妇孤儿;字体大小:11.0pt; font-family:“ Calibri”,“ sans -serif“; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:” Times New Roman“; mso-fareast-theme-font:minor-远东; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:“ Times New Roman”; mso-bidi-theme-font:minor-bidi; }

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