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2. Beijing Engineering Research Center of Food Environment and Public Health, Beijing 100081, China;
3. Liaoning Entry-Exit Inspection and Quarantine Bureau, Dalian 116001, China, fund=null, authors=JIANG Dan1,2,3 , JIN Weilin1,2 , SU Deshan1,2 , HUANG Yaojiang1,2 , authorsList=JIANG Dan, JIN Weilin, SU Deshan, HUANG Yaojiang), CN=ArticleExt(id=1242131980645643207, articleId=1242131977898374078, tenantId=1146029695717560320, journalId=1146031591421210625, language=CN, title=曲霉属产毒真菌DNA的制备及其毒素相关基因aflR 的PCR 检测, columnId=1146540929516700224, journalTitle=科技导报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=研究了用改良的CTAB 法提取曲霉属产毒真菌DNA 的方法,并与试剂盒提取法进行比较。经过改良的CTAB 法能够成功提取出曲霉属产毒真菌的DNA,且浓度和纯度均可达到PCR 扩增的标准。根据合成黄曲霉毒素的aflR 基因设计两对引物,运用PCR 方法进行扩增鉴定,结果表明黄曲霉、寄生曲霉和溜曲霉基因中可检出aflR 基因,烟曲霉和杂色曲霉中并未检出,达到对黄曲霉毒素产生菌进行鉴定的目的。这种方法可为产毒真菌的快速检测提供参考。, correspAuthors=null, authorNote=蒋丹,副研究员,研究方向为食品安全与健康,电子信箱:jiangdan66@163.com;靳卫林(共同第一作者),硕士研究生,研究方向为分子生态学,电子信箱:jwldsg@126.com, correspAuthorsNote=黄耀江,教授,研究方向为生物化学与分子生物学、食品安全与公众健康,电子信箱:yaojiangh@hotmail.com, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=t3lsxln1JSJ1f9Qo9IXcXw==, pdfFileSize=1229527, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, authorCompany=1. 中央民族大学, 北京 100081;
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科技导报
| 研究论文 2014, 32(14): 31-34
曲霉属产毒真菌DNA的制备及其毒素相关基因
aflR 的PCR 检测
全屏
蒋丹, 靳卫林, 苏德山, 黄耀江
作者信息
通讯作者:
黄耀江,教授,研究方向为生物化学与分子生物学、食品安全与公众健康,电子信箱:yaojiangh@hotmail.com
DNA Preparation of Toxigenic Aspergillus and PCR Detection of aflR Toxin Gene
JIANG Dan, JIN Weilin, SU Deshan, HUANG Yaojiang
Affiliations
出版时间: 2014-05-18
doi: 10.3981/j.issn.1000-7857.2014.14.004
文章导航
研究了用改良的CTAB 法提取曲霉属产毒真菌DNA 的方法,并与试剂盒提取法进行比较。经过改良的CTAB 法能够成功提取出曲霉属产毒真菌的DNA,且浓度和纯度均可达到PCR 扩增的标准。根据合成黄曲霉毒素的aflR 基因设计两对引物,运用PCR 方法进行扩增鉴定,结果表明黄曲霉、寄生曲霉和溜曲霉基因中可检出aflR 基因,烟曲霉和杂色曲霉中并未检出,达到对黄曲霉毒素产生菌进行鉴定的目的。这种方法可为产毒真菌的快速检测提供参考。
产毒真菌
/
DNA 提取
/
黄曲霉毒素
/
RCR 检测
This paper discusses the modified CTAB method for DNA extraction of toxigenic Aspergillus and compares it with the kit extraction method. The modified CTAB method successfully extracted DNA of toxigenic Aspergillus. The concentration and purity reached the standard of PCR amplification. Two pairs of primers were designed based on the aflR gene for aflatoxin biosynthesis regulation, and the toxigenic Aspergillus aflR gene was identified by using PCR amplification. The results show that the aflR gene is contained in the genome of Aspergillus flavus , Aspergillus parasitic and Aspergillus tamarii , Aspergillus fumigates and Aspergillus versicolor are not detected, realizing the purpose for identifying aflatoxin producing strains. This method provides a reference for rapid detection of toxigenic fungi.
toxic fungi
/
DNA extraction
/
aflatoxin
/
PCR detection
蒋丹, 靳卫林, 苏德山, 黄耀江.
曲霉属产毒真菌DNA的制备及其毒素相关基因aflR 的PCR 检测.
科技导报,
2014
, 32
(14)
: 31
-34
.
DOI: 10.3981/j.issn.1000-7857.2014.14.004
JIANG Dan, JIN Weilin, SU Deshan, HUANG Yaojiang.
DNA Preparation of Toxigenic Aspergillus and PCR Detection of aflR Toxin Gene[J].
Science & Technology Review ,
2014
, 32
(14)
: 31
-34
.
DOI: 10.3981/j.issn.1000-7857.2014.14.004
2014年第32卷第14期
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文章信息
doi: 10.3981/j.issn.1000-7857.2014.14.004
接收时间:2014-01-17
首发时间:2014-05-29
出版时间:2014-05-18
收稿日期:2014-01-17
修回日期:2014-03-26
通讯作者:
黄耀江,教授,研究方向为生物化学与分子生物学、食品安全与公众健康,电子信箱:yaojiangh@hotmail.com
https://castjournals.cast.org.cn/joweb/kjdb/CN/10.3981/j.issn.1000-7857.2014.14.004
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2种不同金属材料的力学参数
科 Family 属数 Number of genus 种数 Number of species 占总种数比例 Percentage of total species (%) 属 Genus 种数 Number of species 占总种数比例 Percentage of total species (%) 鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78 小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39 多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39 红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87 小菇属 Mycena 11 5.26 光柄菇属 Pluteus 5 2.39 红菇属 Russula 17 8.13 栓菌属 Trametes 5 2.39
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